Functional characterization of the Opitz syndrome gene product (midin): Evidence for homodimerization and association with microtubules throughout the cell cycle

Human Molecular Genetics

Volumn 8, Issue 8, 1999, Pages 1387-1396

  Cainarca, Silvia ^a   Messali, Silvia ^a   Ballabio, Andrea ^a,b   Meroni, Germana ^a  

^a TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

^b VITA SALUTE SAN RAFFAELE UNIVERSITY   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; CYTOPLASM PROTEIN; GENE PRODUCT; MICROTUBULE ASSOCIATED PROTEIN; MIDIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL CYCLE; CELL MATURATION; CELL PROLIFERATION; CONGENITAL MALFORMATION; CONTROLLED STUDY; CYTOKINESIS; DIMERIZATION; GEL FILTRATION; GENE FUNCTION; GENE MUTATION; HUMAN; HUMAN CELL; IMMUNOPRECIPITATION; INTERPHASE; MICROTUBULE; MITOSIS; MITOSIS SPINDLE; NONHUMAN; OPITZ SYNDROME; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; SITE DIRECTED MUTAGENESIS; X CHROMOSOME LINKAGE;

ANIMALS; CELL CYCLE; COS CELLS; DIMERIZATION; HUMANS; MICROTUBULE PROTEINS; MICROTUBULES; MUTATION; NUCLEAR PROTEINS; PROTEIN BINDING; SMITH-LEMLI-OPITZ SYNDROME; TRANSCRIPTION FACTORS;

ANIMALIA;

EID: 0032854670     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.8.1387     Document Type: Article

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