Literature DB >> 7698270

The roles of collagen genes in skeletal development and morphogenesis.

B R Olsen1.   

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Year:  1995        PMID： 7698270     DOI： 10.1007/bf01931087

Source DB:  PubMed          Journal:  Experientia        ISSN： 0014-4754


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  7 in total

1.  Studies on cartilage. VI. A genetically determined defect in tracheal cartilage.

Authors:  R Seegmiller; C C Ferguson; H Sheldon
Journal:  J Ultrastruct Res       Date:  1972-02

2.  A type X collagen mutation causes Schmid metaphyseal chondrodysplasia.

Authors:  M L Warman; M Abbott; S S Apte; T Hefferon; I McIntosh; D H Cohn; J T Hecht; B R Olsen; C A Francomano
Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

3.  The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.

Authors:  J Hästbacka; A de la Chapelle; M M Mahtani; G Clines; M P Reeve-Daly; M Daly; B A Hamilton; K Kusumi; B Trivedi; A Weaver
Journal:  Cell       Date:  1994-09-23       Impact factor: 41.582

4.  A Stickler syndrome gene is linked to chromosome 6 near the COL11A2 gene.

Authors:  H G Brunner; S E van Beersum; M L Warman; B R Olsen; H H Ropers; E C Mariman
Journal:  Hum Mol Genet       Date:  1994-09       Impact factor: 6.150

5.  Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia.

Authors:  R Shiang; L M Thompson; Y Z Zhu; D M Church; T J Fielder; M Bocian; S T Winokur; J J Wasmuth
Journal:  Cell       Date:  1994-07-29       Impact factor: 41.582

6.  Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome.

Authors:  W Reardon; R M Winter; P Rutland; L J Pulleyn; B M Jones; S Malcolm
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

7.  A new chondrodystrophic mutant in mice. Electron microscopy of normal and abnormal chondrogenesis.

Authors:  R Seegmiller; F C Fraser; H Sheldon
Journal:  J Cell Biol       Date:  1971-03       Impact factor: 10.539
  7 in total
  5 in total

1.  Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development.

Authors:  X Liu; H Wu; M Byrne; S Krane; R Jaenisch
Journal:  Proc Natl Acad Sci U S A       Date:  1997-03-04       Impact factor: 11.205

2.  Gene expression analysis of cultured amniotic fluid cell with Down syndrome by DNA microarray.

Authors:  In-Hyuk Chung; Sook-Hwan Lee; Kyo-Won Lee; Sang-hee Park; Kwang-Yul Cha; Nam-Soon Kim; Hyang-Sook Yoo; Yong Sung Kim; Suman Lee
Journal:  J Korean Med Sci       Date:  2005-02       Impact factor: 2.153

3.  Secretion of collagen I and tenascin is modulated by laminin-111 in 3D culture of human adenoid cystic carcinoma cells.

Authors:  Ruy G Jaeger; Normando Scarabotto-Neto; Nilton Azambuja; Vanessa M Freitas
Journal:  Int J Exp Pathol       Date:  2008-04       Impact factor: 1.925

4.  Hydrolyzed eggshell membrane immobilized on phosphorylcholine polymer supplies extracellular matrix environment for human dermal fibroblasts.

Authors:  Eri Ohto-Fujita; Tomohiro Konno; Miho Shimizu; Kazuhiko Ishihara; Toshihiro Sugitate; Jun Miyake; Kotaro Yoshimura; Kaori Taniwaki; Takashi Sakurai; Yukio Hasebe; Yoriko Atomi
Journal:  Cell Tissue Res       Date:  2011-05-20       Impact factor: 5.249

5.  Redox imbalance and morphological changes in skin fibroblasts in typical Rett syndrome.

Authors:  Cinzia Signorini; Silvia Leoncini; Claudio De Felice; Alessandra Pecorelli; Ilaria Meloni; Francesca Ariani; Francesca Mari; Sonia Amabile; Eugenio Paccagnini; Mariangela Gentile; Giuseppe Belmonte; Gloria Zollo; Giuseppe Valacchi; Thierry Durand; Jean-Marie Galano; Lucia Ciccoli; Alessandra Renieri; Joussef Hayek
Journal:  Oxid Med Cell Longev       Date:  2014-05-29       Impact factor: 6.543
  5 in total

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