Author: claimsbot

1-12. (canceled)
13. A method of promoting recruitment, proliferation, differentiation, migration or survival of neural cells or neural precursor cells in a mammalian subject comprising:
identifying a mammalian subject in need of treatment to promote recruitment, proliferation, differentiation, migration, or survival of neural cells or neural precursor cells, and
administering to the subject a composition comprising a vascular endothelial growth factor C (VEGF-C) product or a vascular endothelial growth factor D (VEGF-D) product in an amount effective to stimulate recruitment, proliferation, differentiation, migration or survival of neural cells or neural precursor cells in said subject.
14. A method according to claim 13 wherein the identifying comprises identifying a mammalian subject in need of treatment to promote recruitment, proliferation, differentiation, migration or survival of neuronal cells or neuronal precursor cells.
15. A method according to claim 13, wherein the identifying comprises identifying a mammalian subject in need of oligodendrocyte or oligodendrocyte precursor cell recruitment, proliferation, or differentiation.
16. A method of promoting proliferation, differentiation, migration or survival of neural stem cells or neural precursor cells comprising:
contacting purified neural stem cells or neural precursor cells with a composition comprising a vascular endothelial growth factor C (VEGF-C) product or a vascular endothelial growth factor D (VEGF-D) product in an amount effective to promote survival or stimulate proliferation or differentiation of said cells.
17. A method according to claim 16, wherein the neural stem cell is selected from the group consisting of C17.2, purified neural stem cells, HSN-1 cells, fetal pig cells, neural crest cells, bone marrow derived neural stem cells, hNT cells and a human neuronal progenitor cell line.
18. A method of inducing oligodendrocyte precursor cell proliferation in vitro comprising contacting the oligodendrocyte or oligodendrocyte precursor cell with a composition comprising a VEGF-C product or a VEGF-D product, wherein the oligodendrocyte precursor cell is selected from the group consisting of CG-4 cells, SVG p12 fetal glial cell line, DBTRG-05MG glial cell line, purified oligodendrocyte precursor cells, isolated NG2 proteoglycan (NG2+ cells), bone marrow derived neural stem cells, a human neuronal progenitor cell line.
19. A method of stimulating neural stem cell or neuronal precursor cell proliferation or differentiation, comprising,
obtaining a biological sample from a Mammalian subject, wherein said sample comprises neural stem cells or neuronal precursor cells, and
contacting the neural stem cells or neuronal precursor cells with a composition comprising a vascular endothelial growth factor C (VEGF-C) product or a vascular endothelial growth factor D (VEGF-D) product.
20. (canceled)
21. A method of stimulating oligodendrocyte precursor cell proliferation or differentiation, comprising,
obtaining a biological sample from a mammalian subject, wherein said sample comprises oligodendrocyte precursor cells, and
contacting the oligodendrocyte precursor cells with a composition comprising a vascular endothelial growth factor C (VEGF-C) product or a vascular endothelial growth factor D (VEGF-D) product.
22. A method according to any one of claims 16-19 or 21, wherein the contacting comprises culturing the cells in a culture containing the VEGF-C product or the VEGF-D product.
23. A method according to claim 19 or 21, further comprising a step of purifying and isolating the cells from the sample before the contacting step.
24. A method according to claim 22, further comprising a step of purifying and isolating the cells after the contacting step.
25. Purified and isolated neural cells cultured according to claim 24.
26. The method according to claim 24, further comprising a step of administering the cells to the mammalian subject after the contacting step.
27. The method according to claim 24 further comprising a step of transplanting the cells into a different mammalian subject after the contacting step.
28. (canceled)
29. The method according to claim 24, wherein the cells are seeded into a tissue, organ, or artificial matrix ex vivo, and said tissue, organ, or artificial matrix is attached, implanted, or transplanted into the mammalian subject.
30. A method according to any one of claims 13-15 or 29, wherein the subject has a disease or condition characterized by aberrant growth of neuronal cells, neuronal scarring, or neural degeneration.
31. A method according to claim 30, wherein the neural degeneration is caused by a neurodegenerative disorder selected from the group consisting of Alzheimer’s disease, Parkinson’s disease, Huntington’s disease, motor neuron disease, Amyotrophic Lateral Sclerosis (ALS), dementia and cerebral palsy.
