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Guillaume Smits

Showing results (11-20 of 60) with videos related to

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Experimental Dermatology|July 24, 2022
Comparative study of keratinocyte primary culture methods from paediatric skin biopsies for RNA-sequencingDéborah Salik, Yousra El Kaderi, Christine Hans, et al.
Pulmonary Circulation|June 23, 2022
Early-onset and severe pulmonary arterial hypertension due to a novel compound heterozygous association of rare <i>VHL</i> mutations: A case report and review of existing dataLaura Chomette, Isabelle Migeotte, Céline Dewachter, et al.
Clinical Epigenetics|December 16, 2022
Identification of differentially methylated regions in rare diseases from a single-patient perspectiveRobin Grolaux, Alexis Hardy, Catharina Olsen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 16, 2005
Premature ovarian aging in mice deficient for Gpr3Catherine Ledent, Isabelle Demeestere, David Blum, et al.
Artificial Intelligence in Medicine|October 14, 2019
Using game theory and decision decomposition to effectively discern and characterise bi-locus diseasesNassim Versbraegen, Aziz Fouché, Charlotte Nachtegael, et al.
Database : the Journal of Biological Databases and Curation|April 12, 2022
Scaling up oligogenic diseases research with OLIDA: the Oligogenic Diseases DatabaseCharlotte Nachtegael, Barbara Gravel, Arnau Dillen, et al.
Journal of Perinatal Medicine|January 1, 2022
Rarity of fetal cells in exocervical samples for noninvasive prenatal diagnosisLaura Bourlard, Yannick Manigart, Catherine Donner, et al.
Nature Cell Biology|June 12, 2012
The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1rAndrew Keniry, David Oxley, Paul Monnier, et al.
The Journal of Clinical Endocrinology and Metabolism|December 8, 2004
Prediction of severity of symptoms in iatrogenic ovarian hyperstimulation syndrome by follicle-stimulating hormone receptor Ser680Asn polymorphismCaroline Daelemans, Guillaume Smits, Viviane de Maertelaer, et al.
The Journal of Clinical Endocrinology and Metabolism|March 6, 2004
A mutation in the follicle-stimulating hormone receptor as a cause of familial spontaneous ovarian hyperstimulation syndromeLucia Montanelli, Anne Delbaere, Costantino Di Carlo, et al.
Pageof 6

Showing results (11-20 of 60) with videos related to

Sort By:
Pageof 6
Experimental Dermatology|July 24, 2022
Comparative study of keratinocyte primary culture methods from paediatric skin biopsies for RNA-sequencingDéborah Salik, Yousra El Kaderi, Christine Hans, et al.
Pulmonary Circulation|June 23, 2022
Early-onset and severe pulmonary arterial hypertension due to a novel compound heterozygous association of rare <i>VHL</i> mutations: A case report and review of existing dataLaura Chomette, Isabelle Migeotte, Céline Dewachter, et al.
Clinical Epigenetics|December 16, 2022
Identification of differentially methylated regions in rare diseases from a single-patient perspectiveRobin Grolaux, Alexis Hardy, Catharina Olsen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 16, 2005
Premature ovarian aging in mice deficient for Gpr3Catherine Ledent, Isabelle Demeestere, David Blum, et al.
Artificial Intelligence in Medicine|October 14, 2019
Using game theory and decision decomposition to effectively discern and characterise bi-locus diseasesNassim Versbraegen, Aziz Fouché, Charlotte Nachtegael, et al.
Database : the Journal of Biological Databases and Curation|April 12, 2022
Scaling up oligogenic diseases research with OLIDA: the Oligogenic Diseases DatabaseCharlotte Nachtegael, Barbara Gravel, Arnau Dillen, et al.
Journal of Perinatal Medicine|January 1, 2022
Rarity of fetal cells in exocervical samples for noninvasive prenatal diagnosisLaura Bourlard, Yannick Manigart, Catherine Donner, et al.
Nature Cell Biology|June 12, 2012
The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1rAndrew Keniry, David Oxley, Paul Monnier, et al.
The Journal of Clinical Endocrinology and Metabolism|December 8, 2004
Prediction of severity of symptoms in iatrogenic ovarian hyperstimulation syndrome by follicle-stimulating hormone receptor Ser680Asn polymorphismCaroline Daelemans, Guillaume Smits, Viviane de Maertelaer, et al.
The Journal of Clinical Endocrinology and Metabolism|March 6, 2004
A mutation in the follicle-stimulating hormone receptor as a cause of familial spontaneous ovarian hyperstimulation syndromeLucia Montanelli, Anne Delbaere, Costantino Di Carlo, et al.
Pageof 6