MID2, a Homologue of the Opitz Syndrome Gene MID1: Similarities in Subcellular Localization and Differences in Expression During Development

The B-box family is an expanding new family of genes encoding proteins involved in diverse cellular functions such as developmental patterning and oncogenesis. A member of this protein family, MID1, is the gene responsible for the X-linked form of Opitz G/BBB syndrome, a developmental disorder chara...

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Veröffentlicht in:	Human molecular genetics 1999-08, Vol.8 (8), p.1397-1407
Hauptverfasser:	Buchner, Georg, Montini, Eugenio, Andolfi, Grazia, Quaderi, Nandita, Cainarca, Silvia, Messali, Silvia, Bassi, Maria Teresa, Ballabio, Andrea, Meroni, Germana, Franco, Brunella
Format:	Artikel
Sprache:	eng
Schlagworte:	Amino Acid Sequence Animals Base Sequence Biological and medical sciences Calcium-Binding Proteins - genetics Cell structures and functions Chromosome Mapping COS Cells Cytoskeleton, cytoplasm. Intracellular movements DNA - chemistry DNA - genetics DNA, Complementary - chemistry DNA, Complementary - genetics Embryo, Mammalian - metabolism Embryonic and Fetal Development Exons Fluorescent Antibody Technique, Direct Fundamental and applied biological sciences. Psychology Gene Expression Regulation, Developmental Humans In Situ Hybridization Intracellular Signaling Peptides and Proteins Introns Membrane Glycoproteins Membrane Proteins - genetics Mice Mice, Inbred C57BL Microtubule Proteins Microtubules - metabolism Molecular and cellular biology Molecular Sequence Data Muridae Nuclear Proteins RNA - genetics RNA - metabolism Saccharomyces cerevisiae Proteins Sequence Alignment Sequence Analysis, DNA Sequence Homology, Amino Acid Smith-Lemli-Opitz Syndrome - genetics Tissue Distribution Transcription Factors - genetics Ubiquitin-Protein Ligases X Chromosome - genetics
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