RAB7A wt Allele

Known as: PRO2706, RAB7, Member RAS Oncogene Family Gene, CMT2B 
Human RAB7A wild-type allele is located in the vicinity of 3q21 and is approximately 89 kb in length. This allele, which encodes ras-related protein… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

2000-2012
0120002012

Papers overview

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2013
2013
Hormone-stimulated lipolysis is a rapid way to mobilize fat from its storage depot for use in peripheral tissues. By convention… (More)
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2013
2013
Charcot-Marie-Tooth type 2B (CMT2B) disease is a hereditary motor and sensory neuropathy subtype characterized by prominent loss… (More)
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2012
2012
CMT2B (Charcot-Marie-Tooth type 2B) disease is an autosomal dominant peripheral neuropathy whose onset is in the second or third… (More)
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2006
2006
We report a 32-year-old patient with Charcot-Marie-Tooth (CMT2B) including foot ulcerations. Genetic analysis identified a de… (More)
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2005
2005
BACKGROUND The variable clinical features of hereditary sensory and autonomic neuropathy (HSAN I) suggest heterogeneity. Some… (More)
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Highly Cited
2004
Highly Cited
2004
There are two known autosomal dominant genes for the hereditary ulcero-mutilating neuropathies: SPTLC1 (hereditary sensory… (More)
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2000
2000
Members of the Sox gene family encode transcription factors that have diverse and important functions during development. We have… (More)
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