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Monnot

Showing results (271-280 of 338) with videos related to

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JBMR Plus|April 7, 2026
A rare coexistence: Ollier disease and primary hyperparathyroidism-mere coincidence or expanding the spectrum of Ollier disease?Justine Luciano, Astrid Dauchez, Beatrix Cochand-Priollet, et al.
JCI Insight|July 21, 2017
TCR-ligand dissociation rate is a robust and stable biomarker of CD8+ T cell potencyMathilde Allard, Barbara Couturaud, Laura Carretero-Iglesia, et al.
The American Journal of Pathology|April 23, 2003
Angiopoietin-like 4 is a proangiogenic factor produced during ischemia and in conventional renal cell carcinomaSébastien Le Jan, Céline Amy, Aurélie Cazes, et al.
Cutaneous and Ocular Toxicology|March 4, 2020
Tolerability of hair cleansing conditioners: a double-blind randomized, controlled trial designed to evaluate consumer complaints to the U.S. Food and Drug AdministrationErin M Warshaw, Jamie P Schlarbaum, Yujie L Liou, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 21, 2008
Interaction of the coiled-coil domain with glycosaminoglycans protects angiopoietin-like 4 from proteolysis and regulates its antiangiogenic activityClémence Chomel, Aurélie Cazes, Clément Faye, et al.
Journal of Assisted Reproduction and Genetics|February 5, 2026
Effectiveness of preimplantation genetic testing in sickle cell disease: insights from a single-center experienceA Aganahi, F Souare, A Mayeur, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndromeA Cano, C Rouzier, S Monnot, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 18, 2020
Homozygous Loss-of-Function Mutations in CCDC134 Are Responsible for a Severe Form of Osteogenesis ImperfectaJohanne Dubail, Perrine Brunelle, Geneviève Baujat, et al.
Prenatal Diagnosis|February 20, 2019
Prenatal diagnosis of fragile X syndrome: Small meiotic recombination events at the FMR1 locusSéverine Bacrot, Sophie Monnot, Georges Haddad, et al.
Development (Cambridge, England)|October 18, 2013
Knockdown of col22a1 gene in zebrafish induces a muscular dystrophy by disruption of the myotendinous junctionBenjamin Charvet, Alexandre Guiraud, Marilyne Malbouyres, et al.
Pageof 34

Showing results (271-280 of 338) with videos related to

Sort By:
Pageof 34
JBMR Plus|April 7, 2026
A rare coexistence: Ollier disease and primary hyperparathyroidism-mere coincidence or expanding the spectrum of Ollier disease?Justine Luciano, Astrid Dauchez, Beatrix Cochand-Priollet, et al.
JCI Insight|July 21, 2017
TCR-ligand dissociation rate is a robust and stable biomarker of CD8+ T cell potencyMathilde Allard, Barbara Couturaud, Laura Carretero-Iglesia, et al.
The American Journal of Pathology|April 23, 2003
Angiopoietin-like 4 is a proangiogenic factor produced during ischemia and in conventional renal cell carcinomaSébastien Le Jan, Céline Amy, Aurélie Cazes, et al.
Cutaneous and Ocular Toxicology|March 4, 2020
Tolerability of hair cleansing conditioners: a double-blind randomized, controlled trial designed to evaluate consumer complaints to the U.S. Food and Drug AdministrationErin M Warshaw, Jamie P Schlarbaum, Yujie L Liou, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 21, 2008
Interaction of the coiled-coil domain with glycosaminoglycans protects angiopoietin-like 4 from proteolysis and regulates its antiangiogenic activityClémence Chomel, Aurélie Cazes, Clément Faye, et al.
Journal of Assisted Reproduction and Genetics|February 5, 2026
Effectiveness of preimplantation genetic testing in sickle cell disease: insights from a single-center experienceA Aganahi, F Souare, A Mayeur, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndromeA Cano, C Rouzier, S Monnot, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 18, 2020
Homozygous Loss-of-Function Mutations in CCDC134 Are Responsible for a Severe Form of Osteogenesis ImperfectaJohanne Dubail, Perrine Brunelle, Geneviève Baujat, et al.
Prenatal Diagnosis|February 20, 2019
Prenatal diagnosis of fragile X syndrome: Small meiotic recombination events at the FMR1 locusSéverine Bacrot, Sophie Monnot, Georges Haddad, et al.
Development (Cambridge, England)|October 18, 2013
Knockdown of col22a1 gene in zebrafish induces a muscular dystrophy by disruption of the myotendinous junctionBenjamin Charvet, Alexandre Guiraud, Marilyne Malbouyres, et al.
Pageof 34