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searching for NRXN1 7 found (20 total)

alternate case: nRXN1

1q21.1 deletion syndrome (2,681 words) [view diff] exact match in snippet view article find links to article

schizophrenia and deletions at 1q21.1, 3q29, 15q13.3, 22q11.21 en Neurexin 1 (NRXN1) and duplications at 16p11.2 are at 7.5% or higher. Common variations in

CNTNAP2 (1,398 words) [view diff] exact match in snippet view article find links to article

Orrico A, Ousager LB, Collins AL, et al. (November 2009). "CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation

1q21.1 duplication syndrome (1,999 words) [view diff] exact match in snippet view article find links to article

schizophrenia and deletions at 1q21.1, 3q29, 15q13.3, 22q11.21 en Neurexin 1 (NRXN1) and duplications at 16p11.2 are at 7.5% or higher. Common variations in

Anti-VGKC-complex encephalitis (1,570 words) [view diff] exact match in snippet view article find links to article

"Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1". BMC Med Genet. 12: 106. doi:10.1186/1471-2350-12-106. PMC 3162517. PMID 21827697

Epigenetics of schizophrenia (5,482 words) [view diff] exact match in snippet view article find links to article

chromosomal regions with large amounts of CNVs. A CNV located at the gene NRXN1, which encodes a neurexin protein involved in synaptic transmission, is

Epigenetics of autism (6,257 words) [view diff] exact match in snippet view article find links to article

candidate genes relating to ASD in mice exposed to valproate in utero are NRXN1, NRXN2, NRXN3, NLGN1, NLGN2, and NLGN3. In the somatosensory cortex, CA1

Risk factors of schizophrenia (14,999 words) [view diff] exact match in snippet view article find links to article

examined CNVs in neurexins, and found that exon-affecting deletions in the NRXN1 gene conferred risk of schizophrenia. An updated meta-analysis on CNVs for