32. A method according to any one of claims 13-15 or 29, wherein the subject has a disease or condition characterized by aberrant growth of oligodendrocyte or oligodendrocyte precursor cells.
33. A method according to any one of claims 13-15 or 29, wherein the subject has a condition selected from the group consisting of demyelination in the nervous system, chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), neural trauma or neural injury.
34. The method of claim 33 wherein the condition is multiple sclerosis, phenylketonuria, periventricular leukomalacia (PVL) HIV-1 encephalitis (HIVE), Guillian Barre Syndrome (GBS), acute inflammatory demyelinating polyneuropathy (AIDP), acute motor axonal neuropathy (AMAN), acute motor sensory axonal neuropathy (AMSAN), Fisher syndrome, acute pandysautonomia, and Krabbe’s disease.
35. (canceled)
36. The method of claim 33 wherein the CIPD is selected from the group consisting of MADSAM (multifocal acquired demyelinating sensory and motor neuropathy, also know as Lewis-Sumner syndrome) and DADS (distal acquired demyelinating symmetric neuropathy).
37. (canceled)
38. The method of claim 33, wherein the neural trauma is selected from the group consisting of stroke-related injury, spinal cord injury, post-operative injury and brain ischemia.
39. The method of claim 13, wherein the mammalian subject is human.
40. The method according to claim 39, wherein the product is a VEGF-C product.
41. The method according to claim 40, wherein the VEGF-C product comprises a purified mammalian prepro-VEGF-C polypeptide or fragment thereof that binds VEGFR-3 or neuropilin-2.
42. The method according to claim 40, wherein the VEGF-C product comprises a VEGF-C \u0394C156 polypeptide.
43. The method according to claim 40, wherein the VEGF-C product comprises a chimeric heparin-binding VEGF-C polypeptide.
44. The method of claim 40, wherein the subject and the prepro-VEGF-C polypeptide are human.
45. The method according to claim 40, wherein the VEGF-C product comprises a polypeptide that comprises an amino acid sequence at least 95% identical to amino acids 32-227 of SEQ ID NO: 24, wherein the polypeptide binds VEGFR-3.
46. The method according to claim 40, wherein the VEGF-C product comprises a polypeptide that comprises an amino acid sequence at least 95% identical to amino acids 103-227 of SEQ ID NO: 24, wherein the polypeptide binds VEGFR-3.
47. The method of claim 40, wherein the VEGF-C product comprises a polynucleotide selected from:
(a) a polynucleotide comprising a nucleotide sequence at least 90% identical to the nucleotide sequence of SEQ ID NO: 23 and encoding a polypeptide that binds VEGFR-3;
(b) a polynucleotide comprising a nucleotide sequence that encodes a polypeptide comprising an amino acid sequence at least 90% identical to SEQ ID NO: 24, wherein the polypeptide binds VEGFR-3;
(c) a polynucleotide that hybridizes to the complement of SEQ ID NO: 23 under the following hybridization and washing conditions and encodes a polypeptide that binds VEGFR-3: hybridization in 0.5 M NaHPO4, 7% sodium dodecyl sulfate (SDS), 1 mM EDTA at 65\xb0 C. and washing in 0.2\xd7SSC0.1% SDS at 42\xb0 C.
(d) a polynucleotide comprising a nucleotide sequence that encodes the human VEGF-C amino acid sequence of SEQ ID NO: 24;
(e) a polynucleotide that encodes a VEGF-C \u0394C156, polypeptide:
(f) a nucleotide sequence that encodes a chimeric heparin binding VEGF-C polypeptide; and
(g) fragments of (a), (b) or (d) that encode a polypeptide that binds VEGFR-3.
48-49. (canceled)
50. The method or use of claim 40, wherein the VEGF-C product comprises a polynucleotide selected from:
(a) a polynucleotide comprising a nucleotide sequence that encodes the human VEGF-C amino acid sequence of SEQ ID NO: 24; and
(b) fragments of (a) that encode a polypeptide that binds VEGFR-3.
