Search Results

Filter
  • 1-2 of  2 results for ""ENDOCHONDRAL ossification""
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia.

  • Authors : Campos-Xavier AB; Division of Molecular Pediatrics, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.; Martinet D

Subjects: Abnormalities, Multiple/Abnormalities, Multiple/Abnormalities, Multiple/*genetics ; Chondrocytes/Chondrocytes/Chondrocytes/*metabolism ; Dwarfism/Dwarfism/Dwarfism/*genetics

  • Source: American journal of human genetics [Am J Hum Genet] 2009 Jun; Vol. 84 (6), pp. 760-70. Date of Electronic Publication: 2009 May 28.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium:

Record details

×
Academic Journal

FoxA family members are crucial regulators of the hypertrophic chondrocyte differentiation program.

  • Authors : Ionescu A; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.; Kozhemyakina E

Subjects: Cell Enlargement*; Chondrocytes/Chondrocytes/Chondrocytes/*metabolism ; Chondrogenesis/Chondrogenesis/Chondrogenesis/*genetics

  • Source: Developmental cell [Dev Cell] 2012 May 15; Vol. 22 (5), pp. 927-39.Publisher: Cell Press Country of Publication: United States NLM ID: 101120028 Publication Model: Print Cited Medium:

Record details

×
  • 1-2 of  2 results for ""ENDOCHONDRAL ossification""