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Cell Death & Disease
|
March 22, 2014
Homozygous mutation of MTPAP causes cellular radiosensitivity and persistent DNA double-strand breaks
N T Martin, K Nakamura, U Paila, et al.
American Journal of Human Genetics
|
June 23, 1998
Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype
K M Cerosaletti, E Lange, H M Stringham, et al.
Nature Genetics
|
July 14, 1998
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus
P Concannon, K J Gogolin-Ewens, D A Hinds, et al.
American Journal of Human Genetics
|
March 7, 1998
Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations
M Telatar, S Teraoka, Z Wang, et al.
Neuropediatrics
|
November 24, 1999
Physical map of the region surrounding the ataxia-telangiectasia gene on human chromosome 11q22-23
N S Udar, S Xu, J O Bay, et al.
Molecular Cell
|
January 10, 2002
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency
M O'Driscoll, K M Cerosaletti, P M Girard, et al.
British Journal of Cancer
|
October 17, 2003
ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancer
J L Bernstein, L Bernstein, W D Thompson, et al.
American Journal of Human Genetics
|
December 1, 1991
Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium
T Foroud, S Wei, Y Ziv, et al.
Cell
|
May 20, 1998
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome
R Varon, C Vissinga, M Platzer, et al.
British Journal of Cancer
|
February 7, 2008
Risk for contralateral breast cancer among carriers of the CHEK2*1100delC mutation in the WECARE Study
L Mellemkjaer, C Dahl, J H Olsen, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 186) with videos related to
Sort By:
Page
of 19
Cell Death & Disease
|
March 22, 2014
Homozygous mutation of MTPAP causes cellular radiosensitivity and persistent DNA double-strand breaks
N T Martin, K Nakamura, U Paila, et al.
American Journal of Human Genetics
|
June 23, 1998
Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype
K M Cerosaletti, E Lange, H M Stringham, et al.
Nature Genetics
|
July 14, 1998
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus
P Concannon, K J Gogolin-Ewens, D A Hinds, et al.
American Journal of Human Genetics
|
March 7, 1998
Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations
M Telatar, S Teraoka, Z Wang, et al.
Neuropediatrics
|
November 24, 1999
Physical map of the region surrounding the ataxia-telangiectasia gene on human chromosome 11q22-23
N S Udar, S Xu, J O Bay, et al.
Molecular Cell
|
January 10, 2002
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency
M O'Driscoll, K M Cerosaletti, P M Girard, et al.
British Journal of Cancer
|
October 17, 2003
ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancer
J L Bernstein, L Bernstein, W D Thompson, et al.
American Journal of Human Genetics
|
December 1, 1991
Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium
T Foroud, S Wei, Y Ziv, et al.
Cell
|
May 20, 1998
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome
R Varon, C Vissinga, M Platzer, et al.
British Journal of Cancer
|
February 7, 2008
Risk for contralateral breast cancer among carriers of the CHEK2*1100delC mutation in the WECARE Study
L Mellemkjaer, C Dahl, J H Olsen, et al.
Page
of 19