Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

[1]  J. Haines,et al.  A second locus for Rieger syndrome maps to chromosome 13q14. , 1996, American journal of human genetics.

[2]  J. Seidman,et al.  A human MSX1 homeodomain missense mutation causes selective tooth agenesis , 1996, Nature Genetics.

[3]  M. Rosenfeld,et al.  P-OTX: a PIT-1-interacting homeodomain factor expressed during anterior pituitary gland development. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[4]  M. Therrien,et al.  Ptx1, a bicoid-related homeo box transcription factor involved in transcription of the pro-opiomelanocortin gene. , 1996, Genes & development.

[5]  J. Hurst,et al.  Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome. , 1996, American journal of human genetics.

[6]  S. Mundlos,et al.  Altered Growth and Branching Patterns in Synpolydactyly Caused by Mutations in HOXD13 , 1996, Science.

[7]  N. Copeland,et al.  Good genes in bad neighbourhoods , 1996, Nature Genetics.

[8]  J. Dubnau,et al.  RNA recognition and translational regulation by a homeodomain protein , 1996, Nature.

[9]  J. Wasmuth,et al.  Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome , 1996, Nature Genetics.

[10]  R. Winter What's in a face? , 1996, Nature Genetics.

[11]  V. Kaartinen,et al.  Abnormal lung development and cleft palate in mice lacking TGF–β3 indicates defects of epithelial–mesenchymal interaction , 1995, Nature Genetics.

[12]  M. Ferguson,et al.  Transforming growth factor–β3 is required for secondary palate fusion , 1995, Nature Genetics.

[13]  J. Rubenstein,et al.  Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain. , 1995, Genes & development.

[14]  V. Sheffield,et al.  Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25). , 1995, Human molecular genetics.

[15]  J. Murray Face facts: genes, environment, and clefts. , 1995, American journal of human genetics.

[16]  Adriana C. Gittenberger-de Groot,et al.  Expression patterns of the paired-related homeobox genes MHox/Prx1 and S8/Prx2 suggest roles in development of the heart and the forebrain , 1995, Mechanisms of Development.

[17]  David J. Anderson,et al.  Identification by Differential RT-PCR of a Novel Paired Homeodomain Protein Specifically Expressed in Sensory Neurons and a Subset of Their CNS Targets , 1995, Molecular and Cellular Neuroscience.

[18]  Roy Parker,et al.  Degradation of mRNA in eukaryotes , 1995, Cell.

[19]  W. Dobyns,et al.  Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux , 1995, Nature Genetics.

[20]  Francis S. Collins,et al.  Positional cloning moves from perditional to traditional , 1995, Nature Genetics.

[21]  Yishi Jin,et al.  Control of type-D GABAergic neuron differentiation by C. elegans UNC-30 homeodomain protein , 1994, Nature.

[22]  M. Seldin,et al.  The gene for the homeodomain-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development , 1994, Mechanisms of Development.

[23]  R. Stevenson,et al.  Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: A putative Rho Rac guanine nucleotide exchange factor , 1994, Cell.

[24]  V. P. Johnson,et al.  Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[25]  D. Kooy,et al.  Developmental expression of a novel murine homeobox gene (Chx10): Evidence for roles in determination of the neuroretina and inner nuclear layer , 1994, Neuron.

[26]  R. Krumlauf Hox genes in vertebrate development , 1994, Cell.

[27]  A. Simeone,et al.  Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and drosophila , 1994, Neuron.

[28]  R. Brent,et al.  Specific DNA recognition and intersite spacing are critical for action of the bicoid morphogen , 1994, Molecular and cellular biology.

[29]  R. Maas,et al.  Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development , 1994, Nature Genetics.

[30]  J. Diaz,et al.  Evolutionary conservation of the AU-rich 3' untranslated region of messenger RNA. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[31]  E. Jabs,et al.  A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis , 1993, Cell.

[32]  H. Slavkin Rieger syndrome revisited: experimental approaches using pharmacologic and antisense strategies to abrogate EGF and TGF-alpha functions resulting in dysmorphogenesis during embryonic mouse craniofacial morphogenesis. , 1993, American journal of medical genetics.

