Skip to search formSkip to main contentSkip to account menu

NGF wt Allele

Known as: Nerve Growth Factor (Beta Polypeptide) wt Allele, Beta-NGF, NGFB 
Human NGF wild-type allele is located in the vicinity of 1p13.1 and is approximately 52 kb in length. This allele, which encodes beta-nerve growth… 
National Institutes of Health

Related topics

Related topics

14 relations
1p13.1ApoptosisCell Proliferation Regulatory ProcessHereditary Sensory Autonomic Neuropathy, Type 5

Broader (1)

NGF gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Rare human nerve growth factor-β mutation reveals relationship between C-afferent density and acute pain evaluation.
The rare nerve growth factor-β (NGFB) mutation R221W causes a selective loss of thinly myelinated fibers and especially… 
2015
2015
Effects of a human nerve growth factor beta (NGFB) mutation on cerebral structure and function in pain.
Effects of a human nerve growth factor beta (NGFB) mutation on cerebral structure and function in pain. 
2011
2011
X-inactivation pattern in females with CMTX 1
known HSN genes, RAB7, WNK1/HSN2, NTRK1, NGFB, FAM134B and SPTLC1. We found mutations in 24 (16%) index cases, a similar… 
2009
2009
Haploinsufficiency of the nerve growth factor beta gene in a 1p13 deleted female child with an insensitivity to pain
Pain insensitivity is mediated at the genetic level by the disruption of specific genes associated with neuronal development… 
1996
1996
Integrated physical, genetic, and genic map covering 3 Mb around the human NGF gene (NGFB) at 1p13.
We have characterized 11 overlapping yeast artificial chromosomes (YACs) in the 1p13 region, 8 of them containing the human nerve… 
1995
1995
Four loci from human Chromosome 1 are physically assigned to sheep Chromosome 1p
Phosphoglucomutase 1 (PGM1), thyroid stimulating hormone beta (TSHB), and urate oxidase (UOX) were newly assigned to sheep… 
1988
1988
Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type I.
Charcot-Marie-Tooth neuropathy type 1 (CMT1) is an autosomal dominant disorder of peripheral nerve. The gene for CMT1 was… 
1988
1988
Two thyroid hormone regulated genes, the beta-subunits of nerve growth factor (NGFB) and thyroid stimulating hormone (TSHB), are located less than 310 kb apart in both human and mouse genomes.
1986
1986
DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia.
Alleles for the single human nerve growth factor receptor gene (NGFR) on chromosome 17q can be distinguished by two polymorphic… 
1984
1984
Comparative analysis of mouse-human hybrids with rearranged chromosomes 1 by in situ hybridization and southern blotting: High-resolution mapping of NRAS, NGFB, and AMY on human chromosome 1
The human protooncogene NRASand the genes for the β-subunit of nerve growth factor (NGFB)and for amylase (AMY)have previously… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)