51-52. (canceled)
53. The method according to claim 47, wherein the VEGF-C product comprises a viral vector containing the polynucleotide.
54. The method of claim 53, wherein the vector comprises a replication-deficient adenovirus, adeno-associated virus, or lentivirus.
55. The method according to claim 39, wherein the product is a VEGF-D product.
56. A method according to any one of claims 40 or 55, wherein the composition further comprises a pharmaceutically acceptable carrier.
57. The method of any one of claims 40 or 55, further comprising administering to the mammalian subject a neurotherapeutic agent.
58. (canceled)
59. The method according to claim 57 wherein the neurotherapeutic agent comprises a neural growth factor selected from the group consisting of interferon gamma, nerve growth factor, epidermal growth factor (EGF), basic fibroblast growth factor (bFGF), neurogenin, brain derived neurotrophic factor (BDNF), thyroid hormone, bone morphogenic proteins (BMPs), leukemia inhibitory factor (LIF), sonic hedgehog, glial cell line-derived neurotrophic factor (GDNFs), vascular endothelial growth factor (VEGF), interleukins, interferons, stem cell factor (SCF), activins, inhibins, chemokines, retinoic acid and ciliary neurotrophic factor (CNTF).
60. The method according to claim 57, wherein the neurotherapeutic agent comprises a polynucleotide comprising a nucleotide sequence that encodes a neural growth factor selected from the group consisting of interferon gamma, nerve growth factor, epidermal growth factor (EGF), basic fibroblast growth factor (bFGF), neurogenin, brain derived neurotrophic factor (BDNF), thyroid hormone, bone morphogenic proteins (BMPs), leukemia inhibitory factor (LIF), sonic hedgehog, glial cell line-derived neurotrophic factor (GDNFs), vascular endothelial growth factor (VEGF), interleukins, interferons, stem cell factor (SCF), activins, inhibins, chemokines, retinoic acid and ciliary neurotrophic factor (CNTF).
61. The method according to claim 57, wherein the neurotherapeutic agent is selected form the group consisting of tacrine, donepezil, rivastigmine, galantamine, cholinesterase inhibitors and anti-inflammatory drugs.
62. The method of claim 57 wherein the neurotherapeutic agent is selected form the group consisting of anti-cholinergics, dopamine agonists, catechol-0-methyl-transterases (COMTs), amantadine, Selegiline, carbidopa, ropinirole, coenzyme Q10, Pramipexole and levodopa (L-dopa).
63. The method of any one of claims 40 or 55 wherein the VEGF-C or VEGF-D product is used or administered in combination with PDGF-A or PDGF-C.
64. A composition comprising a VEGF-C product or a VEGF-D product and a neural growth factor in a pharmaceutically acceptable diluent or carrier.
65. A composition comprising a VEGF-C product or a VEGF-D product and a neurotherapeutic agent in a pharmaceutically acceptable diluent or carrier.
66-67. (canceled)
68. A composition of claim 64 or 65, further comprising a PDGF-A product or a PDGF-C product.
69. (canceled)
70. A method of inhibiting growth and progression and of neuroblastoma and neural tumors comprising administering to a subject having a neuroblastoma or neuronal tumor a composition comprising a VEGF-C inhibitor.
71. The method of claim 70 wherein the VEGF-C inhibitor is selected from the group consisting of:
(a) a polypeptide comprising an extracellular fragment of VEGFR-2 that binds to VEGF-C;
(b) a polypeptide comprising an extracellular fragment of VEGFR-3 that binds to VEGF-C;
(c) an antibody substance that immunoreacts with a VEGF-C polypeptide;
(d) a VEGF-C antisense molecule, and
(e) a VEGF-C siRNA.
72. The method of claim 70, wherein the VEGF-C inhibitor is selected from the group consisting of a polypeptide comprising an extracellular fragment of VEGFR-3 that binds to VEGF-C, an extracellular fragment of NRP-1 that binds to VEGF-C, and an extracellular fragment of NRP-2 that binds to VEGF-C.
73. The method of any one of claims 70-72 wherein the VEGF-C or VEGF-D inhibitor is administered in combination with a PDGF-A inhibitor or a PDGF-C inhibitor.
