scholarly article | Q13442814 |
P50 | author | Vincenzo Zappavigna | Q43722187 |
Danila Baldessari | Q51887661 | ||
Gian Giacomo Consalez | Q60325005 | ||
P2093 | author name string | M Rocchi | |
M Mariani | |||
L Viggiano | |||
N Malgaretti | |||
S Francisconi | |||
P2860 | cites work | TGF-beta signal transduction | Q22003891 |
cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeat | Q24314231 | ||
Epithelial V-like antigen (EVA), a novel member of the immunoglobulin superfamily, expressed in embryonic epithelia with a potential role as homotypic adhesion molecule in thymus histogenesis | Q24315853 | ||
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13 | Q24336093 | ||
Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes | Q27860600 | ||
SH2 domains recognize specific phosphopeptide sequences | Q27860748 | ||
Mutations affecting segment number and polarity in Drosophila | Q28273492 | ||
Mmot1, a new helix-loop-helix transcription factor gene displaying a sharp expression boundary in the embryonic mouse brain | Q28508895 | ||
Synpolydactyly in mice with a targeted deficiency in the HoxD complex | Q28593833 | ||
Specific motifs recognized by the SH2 domains of Csk, 3BP2, fps/fes, GRB-2, HCP, SHC, Syk, and Vav | Q29615971 | ||
The molecular biology of axon guidance | Q29617857 | ||
RI manager, a microcomputer program for analysis of data from recombinant inbred strains | Q33305406 | ||
Meiotic instability associated with the CAGR1 trinucleotide repeat at 13q13. | Q33678843 | ||
Mechanisms of Neural Patterning and Specification in the Development Cerebellum | Q34299482 | ||
Characterization of dominant and recessive assembly-defective mutations in mouse neurofilament NF-M. | Q36223914 | ||
Maps from two interspecific backcross DNA panels available as a community genetic mapping resource | Q36738873 | ||
Arbitrarily primed PCR fingerprinting of RNA. | Q40534468 | ||
GKLF in thymus epithelium as a developmentally regulated element of thymocyte-stroma cross-talk | Q40953848 | ||
Genes involved in cerebellar cell specification and differentiation | Q41353344 | ||
Changes in gene expression during the growth arrest of HepG2 hepatoma cells induced by reducing agents or TGFbeta1. | Q47814038 | ||
Mab21, the mouse homolog of a C. elegans cell-fate specification gene, participates in cerebellar, midbrain and eye development | Q47959796 | ||
cDNA sequence, map, and expression of the murine homolog of GTBP, a DNA mismatch repair gene. | Q48060657 | ||
A computer-driven approach to PCR-based differential screening, alternative to differential display | Q48703186 | ||
A new method to screen clones from differential display experiments prior to RNA studies | Q48870510 | ||
HOX-4 genes and the morphogenesis of mammalian genitalia | Q68317843 | ||
P433 | issue | 13 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Caenorhabditis elegans | Q91703 |
nervous system development | Q1345738 | ||
Mab-21 like 2 | Q21118960 | ||
Mab-21-like 1 | Q21980000 | ||
Mab-21-like 2 | Q21988649 | ||
P304 | page(s) | 2397-2406 | |
P577 | publication date | 1999-12-01 | |
P1433 | published in | Human Molecular Genetics | Q2720965 |
P1476 | title | Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural development | |
P478 | volume | 8 |
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Q34920512 | Analysis of the eye developmental pathway in Drosophila using DNA microarrays |
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Q36750102 | Comparative gene expression analysis of the human periodontal ligament in deciduous and permanent teeth. |
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Q30587477 | In vivo analysis of hyaloid vasculature morphogenesis in zebrafish: A role for the lens in maturation and maintenance of the hyaloid. |
Q24808927 | MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1 |
Q34193595 | Mab21l2 is essential for embryonic heart and liver development |
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Q41913422 | Structural and biochemical characterization of the cell fate determining nucleotidyltransferase fold protein MAB21L1. |
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