Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
Cancer Research
|
June 11, 1998
Characterization of cell cycle checkpoint responses after ionizing radiation in Nijmegen breakage syndrome cells
V Yamazaki, R D Wegner, C U Kirchgessner
Cancer Research
|
April 6, 2001
Severe combined immunodeficient cells expressing mutant hRAD54 exhibit a marked DNA double-strand break repair and error-prone chromosome repair defect
J M Pluth, L M Fried, C U Kirchgessner
Radiation Research
|
January 12, 2000
Complementation of the radiosensitive M059J cell line
B S Hoppe, R B Jensen, C U Kirchgessner
Journal of Medical Genetics
|
December 1, 1995
X inactivation of the FMR1 fragile X mental retardation gene
C U Kirchgessner, S T Warren, H F Willard
Radiation Research
|
January 1, 1996
Induction and repair of chromosome aberrations in scid cells measured by premature chromosome condensation
J W Evans, X F Liu, C U Kirchgessner, et al.
Radiation Research
|
May 20, 1998
Higher-order chromatin structure-dependent repair of DNA double-strand breaks: involvement of the V(D)J recombination double-strand break repair pathway
P J Johnston, S H MacPhail, T D Stamato, et al.
Brain & Development
|
January 1, 1987
Molecular analysis of synapsin I, a candidate gene for Rett syndrome
L J DeGennaro, C A McCaffery, C U Kirchgessner, et al.
American Journal of Human Genetics
|
July 1, 1991
A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes
C U Kirchgessner, J A Trofatter, M M Mahtani, et al.
Current Biology : CB
|
August 26, 2000
A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage
T T Paull, E P Rogakou, V Yamazaki, et al.
Cancer Research
|
December 15, 1993
Complementation of the radiosensitive phenotype in severe combined immunodeficient mice by human chromosome 8
C U Kirchgessner, L M Tosto, K A Biedermann, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Cancer Research
|
June 11, 1998
Characterization of cell cycle checkpoint responses after ionizing radiation in Nijmegen breakage syndrome cells
V Yamazaki, R D Wegner, C U Kirchgessner
Cancer Research
|
April 6, 2001
Severe combined immunodeficient cells expressing mutant hRAD54 exhibit a marked DNA double-strand break repair and error-prone chromosome repair defect
J M Pluth, L M Fried, C U Kirchgessner
Radiation Research
|
January 12, 2000
Complementation of the radiosensitive M059J cell line
B S Hoppe, R B Jensen, C U Kirchgessner
Journal of Medical Genetics
|
December 1, 1995
X inactivation of the FMR1 fragile X mental retardation gene
C U Kirchgessner, S T Warren, H F Willard
Radiation Research
|
January 1, 1996
Induction and repair of chromosome aberrations in scid cells measured by premature chromosome condensation
J W Evans, X F Liu, C U Kirchgessner, et al.
Radiation Research
|
May 20, 1998
Higher-order chromatin structure-dependent repair of DNA double-strand breaks: involvement of the V(D)J recombination double-strand break repair pathway
P J Johnston, S H MacPhail, T D Stamato, et al.
Brain & Development
|
January 1, 1987
Molecular analysis of synapsin I, a candidate gene for Rett syndrome
L J DeGennaro, C A McCaffery, C U Kirchgessner, et al.
American Journal of Human Genetics
|
July 1, 1991
A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes
C U Kirchgessner, J A Trofatter, M M Mahtani, et al.
Current Biology : CB
|
August 26, 2000
A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage
T T Paull, E P Rogakou, V Yamazaki, et al.
Cancer Research
|
December 15, 1993
Complementation of the radiosensitive phenotype in severe combined immunodeficient mice by human chromosome 8
C U Kirchgessner, L M Tosto, K A Biedermann, et al.
Page
of 2