Zobrazeno 1 - 5
of 5
pro vyhledávání: '"A. V. Perez-Castro"'
Autor:
Ana V. Perez-Castro, Kathryn G. Vogel
Publikováno v:
Journal of Orthopaedic Research. 17:139-148
A region of fibrocartilage develops in bovine deep flexor tendon where the tissue wraps around bone and is subjected to compressive and shear forces in addition to tension. There is no fibrocartilage at this location in fetal tendon or in adjacent ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d78c9d1c555a262f2d047e60b5486c5
https://doi.org/10.1002/jor.1100170120
https://doi.org/10.1002/jor.1100170120
Publikováno v:
American Journal of Medical Genetics. 71:47-53
Wolf-Hirschhorn syndrome (WHS) is a multiple anomaly condition characterized by mental and developmental defects, resulting from the absence of the distal segment of one chromosome 4 short arm (4p16.3). Owing to the complex and variable expression of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ba4e780bb0d44336dc6837f8c9ec789
https://doi.org/10.1002/(sici)1096-8628(19970711)71:1<47::aid-ajmg9>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19970711)71:1<47::aid-ajmg9>3.0.co
Publikováno v:
Genomics. 41:10-16
Fibroblast growth factor receptor 3 (FGFR3) is a developmentally regulated transmembrane protein. Three other FGFRs (1, 2, and 4) in conjunction with FGFR3 are part of the receptor tyrosine kinase super-family. Mutations in three of these genes (FGFR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53c6b1d9b01c7956e835b07bda888f74
https://doi.org/10.1006/geno.1997.4616
https://doi.org/10.1006/geno.1997.4616
Publikováno v:
American journal of medical genetics. 71(1)
Wolf-Hirschhorn syndrome (WHS) is a multiple anomaly condition characterized by mental and developmental defects, resulting from the absence of the distal segment of one chromosome 4 short arm (4p16.3). Owing to the complex and variable expression of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e1508af0c182a7916bf0fb22faa5f65c
https://pubmed.ncbi.nlm.nih.gov/9215768
https://pubmed.ncbi.nlm.nih.gov/9215768
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 7(9)
The mouse XPG gene is a homolog of the human DNA excision repair gene known to be defective in the hereditary sun-sensitive disorder xeroderma pigmentosum (group-G). Defects in mouse XPG have been shown to directly affect the sensitivity of cultured
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75f86cfe0f529a9497d78fb234685dcd
https://pubmed.ncbi.nlm.nih.gov/8703115
https://pubmed.ncbi.nlm.nih.gov/8703115