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Stanescu

Showing results (671-680 of 940) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 31, 2017
PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and PrognosisEmilie Cornec-Le Gall, Marie-Pierre Audrézet, Eric Renaudineau, et al.
Nature Communications|August 16, 2022
Skyrmions in synthetic antiferromagnets and their nucleation via electrical current and ultra-fast laser illuminationRoméo Juge, Naveen Sisodia, Joseba Urrestarazu Larrañaga, et al.
Nature Communications|October 26, 2018
A crowdsourced analysis to identify ab initio molecular signatures predictive of susceptibility to viral infectionSlim Fourati, Aarthi Talla, Mehrad Mahmoudian, et al.
The New England Journal of Medicine|May 8, 2009
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutationsDetlef Bockenhauer, Sally Feather, Horia C Stanescu, et al.
Social Science & Medicine (1982)|May 23, 2022
Interventions to promote physical distancing behaviour during infectious disease pandemics or epidemics: A systematic reviewTracy Epton, Daniela Ghio, Lisa M Ballard, et al.
The New England Journal of Medicine|February 18, 2011
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathyHoria C Stanescu, Mauricio Arcos-Burgos, Alan Medlar, et al.
Clinical Kidney Journal|February 10, 2025
Multiethnic prevalence of the <i>APOL1</i> G1 and G2 variants among the Israeli dialysis populationDror Ben-Ruby, Danit Atias-Varon, Maayan Kagan, et al.
European Journal of Human Genetics : EJHG|January 11, 2019
Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening programRosa Navarrete, Fátima Leal, Ana I Vega, et al.
Journal of the American Society of Nephrology : JASN|April 7, 2017
A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations <i>via</i> Dysregulation of Retinoic Acid SignalingAsaf Vivante, Nina Mann, Hagith Yonath, et al.
Journal of Medical Genetics|January 8, 2015
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypesAoife M Waters, Rowan Asfahani, Paula Carroll, et al.
Pageof 94

Showing results (671-680 of 940) with videos related to

Sort By:
Pageof 94
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 31, 2017
PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and PrognosisEmilie Cornec-Le Gall, Marie-Pierre Audrézet, Eric Renaudineau, et al.
Nature Communications|August 16, 2022
Skyrmions in synthetic antiferromagnets and their nucleation via electrical current and ultra-fast laser illuminationRoméo Juge, Naveen Sisodia, Joseba Urrestarazu Larrañaga, et al.
Nature Communications|October 26, 2018
A crowdsourced analysis to identify ab initio molecular signatures predictive of susceptibility to viral infectionSlim Fourati, Aarthi Talla, Mehrad Mahmoudian, et al.
The New England Journal of Medicine|May 8, 2009
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutationsDetlef Bockenhauer, Sally Feather, Horia C Stanescu, et al.
Social Science & Medicine (1982)|May 23, 2022
Interventions to promote physical distancing behaviour during infectious disease pandemics or epidemics: A systematic reviewTracy Epton, Daniela Ghio, Lisa M Ballard, et al.
The New England Journal of Medicine|February 18, 2011
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathyHoria C Stanescu, Mauricio Arcos-Burgos, Alan Medlar, et al.
Clinical Kidney Journal|February 10, 2025
Multiethnic prevalence of the <i>APOL1</i> G1 and G2 variants among the Israeli dialysis populationDror Ben-Ruby, Danit Atias-Varon, Maayan Kagan, et al.
European Journal of Human Genetics : EJHG|January 11, 2019
Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening programRosa Navarrete, Fátima Leal, Ana I Vega, et al.
Journal of the American Society of Nephrology : JASN|April 7, 2017
A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations <i>via</i> Dysregulation of Retinoic Acid SignalingAsaf Vivante, Nina Mann, Hagith Yonath, et al.
Journal of Medical Genetics|January 8, 2015
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypesAoife M Waters, Rowan Asfahani, Paula Carroll, et al.
Pageof 94