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Journal of Medical Genetics
|
October 21, 1999
Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome
S Manouvrier-Hanu, J Amiel, S Jacquot, et al.
Human Genetics
|
July 1, 1995
Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature
S Demczuk, A Lévy, M Aubry, et al.
Nucleic Acids Research
|
December 8, 2022
Displacement and dissociation of oligonucleotides during DNA hairpin closure under strain
Fangyuan Ding, Simona Cocco, Saurabh Raj, et al.
American Journal of Human Genetics
|
July 1, 1995
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region
Z Chettouh, M F Croquette, B Delobel, et al.
Archives of Internal Medicine
|
March 24, 2010
Substitution of (R,S)-methadone by (R)-methadone: Impact on QTc interval
Nicolas Ansermot, Ozgür Albayrak, Jürg Schläpfer, et al.
Clinical Pharmacology and Therapeutics
|
December 13, 2005
Methadone enantiomer plasma levels, CYP2B6, CYP2C19, and CYP2C9 genotypes, and response to treatment
Séverine Crettol, Jean-Jacques Déglon, Jacques Besson, et al.
Nature Communications
|
March 18, 2018
Asymmetric adhesion of rod-shaped bacteria controls microcolony morphogenesis
Marie-Cécilia Duvernoy, Thierry Mora, Maxime Ardré, et al.
The New England Journal of Medicine
|
December 12, 1991
Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation
F Rousseau, D Heitz, V Biancalana, et al.
ERJ Open Research
|
July 1, 2025
Femoral venous stasis index predicts elevated right atrial pressure and mortality in pulmonary hypertension
Magali Croquette, Elisa Larrieu Ardilouze, Corinne Beaufort, et al.
Journal of Molecular Biology
|
February 21, 2022
Nucleosome Positioning on Large Tandem DNA Repeats of the '601' Sequence Engineered in Saccharomyces cerevisiae
Astrid Lancrey, Alexandra Joubert, Evelyne Duvernois-Berthet, et al.
Page
of 20
Search research articles
Search
Showing results (151-160 of 197) with videos related to
Sort By:
Page
of 20
Journal of Medical Genetics
|
October 21, 1999
Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome
S Manouvrier-Hanu, J Amiel, S Jacquot, et al.
Human Genetics
|
July 1, 1995
Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature
S Demczuk, A Lévy, M Aubry, et al.
Nucleic Acids Research
|
December 8, 2022
Displacement and dissociation of oligonucleotides during DNA hairpin closure under strain
Fangyuan Ding, Simona Cocco, Saurabh Raj, et al.
American Journal of Human Genetics
|
July 1, 1995
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region
Z Chettouh, M F Croquette, B Delobel, et al.
Archives of Internal Medicine
|
March 24, 2010
Substitution of (R,S)-methadone by (R)-methadone: Impact on QTc interval
Nicolas Ansermot, Ozgür Albayrak, Jürg Schläpfer, et al.
Clinical Pharmacology and Therapeutics
|
December 13, 2005
Methadone enantiomer plasma levels, CYP2B6, CYP2C19, and CYP2C9 genotypes, and response to treatment
Séverine Crettol, Jean-Jacques Déglon, Jacques Besson, et al.
Nature Communications
|
March 18, 2018
Asymmetric adhesion of rod-shaped bacteria controls microcolony morphogenesis
Marie-Cécilia Duvernoy, Thierry Mora, Maxime Ardré, et al.
The New England Journal of Medicine
|
December 12, 1991
Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation
F Rousseau, D Heitz, V Biancalana, et al.
ERJ Open Research
|
July 1, 2025
Femoral venous stasis index predicts elevated right atrial pressure and mortality in pulmonary hypertension
Magali Croquette, Elisa Larrieu Ardilouze, Corinne Beaufort, et al.
Journal of Molecular Biology
|
February 21, 2022
Nucleosome Positioning on Large Tandem DNA Repeats of the '601' Sequence Engineered in Saccharomyces cerevisiae
Astrid Lancrey, Alexandra Joubert, Evelyne Duvernois-Berthet, et al.
Page
of 20