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YY1 - Wikipedia
YY1 is a ubiquitously distributed transcription factor belonging to the GLI-Kruppel class of zinc finger proteins. The protein is involved in repressing and activating a diverse number of promoters. Hence, the YY in the name stands for "yin-yang."
YY1 Haploinsufficiency Causes an Intellectual Disability …
Jun 1, 2017 · Yin and yang 1 (YY1) is a well-known zinc-finger transcription factor with crucial roles in normal development and malignancy. YY1 acts both as a repressor and as an activator of gene expression.
The Protective Role of Yin‐Yang 1 in Cardiac Injury and …
Oct 29, 2021 · YY1 ameliorates cardiac injury and remodeling after MI by repressing cardiomyocyte apoptosis and boosting angiogenesis, which might be ascribed to the enhancement of Akt phosphorylation and the subsequent vascular …
Yin Yang 1 is critical for mid-hindbrain neuroepithelium …
Jul 23, 2020 · Yin Yang 1 (YY1) is a ubiquitously expressed transcription factor which exerts multiple functions in various cellular events by activating or repressing gene transcription, modifying DNA conformation and controlling protein activity [1, 2, 3, 4].
Yin Yang 1 sustains biosynthetic demands during brain ... - Nature
May 16, 2019 · Here, we show that Yy1 controls murine cerebral cortex development in a stage-dependent manner. By regulating a wide range of metabolic pathways and protein translation, Yy1 maintains...
YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome ...
Jun 6, 2017 · We have identified 23 individuals with de novo mutations or deletions of YY1 and phenotypic features that define a syndrome of cognitive impairment, behavioral alterations, intrauterine growth restriction, feeding problems, and various congenital malformations.
Transcription factor YY1: structure, function, and therapeutic ...
Nov 28, 2005 · YY1 is a ubiquitous and multifunctional zinc-finger transcription factor (also known as δ, NF-E1, UCRBP, and CF1) member of the Polycomb Group protein family, a group of homeobox gene...
We have identified 23 individuals with de novo mutations or deletions of YY1 and phenotypic features that define a syndrome of cognitive impairment, behavioral alterations, intrauterine growth restriction, feeding problems, and various congenital malformations.