Mutations in the gene that encodes the F-Actin binding protein anillin cause FSGS

Journal of the American Society of Nephrology

Volumn 25, Issue 9, 2014, Pages 1991-2002

  Gbadegesin, Rasheed A ^a   Hall, Gentzon ^a   Adeyemo, Adebowale ^b   Hanke, Nils ^c,d   Tossidou, Irini ^c   Burchette, James ^a   Wu, Guanghong ^a   Homstad, Alison ^a   Sparks, Matthew A ^a   Gomez, Jose ^a   Jiang, Ruiji ^a   Alonso, Andrea ^a   Lavin, Peter ^a,e   Conlon, Peter ^f   Korstanje, Ron ^d,g   Christine Stander, M ^h   Shamsan, Ghaidan ^h   Barua, Moumita ⁱ   Spurney, Robert ^a   Singhal Jeffrey B Kopp, Pravin C ^j,k   Haller, Hermann ^c,d   Howell, David ^a   Pollak, Martin R ⁱ   Shaw, Andrey S ^h   Schiffer, Mario ^c,d   Winn, Michelle P ^a   more..

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c HANNOVER MEDICAL SCHOOL   (Germany)

^d MOUNT DESERT ISLAND BIOLOGICAL LABORATORY   (United States)

^e ADELAIDE AND MEATH HOSPITAL   (Ireland)

^f BEAUMONT HOSPITAL   (Ireland)

^g JACKSON LABORATORY   (United States)

^h WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

ⁱ BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

^j FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH   (United States)

^k NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN BINDING PROTEIN; BIOLOGICAL MARKER; CD2 ASSOCIATED PROTEIN; F ACTIN BINDING PROTEIN ANILLIN; UNCLASSIFIED DRUG; ACTIN-BINDING PROTEIN ANILLIN, HUMAN; ANILLIN; CD2-ASSOCIATED PROTEIN; CONTRACTILE PROTEIN; CYTOSKELETON PROTEIN; MUTANT PROTEIN; SIGNAL TRANSDUCING ADAPTOR PROTEIN; ZEBRAFISH PROTEIN;

ACTIN FILAMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL MIGRATION; CELL MOTILITY; CONTROLLED STUDY; EDEMA; EMBRYO; FEMALE; FOCAL GLOMERULOSCLEROSIS; GENE OVEREXPRESSION; GENE SEGREGATION; GENE SILENCING; GENETIC VARIABILITY; GENOME-WIDE ASSOCIATION STUDY; GLOMERULAR FILTRATION BARRIER; HIV ASSOCIATED NEPHROPATHY; HUMAN; HUMAN CELL; HUMAN TISSUE; KIDNEY BIOPSY; LINKAGE ANALYSIS; LOSS OF FUNCTION MUTATION; MAJOR CLINICAL STUDY; MALE; MEMBRANE DAMAGE; MISSENSE MUTATION; MUTANT; NONHUMAN; PHENOTYPE; PODOCYTE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; TRANSGENIC ZEBRAFISH; UPREGULATION; WHOLE EXOME SEQUENCING; WILD TYPE; ADULT; AGED; AMINO ACID SEQUENCE; ANIMAL; CELL MOTION; DISEASE MODEL; EXOME; GENETICS; METABOLISM; MIDDLE AGED; MOLECULAR GENETICS; MOUSE; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PEDIGREE; SEQUENCE HOMOLOGY; ZEBRA FISH;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ADULT; AGED; AMINO ACID SEQUENCE; ANIMALS; CELL MOVEMENT; CONSERVED SEQUENCE; CONTRACTILE PROTEINS; CYTOSKELETAL PROTEINS; DISEASE MODELS, ANIMAL; DNA MUTATIONAL ANALYSIS; EXOME; FEMALE; GENE KNOCKDOWN TECHNIQUES; GLOMERULAR FILTRATION BARRIER; GLOMERULOSCLEROSIS, FOCAL SEGMENTAL; HUMANS; MALE; MICE; MICROFILAMENT PROTEINS; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTANT PROTEINS; MUTATION; PEDIGREE; PODOCYTES; SEQUENCE HOMOLOGY, AMINO ACID; UP-REGULATION; ZEBRAFISH; ZEBRAFISH PROTEINS;

EID: 84920173095     PISSN: 10466673     EISSN: 15333450     Source Type: Journal    
DOI: 10.1681/ASN.2013090976     Document Type: Article

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