GTF2IRD1 抗体
(General Transcription Factor II I Repeat Domain-Containing 1 (GTF2IRD1))
may act as a muscle specific transcription factor\; human homolog may be associated with the Williams-Beuren microdeletion syndrome [RGD, Feb 2006]..
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Latest Publications for our GTF2IRD1 抗体
: "Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models." in: Human molecular genetics, (2019) (PubMed).: "Repression of Adipose Tissue Fibrosis through a PRDM16-GTF2IRD1 Complex Improves Systemic Glucose Homeostasis." in: Cell metabolism, Vol. 27, Issue 1, pp. 180-194.e6, (2018) (PubMed).
: "GTF2IRD1 in craniofacial development of humans and mice." in: Science (New York, N.Y.), Vol. 310, Issue 5751, pp. 1184-7, (2005) (PubMed).
Aliases for GTF2IRD1 抗体
GTF2I repeat domain containing 1 (GTF2IRD1) 抗体GTF2I repeat domain containing 1 (Gtf2ird1) 抗体
general transcription factor II I repeat domain-containing 1 (Gtf2ird1) 抗体
GTF2I repeat domain containing 1 (gtf2ird1) 抗体
general transcription factor II-I repeat domain-containing protein 1 (LOC100461122) 抗体
GTF2I repeat domain containing 1 S homeolog (gtf2ird1.S) 抗体
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