PMC Links for Protein (Select 1008909354) - PMC - NCBI

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Items: 3

Select item 65087381.

Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction

Dov Tiosano, Hagit N. Baris, Anlu Chen, Marrit M. Hitzert, Markus Schueler, Federico Gulluni, Antje Wiesener, Antonio Bergua, Adi Mory, Brett Copeland, Joseph G. Gleeson, Patrick Rump, Hester van Meer, Deborah A. Sival, Volker Haucke, Josh Kriwinsky, Karl X. Knaup, André Reis, Nadine N. Hauer, Emilio Hirsch, Ronald Roepman, Rolph Pfundt, Christian T. Thiel, Michael S. Wiesener, Mariam G. Aslanyan, David A. Buchner

PLoS Genet. 2019 Apr; 15(4): e1008088. Published online 2019 Apr 29. doi: 10.1371/journal.pgen.1008088

PMCID:: PMC6508738

Abstract Article PDF–2.3M

Select item 64560272.

Low expression of PIK3C2A gene: A potential biomarker to predict the risk of acute myocardial infarction

Buchuan Tan, Miao Liu, Yushuang Yang, Long Liu, Fanbo Meng

Medicine (Baltimore) 2019 Jun; 98(14): e15061. Published online 2019 Apr 5. doi: 10.1097/MD.0000000000015061

PMCID:: PMC6456027

Abstract Article PDF–234K

Select item 12186473.

Cloning of a human phosphoinositide 3-kinase with a C2 domain that displays reduced sensitivity to the inhibitor wortmannin.

J Domin, F Pages, S Volinia, S E Rittenhouse, M J Zvelebil, R C Stein, M D Waterfield

Biochem J. 1997 Aug 15; 326(Pt 1): 139–147. doi: 10.1042/bj3260139

PMCID:: PMC1218647

Summary PDF–876K

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