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British Journal of Cancer
|
June 2, 2005
Search for germline alterations in CDKN2A/ARF and CDK4 of 42 Jewish melanoma families with or without neural system tumours
C Marian, A Scope, K Laud, et al.
British Journal of Cancer
|
March 25, 2000
Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16INK4A, P14ARF or cdk4 genes
N Soufir, B Bressac-de Paillerets, L Desjardins, et al.
British Journal of Cancer
|
November 21, 1998
Absence of somatic alterations of the EB1 gene adenomatous polyposis coli-associated protein in human sporadic colorectal cancers
P Jaïs, J C Sabourin, J Bombled, et al.
Leukemia
|
July 17, 1998
Non-Hodgkin's lymphomas and myeloid disorders: deletions associated with t(2;5) and t(3;5) detected by FISH
M A Dragon-Durey, A F Goguel, C Leonard, et al.
Annales De Dermatologie Et De Venereologie
|
October 26, 1999
[Muir-Torre syndrome and familial colorectal cancer: 2 families with molecular genetic analysis]
M X Doré, B Dieumegard, S Grandjouan, et al.
Cancer
|
October 1, 1996
Genetic transmission of susceptibility to cancer in families of children with soft tissue sarcomas
C Moutou, C Le Bihan, A Chompret, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
November 1, 1993
Retinoblastoma and p53 tumor suppressor genes in human hepatoma cell lines
A Puisieux, K Galvin, F Troalen, et al.
Oncogene
|
June 15, 1995
Genomic stability and wild-type p53 function of lymphoblastoid cells with germ-line p53 mutation
P Lalle, C Moyret-Lalle, Q Wang, et al.
Pigment Cell & Melanoma Research
|
November 22, 2012
Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history
P Ghiorzo, L Pastorino, P Queirolo, et al.
Human Molecular Genetics
|
March 21, 1998
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group
N Soufir, M F Avril, A Chompret, et al.
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Search research articles
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Showing results (21-30 of 64) with videos related to
Sort By:
Page
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British Journal of Cancer
|
June 2, 2005
Search for germline alterations in CDKN2A/ARF and CDK4 of 42 Jewish melanoma families with or without neural system tumours
C Marian, A Scope, K Laud, et al.
British Journal of Cancer
|
March 25, 2000
Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16INK4A, P14ARF or cdk4 genes
N Soufir, B Bressac-de Paillerets, L Desjardins, et al.
British Journal of Cancer
|
November 21, 1998
Absence of somatic alterations of the EB1 gene adenomatous polyposis coli-associated protein in human sporadic colorectal cancers
P Jaïs, J C Sabourin, J Bombled, et al.
Leukemia
|
July 17, 1998
Non-Hodgkin's lymphomas and myeloid disorders: deletions associated with t(2;5) and t(3;5) detected by FISH
M A Dragon-Durey, A F Goguel, C Leonard, et al.
Annales De Dermatologie Et De Venereologie
|
October 26, 1999
[Muir-Torre syndrome and familial colorectal cancer: 2 families with molecular genetic analysis]
M X Doré, B Dieumegard, S Grandjouan, et al.
Cancer
|
October 1, 1996
Genetic transmission of susceptibility to cancer in families of children with soft tissue sarcomas
C Moutou, C Le Bihan, A Chompret, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
November 1, 1993
Retinoblastoma and p53 tumor suppressor genes in human hepatoma cell lines
A Puisieux, K Galvin, F Troalen, et al.
Oncogene
|
June 15, 1995
Genomic stability and wild-type p53 function of lymphoblastoid cells with germ-line p53 mutation
P Lalle, C Moyret-Lalle, Q Wang, et al.
Pigment Cell & Melanoma Research
|
November 22, 2012
Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history
P Ghiorzo, L Pastorino, P Queirolo, et al.
Human Molecular Genetics
|
March 21, 1998
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group
N Soufir, M F Avril, A Chompret, et al.
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of 7