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CHGA wt Allele

Known as: Chromogranin A (Parathyroid Secretory Protein 1) wt Allele, CHGA, CGA 
Human CHGA wild-type allele is located in the vicinity of 14q32 and is approximately 12 kb in length. This allele, which encodes chromogranin A… 
National Institutes of Health

Related topics

Related topics

5 relations
14q32Chromogranin AIntercellular Communication ProcessTumor Markers

Broader (1)

CHGA gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
A Risk PRODH Haplotype Affects Sensorimotor Gating, Memory, Schizotypy, and Anxiety in Healthy Male Subjects
2008
2008
Genotypes and haplotypes of ERCC1 and ERCC2/XPD genes predict levels of benzo[a]pyrene diol epoxide-induced DNA adducts in cultured primary lymphocytes from healthy individuals: a genotype-phenotype…
Benzo[a]pyrene diol epoxide (BPDE)-induced DNA adducts are a risk factor for tobacco-related cancers. Excision repair cross… 
Highly Cited
2002
Highly Cited
2002
Co-localisation of gonadotrophins and granins in gonadotrophs at different stages of the oestrous cycle in sheep.
Associations between granins (secretogranin II (SgII) and chromogranin A and B (CgA and CgB)) and gonadotrophins (LH and FSH… 
Highly Cited
2002
Highly Cited
2002
Activation of the Inositol 1,4,5-Trisphosphate Receptor by the Calcium Storage Protein Chromogranin A*
Secretory granules of neuroendocrine cells are inositol 1,4,5-trisphosphate (InsP3)-sensitive Ca2+ stores in which the Ca2… 
2000
2000
Mutations of ras Protooncogenes and p53 Tumor Suppressor Gene in Cardiac Hemangiosarcomas from B6C3F1 Mice Exposed to 1,3-Butadiene for 2 Years
1,3-Butadiene is a multisite carcinogen in rodents. Incidences of cardiac hemangiosarcomas were significantly increased in male… 
1999
1999
Ribosomal −1 Frameshifting during Decoding ofBacillus subtilis cdd Occurs at the Sequence CGA AAG
ABSTRACT During translation of the Bacillus subtilis cdd gene, encoding cytidine deaminase (CDA), a ribosomal −1 frameshift… 
1999
1999
A case of complete adenylate kinase deficiency due to a nonsense mutation in AK‐1 gene (Arg 107 → Stop, CGA → TGA) associated with chronic haemolytic anaemia
Two siblings of Italian origin with mild chronic haemolytic anaemia, psychomotor impairment and undetectable adenylate kinase (AK… 
Highly Cited
1998
Highly Cited
1998
Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients.
Lowe syndrome (OCRL) is an X-linked disorder involving the eyes, kidney, and nervous system that is caused by loss of function in… 
1996
1996
Improved cloning of antibody variable regions from hybridomas by an antisense-directed RNase H digestion of the P3-X63-Ag8.653 derived pseudogene mRNA.
When antibody variable regions (VL or VH) are cloned from hybridoma cell lines using standard methods (1), often sequences of non… 
Highly Cited
1992
Highly Cited
1992
Mutations in Severe, Type III von Willebrand’s Disease in the Dutch Population: Candidate Missense and Nonsense Mutations Associated with Reduced Levels of von Willebrand Factor Messenger RNA
Summary The von Willebrand factor (vWF) genes of nine unrelated, severe, type III von Willebrand’s disease (vWD) patients (six of… 
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