Literature DB >> 8304335

Of mice and men: heritable skeletal disorders.

O Jacenko, B R Olsen, M L Warman.   

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Year:  1994        PMID： 8304335      PMCID： PMC1918165     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  29 in total

1.  Transgenic mouse model of the mild dominant form of osteogenesis imperfecta.

Authors:  J Bonadio; T L Saunders; E Tsai; S A Goldstein; J Morris-Wiman; L Brinkley; D F Dolan; R A Altschuler; J E Hawkins; J F Bateman
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

2.  Pattern recognition in bone dysplasias.

Authors:  J Spranger
Journal:  Prog Clin Biol Res       Date:  1985

3.  Association of pancreatic insufficiency and chronic neutropenia in childhood.

Authors:  V Burke; J H Colebatch; C M Anderson; M J Simons
Journal:  Arch Dis Child       Date:  1967-04       Impact factor: 3.791

4.  Gli3 expression is affected in the morphogenetic mouse mutants add and Xt.

Authors:  T Schimmang; F van der Hoeven; U Rüther
Journal:  Prog Clin Biol Res       Date:  1993

5.  Amino acid substitutions of conserved residues in the carboxyl-terminal domain of the alpha 1(X) chain of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type Schmid.

Authors:  G A Wallis; B Rash; W A Sweetman; J T Thomas; M Super; G Evans; M E Grant; R P Boot-Handford
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

Review 6.  Cartilage hair hypoplasia: immunological aspects and their clinical implications.

Authors:  S H Polmar; G F Pierce
Journal:  Clin Immunol Immunopathol       Date:  1986-07

7.  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

8.  Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis.

Authors:  T Sulisalo; P Sistonen; J Hästbacka; C Wadelius; O Mäkitie; A de la Chapelle; I Kaitila
Journal:  Nat Genet       Date:  1993-04       Impact factor: 38.330

9.  Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect.

Authors:  A Winterpacht; M Hilbert; U Schwarze; S Mundlos; J Spranger; B U Zabel
Journal:  Nat Genet       Date:  1993-04       Impact factor: 38.330

10.  Patients with Ehlers-Danlos syndrome type IV lack type III collagen.

Authors:  F M Pope; G R Martin; J R Lichtenstein; R Penttinen; B Gerson; D W Rowe; V A McKusick
Journal:  Proc Natl Acad Sci U S A       Date:  1975-04       Impact factor: 11.205
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  3 in total

Review 1.  Molecular basis for skeletal variation: insights from developmental genetic studies in mice.

Authors:  C Kappen; A Neubüser; R Balling; R Finnell
Journal:  Birth Defects Res B Dev Reprod Toxicol       Date:  2007-12

2.  Chicken collagen X regulatory sequences restrict transgene expression to hypertrophic cartilage in mice.

Authors:  Michelle R Campbell; Catherine J Gress; Elizabeth H Appleman; Olena Jacenko
Journal:  Am J Pathol       Date:  2004-02       Impact factor: 4.307

3.  Growth plate compressions and altered hematopoiesis in collagen X null mice.

Authors:  C J Gress; O Jacenko
Journal:  J Cell Biol       Date:  2000-05-15       Impact factor: 10.539
  3 in total

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