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Gerard Pals

Showing results (61-70 of 90) with videos related to

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Scientific Reports|August 29, 2022
Osteogenic transdifferentiation of primary human fibroblasts to osteoblast-like cells with human platelet lysateFerdy K Cayami, Lauria Claeys, Ruben de Ruiter, et al.
European Journal of Human Genetics : EJHG|November 11, 2010
The clinical spectrum of complete FBN1 allele deletionsYvonne Hilhorst-Hofstee, Ben C J Hamel, Joke B G M Verheij, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
Familial Ehlers-Danlos syndrome with lethal arterial events caused by a mutation in COL5A1Glen R Monroe, Magdalena Harakalova, Saskia N van der Crabben, et al.
Scientific Reports|May 27, 2018
An in vitro method to keep human aortic tissue sections functionally and structurally intactJorn P Meekel, Menno E Groeneveld, Natalija Bogunovic, et al.
Bone|March 13, 2019
Evolution of heterotopic bone in fibrodysplasia ossificans progressiva: An [<sup>18</sup>F]NaF PET/CT studyEsmée Botman, Pieter G H M Raijmakers, Maqsood Yaqub, et al.
Circulation. Cardiovascular Genetics|January 24, 2015
Beneficial Outcome of Losartan Therapy Depends on Type of FBN1 Mutation in Marfan SyndromeRomy Franken, Alexander W den Hartog, Teodora Radonic, et al.
Cancer Research|April 3, 2003
Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative methodFrans B L Hogervorst, Petra M Nederlof, Johan J P Gille, et al.
American Journal of Human Genetics|December 25, 2012
Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesiaAlexandros Onoufriadis, Tamara Paff, Dinu Antony, et al.
American Journal of Human Genetics|January 3, 2017
Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm DefectsTamara Paff, Niki T Loges, Isabella Aprea, et al.
Molecular Human Reproduction|June 23, 2004
The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentasCees B M Oudejans, Joyce Mulders, Augusta M A Lachmeijer, et al.
Pageof 9

Showing results (61-70 of 90) with videos related to

Sort By:
Pageof 9
Scientific Reports|August 29, 2022
Osteogenic transdifferentiation of primary human fibroblasts to osteoblast-like cells with human platelet lysateFerdy K Cayami, Lauria Claeys, Ruben de Ruiter, et al.
European Journal of Human Genetics : EJHG|November 11, 2010
The clinical spectrum of complete FBN1 allele deletionsYvonne Hilhorst-Hofstee, Ben C J Hamel, Joke B G M Verheij, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
Familial Ehlers-Danlos syndrome with lethal arterial events caused by a mutation in COL5A1Glen R Monroe, Magdalena Harakalova, Saskia N van der Crabben, et al.
Scientific Reports|May 27, 2018
An in vitro method to keep human aortic tissue sections functionally and structurally intactJorn P Meekel, Menno E Groeneveld, Natalija Bogunovic, et al.
Bone|March 13, 2019
Evolution of heterotopic bone in fibrodysplasia ossificans progressiva: An [<sup>18</sup>F]NaF PET/CT studyEsmée Botman, Pieter G H M Raijmakers, Maqsood Yaqub, et al.
Circulation. Cardiovascular Genetics|January 24, 2015
Beneficial Outcome of Losartan Therapy Depends on Type of FBN1 Mutation in Marfan SyndromeRomy Franken, Alexander W den Hartog, Teodora Radonic, et al.
Cancer Research|April 3, 2003
Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative methodFrans B L Hogervorst, Petra M Nederlof, Johan J P Gille, et al.
American Journal of Human Genetics|December 25, 2012
Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesiaAlexandros Onoufriadis, Tamara Paff, Dinu Antony, et al.
American Journal of Human Genetics|January 3, 2017
Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm DefectsTamara Paff, Niki T Loges, Isabella Aprea, et al.
Molecular Human Reproduction|June 23, 2004
The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentasCees B M Oudejans, Joyce Mulders, Augusta M A Lachmeijer, et al.
Pageof 9