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The Journal of Investigative Dermatology
|
March 18, 2019
Chronic UVA1 Irradiation of Human Dermal Fibroblasts: Persistence of DNA Damage and Validation of a Cell Cultured-Based Model of Photoaging
Alicia Montoni, Kelly M George, Jérémie Soeur, et al.
Mutation Research
|
May 12, 2009
Influence of cytosine methylation on ultraviolet-induced cyclobutane pyrimidine dimer formation in genomic DNA
Patrick J Rochette, Sandrine Lacoste, Jean-Philippe Therrien, et al.
Genetic Testing
|
August 23, 2000
Geography of HFE C282Y and H63D mutations
A T Merryweather-Clarke, J J Pointon, A M Jouanolle, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1984
[Erythrocytosis due to a high-affinity hemoglobulin: mutant hemoglobin Saint-Jacques beta 140 (H18) Ala----Thr with a change in the 2,3-diphosphoglycerate binding site]
J Rochette, J P Boissel, D Labie, et al.
Plos One
|
August 30, 2016
Association of Telomere Length with Breast Cancer Prognostic Factors
Kaoutar Ennour-Idrissi, Bernard Têtu, Elizabeth Maunsell, et al.
The Journal of Peptide Research : Official Journal of the American Peptide Society
|
February 27, 2004
Development of H1e histone linker-specific antibodies by means of synthetic peptides
K Foulon, S Baltora-Rosset, V Fuentes, et al.
Biology of the Neonate
|
October 24, 1998
Effect of two types of fish oil supplementation on plasma and erythrocyte phospholipids in formula-fed term infants
C Maurage, P Guesnet, M Pinault, et al.
Oncogene
|
August 13, 2002
Human cells bearing homozygous mutations in the DNA mismatch repair genes hMLH1 or hMSH2 are fully proficient in transcription-coupled nucleotide excision repair
Patrick J Rochette, Nathalie Bastien, Bruce C McKay, et al.
Revue Medicale De Bruxelles
|
May 1, 1985
[Polycythemia associated with a hemoglobinopathy: apropos of a case of hemoglobin San Diego]
F Vertongen, J Rochette, Y Grégoire, et al.
American Journal of Human Genetics
|
February 1, 1994
Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers
S L Thein, M Sampietro, K Rohde, et al.
Page
of 12
Search research articles
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Showing results (71-80 of 118) with videos related to
Sort By:
Page
of 12
The Journal of Investigative Dermatology
|
March 18, 2019
Chronic UVA1 Irradiation of Human Dermal Fibroblasts: Persistence of DNA Damage and Validation of a Cell Cultured-Based Model of Photoaging
Alicia Montoni, Kelly M George, Jérémie Soeur, et al.
Mutation Research
|
May 12, 2009
Influence of cytosine methylation on ultraviolet-induced cyclobutane pyrimidine dimer formation in genomic DNA
Patrick J Rochette, Sandrine Lacoste, Jean-Philippe Therrien, et al.
Genetic Testing
|
August 23, 2000
Geography of HFE C282Y and H63D mutations
A T Merryweather-Clarke, J J Pointon, A M Jouanolle, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1984
[Erythrocytosis due to a high-affinity hemoglobulin: mutant hemoglobin Saint-Jacques beta 140 (H18) Ala----Thr with a change in the 2,3-diphosphoglycerate binding site]
J Rochette, J P Boissel, D Labie, et al.
Plos One
|
August 30, 2016
Association of Telomere Length with Breast Cancer Prognostic Factors
Kaoutar Ennour-Idrissi, Bernard Têtu, Elizabeth Maunsell, et al.
The Journal of Peptide Research : Official Journal of the American Peptide Society
|
February 27, 2004
Development of H1e histone linker-specific antibodies by means of synthetic peptides
K Foulon, S Baltora-Rosset, V Fuentes, et al.
Biology of the Neonate
|
October 24, 1998
Effect of two types of fish oil supplementation on plasma and erythrocyte phospholipids in formula-fed term infants
C Maurage, P Guesnet, M Pinault, et al.
Oncogene
|
August 13, 2002
Human cells bearing homozygous mutations in the DNA mismatch repair genes hMLH1 or hMSH2 are fully proficient in transcription-coupled nucleotide excision repair
Patrick J Rochette, Nathalie Bastien, Bruce C McKay, et al.
Revue Medicale De Bruxelles
|
May 1, 1985
[Polycythemia associated with a hemoglobinopathy: apropos of a case of hemoglobin San Diego]
F Vertongen, J Rochette, Y Grégoire, et al.
American Journal of Human Genetics
|
February 1, 1994
Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers
S L Thein, M Sampietro, K Rohde, et al.
Page
of 12