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Gerard Pals

Showing results (21-30 of 90) with videos related to

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Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|December 5, 2017
Betaglycan (TGFBR3) up-regulation correlates with increased TGF-β signaling in Marfan patient fibroblasts in vitroMenno Evert Groeneveld, Natalija Bogunovic, René John Philip Musters, et al.
Archives of Otolaryngology--Head & Neck Surgery|July 23, 2003
Delineating genetic pathways of disease progression in head and neck squamous cell carcinomaMaria J Worsham, Gerard Pals, Jan P Schouten, et al.
Frontiers in Endocrinology|March 27, 2023
Exploration of the skeletal phenotype of the <i>Col1a1</i> <sup>+/Mov13</sup> mouse model for haploinsufficient osteogenesis imperfecta type 1Lauria Claeys, Lidiia Zhytnik, Lisanne E Wisse, et al.
European Journal of Human Genetics : EJHG|August 11, 2011
EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfectaFleur S van Dijk, Peter H Byers, Raymond Dalgleish, et al.
International Journal of Molecular Sciences|March 28, 2024
In Vitro Modelling of Osteogenesis Imperfecta with Patient-Derived Induced Mesenchymal Stem CellsLauria Claeys, Lidiia Zhytnik, Laura Ventura, et al.
The Journal of Biological Chemistry|February 25, 2005
Mutations near amino end of alpha1(I) collagen cause combined osteogenesis imperfecta/Ehlers-Danlos syndrome by interference with N-propeptide processingWayne A Cabral, Elena Makareeva, Alain Colige, et al.
Genes|March 25, 2022
Phenotypic Variation in Vietnamese Osteogenesis Imperfecta Patients Sharing a Recessive <i>P3H1</i> Pathogenic VariantLidiia Zhytnik, Binh Ho Duy, Marelise Eekhoff, et al.
Molecular Genetics & Genomic Medicine|June 18, 2019
The first family with adult osteogenesis imperfecta caused by a novel homozygous mutation in CREB3L1Ferdy K Cayami, Alessandra Maugeri, Sanne Treurniet, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 16, 2010
Lethal/severe osteogenesis imperfecta in a large family: a novel homozygous LEPRE1 mutation and bone histological findingsFleur S van Dijk, Peter G J Nikkels, Nicolette S den Hollander, et al.
Bone|July 15, 2017
Periodontal ligament fibroblasts as a cell model to study osteogenesis and osteoclastogenesis in fibrodysplasia ossificans progressivaTeun J de Vries, Ton Schoenmaker, Dimitra Micha, et al.
Pageof 9

Showing results (21-30 of 90) with videos related to

Sort By:
Pageof 9
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|December 5, 2017
Betaglycan (TGFBR3) up-regulation correlates with increased TGF-β signaling in Marfan patient fibroblasts in vitroMenno Evert Groeneveld, Natalija Bogunovic, René John Philip Musters, et al.
Archives of Otolaryngology--Head & Neck Surgery|July 23, 2003
Delineating genetic pathways of disease progression in head and neck squamous cell carcinomaMaria J Worsham, Gerard Pals, Jan P Schouten, et al.
Frontiers in Endocrinology|March 27, 2023
Exploration of the skeletal phenotype of the <i>Col1a1</i> <sup>+/Mov13</sup> mouse model for haploinsufficient osteogenesis imperfecta type 1Lauria Claeys, Lidiia Zhytnik, Lisanne E Wisse, et al.
European Journal of Human Genetics : EJHG|August 11, 2011
EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfectaFleur S van Dijk, Peter H Byers, Raymond Dalgleish, et al.
International Journal of Molecular Sciences|March 28, 2024
In Vitro Modelling of Osteogenesis Imperfecta with Patient-Derived Induced Mesenchymal Stem CellsLauria Claeys, Lidiia Zhytnik, Laura Ventura, et al.
The Journal of Biological Chemistry|February 25, 2005
Mutations near amino end of alpha1(I) collagen cause combined osteogenesis imperfecta/Ehlers-Danlos syndrome by interference with N-propeptide processingWayne A Cabral, Elena Makareeva, Alain Colige, et al.
Genes|March 25, 2022
Phenotypic Variation in Vietnamese Osteogenesis Imperfecta Patients Sharing a Recessive <i>P3H1</i> Pathogenic VariantLidiia Zhytnik, Binh Ho Duy, Marelise Eekhoff, et al.
Molecular Genetics & Genomic Medicine|June 18, 2019
The first family with adult osteogenesis imperfecta caused by a novel homozygous mutation in CREB3L1Ferdy K Cayami, Alessandra Maugeri, Sanne Treurniet, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 16, 2010
Lethal/severe osteogenesis imperfecta in a large family: a novel homozygous LEPRE1 mutation and bone histological findingsFleur S van Dijk, Peter G J Nikkels, Nicolette S den Hollander, et al.
Bone|July 15, 2017
Periodontal ligament fibroblasts as a cell model to study osteogenesis and osteoclastogenesis in fibrodysplasia ossificans progressivaTeun J de Vries, Ton Schoenmaker, Dimitra Micha, et al.
Pageof 9