74. A method for screening for modulators of VEGF-C or VEGF-D stimulation of neural stem cell or neural precursor cell growth, migration, differentiation, or survival, comprising:
contacting a composition comprising a VEGF-C polypeptide or a VEGF-D polypeptide and a neural cell or neural precursor cell in the presence and absence of a test agent;
measuring growth, migration, differentiation, or survival of the cell in the presence and absence of the agent; and
identifying the test agent as a modulator of VEGF-C or VEGF-D effects on neural cells or neural precursor cells from differential measurements in the presence versus the absence of the test agent.
75. (canceled)
76. The method of claim 74 wherein the cell comprises a neural stem cell line.
77. The method of claim 74 wherein the cell comprises neural cell or neural progenitor cell that expresses VEGFR-3.
78. The method of claim 74 wherein the cell expresses neuropilin 2.
79. The method of claim 74 for detecting a modulator that is an agonist of stimulation of neural stem cell or neural precursor cell growth, migration, differentiation, or survival,
wherein an agonist is detected by an increase in staining of neural cell markers on the cell surface or increased detection of proliferative markers in the cell.
80. The method of claim 74 for detecting a modulator that is an antagonist of stimulation of neural stem cell or neural precursor cell growth, migration, differentiation, or survival,
wherein an antagonist is detected by a decrease in staining of neural cell markers on the cell surface or decreased detection of proliferative markers in the cell.
81. A method according to claim 23, further comprising a step of purifying and isolating the cells after the contacting step.

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1. An inverter output current detection method for an inverter, the inverter having an LC filter made up of a reactor and a capacitor at an output side of an inverter circuit and supplying a load with a terminal voltage of the capacitor as an output voltage vo, the detection method detecting as an output current a current io obtained by subtracting a capacitor current ic flowing through the capacitor from a reactor current iL flowing through the reactor, comprising the steps of:
detecting the output voltage vo for obtaining its effective value or average value V;
obtaining cosine wave digital data (cos WaveData) by advancing by 90 degrees a phase of an inverter sine wave data used to obtain the output voltage vo; and
digitally calculating a current ic\u2032 equivalent to the capacitor current ic by an expression shown below
ic\u2032=V\xd7\u03c90\xd7C\xd7cos WaveData\xd7K
where the \u03c90 is an angular frequency of the output voltage, the C is a capacitance of the capacitor, and the K is a value obtained by multiplying a detection ratio for detecting the output voltage vo, a conversion ratio for converting an analog value to a digital value and a conversion ratio for converting the effective value or average value V into a maximum value;
using the current ic\u2032 equivalent in place of the capacitor curent ic to determine the output current; and outputting the inverter output current.
2. The inverter output current detection method for an inverter according to claim 1, further comprises a step of obtaining the angular frequency \u03c90 of the output voltage vo from the output voltage.
3. The inverter output current detection method for an inverter according to claim 1, comprising the further step of using the output current to determine one of load factor information and current value information to assist in monitoring operation of the inverter.
4. An inverter output current detection method for an inverter, the inverter having an LC filter made up of a reactor and a capacitor on an output side of an inverter circuit and supplying a load with a terminal voltage of the capacitor as an output voltage, the detection method detecting as an output current a current io obtained by subtracting a capacitor current ic flowing through the capacitor from a reactor current iL flowing through the reactor, comprising the steps of:
detecting the output voltage vo for obtaining its effective value or average value V;
determining an angular frequency \u03c90 of the output voltage vo from the output voltage;
obtaining in advance cosine wave digital data (cos Wave Data) by advancing by 90 degrees a phase of inverter sine wave data used to obtain the output voltage vo; and
digitally calculating a current ic\u2032 equivalent to the capacitor current ic according to an expression below
ic\u2032=V\xd7\u03c90\xd7C\xd7(cos WaveData)\xd7K
where the C is a capacitance of the capacitor, and the K is a value obtained by multiplying a detection ratio for detecting the output voltage vo, a conversion ratio for converting an analog value into a digital value and a conversion ratio for converting the effective value or average value V into a maximum value;
using the current ic\u2032 equivalent in place of the capacitor current ic to determine the output current; and outputting the inverter output current.
5. The inverter output current detection method for an inverter according to claim 4, wherein the cos WaveData is stored in a memory in advance.
