نتایج جستجو برای: rab23

تعداد نتایج: 78  

Journal: :American journal of human genetics 2012
Stephen R F Twigg Deborah Lloyd Dagan Jenkins Nursel E Elçioglu Christopher D O Cooper Nouriya Al-Sannaa Ali Annagür Gabriele Gillessen-Kaesbach Irina Hüning Samantha J L Knight Judith A Goodship Bernard D Keavney Philip L Beales Opher Gileadi Simon J McGowan Andrew O M Wilkie

Carpenter syndrome is an autosomal-recessive multiple-congenital-malformation disorder characterized by multisuture craniosynostosis and polysyndactyly of the hands and feet; many other clinical features occur, and the most frequent include obesity, umbilical hernia, cryptorchidism, and congenital heart disease. Mutations of RAB23, encoding a small GTPase that regulates vesicular transport, are...

Journal: :Human Molecular Genetics 2009
Victoria L. Patterson Christine Damrau Anju Paudyal Benjamin Reeve Daniel T. Grimes Michelle E. Stewart Debbie J. Williams Pam Siggers Andy Greenfield Jennifer N. Murdoch

The mammalian Sonic hedgehog (Shh) signalling pathway is essential for embryonic development and the patterning of multiple organs. Disruption or activation of Shh signalling leads to multiple birth defects, including holoprosencephaly, neural tube defects and polydactyly, and in adults results in tumours of the skin or central nervous system. Genetic approaches with model organisms continue to...

2015
Carolini Kaid Patrícia B G Silva Beatriz A Cortez Carolina O Rodini Patricia Semedo-Kuriki Oswaldo K Okamoto

In medulloblastoma, abnormal expression of pluripotency factors such as LIN28 and OCT4 has been correlated with poor patient survival. The miR-302/367 cluster has also been shown to control self-renewal and pluripotency in human embryonic stem cells and induced pluripotent stem cells, but there is limited, mostly correlational, information about these pluripotency-related miRNA in cancer. We ev...

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