Search research articles
Contact Us
Filters
Showing results (141-150 of 246) with videos related to
Page
of 25
Sort By:
Prenatal Diagnosis
|
July 1, 1986
Prenatal identification of a Y-chromosome deletion by Y-specific single copy DNA probes
S Gilgenkrantz, P Droulle, E Seboun, et al.
Microbes and Infection
|
December 30, 1999
Differential expression of MHC class II isotype chains
C Alcaïde-Loridan, A M Lennon, M R Bono, et al.
The Journal of Cell Biology
|
November 17, 1998
Interferon alpha inhibits a Src-mediated pathway necessary for Shigella-induced cytoskeletal rearrangements in epithelial cells
G Duménil, J C Olivo, S Pellegrini, et al.
Bulletin De L'Association Des Anatomistes
|
March 1, 1991
[Genetic factor of sex determination]
N Abbas, J Toublanc, R Rappaport, et al.
Immunogenetics
|
August 26, 1998
CIITA B-cell-specific promoter suppression in MHC class II-silenced cell hybrids
A M Lennon, C Ottone, M Rosemblatt, et al.
Birth Defects Original Article Series
|
January 1, 1975
Mapping the Xga red blood cell antigen in human-Chinese hamster cell hybrids. The Xg locus is possibly located on the short arm of the X chromosome
M Fellous, P L Pearson, A G van der Linden, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles
|
December 18, 1972
[Linkage between the HL-A histocompatibility system and the thymidine kinase activity in a human-mouse hybrid]
M C Hors-Cayla, M Fellous, J Y Picard, et al.
Research in Immunology
|
November 1, 1991
The recombinant human interferon-gamma receptor is fully functional in a human x murine hybrid containing human chromosome 21
M R Bono, C Alcaïde-Loridan, B Letouzé, et al.
Cytogenetics and Cell Genetics
|
January 1, 1975
Mapping the Xga red blood cell antigen in human-Chinese hamster cell hybrids. The Xg locus is possibly located on the short arm of the X chromosome
M Fellous, P L Pearson, A G van der Linden, et al.
American Journal of Human Genetics
|
June 1, 1996
A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome
A Ion, L Telvi, J L Chaussain, et al.
Page
of 25
Search research articles
Search
Showing results (141-150 of 246) with videos related to
Sort By:
Page
of 25
Prenatal Diagnosis
|
July 1, 1986
Prenatal identification of a Y-chromosome deletion by Y-specific single copy DNA probes
S Gilgenkrantz, P Droulle, E Seboun, et al.
Microbes and Infection
|
December 30, 1999
Differential expression of MHC class II isotype chains
C Alcaïde-Loridan, A M Lennon, M R Bono, et al.
The Journal of Cell Biology
|
November 17, 1998
Interferon alpha inhibits a Src-mediated pathway necessary for Shigella-induced cytoskeletal rearrangements in epithelial cells
G Duménil, J C Olivo, S Pellegrini, et al.
Bulletin De L'Association Des Anatomistes
|
March 1, 1991
[Genetic factor of sex determination]
N Abbas, J Toublanc, R Rappaport, et al.
Immunogenetics
|
August 26, 1998
CIITA B-cell-specific promoter suppression in MHC class II-silenced cell hybrids
A M Lennon, C Ottone, M Rosemblatt, et al.
Birth Defects Original Article Series
|
January 1, 1975
Mapping the Xga red blood cell antigen in human-Chinese hamster cell hybrids. The Xg locus is possibly located on the short arm of the X chromosome
M Fellous, P L Pearson, A G van der Linden, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles
|
December 18, 1972
[Linkage between the HL-A histocompatibility system and the thymidine kinase activity in a human-mouse hybrid]
M C Hors-Cayla, M Fellous, J Y Picard, et al.
Research in Immunology
|
November 1, 1991
The recombinant human interferon-gamma receptor is fully functional in a human x murine hybrid containing human chromosome 21
M R Bono, C Alcaïde-Loridan, B Letouzé, et al.
Cytogenetics and Cell Genetics
|
January 1, 1975
Mapping the Xga red blood cell antigen in human-Chinese hamster cell hybrids. The Xg locus is possibly located on the short arm of the X chromosome
M Fellous, P L Pearson, A G van der Linden, et al.
American Journal of Human Genetics
|
June 1, 1996
A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome
A Ion, L Telvi, J L Chaussain, et al.
Page
of 25