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Biochemical and Biophysical Research Communications
|
July 16, 1980
Viral glycoproteins synthesis in Friend cell lines producing polycythemic (FV-P) and anemic (FV-A) Friend viruses
D Mathieu-Mahul, D Weil-Barbieri, F Wendling, et al.
European Journal of Immunology
|
January 1, 1977
The expression and relation of HLA, beta2-microglobulin and receptor for marmoset red blood cells on man/mouse and man/Chinese hamster hybrid cells
M Fellous, M C Hors, R Rebourcet, et al.
Human Molecular Genetics
|
November 1, 1993
A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata
D Weil, M F Portnoï, J Levilliers, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Isolation and characterization of the human fibrillar collagen genes
F Ramirez, M Bernard, M L Chu, et al.
Surgical Endoscopy
|
April 5, 2001
Laparoscopic adrenalectomy in children
E Mirallié, M D Leclair, P de Lagausie, et al.
Human Genetics
|
September 1, 1986
Ehlers-Danlos syndrome type IV: cosegregation of the phenotype to a COL3A1 allele of type III procollagen
P Tsipouras, P H Byers, R C Schwartz, et al.
The Journal of Investigative Dermatology
|
February 1, 1988
Growth and phenotypic characteristics of human nevus cells in culture
M L Mancianti, M Herlyn, D Weil, et al.
Experimental Hematology
|
December 1, 1990
Secretion of tumor necrosis factor-alpha by fresh human acute nonlymphoblastic leukemic cells: role in the disappearance of normal CFU-GM progenitors
L Kobari, D Weil, F M Lemoine, et al.
Genomics
|
September 1, 1995
A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C)
P Guilford, C Dodé, F Crozet, et al.
Annales De Genetique
|
January 1, 1985
Assignment to chromosome 12 of the gene coding for the human cell surface antigen CD9(p24) using the monoclonal antibody ALB6
C Boucheix, Nguyen-van-Cong, J Y Perrot, et al.
Page
of 21
Search research articles
Search
Showing results (161-170 of 203) with videos related to
Sort By:
Page
of 21
Biochemical and Biophysical Research Communications
|
July 16, 1980
Viral glycoproteins synthesis in Friend cell lines producing polycythemic (FV-P) and anemic (FV-A) Friend viruses
D Mathieu-Mahul, D Weil-Barbieri, F Wendling, et al.
European Journal of Immunology
|
January 1, 1977
The expression and relation of HLA, beta2-microglobulin and receptor for marmoset red blood cells on man/mouse and man/Chinese hamster hybrid cells
M Fellous, M C Hors, R Rebourcet, et al.
Human Molecular Genetics
|
November 1, 1993
A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata
D Weil, M F Portnoï, J Levilliers, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Isolation and characterization of the human fibrillar collagen genes
F Ramirez, M Bernard, M L Chu, et al.
Surgical Endoscopy
|
April 5, 2001
Laparoscopic adrenalectomy in children
E Mirallié, M D Leclair, P de Lagausie, et al.
Human Genetics
|
September 1, 1986
Ehlers-Danlos syndrome type IV: cosegregation of the phenotype to a COL3A1 allele of type III procollagen
P Tsipouras, P H Byers, R C Schwartz, et al.
The Journal of Investigative Dermatology
|
February 1, 1988
Growth and phenotypic characteristics of human nevus cells in culture
M L Mancianti, M Herlyn, D Weil, et al.
Experimental Hematology
|
December 1, 1990
Secretion of tumor necrosis factor-alpha by fresh human acute nonlymphoblastic leukemic cells: role in the disappearance of normal CFU-GM progenitors
L Kobari, D Weil, F M Lemoine, et al.
Genomics
|
September 1, 1995
A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C)
P Guilford, C Dodé, F Crozet, et al.
Annales De Genetique
|
January 1, 1985
Assignment to chromosome 12 of the gene coding for the human cell surface antigen CD9(p24) using the monoclonal antibody ALB6
C Boucheix, Nguyen-van-Cong, J Y Perrot, et al.
Page
of 21