Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Daniel Halperin

Showing results (41-50 of 57) with videos related to

Pageof 6
Sort By:
Journal of Medical Genetics|July 3, 2023
<i>SMARCA4</i> mutation causes human otosclerosis and a similar phenotype in miceMax Drabkin, Matan M Jean, Yael Noy, et al.
Brain : a Journal of Neurology|March 24, 2017
SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndromeYonatan Perez, Zamir Shorer, Keren Liani-Leibson, et al.
Annals of Surgical Oncology|April 8, 2018
Preoperative Fluorouracil, Doxorubicin, and Streptozocin for the Treatment of Pancreatic Neuroendocrine Liver MetastasesJordan M Cloyd, Kiyohiko Omichi, Takashi Mizuno, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 28, 2025
Phase II Trial of Atezolizumab and Bevacizumab for Treatment of HPV-Positive Unresectable or Metastatic Squamous Cell Carcinoma of the Anal CanalVan K Morris, Suyu Liu, Kangyu Lin, et al.
NPJ Genomic Medicine|August 14, 2023
IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and colobomaOhad Wormser, Yonatan Perez, Vadim Dolgin, et al.
British Journal of Haematology|March 23, 2023
Venetoclax ramp-up strategies for chronic lymphocytic leukaemia in the United Kingdom: a real world multicentre retrospective studyRocio Figueroa-Mora, Alexandros Rampotas, Daniel Halperin, et al.
European Journal of Human Genetics : EJHG|February 7, 2019
SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndromeOhad Wormser, Libe Gradstein, Yuval Yogev, et al.
Human Genetics|April 12, 2024
VARista: a free web platform for streamlined whole-genome variant analysis across T2T, hg38, and hg19Noam Hadar, Vadim Dolgin, Katya Oustinov, et al.
Lancet (London, England)|June 8, 2024
[<sup>177</sup>Lu]Lu-DOTA-TATE plus long-acting octreotide versus high‑dose long-acting octreotide for the treatment of newly diagnosed, advanced grade 2-3, well-differentiated, gastroenteropancreatic neuroendocrine tumours (NETTER-2): an open-label, randomised, phase 3 studySimron Singh, Daniel Halperin, Sten Myrehaug, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Cortical tension as a mechanical barrier to safeguard against premature differentiation during neurogenesisDaniel Halperin, Chrystian Junqueira Alves, Marcelle Rodrigues Lemos, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|July 3, 2023
<i>SMARCA4</i> mutation causes human otosclerosis and a similar phenotype in miceMax Drabkin, Matan M Jean, Yael Noy, et al.
Brain : a Journal of Neurology|March 24, 2017
SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndromeYonatan Perez, Zamir Shorer, Keren Liani-Leibson, et al.
Annals of Surgical Oncology|April 8, 2018
Preoperative Fluorouracil, Doxorubicin, and Streptozocin for the Treatment of Pancreatic Neuroendocrine Liver MetastasesJordan M Cloyd, Kiyohiko Omichi, Takashi Mizuno, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 28, 2025
Phase II Trial of Atezolizumab and Bevacizumab for Treatment of HPV-Positive Unresectable or Metastatic Squamous Cell Carcinoma of the Anal CanalVan K Morris, Suyu Liu, Kangyu Lin, et al.
NPJ Genomic Medicine|August 14, 2023
IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and colobomaOhad Wormser, Yonatan Perez, Vadim Dolgin, et al.
British Journal of Haematology|March 23, 2023
Venetoclax ramp-up strategies for chronic lymphocytic leukaemia in the United Kingdom: a real world multicentre retrospective studyRocio Figueroa-Mora, Alexandros Rampotas, Daniel Halperin, et al.
European Journal of Human Genetics : EJHG|February 7, 2019
SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndromeOhad Wormser, Libe Gradstein, Yuval Yogev, et al.
Human Genetics|April 12, 2024
VARista: a free web platform for streamlined whole-genome variant analysis across T2T, hg38, and hg19Noam Hadar, Vadim Dolgin, Katya Oustinov, et al.
Lancet (London, England)|June 8, 2024
[<sup>177</sup>Lu]Lu-DOTA-TATE plus long-acting octreotide versus high‑dose long-acting octreotide for the treatment of newly diagnosed, advanced grade 2-3, well-differentiated, gastroenteropancreatic neuroendocrine tumours (NETTER-2): an open-label, randomised, phase 3 studySimron Singh, Daniel Halperin, Sten Myrehaug, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Cortical tension as a mechanical barrier to safeguard against premature differentiation during neurogenesisDaniel Halperin, Chrystian Junqueira Alves, Marcelle Rodrigues Lemos, et al.
Pageof 6