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searching for ARG1 (gene) 7 found (9 total)

alternate case: aRG1 (gene)

Argininemia (547 words) [view diff] no match in snippet view article find links to article

Hypotonia Growth is stunted Microcephaly Seizures Mutations in the ARG1 gene cause argininemia, which belongs to a class of genetic diseases called
TINAGL1 (604 words) [view diff] no match in snippet view article find links to article
nephritis antigen-like is a protein that in humans is encoded by the TINAGL1 gene. GRCh38: Ensembl release 89: ENSG00000142910 - Ensembl, May 2017 GRCm38:
XPNPEP2 (574 words) [view diff] no match in snippet view article find links to article
F, et al. (1992). "Kininase activity in human platelets: cleavage of the Arg1-Pro2 bond of bradykinin by aminopeptidase P". Biochem. Pharmacol. 44 (3):
XPNPEP1 (797 words) [view diff] no match in snippet view article find links to article
Yaron A (Aug 1992). "Kininase activity in human platelets: cleavage of the Arg1-Pro2 bond of bradykinin by aminopeptidase P". Biochemical Pharmacology. 44
P-bodies (1,778 words) [view diff] no match in snippet view article find links to article
components. The evidence being that GW182 and Ago2, both associated with miRNA gene silencing, are found exclusively in multivesicular bodies or GW-bodies and
Substance P (4,863 words) [view diff] no match in snippet view article find links to article
PMID 21226668.  Seckl MJ, Higgins T, Widmer F, Rozengurt E (Jan 1997). "[D-Arg1,D-Trp5,7,9,Leu11]substance P: a novel potent inhibitor of signal transduction
Arginase (1,441 words) [view diff] no match in snippet view article find links to article
Arginase at the US National Library of Medicine Medical Subject Headings (MeSH) GeneReviews/NIH/NCBI/UW entry on Arginase Deficiency Arginase family signature