Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Polymorphic variants of genes related to arginine metabolism and the risk of orofacial clefts.

Archives of oral biology - 1 Nov 2010

Hozyasz Kamil K, Mostowska Adrianna, Wojcicki Piotr, Lianeri Margarita, Jagodzinski Pawel P

Abstract excerpt

OBJECTIVE: Maternal mid-pregnancy low levels of symmetric dimethylarginine and newborn low levels of citrulline are suspected to be risk factors for orofacial clefts. This study was undertaken to investigate the involvement of polymorphic variants of genes related to arginine metabolism in the su...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Argininosuccinate Synthase
Share to Chi-Square Distribution
Share to Cleft Lip

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cleft Palate

Share to Infant, Newborn

Share to Mitochondrial Membrane Transport Proteins

Share to Polymorphism, Restriction Fragment Length

Share to Statistics, Nonparametric

Source

Identifiers

PMID: 20739017
DOI: 10.1016/j.archoralbio.2010.07.012

Genes

ASS1
ASL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20739017-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Polymorphic variants of genes related to arginine metabolism and the risk of orofacial clefts.PMID 20739017Read ↗

Genetic variants in S-adenosyl-methionine synthesis pathway and nonsyndromic cleft lip with or without cleft palate in Chile.Semantic proximity Read ↗

Genetic variants of MGMT, RHPN2, and FAM49A contributed to susceptibility of nonsyndromic orofacial clefts in a Chinese population.Semantic proximity Read ↗

Association of MSX1 Gene Variants with Nonsyndromic Cleft Lip and/or Palate in the Pakistani Population.Semantic proximity Read ↗

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population.Semantic proximity Read ↗

Arginase I gene single-nucleotide polymorphism is associated with decreased risk of pulmonary hypertension in bronchopulmonary dysplasia.Semantic proximity Read ↗

Association of Genetic Polymorphisms of GREM1 Gene with Susceptibility to Non-Syndromic Cleft Lip with or without Cleft Palate in an Iranian Population.Semantic proximity Read ↗

Spastic gait, intellectual disability and seizures due to a rare mutation causing hyperargininemia.Semantic proximity Read ↗

Association between a single-nucleotide polymorphism in the GREM1 gene and non-syndromic orofacial cleft in the Chinese population.Semantic proximity Read ↗

Association of common variants in PAH and LAT1 with non-syndromic cleft lip with or without cleft palate (NSCL/P) in the Polish population.Semantic proximity Read ↗

Case series of arginase 1 deficiency: Expanding the spectrum in hyperargininemia.Semantic proximity Read ↗

Polymorphisms of stress-related genes and the risk of nonsyndromic cleft lip with or without cleft palate.Semantic proximity Read ↗

Association of Ugrp2 gene polymorphisms with adenoid hypertrophy in the pediatric population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.