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Monnot

Showing results (331-340 of 338) with videos related to

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American Journal of Human Genetics|December 11, 2012
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephalySandrine Vuillaumier-Barrot, Céline Bouchet-Séraphin, Malika Chelbi, et al.
Molecular Genetics and Metabolism|October 4, 2015
Molecular diagnosis of hypophosphatasia and differential diagnosis by targeted Next Generation SequencingAgnès Taillandier, Christelle Domingues, Clémence De Cazanove, et al.
BMC Medicine|January 15, 2026
Determinants of long-term SARS-CoV-2 immune responses in asymptomatic-to-moderate COVID-19 patients in sub-Saharan AfricaVíctor L de Rioja, Odin Goovaerts, Marta Vidal, et al.
Regulatory Toxicology and Pharmacology : RTP|July 13, 2021
An integrated benefit-risk assessment of cobalt-containing alloys used in medical devices: Implications for regulatory requirements in the European UnionGary Eichenbaum, Jared T Wilsey, Gion Fessel, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 28, 2022
Agonists of prostaglandin E<sub>2</sub> receptors as potential first in class treatment for nephronophthisis and related ciliopathiesHugo Garcia, Alice S Serafin, Flora Silbermann, et al.
Nature Immunology|December 22, 2022
Staphylococcal phosphatidylglycerol antigens activate human T cells via CD1aGwennaëlle C Monnot, Marcin Wegrecki, Tan-Yun Cheng, et al.
Journal of Dental Research|March 23, 2023
Unequal Impact of <i>COL1A1</i> and <i>COL1A2</i> Variants on Dentinogenesis ImperfectaP M Yamaguti, M de La Dure-Molla, S Monnot, et al.
American Journal of Human Genetics|June 11, 2013
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathyGianina Ravenscroft, Satoko Miyatake, Vilma-Lotta Lehtokari, et al.
Pageof 34

Showing results (331-340 of 338) with videos related to

Sort By:
Pageof 34
You have reached the last page of results.This site can display upto 338 results.
American Journal of Human Genetics|December 11, 2012
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephalySandrine Vuillaumier-Barrot, Céline Bouchet-Séraphin, Malika Chelbi, et al.
Molecular Genetics and Metabolism|October 4, 2015
Molecular diagnosis of hypophosphatasia and differential diagnosis by targeted Next Generation SequencingAgnès Taillandier, Christelle Domingues, Clémence De Cazanove, et al.
BMC Medicine|January 15, 2026
Determinants of long-term SARS-CoV-2 immune responses in asymptomatic-to-moderate COVID-19 patients in sub-Saharan AfricaVíctor L de Rioja, Odin Goovaerts, Marta Vidal, et al.
Regulatory Toxicology and Pharmacology : RTP|July 13, 2021
An integrated benefit-risk assessment of cobalt-containing alloys used in medical devices: Implications for regulatory requirements in the European UnionGary Eichenbaum, Jared T Wilsey, Gion Fessel, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 28, 2022
Agonists of prostaglandin E<sub>2</sub> receptors as potential first in class treatment for nephronophthisis and related ciliopathiesHugo Garcia, Alice S Serafin, Flora Silbermann, et al.
Nature Immunology|December 22, 2022
Staphylococcal phosphatidylglycerol antigens activate human T cells via CD1aGwennaëlle C Monnot, Marcin Wegrecki, Tan-Yun Cheng, et al.
Journal of Dental Research|March 23, 2023
Unequal Impact of <i>COL1A1</i> and <i>COL1A2</i> Variants on Dentinogenesis ImperfectaP M Yamaguti, M de La Dure-Molla, S Monnot, et al.
American Journal of Human Genetics|June 11, 2013
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathyGianina Ravenscroft, Satoko Miyatake, Vilma-Lotta Lehtokari, et al.
Pageof 34