Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural development

scientific article

Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural development is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1093/HMG/8.13.2397
P3181OpenCitations bibliographic resource ID947186
P698PubMed publication ID10556287

P50authorVincenzo ZappavignaQ43722187
Danila BaldessariQ51887661
Gian Giacomo ConsalezQ60325005
P2093author name stringM Rocchi
M Mariani
L Viggiano
N Malgaretti
S Francisconi
P2860cites workTGF-beta signal transductionQ22003891
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 repeatQ24314231
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 histogenesisQ24315853
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13Q24336093
Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomesQ27860600
SH2 domains recognize specific phosphopeptide sequencesQ27860748
Mutations affecting segment number and polarity in DrosophilaQ28273492
Mmot1, a new helix-loop-helix transcription factor gene displaying a sharp expression boundary in the embryonic mouse brainQ28508895
Synpolydactyly in mice with a targeted deficiency in the HoxD complexQ28593833
Specific motifs recognized by the SH2 domains of Csk, 3BP2, fps/fes, GRB-2, HCP, SHC, Syk, and VavQ29615971
The molecular biology of axon guidanceQ29617857
RI manager, a microcomputer program for analysis of data from recombinant inbred strainsQ33305406
Meiotic instability associated with the CAGR1 trinucleotide repeat at 13q13.Q33678843
Mechanisms of Neural Patterning and Specification in the Development CerebellumQ34299482
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 resourceQ36738873
Arbitrarily primed PCR fingerprinting of RNA.Q40534468
GKLF in thymus epithelium as a developmentally regulated element of thymocyte-stroma cross-talkQ40953848
Genes involved in cerebellar cell specification and differentiationQ41353344
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 developmentQ47959796
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 displayQ48703186
A new method to screen clones from differential display experiments prior to RNA studiesQ48870510
HOX-4 genes and the morphogenesis of mammalian genitaliaQ68317843
P433issue13
P407language of work or nameEnglishQ1860
P921main subjectCaenorhabditis elegansQ91703
nervous system developmentQ1345738
Mab-21 like 2Q21118960
Mab-21-like 1Q21980000
Mab-21-like 2Q21988649
P304page(s)2397-2406
P577publication date1999-12-01
P1433published inHuman Molecular GeneticsQ2720965
P1476titleTwo murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural development
P478volume8

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cites work (P2860)
Q43169412A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3.
Q47690034An evolutionarily conserved nested gene pair - Mab21 and Lrba/Nbea in metazoan.
Q34920512Analysis of the eye developmental pathway in Drosophila using DNA microarrays
Q24288734Ancient origin of the new developmental superfamily DANGER
Q50518606Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis.
Q36750102Comparative gene expression analysis of the human periodontal ligament in deciduous and permanent teeth.
Q45714503Depletion of Mab21l1 and Mab21l2 messages in mouse embryo arrests axial turning, and impairs notochord and neural tube differentiation
Q28656367Differential expression of Meis2, Mab21l2 and Tbx3 during limb development associated with diversification of limb morphology in mammals
Q36109601First insights into the nature and evolution of antisense transcription in nematodes
Q58095195Generation and characterization of Pathogenic Mab21l2(R51C) mouse model
Q30587477In vivo analysis of hyaloid vasculature morphogenesis in zebrafish: A role for the lens in maturation and maintenance of the hyaloid.
Q24808927MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1
Q34193595Mab21l2 is essential for embryonic heart and liver development
Q49321805Mapping the Chromatin State Dynamics in Myoblasts
Q33983673Molecular evolutionary and structural analysis of the cytosolic DNA sensor cGAS and STING
Q35125578Mutations in MAB21L2 result in ocular Coloboma, microcornea and cataracts
Q34086564Postembryonic expression of Caenorhabditis elegans mab-21 and its requirement in sensory ray differentiation
Q28585119Requirement for Mab21l2 during development of murine retina and ventral body wall
Q41913422Structural and biochemical characterization of the cell fate determining nucleotidyltransferase fold protein MAB21L1.
Q28262421Thalamic development induced by Shh in the chick embryo
Q48719124The neurobeachin gene spans the common fragile site FRA13A.
Q37978029Transcription factors involved in lens development from the preplacodal ectoderm
Q51562273Whole genome microarray analysis of chicken embryo facial prominences.
Q42020814Xmab21l3 mediates dorsoventral patterning in Xenopus laevis
Q48733539Zebrafish mab21l2 is specifically expressed in the presumptive eye and tectum from early somitogenesis onwards
Q91630796Zebrafish mab21l2 mutants possess severe defects in optic cup morphogenesis, lens and cornea development
Q44926511Zebrafish rx3 and mab21l2 are required during eye morphogenesis
Q38918879mab21-l3 regulates cell fate specification of multiciliate cells and ionocytes
Q43890453mab21l2 transgenics reveal novel expression patterns of mab21l1 and mab21l2, and conserved promoter regulation without sequence conservation

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