A genetically heterogeneous developmental disorder some forms of which are caused by mutation in the ROR2 gene (neurotrophic tyrosine kinase receptor-2, NTRKR2) which can also cause brachydactyly type B. NTRKR2 is involved in the early formation of chondrocytes. Robinow-Sorauf syndrome A phenotyp...
(3) If the Director-General fails to determine the application for renewal before the date the harvest operator’s current registration expires, the operator is nevertheless deemed to be registered under this scheme until the date the Director-General notifies the operator of his or her determinatio...
(3) If the Director-General fails to determine the application for renewal before the date the vessel's current registration expires, the vessel is nevertheless deemed to be registered under this Part until the date the Director-General notifies the operator of his or her determination on the ap...
To circumvent these general developmental effects of global srpra gene disruption in vivo, we selectively knocked down srpra in neutrophils using our neutrophil-specific gene editing line Tg(mpx:KalTA4)× (UAS:Cas9)× (UAS:NTR-mCherry), in which Cas9 expression is confined to mCherry-marked ...
Global DNA methylome analysis of sperm cells revealed that the sperm epigenome was affected by prior ofDetrSheSen-rtinicaedllluyl ctmeydpeetch,oymlilataitsses.diSvaiemnediplaeigrxlepyn,reethstsiecemdchgeaethnnygelesoscmotamekapenapdrleatdrcaetnodsFuc1rrCiipntrltgomsmipceeer.omIftIahEtaoCdgseaon...