6. The inverter output current detection method for an inverter according to claim 4, comprising the further step of using the output current to determine one of load factor information and current value information to assist in monitoring operation of the inverter.
7. An inverter output current detection device for an inverter, the inverter having an LC filter made up of a reactor and a capacitor at an output side of an inverter circuit and supplying a load with a terminal voltage of the capacitor as an output voltage, the detection device detecting as an output current a current io obtained by subtracting a capacitor current ic flowing through the capacitor from a reactor current iL flowing through the reactor, comprising:
a voltage calculation means for detecting the output voltage vo and calculating its effective value or average value V;
a data memory means to store in advance cosine wave digital data (cos WaveData) obtained by advancing by 90 degrees a phase of inverter sine wave data used to obtain the output voltage vo; and
a capacitor current calculation means to digitally calculate a current ic\u2032 equivalent to the capacitor current ic according to an expression below
ic\u2032=V\xd7\u03c90\xd7C\xd7(cos WaveData)\xd7K
where the \u03c90 is an angular frequency of the output voltage, the C is a capacitance of the capacitor, and the K is a value obtained by multiplying a detection ratio for detecting the output voltage vo, a conversion ratio for converting an analog value into a digital value and a conversion ratio for converting the effective value or average value V into a maximum value.
8. The inverter output current detection device for an inverter according to claim 7, further comprises an angular frequency calculation means to obtain the angular frequency \u03c90 of the output voltage vo from the output voltage.

1. A mass spectrometer comprising:
an ion source for ionizing a sample;
an ion storage-and-ejection portion for performing a storing operation for storing at least some of the ions generated in the ion source and then performing an ejecting operation for ejecting the stored ions;
a mass analyzer for selecting desired ions according to mass-to-charge ratio from the ions ejected from the ion storage-and-ejection portion;
a detector for detecting the desired ions;
analog signal processing circuitry for converting a signal from the detector into a voltage; and
an AD converter for sampling and converting the output voltage from the analog signal processing circuitry into a digital signal;
wherein two signals delivered from the analog signal processing circuitry in response to two pulsed ions produced by two successive ejecting operations of the ion storage-and-ejection portion are at least partially overlapped temporally.
2. The mass spectrometer as set forth in claim 1, wherein said ejecting operations of said ion storage-and-ejection portion have a frequency greater than a frequency bandwidth of said analog signal processing circuitry.
3. The mass spectrometer as set forth in claim 1, wherein at least some of said desired ions contained in the ions ejected by a latter one of said two successive ejecting operations of said ion storage-and-ejection portion enter said detector earlier than at least some of the desired ions contained in the ions ejected by a former one of said two successive ejecting operations.
4. The mass spectrometer as set forth in claim 1, wherein there is further provided a control section for controlling timings of storage and ejection of ions performed by said ion storage-and-ejection portion, and wherein said control section causes the storage-and-ejection portion to perform said storing operation and said ejecting operation by applying a voltage varying like a rectangular, sinusoidal, or triangular wave to an exit electrode of the ion storage-and-ejection portion.
5. The mass spectrometer as set forth in claim 1,
wherein there is further provided a cooling chamber for lowering kinetic energies of the ions generated in said ion source,
wherein said cooling chamber operates as said ion storage-and-ejection portion, performs the storing operation for storing the ions generated in the ion source, and then performs the ejecting operation for ejecting the stored ions, and
wherein said mass analyzer selects said desired ions according to mass-to-charge ratio from the ions ejected by the cooling chamber.
6. The mass spectrometer as set forth in claim 5, wherein said mass analyzer includes a quadrupole mass filter.
7. The mass spectrometer as set forth in claim 1,
wherein there are further provided a first mass analyzer for selecting first desired ions according to mass-to-charge ratio from the ions generated in said ion source, a collisional cell for fragmenting some or all of the first desired ions into product ions, and a second mass analyzer for selecting second desired ions according to mass-to-charge ratio from the first desired ions and the product ions,
wherein the collisional cell operates as said ion storage-and-ejection portion, performs a storing operation for storing the first desired ions and the product ions, and then performs an ejecting operation for ejecting the stored ions, and
wherein the second mass analyzer operates as the first-mentioned mass analyzer and selects the second desired ions according to mass-to-charge ratio from the ions ejected from the collisional cell.
