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Gerard Pals

Showing results (31-40 of 90) with videos related to

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Human Mutation|October 11, 2007
Genetic subtyping of Fanconi anemia by comprehensive mutation screeningNajim Ameziane, Abdellatif Errami, France Léveillé, et al.
Heart (British Cardiac Society)|May 5, 2017
Relationship between fibrillin-1 genotype and severity of cardiovascular involvement in Marfan syndromeRomy Franken, Gisela Teixido-Tura, Maria Brion, et al.
Bone|January 16, 2016
Inhibition of TGFβ signaling decreases osteogenic differentiation of fibrodysplasia ossificans progressiva fibroblasts in a novel in vitro model of the diseaseDimitra Micha, Elise Voermans, Marelise E W Eekhoff, et al.
American Journal of Medical Genetics. Part A|July 15, 2005
Should chromosome breakage studies be performed in patients with VACTERL association?Laurence Faivre, Marie France Portnoï, Gerard Pals, et al.
Cells|September 14, 2024
Functional Insights in PLS3-Mediated Osteogenic RegulationWenchao Zhong, Janine Neugebauer, Janak L Pathak, et al.
Frontiers in Endocrinology|May 13, 2022
Prevalence and Hospital Admissions in Patients With Osteogenesis Imperfecta in The Netherlands: A Nationwide Registry StudySilvia Storoni, Sanne Treurniet, Alessandra Maugeri, et al.
Human Mutation|June 26, 2014
RNA sequencing of creatine transporter (SLC6A8) deficient fibroblasts reveals impairment of the extracellular matrixBenjamin Nota, Joseph D T Ndika, Jiddeke M van de Kamp, et al.
Peerj|January 10, 2020
Bioactivity of compounds secreted by symbiont bacteria of Nudibranchs from IndonesiaRhesi Kristiana, Gilles Bedoux, Gerard Pals, et al.
Open Heart|December 21, 2022
Growth of the aortic root in children and young adults with Marfan syndromeElroy van Elsäcker, Arja S Vink, Leonie A Menke, et al.
Community Genetics|May 16, 2003
Offering preconceptional cystic fibrosis carrier couple screening in the absence of established preconceptional care servicesLidewij Henneman, Inge Bramsen, Linda van Kempen, et al.
Pageof 9

Showing results (31-40 of 90) with videos related to

Sort By:
Pageof 9
Human Mutation|October 11, 2007
Genetic subtyping of Fanconi anemia by comprehensive mutation screeningNajim Ameziane, Abdellatif Errami, France Léveillé, et al.
Heart (British Cardiac Society)|May 5, 2017
Relationship between fibrillin-1 genotype and severity of cardiovascular involvement in Marfan syndromeRomy Franken, Gisela Teixido-Tura, Maria Brion, et al.
Bone|January 16, 2016
Inhibition of TGFβ signaling decreases osteogenic differentiation of fibrodysplasia ossificans progressiva fibroblasts in a novel in vitro model of the diseaseDimitra Micha, Elise Voermans, Marelise E W Eekhoff, et al.
American Journal of Medical Genetics. Part A|July 15, 2005
Should chromosome breakage studies be performed in patients with VACTERL association?Laurence Faivre, Marie France Portnoï, Gerard Pals, et al.
Cells|September 14, 2024
Functional Insights in PLS3-Mediated Osteogenic RegulationWenchao Zhong, Janine Neugebauer, Janak L Pathak, et al.
Frontiers in Endocrinology|May 13, 2022
Prevalence and Hospital Admissions in Patients With Osteogenesis Imperfecta in The Netherlands: A Nationwide Registry StudySilvia Storoni, Sanne Treurniet, Alessandra Maugeri, et al.
Human Mutation|June 26, 2014
RNA sequencing of creatine transporter (SLC6A8) deficient fibroblasts reveals impairment of the extracellular matrixBenjamin Nota, Joseph D T Ndika, Jiddeke M van de Kamp, et al.
Peerj|January 10, 2020
Bioactivity of compounds secreted by symbiont bacteria of Nudibranchs from IndonesiaRhesi Kristiana, Gilles Bedoux, Gerard Pals, et al.
Open Heart|December 21, 2022
Growth of the aortic root in children and young adults with Marfan syndromeElroy van Elsäcker, Arja S Vink, Leonie A Menke, et al.
Community Genetics|May 16, 2003
Offering preconceptional cystic fibrosis carrier couple screening in the absence of established preconceptional care servicesLidewij Henneman, Inge Bramsen, Linda van Kempen, et al.
Pageof 9