Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tamar, Erlich"'
Autor:
Sat Dev Batish, Neiva Magdalena, Orna Levran, Arleen D. Auerbach, Tamar Erlich, John J. Gregory, Peter C. Verlander
Publikováno v:
Proceedings of the National Academy of Sciences. 94:13051-13056
Fanconi anemia (FA) is a genetically heterogeneous autosomal recessive syndrome associated with chromosomal instability, hypersensitivity to DNA crosslinking agents, and predisposition to malignancy. The gene for FA complementation group A ( FAA ) re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c03f19cd1a6ffacab801372492058449
https://doi.org/10.1073/pnas.94.24.13051
https://doi.org/10.1073/pnas.94.24.13051
Autor:
Joshua, Shachor, Ziv, Chana, Shabtai, Varsano, Tamar, Erlich, Elizabeth, Goldman, Yigal, Dror, Ilana, Yakovy, Ruth, Navon
Publikováno v:
The Israel Medical Association journal : IMAJ. 5(11)
It has been argued that arginine replacement in locus 16 (Arg16) of beta 2 adrenergic receptor with glycin (Gly16) increases asthma severity, while glutamin replacement in locus 27 (Gln27) with glutamic acid (Glu27) decreases it. In addition, ethnic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::156f9ba4bf5d11e61c1fb21fbf4f1938
https://pubmed.ncbi.nlm.nih.gov/14650112
https://pubmed.ncbi.nlm.nih.gov/14650112
Autor:
Leopoldo Zelante, Sinoula Apostolou, Peter C. Verlander, Elna W. Moerland, Douglas F. Easton, Maria Savino, Alex J. Tipping, Gregory G. Lennon, Leonarda lanzano, Neil V. Morgan, Anne-Marie Cleton-Jansen, S.A. Whitmore, Larry L. Deaven, Tamar Erlich, David F. Callen, Sheila Hassock, Christopher G. Mathew, Arleen D. Auerbach, Orna Levran, Joanna Crawford, Anna Savoia, Norman A. Doggett, Maria D'Apolito, Robert K. Moyzis, Thomy J. L. de Ravel, Jan C. Pronk, Stander Jansen, Rachel A. Gibson, Sat Dev Batish, Carola Van Berkell, Elena Memeo, Grant R. Sutherland, Angelo Notarangeio, Maria Rosaria Piemontese, Cees J. Cornelisse
Publikováno v:
Nature genetics. 14(3)
The Fanconi anaemia/Breast cancer consortium* Fanconi anaemia (FA) is an autosomal recessive disorder associated with progressive bone-marrow failure, a variety of congenital abnormalities, and predisposition to acute myeloid leukaemia1. Cells from F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34be34c3e987319dd16130ddd1e53194
https://pubmed.ncbi.nlm.nih.gov/8896564
https://pubmed.ncbi.nlm.nih.gov/8896564