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Daniel Grinberg

Showing results (141-150 of 181) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 8, 2013
Analyses of RANK and RANKL in the post-GWAS context: functional evidence of vitamin D stimulation through a RANKL distal regionGuy Yoskovitz, Natalia Garcia-Giralt, Maria Rodriguez-Sanz, et al.
Archivos Argentinos De Pediatria|March 3, 2015
[Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses]Francisco Cammarata-Scalisi, Mónica Cozar, Daniel Grinberg, et al.
European Journal of Human Genetics : EJHG|March 17, 2019
DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patientsRoser Urreizti, Klaus Mayer, Gilad D Evrony, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 23, 2011
COL1A1 haplotypes and hip fractureRoser Urreizti, Natàlia Garcia-Giralt, José A Riancho, et al.
European Journal of Human Genetics : EJHG|September 4, 2019
Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patientsRoser Urreizti, Klaus Mayer, Gilad D Evrony, et al.
American Journal of Medical Genetics. Part A|January 16, 2016
Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromesRoser Urreizti, Neus Roca-Ayats, Judith Trepat, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|September 15, 2022
Carbon footprint of atrial fibrillation catheter ablationGeoffroy Ditac, Pierre-Jean Cottinet, Minh Quyen Le, et al.
The International Journal of Biochemistry & Cell Biology|August 2, 2014
Selective chaperone effect of aminocyclitol derivatives on G202R and other mutant glucocerebrosidases causing Gaucher diseaseJenny Serra-Vinardell, Lucía Díaz, Hugo Gutiérrez-de Terán, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 5, 2011
Functional relevance of the BMD-associated polymorphism rs312009: novel involvement of RUNX2 in LRP5 transcriptional regulationLídia Agueda, Rafael Velázquez-Cruz, Roser Urreizti, et al.
JBMR Plus|December 23, 2020
Functional Assessment of Coding and Regulatory Variants From the <i>DKK1</i> LocusNúria Martínez-Gil, Neus Roca-Ayats, Nurgül Atalay, et al.
Pageof 19

Showing results (141-150 of 181) with videos related to

Sort By:
Pageof 19
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 8, 2013
Analyses of RANK and RANKL in the post-GWAS context: functional evidence of vitamin D stimulation through a RANKL distal regionGuy Yoskovitz, Natalia Garcia-Giralt, Maria Rodriguez-Sanz, et al.
Archivos Argentinos De Pediatria|March 3, 2015
[Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses]Francisco Cammarata-Scalisi, Mónica Cozar, Daniel Grinberg, et al.
European Journal of Human Genetics : EJHG|March 17, 2019
DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patientsRoser Urreizti, Klaus Mayer, Gilad D Evrony, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 23, 2011
COL1A1 haplotypes and hip fractureRoser Urreizti, Natàlia Garcia-Giralt, José A Riancho, et al.
European Journal of Human Genetics : EJHG|September 4, 2019
Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patientsRoser Urreizti, Klaus Mayer, Gilad D Evrony, et al.
American Journal of Medical Genetics. Part A|January 16, 2016
Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromesRoser Urreizti, Neus Roca-Ayats, Judith Trepat, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|September 15, 2022
Carbon footprint of atrial fibrillation catheter ablationGeoffroy Ditac, Pierre-Jean Cottinet, Minh Quyen Le, et al.
The International Journal of Biochemistry & Cell Biology|August 2, 2014
Selective chaperone effect of aminocyclitol derivatives on G202R and other mutant glucocerebrosidases causing Gaucher diseaseJenny Serra-Vinardell, Lucía Díaz, Hugo Gutiérrez-de Terán, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 5, 2011
Functional relevance of the BMD-associated polymorphism rs312009: novel involvement of RUNX2 in LRP5 transcriptional regulationLídia Agueda, Rafael Velázquez-Cruz, Roser Urreizti, et al.
JBMR Plus|December 23, 2020
Functional Assessment of Coding and Regulatory Variants From the <i>DKK1</i> LocusNúria Martínez-Gil, Neus Roca-Ayats, Nurgül Atalay, et al.
Pageof 19