8. The mass spectrometer as set forth in claim 1,
wherein there are further provided a cooling chamber for lowering kinetic energies of the ions generated in said ion source, a first mass analyzer for selecting first desired ions according to mass-to-charge ratio from the ions ejected by the cooling chamber, a collisional cell for fragmenting some or all of the first desired ions into product ions, and a second mass analyzer for selecting second desired ions according to mass-to-charge ratio from the first desired ions and the product ions,
wherein the cooling chamber operates as said ion storage-and-ejection portion, performs a storing operation for storing the ions generated in the ion source, and then performs an ejecting operation for ejecting the stored ions, and
wherein the first mass analyzer operates as the first-mentioned mass analyzer.
9. The mass spectrometer as set forth in claim 7, wherein at least one of said first mass analyzer and said second mass analyzer includes a quadrupole mass filter.
10. A method of controlling a mass spectrometer having: an ion source for ionizing a sample; an ion storage-and-ejection portion for performing a storing operation for storing at least some of the ions generated in the ion source and then performing an ejecting operation for ejecting the stored ions; a mass analyzer for selecting desired ions according to mass-to-charge ratio from the ions ejected from the ion storage-and-ejection portion; a detector for detecting the desired ions; analog signal processing circuitry for converting a signal from the detector into a voltage; and an AD converter for sampling and converting the output voltage from the analog signal processing circuitry into a digital signal, said method comprising the step of:
controlling timings of storage and ejection of ions performed by the ion storage-and-ejection portion in response to two pulsed ions produced by two successive ejecting operations of the ion storage-and-ejection portion such that two signals delivered from the analog signal processing circuitry are at least partially overlapped temporally.

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1. A method for controlling a temperature of a terminal, the method comprising:
detecting a temperature of the terminal; and
performing at least one of:
a temperature based first throttle procedure including driving a controller with a first preset driving frequency when the temperature of the terminal is a first preset temperature, and driving the controller with a second driving frequency higher than the first driving frequency when the temperature of the terminal is reduced to a second preset temperature lower than the first preset temperature according to the driving of the controller with the first driving frequency; and
a time based second throttle procedure including repeatedly driving the controller with the first driving frequency for a first time when the temperature of the terminal is the first preset temperature, and driving the controller with the second driving frequency for a second time after the first time elapses.
2. The method of claim 1, further comprising performing a temperature based second throttle procedure including:
driving the controller with a third driving frequency lower than the first driving frequency when the temperature of the terminal increases to a third preset temperature greater than the first preset temperature, and
driving the controller with a fourth driving frequency greater than the third driving frequency and lower than the first driving frequency when the temperature of the terminal is reduced to a fourth preset temperature lower than the third preset temperature according to the driving of the controller with the third driving frequency.
3. The method of claim 1, further comprising performing a time based second throttle procedure including:
driving the controller with a third driving frequency lower than the first driving frequency for a third time when the temperature of the terminal increases to a third preset temperature greater than the first preset temperature, and
driving the controller with a fourth driving frequency greater than the third driving frequency and lower than the first driving frequency for a predetermined time.
4. The method of claim 1, further comprising shutting down the terminal when the temperature of the terminal increases to a fifth preset temperature being a preset maximum increased value.
5. The method of claim 1, further comprising: restricting a limited number or a function of currently activated application programs when the temperature of the terminal increases to the first preset temperature.
6. The method of claim 5, wherein the restricting of the limited number or the function of the currently activated application programs comprises:
determining priority information of the currently activated application program; and
terminating at least one application program having relatively low priority information among the currently activated application programs or restricting a function of an application according to the limited number of the currently activated application programs.
7. The method of claim 6, wherein the restricting of the limited number or the function of the currently activated programs further comprises:
limiting the number of currently activated application programs based on the limited number to fewer than the limited number of the currently activated application programs when the temperature of the terminal increases to another preset temperature higher than the first preset temperature; and
limiting the number of currently activated application programs based on the limited number to more than the limited number of the application programs when the temperature of the terminal is reduced from the first preset temperature to another preset temperature lower than the first preset temperature.
