Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes

[1]  L. Peck,et al.  Maxillary canine-first premolar transposition, associated dental anomalies and genetic basis. , 2009, The Angle orthodontist.

[2]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[3]  A. Vaahtokari,et al.  Regulation of organogenesis. Common molecular mechanisms regulating the development of teeth and other organs. , 1995, The International journal of developmental biology.

[4]  I. Thesleff,et al.  Evidence for the role of the enamel knot as a control center in mammalian tooth cusp formation: non-dividing cells express growth stimulating Fgf-4 gene. , 1994, The International journal of developmental biology.

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

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

[7]  I. Thesleff,et al.  Identification of BMP-4 as a signal mediating secondary induction between epithelial and mesenchymal tissues during early tooth development , 1993, Cell.

[8]  D. Schlessinger,et al.  Anhidrotic ectodermal dysplasia gene region cloned in yeast artificial chromosomes. , 1993, Genomics.

[9]  G. Gyapay,et al.  A second-generation linkage map of the human genome , 1992, Nature.

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

[11]  I. Thesleff,et al.  Coordinated induction of cell proliferation and syndecan expression in dental mesenchyme by epithelium: Evidence for diffusible signals , 1992, Developmental dynamics : an official publication of the American Association of Anatomists.

[12]  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.

[13]  D. Duboule,et al.  Expression of the murine Dlx-1 homeobox gene during facial, ocular and limb development. , 1992, Differentiation; research in biological diversity.

[14]  A. Vaahtokari,et al.  Associations between transforming growth factor beta 1 RNA expression and epithelial-mesenchymal interactions during tooth morphogenesis. , 1991, Development.

[15]  E. Kollar,et al.  EGF antisense oligodeoxynucleotides block murine odontogenesis in vitro. , 1991, Developmental biology.

[16]  M. Ferguson,et al.  The homeobox gene Hox 7.1 has specific regional and temporal expression patterns during early murine craniofacial embryogenesis, especially tooth development in vivo and in vitro. , 1991, Development.

[17]  A. Vaahtokari,et al.  Molecular changes during determination and differentiation of the dental mesenchymal cell lineage. , 1990, Journal de biologie buccale.

[18]  A. Ivens,et al.  The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome , 1990, Human Genetics.

[19]  J. Ott.  Computer-simulation methods in human linkage analysis. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[20]  S. Myllärniemi,et al.  Dominant inheritance of tooth malpositions and their association to hypodontia , 1988, Clinical genetics.

[21]  R. Ranta.  A review of tooth formation in children with cleft lip/palate. , 1986, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.

[22]  J. Ott,et al.  Strategies for multilocus linkage analysis in humans. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[23]  C. Mathew,et al.  Blot hybridisation analysis of genomic DNA. , 1984, Journal of medical genetics.

[24]  J. Hobkirk,et al.  The management of patients with severe hypodontia. , 1980, Journal of oral rehabilitation.

[25]  R. Burgersdijk,et al.  Oral symptoms of the Wolf syndrome: report of case. , 1978, ASDC journal of dentistry for children.

[26]  M. Spence,et al.  The Genetics of Hypodontia , 1974, Journal of dental research.

[27]  K. Hunstadbråten.  Hypodontia in the permanent dentition. , 1973, ASDC journal of dentistry for children.

[28]  Cohen Mm.  The oral manifestations of trisomy G-1 (Down syndrome). , 1971 .

[29]  L. Alvesalo,et al.  The inheritance pattern of missing, peg-shaped, and strongly mesio-distally reduced upper lateral incisors. , 1969, Acta odontologica Scandinavica.

[30]  M. Kaye,et al.  IN VIVO AND IN VITRO , 2006 .

[31]  A. Vaahtokari,et al.  The role of growth factors in determination and differentiation of the odontoblastic cell lineage. , 1992, Proceedings of the Finnish Dental Society. Suomen Hammaslaakariseuran toimituksia.

[32]  Y. Weide.  Oligodontia : a clinical radiographic and genetic evaluation , 1992 .

[33]  A. McMahon,et al.  Expression pattern of the FGF-related proto-oncogene int-2 suggests multiple roles in fetal development. , 1989, Development.

[34]  N. Burzynski,et al.  Classification and genetics of numeric anomalies of dentition. , 1983, Birth defects original article series.

[35]  Burzynski Nj,et al.  Classification and genetics of numeric anomalies of dentition. , 1983 .

[36]  Robert J. Gorlin,et al.  Syndromes of the Head and Neck , 1976 .

[37]  M. Cohen.  The oral manifestations of trisomy G-1 (Down syndrome). , 1971, Birth defects original article series.

[38]  S. Keiser-Nielsen.  Federation Dentaire Internationale. Two-Digit System of designating teeth. , 1971, DP. Dental practice.