...LETM1. Thus, manifestations attributable to this deletion are reduced weight for height, minor facial anomalies, ADHD an...
...LETM1) that is deleted in nearly all WHS patients. LETM1 encodes a putative member of the EF-hand family of Ca(2+)-bindi...
...LETM1 and WHSC1. The 2p25.3 microduplication was smaller than 666 kb and encompassed only one OMIM gene, ACP1.,The combi...
...LETM1) in terms of their ability to modulate mitoflash response to hyperosmotic stress. In particular, overexpression or...
...LETM1, WHSC1, and FGFR3.,The combined use of MLPA and array CGH is an effective and specific means to diagnose WHS and a...
...LETM1 induced YAP1 nuclear accumulation, increasing the expression of PDGFB, PDGFRB and THBS4. Consistent with this, LET...
...Letm1-dependent mitochondrial Ca2+ uptake upon intracellular Ca2+ release exclusively in cancer cells. Accordingly, resv...
...LETM1) is located in the mitochondrial inner membrane and is defective in Wolf-Hirschhorn syndrome. LETM1 contains only ...
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