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GLRB gene
Known as:
GLRB
, GLYCINE RECEPTOR, BETA SUBUNIT
, glycine receptor beta
National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Genome-wide selection signatures analysis of litter size in Dazu black goats using single-nucleotide polymorphism
G. E
,
X. Duan
,
+12 authors
Y. Zeng
3 Biotech
2019
Corpus ID: 201041005
Litter size is considered to be the most important index for estimating domestic animal productivity. The number of indigenous…
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2019
2019
Interaction between interferon regulatory factor 6 and glycine receptor beta shows a protective effect on developing nonsyndromic cleft lip with or without cleft palate in the Han Chinese population
Di Wu
,
Mei Wang
,
+4 authors
Zhenmin Zhao
European Journal of Oral Sciences
2019
Corpus ID: 53719055
Single-nucleotide polymorphisms (SNPs) in protein-coding regions of genes which were previously reported to be associated with…
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2017
2017
Modulation of defensive reactivity by GLRB allelic variation: converging evidence from an intermediate phenotype approach
U. Lueken
,
M. Kuhn
,
+12 authors
T. Lonsdorf
Translational Psychiatry
2017
Corpus ID: 12342692
Representing a phylogenetically old and very basic mechanism of inhibitory neurotransmission, glycine receptors have been…
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2014
2014
Novel GLRB Gene Mutation in a Saudi Baby with Hyperekplexia
T. Rizk
2014
Corpus ID: 75289454
Aim: We aim to describe a case of hyperekplexia in a Saudi neonate due to Novel mutation in GLRB. Case Presentation: One month…
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Review
2013
Review
2013
Bilaterally cleft lip and bilateral thumb polydactyly with triphalangeal component in a patient with two De novo deletions of HSA 4q32 and 4q34 involving PDGFC, GRIA2, and FBXO8 genes
A. Calcia
,
G. Gai
,
+6 authors
A. Brusco
American Journal of Medical Genetics. Part A
2013
Corpus ID: 24287049
We report on a newborn boy with a bilateral cleft of the primary palate, duplicated triphalangeal thumbs, and a patent foramen…
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Highly Cited
1994
Highly Cited
1994
Glycine receptor β–subunit gene mutation in spastic mouse associated with LINE–1 element insertion
S. Kingsmore
,
B. Giros
,
D. Suh
,
M. Bieniarz
,
M. Caron
,
M. Seldin
Nature Genetics
1994
Corpus ID: 9843125
Congenital myoclonus is a widespread neurologic disorder characterized by hyperexcitability, muscular spasticity and myoclonus…
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