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Ignaty Leshchiner

Showing results (11-20 of 64) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2014
Summarizing polygenic risks for complex diseases in a clinical whole-genome reportSek Won Kong, In-Hee Lee, Ignaty Leshchiner, et al.
Biomedicines|November 11, 2022
<i>osr1</i> Maintains Renal Progenitors and Regulates Podocyte Development by Promoting <i>wnt2ba</i> via the Antagonism of <i>hand2</i>Bridgette E Drummond, Brooke E Chambers, Hannah M Wesselman, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2016
Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humansVivian S Lee, Carmen M Halabi, Erin P Hoffman, et al.
Nature Cancer|April 20, 2023
Inferring early genetic progression in cancers with unobtainable premalignant diseaseIgnaty Leshchiner, Edmund A Mroz, Justin Cha, et al.
Blood|March 8, 2021
Activation of the MAPK pathway mediates resistance to PI3K inhibitors in chronic lymphocytic leukemiaIshwarya Murali, Siddha Kasar, Aishath Naeem, et al.
Rheumatology (Oxford, England)|October 24, 2015
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhoodChristopher A Cassa, Stacy E Smith, William Docken, et al.
Biorxiv : the Preprint Server for Biology|May 7, 2026
Bloom syndrome helicase is required for efficient HIV-1 reverse transcription in macrophagesAndrew A Leal, Samantha Tafrate, Xianbao He, et al.
Molecular Genetics & Genomic Medicine|October 6, 2015
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative diseaseSameer S Chopra, Ignaty Leshchiner, Hatice Duzkale, et al.
Developmental Biology|June 6, 2017
The zebrafish kidney mutant zeppelin reveals that brca2/fancd1 is essential for pronephros developmentPaul T Kroeger, Bridgette E Drummond, Rachel Miceli, et al.
Genome Research|May 5, 2012
Mutation mapping and identification by whole-genome sequencingIgnaty Leshchiner, Kristen Alexa, Peter Kelsey, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2014
Summarizing polygenic risks for complex diseases in a clinical whole-genome reportSek Won Kong, In-Hee Lee, Ignaty Leshchiner, et al.
Biomedicines|November 11, 2022
<i>osr1</i> Maintains Renal Progenitors and Regulates Podocyte Development by Promoting <i>wnt2ba</i> via the Antagonism of <i>hand2</i>Bridgette E Drummond, Brooke E Chambers, Hannah M Wesselman, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2016
Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humansVivian S Lee, Carmen M Halabi, Erin P Hoffman, et al.
Nature Cancer|April 20, 2023
Inferring early genetic progression in cancers with unobtainable premalignant diseaseIgnaty Leshchiner, Edmund A Mroz, Justin Cha, et al.
Blood|March 8, 2021
Activation of the MAPK pathway mediates resistance to PI3K inhibitors in chronic lymphocytic leukemiaIshwarya Murali, Siddha Kasar, Aishath Naeem, et al.
Rheumatology (Oxford, England)|October 24, 2015
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhoodChristopher A Cassa, Stacy E Smith, William Docken, et al.
Biorxiv : the Preprint Server for Biology|May 7, 2026
Bloom syndrome helicase is required for efficient HIV-1 reverse transcription in macrophagesAndrew A Leal, Samantha Tafrate, Xianbao He, et al.
Molecular Genetics & Genomic Medicine|October 6, 2015
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative diseaseSameer S Chopra, Ignaty Leshchiner, Hatice Duzkale, et al.
Developmental Biology|June 6, 2017
The zebrafish kidney mutant zeppelin reveals that brca2/fancd1 is essential for pronephros developmentPaul T Kroeger, Bridgette E Drummond, Rachel Miceli, et al.
Genome Research|May 5, 2012
Mutation mapping and identification by whole-genome sequencingIgnaty Leshchiner, Kristen Alexa, Peter Kelsey, et al.
Pageof 7