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NLGN4X wt Allele
Known as:
UNQ365/PRO701
, ASPGX2
, NLGN
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Human NLGN4X wild-type allele is located within Xp22.32-p22.31 and is approximately 339 kb in length. This allele, which encodes neuroligin 4, X…
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National Institutes of Health
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Related topics
Related topics
6 relations
Cell Adhesion
Homo sapiens
Ligand Binding
NLGN4X protein, human
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Broader (1)
NLGN4X gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
Neuroimaging Endophenotypes in Animal Models of Autism Spectrum Disorders: Lost or Found in Translation?
M. Petrinovic
,
B. Künnecke
Psychopharmacology
2013
Corpus ID: 253752967
Autism spectrum disorder(s) (ASDs) is a neurodevelopmental disorder characterized by stereotyped behaviours and impairments in…
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2007
2007
possible implications in autism Novel splice isoforms for NLGN3 and NLGN4 with
Z. Talebizadeh
,
D. Y. Lam
,
M. Theodoro
,
D. Bittel
,
G. Lushington
,
M. Butler
2007
Corpus ID: 81794852
Objective: To screen cDNA for NLGN3 and NLGN4 fromlymphoblastoid cells from autistic subjects.Methods and results: 10 young…
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2005
2005
A single mutation near the C-terminus in alpha/beta hydrolase fold protein family causes a defect in protein processing.
A. De Jaco
,
Z. Kovarik
,
+4 authors
P. Taylor
Chemico-Biological Interactions
2005
Corpus ID: 46569111
An Arg to Cys mutation in the extracellular domain of neuroligin-3 (NL3) was recently found in a twin set with autism [S. Jamain…
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