Mutations in Lama1 disrupt retinal vascular development and inner limiting membrane formation

Journal of Biological Chemistry

Volumn 285, Issue 10, 2010, Pages 7697-7711

  Edwards, Malia M ^a,h   Mammadova Bach, Elmina ^b   Alpy, Fabien ^b,c,i   Klein, Annick ^b,c   Hicks, Wanda L ^a   Roux, Michel ^d   Simon Assmann, Patricia ^b,c   Smith, Richard S ^a   Orend, Gertraud ^b,c   Wu, Jiang ^e   Peachey, Neal S ^e,f,g   Naggert, Jürgen K ^a   Lefebvre, Olivier ^b,c   Nishina, Patsy M ^a  

^a JACKSON LABORATORY   (United States)

^b INSERM   (France)

^c UNIVERSITÉ DE STRASBOURG   (France)

^d INSTITUT CLINIQUE DE LA SOURIS   (France)

^e LERNER RESEARCH INSTITUTE   (United States)

^f LOUIS STOKES CLEVELAND VA MEDICAL CENTER   (United States)

^g CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^h JOHNS HOPKINS UNIVERSITY   (United States)

ⁱ INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BASEMENT MEMBRANE; ELECTRORETINOGRAMS; IMMUNOHISTOCHEMICAL CHARACTERIZATION; INNER LIMITING MEMBRANES; INNER NUCLEAR LAYERS; JACKSON; LAMININ; MOUSE MODELS; N-TERMINAL DOMAINS; NULL MUTANT; RETINAL DISEASE; TWO-HYBRID SYSTEM; VASCULAR DEVELOPMENT; VASCULATURE;

AMINO ACIDS; BIOLOGICAL MEMBRANES; BLOOD VESSELS; ORGANIC ACIDS; PHOSPHATASES;

OPHTHALMOLOGY;

CYSTEINE; LAMININ 1; TYROSINE;

AMINO ACID SUBSTITUTION; ANIMAL EXPERIMENT; ARTICLE; ASTROCYTE; CELL MIGRATION; CONTROLLED STUDY; GENE FREQUENCY; GENE FUNCTION; GENE MAPPING; GENE MUTATION; HETEROZYGOSITY; HOMOZYGOSITY; IMMUNOHISTOCHEMISTRY; MISSENSE MUTATION; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; RETINA BLOOD VESSEL; RETINA DEVELOPMENT; SINGLE NUCLEOTIDE POLYMORPHISM; TWO HYBRID SYSTEM; VITREOUS BODY;

ADULT; AMINO ACID SEQUENCE; ANIMALS; ASTROCYTES; BASEMENT MEMBRANE; ELECTRORETINOGRAPHY; FEMALE; GENETIC COMPLEMENTATION TEST; HUMANS; LAMININ; MALE; MICE; MICE, INBRED C57BL; MICE, INBRED DBA; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; PHENOTYPE; PROTEIN ISOFORMS; RETINA; RETINAL DISEASES; RETINAL VESSELS; SEQUENCE ALIGNMENT; TRANSGENES;

BACTERIA (MICROORGANISMS); MUS;

EID: 77951251055     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M109.069575     Document Type: Article

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