[33]  F. Myokai,et al.  A chicken homeobox gene related to Drosophila paired is predominantly expressed in the developing limb. , 1993, Developmental biology.

[34]  A. Simeone,et al.  A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo. , 1993, The EMBO journal.

[35]  R. Maas,et al.  Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene , 1992, Nature Genetics.

[36]  J. Weber,et al.  Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4 , 1992, Nature genetics.

[37]  K. Buetow,et al.  Characterization of the human HOX 7 cDNA and identification of polymorphic markers. , 1992, Human molecular genetics.

[38]  M. Rosenfeld,et al.  Mutation of the POU-Specific Domain of Pit-1 and Hypopituitarism Without Pituitary Hypoplasia , 1992, Science.

[39]  M. Ferguson,et al.  Expression patterns of the homeobox gene, Hox-8, in the mouse embryo suggest a role in specifying tooth initiation and shape. , 1992, Development.

[40]  C. Desplan,et al.  The homeodomain: A new face for the helix‐turn‐helix? , 1992, BioEssays : news and reviews in molecular, cellular and developmental biology.

[41]  C. Baldwin,et al.  An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome , 1992, Nature.

[42]  R. Balling,et al.  Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene , 1992, Nature.

[43]  D. Gasser,et al.  Restriction fragment length polymorphisms, glucocorticoid receptors, and phenytoin-induced cleft palate in congenic strains of mice with steroid susceptibility differences. , 1991, Journal of craniofacial genetics and developmental biology.

[44]  L W Swanson,et al.  Pituitary cell phenotypes involve cell-specific Pit-1 mRNA translation and synergistic interactions with other classes of transcription factors. , 1990, Genes & development.

[45]  P. M. Falk,et al.  Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq. , 1990, American journal of human genetics.

[46]  R. Reed,et al.  The organization of 3' splice-site sequences in mammalian introns. , 1989, Genes & development.

[47]  Roger Brent,et al.  DNA specificity of the bicoid activator protein is determined by homeodomain recognition helix residue 9 , 1989, Cell.

[48]  D Bopp,et al.  The role of localization of bicoid RNA in organizing the anterior pattern of the Drosophila embryo. , 1988, The EMBO journal.

[49]  Marvin B. Shapiro,et al.  RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression. , 1987, Nucleic acids research.

[50]  H. Eiberg,et al.  Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6 , 1987, Clinical genetics.

[51]  M. Farrall,et al.  Linkage of an X-chromosome cleft palate gene , 1987, Nature.

[52]  S. Oppenheimer,et al.  Atlas of embryonic development , 1984 .

[53]  Y. Krespi,et al.  Rieger's syndrome associated with a large Meckel's diverticulum. , 1979, The American journal of gastroenterology.

[54]  M. Kaback,et al.  The Axenfeld syndrome and the Rieger syndrome. , 1978, Journal of medical genetics.

[55]  A. Sadeghi‐Nejad,et al.  Autosomal dominant transmission of isolated growth hormone deficiency in iris-dental dysplasia (Rieger's syndrome). , 1974, The Journal of pediatrics.

[56]  D. Donaldson,et al.  Rieger's syndrome. , 1969, Pediatrics.

[57]  P.P.H. Alkemade,et al.  Dysgenesis Mesodermalis of the Iris and the Cornea: a study of Rieger's syndromeand Peters' Anomaly , 1969 .

[58]  R. Crawford Iris dysgenesis with other anomalies. , 1967, The British journal of ophthalmology.

[59]  A. Simeone,et al.  Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly , 1996, Nature Genetics.

[60]  M. Noll,et al.  Molecular genetics of Aristaless, a prd-type homeo box gene involved in the morphogenesis of proximal and distal pattern elements in a subset of appendages in Drosophila. , 1993, Genes & development.

[61]  D. Sassoon,et al.  Detection of messenger RNA by in situ hybridization. , 1993, Methods in enzymology.

[62]  R. Harland,et al.  In situ hybridization: an improved whole-mount method for Xenopus embryos. , 1991, Methods in cell biology.

[63]  A. Bird,et al.  Use of restriction enzymes to detect potential gene sequences in mammalian DNA , 1987, Nature.