glycerophosphoinositol 4,5-bisphosphate and Genetic Predisposition

glycerophosphoinositol 4,5-bisphosphate has been researched along with Genetic Predisposition in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Conduit, SE; DiTommaso, T; Dyson, JM; Feeney, SJ; Fulcher, AJ; Gurung, R; Hakim, S; Horan, KA; Mitchell, CA; Ramm, G; Smyth, I; Sriratana, A; Wicking, C	1
Behr, E; Bendahhou, S; Cobo, AM; Donaldson, MR; Escolar, DM; Fu, YH; Jensen, JL; Mozaffar, T; Pereira, S; Poza, JJ; Ptácek, LJ; Suarez, WA; Szepetowski, P; Tawil, R; Tristani-Firouzi, M; Wagstaff, J	1

Other Studies

2 other study(ies) available for glycerophosphoinositol 4,5-bisphosphate and Genetic Predisposition

Article	Year
INPP5E regulates phosphoinositide-dependent cilia transition zone function. The Journal of cell biology, 2017, Jan-02, Volume: 216, Issue:1 Topics: Abnormalities, Multiple; Animals; Cell Line; Cerebellum; Cilia; Disease Models, Animal; Embryo, Mammalian; Eye Abnormalities; Gene Expression Regulation, Developmental; Genetic Predisposition to Disease; Hedgehog Proteins; Humans; Kidney Diseases, Cystic; Kruppel-Like Transcription Factors; Mice, Inbred C57BL; Mice, Knockout; Phenotype; Phosphatidylinositol 4,5-Diphosphate; Phosphatidylinositol Phosphates; Phosphoric Monoester Hydrolases; Retina; Retinal Pigment Epithelium; Second Messenger Systems; Smoothened Receptor; Time Factors; Transfection; Zinc Finger Protein Gli2	2017
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome. Neurology, 2003, Jun-10, Volume: 60, Issue:11 Topics: Abnormalities, Multiple; Arrhythmias, Cardiac; Binding Sites; Female; Genetic Predisposition to Disease; Humans; Male; Muscle Weakness; Mutation; Paralysis; Pedigree; Phenotype; Phosphatidylinositol 4,5-Diphosphate; Potassium Channels, Inwardly Rectifying; Syndrome	2003

Article

Year

INPP5E regulates phosphoinositide-dependent cilia transition zone function.

The Journal of cell biology, 2017, Jan-02, Volume: 216, Issue:1

Topics: Abnormalities, Multiple; Animals; Cell Line; Cerebellum; Cilia; Disease Models, Animal; Embryo, Mammalian; Eye Abnormalities; Gene Expression Regulation, Developmental; Genetic Predisposition to Disease; Hedgehog Proteins; Humans; Kidney Diseases, Cystic; Kruppel-Like Transcription Factors; Mice, Inbred C57BL; Mice, Knockout; Phenotype; Phosphatidylinositol 4,5-Diphosphate; Phosphatidylinositol Phosphates; Phosphoric Monoester Hydrolases; Retina; Retinal Pigment Epithelium; Second Messenger Systems; Smoothened Receptor; Time Factors; Transfection; Zinc Finger Protein Gli2

2017

PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome.

Neurology, 2003, Jun-10, Volume: 60, Issue:11

Topics: Abnormalities, Multiple; Arrhythmias, Cardiac; Binding Sites; Female; Genetic Predisposition to Disease; Humans; Male; Muscle Weakness; Mutation; Paralysis; Pedigree; Phenotype; Phosphatidylinositol 4,5-Diphosphate; Potassium Channels, Inwardly Rectifying; Syndrome

2003