8. The method of claim 6, further comprising:
receiving a request to activate a new application program when the number of activated application programs is restricted to the limited number of application programs;
determining priority information of the new application program; and
rejecting activation of the new application program or outputting a rejection guide message together with the rejection when the priority information is lower than that of the currently activated application programs.
9. The method of claim 8, further comprising terminating at least one application program having relatively low priority information among the currently activated application programs and activating the new application program when activation of a new application program is again requested after the rejection.
10. The method of claim 6, further comprising:
receiving a request to activate a new application program when the number of activated application programs is restricted according to the limited number of application programs;
determining priority information of the new application program; and
terminating at least one of the currently activated application programs and activating a new application program when the priority information of the new application program is higher than that of at least one of the currently activated application programs.
11. A terminal for supporting temperature control, the terminal comprising:
a temperature sensor for detecting a temperature of the terminal; and
a controller for performing at least one of:
a temperature based first throttle procedure including driving the controller with a first preset driving frequency when the temperature of the terminal detected by the temperature sensor is a first preset temperature, and driving the controller with a second driving frequency higher than the first driving frequency when the temperature of the terminal is reduced to a second preset temperature lower than the first preset temperature, and
a time based second throttle procedure including driving the controller with the first preset driving frequency for a first time, and driving the controller with the second driving frequency higher than the first driving frequency for a second time after the first time elapses.
12. The terminal of claim 11, wherein the controller comprises a processor driver controller for controlling an operation performed according to a situation of the first preset temperature, for driving the controller with a third driving frequency lower than the first driving frequency when the temperature of the terminal increases from the first preset temperature to a third preset temperature, and for controlling the controller to be operated with a fourth driving frequency higher than the third driving frequency and lower than the first driving frequency when the temperature of the terminal is reduced to a fourth preset temperature lower than the third preset temperature.
13. The terminal of claim 11, wherein the controller comprises a processor drive controller for repeatedly driving the controller with a third driving frequency for a third time when the temperature of the terminal increases to a third preset temperature lower than the first driving frequency, and driving the controller with a fourth driving frequency higher than the third driving frequency and lower than the first driving frequency for a fourth time for a predetermined time.
14. The terminal of claim 11, wherein the controller comprises a processor driver controller for controlling the terminal is to shut down when the temperature of the terminal increases to a fifth preset temperature being a preset maximum increased value.
15. The terminal of claim 11, wherein the controller comprises a function restricting unit for restricting a limited number of functions of currently activated application programs when the temperature of the terminal increases to the first preset temperature.
16. The terminal of claim 15, wherein the function restricting unit obtains priority information of the currently activated application programs, terminates at least one application program having relatively low priority information among the currently activated application programs according to the limited number of the currently activated application programs or restricts functions of the application program having the relatively low priority.
17. The terminal of claim 16, wherein the function restricting unit restricts the number of currently activated application programs based on the limited number to fewer than the limited number of the application when the temperature of the terminal increases to another preset temperature higher than the first preset temperature, and
wherein the function restricting unit restricts the number of currently activated application programs based on the limited number to more than the limited number of the application programs when the temperature of the terminal is reduced from the first preset temperature to another preset temperature lower than the first preset temperature.
18. The terminal of claim 16, further comprising:
an input unit or a display unit of an input function for receiving an input signal requesting activation of a new application program, and
wherein, when the number of the currently activated application programs is limited according to the limited number, the function restricting unit determines priority information of the new application program, and controls such that activation of the new application program is rejected and a rejection guide message is output on the display unit together with the rejection when the priority information is lower than that of the currently activated application programs.
19. The terminal of claim 18, wherein the function restricting unit terminates at least one application program having relatively low priority information among the currently activated application programs and activates the new application program when the activation of the new application program is requested again after the rejection.
20. The terminal of claim 16, further comprising:
an input unit or a display unit having an input function for generating an input signal for requesting activation of a new application program,
wherein, when the number of currently activated application programs is limited according to the limited number of application programs, the function restricting unit determines priority information of the new application program, and controls such that at least one of the activated application programs is terminated and the new application program is activated when the priority information is higher than that of at least one of the currently activated application programs.