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searching for NRXN1 (gene) 20 found (20 total)

NRXN1 (1,321 words) [view diff] no match in snippet view article find links to article

Neurexin-1-alpha is a protein that in humans is encoded by the NRXN1 gene. Neurexins are a family of proteins that function in the vertebrate nervous system

NRXN3 (1,103 words) [view diff] no match in snippet view article find links to article

encoded by several unlinked genes of which two, NRXN1 and NRXN3, are among the largest known human genes. Three of the genes (NRXN1-3) utilize two alternate

NRXN2 (766 words) [view diff] no match in snippet view article find links to article

encoded by several unlinked genes of which two, NRXN1 and NRXN3, are among the largest known human genes. Three of the genes (NRXN1-3) utilize two alternate

Neurexin (2,857 words) [view diff] no match in snippet view article find links to article

and schizophrenia. In mammals, neurexin is encoded by three different genes (NRXN1, NRXN2, and NRXN3) each controlled by two different promoters, an upstream

Verbal intelligence (2,050 words) [view diff] no match in snippet view article find links to article

genes that have been linked to individual linguistic ability. The NRXN1 gene has been linked to general language ability, and mutations of this gene has

NLGN1 (887 words) [view diff] no match in snippet view article find links to article

nervous system synapses. NLGN1 has been shown to interact with NRXN1 and DLG4. Neurexins: NRXN1, NRXN2, NRXN3 GRCh38: Ensembl release 89: ENSG00000169760 –

SNED1 (2,400 words) [view diff] no match in snippet view article find links to article

(NRXN1). Neurexins are cell adhesion molecules and often contain EGF binding domains, enhancing intracellular junction forming between cells. NRXN1 is

CNTNAP2 (1,398 words) [view diff] no 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 deletion syndrome (2,681 words) [view diff] no match in snippet view article find links to article

15q13.3, 22q11.21 en Neurexin 1 (NRXN1) and duplications at 16p11.2 are at 7.5% or higher. Common variations in the BCL9 gene, which is in the distal area

Pitt–Hopkins syndrome (1,449 words) [view diff] no match in snippet view article find links to article

associated protein like 2 (CNTNAP2) gene on the long arm of chromosome 7 (7q33-q36) and the neurexin 1 alpha (NRXN1) gene on the short arm of chromosome 2

1q21.1 duplication syndrome (1,999 words) [view diff] no match in snippet view article find links to article

15q13.3, 22q11.21 en Neurexin 1 (NRXN1) and duplications at 16p11.2 are at 7.5% or higher. Common variations in the BCL9 gene, which is in the distal area

Epigenetics of autism (6,257 words) [view diff] no 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

Epigenetics of schizophrenia (5,482 words) [view diff] no 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

EGF-like domain (3,071 words) [view diff] no match in snippet view article find links to article

NID2; NOTCH1; NOTCH2; NOTCH2NL; NOTCH3; NOTCH4; NRG1; NRG2; NRG3; NRG4; NRXN1; NRXN2; NRXN3; NTNG2; ODZ1; ODZ2; OIT3; PLAT; PP187; PROC; PROS1; PROZ;

Heritability of autism (10,803 words) [view diff] no match in snippet view article find links to article

genes, or between the environment and mutated genes. By identifying genetic markers inherited with autism in family studies, numerous candidate genes

Anti-VGKC-complex encephalitis (1,570 words) [view diff] no 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

Laminin (3,429 words) [view diff] no match in snippet view article find links to article

(FAT1, FAT2, FAT3, FAT4), NEL-like proteins (NELL1, NELL2), neurexins (NRXN1, NRXN2, NRXN3), slit homologs (SLIT1, SLIT2, SLIT3), thrombospondins (THBS1

Risk factors of schizophrenia (15,048 words) [view diff] no 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

Syndromic autism (1,194 words) [view diff] no match in snippet view article find links to article

isodicentric 15q) ASD-risk genes (e.g.: ADNP, ARIDB1B, ANK2, SCN2A) ASD-associated CNVs (e.g.: 16p11.2 deletion/duplication, exonic NRXN1 deletions) Currently

List of human protein-coding genes 3 (17 words) [view diff] no match in snippet view article find links to article

"Statistics & download files". www.genenames.org. HUGO Gene Nomenclature Committee. 12 April 2024. Retrieved 12 April 2024.