The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane

Nature Cell Biology

Volumn 18, Issue 1, 2016, Pages 132-138

  Baskin, Jeremy M ^a,f   Wu, Xudong ^a,f,g   Christiano, Romain ^a,g,h,i,j   Oh, Michael S ^a   Schauder, Curtis M ^a   Gazzerro, Elisabetta ^b   Messa, Mirko ^a   Baldassari, Simona ^b   Assereto, Stefania ^b   Biancheri, Roberta ^b   Zara, Federico ^b   Minetti, Carlo ^b,c   Raimondi, Andrea ^d   Simons, Mikael ^e   Walther, Tobias C ^a,g,h,i,j   Reinisch, Karin M ^a,h   De Camilli, Pietro ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b G GASLINI INSTITUTE   (Italy)

^c UNIVERSITY OF GENOA   (Italy)

^d SAN RAFFAELE HOSPITAL   (Italy)

^e UNIVERSITY OF GÖTTINGEN   (Germany)

^f School of Integrative Plant Sciences   (United States)

^g HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^h HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

ⁱ HARVARD MEDICAL SCHOOL   (United States)

^j BROAD INSTITUTE OF MIT AND HARVARD   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; FAM126A PROTEIN; HYCCIN; PHOSPHATIDYLINOSITOL 4 PHOSPHATE; PHOSPHATIDYLINOSITOL KINASE; PI4KIII ALPHA PROTEIN; UNCLASSIFIED DRUG; FAM126A PROTEIN, HUMAN; MEMBRANE PROTEIN; PHOSPHATIDYLINOSITOL 4-PHOSPHATE; POLYPHOSPHOINOSITIDE; SIGNAL PEPTIDE;

ALPHA HELIX; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL MEMBRANE; COMPLEX FORMATION; CONTROLLED STUDY; CRYSTAL STRUCTURE; FIBROBLAST; HUMAN; HUMAN CELL; HYPOMYELINATION AND CONGENITAL CATARACT; LEUKODYSTROPHY; MALE; MOUSE; MYELINATION; NONHUMAN; OLIGODENDROGLIA; PHOSPHOLIPID SYNTHESIS; PRIORITY JOURNAL; PROTEIN BINDING; REGULATORY MECHANISM; ANIMAL; BIOSYNTHESIS; GENETICS; METABOLISM; MUTATION; PHYSIOLOGY; PROTEIN TERTIARY STRUCTURE; PROTEIN TRANSPORT;

ANIMALS; CELL MEMBRANE; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MEMBRANE PROTEINS; MICE; MUTATION; PHOSPHATIDYLINOSITOL PHOSPHATES; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT;

EID: 84952638705     PISSN: 14657392     EISSN: 14764679     Source Type: Journal    
DOI: 10.1038/ncb3271     Document Type: Article

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