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Article title matches
- Category:Cpvt (35 bytes)
1: List of pages with the keyword Cpvt
Page text matches
- 2vaf (5,609 bytes)
10: ...uced polymorphic ventricular tachycardia (VTSIP). CPVT2 is an autosomal recessive form of arrhythmogenic...
25: ...e mutations. Our data show clearly that all three CPVT-related mutations lead to significant reduction i... - Category:Cpvt (35 bytes)
1: List of pages with the keyword Cpvt - 3qr5 (3,699 bytes)
13: ...holaminergic polymorphic ventricular tachycardia (CPVT). This exon encodes secondary structure elements ... - 4kei (4,962 bytes)
13: .... Taken together, our data suggest that ARVD2 and CPVT mutations have at least two distinct structural c... - 4kej (4,962 bytes)
13: .... Taken together, our data suggest that ARVD2 and CPVT mutations have at least two distinct structural c... - 4kek (5,130 bytes)
14: .... Taken together, our data suggest that ARVD2 and CPVT mutations have at least two distinct structural c... - 2mc2 (4,928 bytes)
13: .... Taken together, our data suggest that ARVD2 and CPVT mutations have at least two distinct structural c... - 6owv (4,424 bytes)
11: ...uced polymorphic ventricular tachycardia (VTSIP). CPVT2 is an autosomal recessive form of arrhythmogenic...
16: ...holaminergic polymorphic ventricular tachycardia (CPVT). In vivo, calsequestrin multimerizes into filame... - 6oww (4,456 bytes)
11: ...uced polymorphic ventricular tachycardia (VTSIP). CPVT2 is an autosomal recessive form of arrhythmogenic...
16: ...holaminergic polymorphic ventricular tachycardia (CPVT). In vivo, calsequestrin multimerizes into filame... - 6xxf (4,560 bytes)
16: ...es novel insight into the molecular mechanisms of CPVT-associated CaM variants and will facilitate the d...
18: CPVT-associated calmodulin variants N53I and A102V dys... - 6xxx (4,556 bytes)
11: ...n this entry. Mutations in CALM1 are the cause of CPVT4. The disease is caused by mutations affecting t...
16: ...es novel insight into the molecular mechanisms of CPVT-associated CaM variants and will facilitate the d...
18: CPVT-associated calmodulin variants N53I and A102V dys... - 6xy3 (4,551 bytes)
11: ...n this entry. Mutations in CALM1 are the cause of CPVT4. The disease is caused by mutations affecting t...
16: ...es novel insight into the molecular mechanisms of CPVT-associated CaM variants and will facilitate the d...
18: CPVT-associated calmodulin variants N53I and A102V dys... - 6y4o (5,337 bytes)
11: ...n this entry. Mutations in CALM1 are the cause of CPVT4. The disease is caused by mutations affecting t...
16: ...a(2+)-coordinating residues. One exception is the CPVT-causing N53I substitution, which resides in the N... - 6y4p (5,350 bytes)
11: ...n this entry. Mutations in CALM1 are the cause of CPVT4. The disease is caused by mutations affecting t...
16: ...a(2+)-coordinating residues. One exception is the CPVT-causing N53I substitution, which resides in the N... - 7u9q (3,554 bytes)
14: .... Together, these studies provide a mechanism for CPVT and for the therapeutic actions of ARM210. - 7u9r (3,413 bytes)
13: .... Together, these studies provide a mechanism for CPVT and for the therapeutic actions of ARM210. - 7u9t (3,585 bytes)
14: .... Together, these studies provide a mechanism for CPVT and for the therapeutic actions of ARM210. - 7u9z (4,530 bytes)
16: .... Together, these studies provide a mechanism for CPVT and for the therapeutic actions of ARM210. - 7ua1 (4,574 bytes)
16: .... Together, these studies provide a mechanism for CPVT and for the therapeutic actions of ARM210. - 7ua3 (4,462 bytes)
16: .... Together, these studies provide a mechanism for CPVT and for the therapeutic actions of ARM210.
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