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Proceedings of the National Academy of Sciences of the United States of America
|
July 15, 1992
Germ-line mutations of the p53 tumor suppressor gene in patients with high risk for cancer inactivate the p53 protein
T Frebourg, J Kassel, K T Lam, et al.
The Journal of Biological Chemistry
|
May 25, 1991
A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuria
C Caillaud, S Lyonnet, F Rey, et al.
Genomics
|
March 20, 1995
The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease
D Campion, C Martin, R Heilig, et al.
Molecular Psychiatry
|
October 22, 2003
The promoter -194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit
E Houy, G Raux, F Thibaut, et al.
Cancer Research
|
June 13, 2000
Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments
F Charbonnier, G Raux, Q Wang, et al.
Oncogene
|
June 29, 2001
p53 mutants can often transactivate promoters containing a p21 but not Bax or PIG3 responsive elements
P Campomenosi, P Monti, A Aprile, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 25, 1995
A simple p53 functional assay for screening cell lines, blood, and tumors
J M Flaman, T Frebourg, V Moreau, et al.
Developmental Biology
|
September 1, 1992
Structure and expression of the Xenopus retinoblastoma gene
O H Destrée, K T Lam, L J Peterson-Maduro, et al.
Leukemia
|
May 15, 2007
Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patients
C Bastard, G Raux, C Fruchart, et al.
Journal of Medical Genetics
|
January 20, 2004
Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC
F Di Fiore, F Charbonnier, C Martin, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 103) with videos related to
Sort By:
Page
of 11
Proceedings of the National Academy of Sciences of the United States of America
|
July 15, 1992
Germ-line mutations of the p53 tumor suppressor gene in patients with high risk for cancer inactivate the p53 protein
T Frebourg, J Kassel, K T Lam, et al.
The Journal of Biological Chemistry
|
May 25, 1991
A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuria
C Caillaud, S Lyonnet, F Rey, et al.
Genomics
|
March 20, 1995
The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease
D Campion, C Martin, R Heilig, et al.
Molecular Psychiatry
|
October 22, 2003
The promoter -194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit
E Houy, G Raux, F Thibaut, et al.
Cancer Research
|
June 13, 2000
Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments
F Charbonnier, G Raux, Q Wang, et al.
Oncogene
|
June 29, 2001
p53 mutants can often transactivate promoters containing a p21 but not Bax or PIG3 responsive elements
P Campomenosi, P Monti, A Aprile, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 25, 1995
A simple p53 functional assay for screening cell lines, blood, and tumors
J M Flaman, T Frebourg, V Moreau, et al.
Developmental Biology
|
September 1, 1992
Structure and expression of the Xenopus retinoblastoma gene
O H Destrée, K T Lam, L J Peterson-Maduro, et al.
Leukemia
|
May 15, 2007
Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patients
C Bastard, G Raux, C Fruchart, et al.
Journal of Medical Genetics
|
January 20, 2004
Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC
F Di Fiore, F Charbonnier, C Martin, et al.
Page
of 11