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J Majewski

Showing results (91-100 of 128) with videos related to

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The Journal of Experimental Medicine|March 15, 2023
Overexpression of Lmo2 initiates T-lymphoblastic leukemia via impaired thymocyte competitionHesham D Abdulla, Raed Alserihi, Christoffer Flensburg, et al.
Cancer Research|December 28, 2012
Epigenetic regulator Smchd1 functions as a tumor suppressorHuei San Leong, Kelan Chen, Yifang Hu, et al.
Blood|May 7, 2010
Opposing roles of polycomb repressive complexes in hematopoietic stem and progenitor cellsIan J Majewski, Matthew E Ritchie, Belinda Phipson, et al.
Kidney International|August 3, 2006
Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndromeP Vylet'al, M Kublová, M Kalbácová, et al.
Clinical Genetics|May 21, 2013
WDR19: an ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior-Loken syndromeR G Coussa, E A Otto, H-Y Gee, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 13, 2006
A mutation in the translation initiation codon of Gata-1 disrupts megakaryocyte maturation and causes thrombocytopeniaIan J Majewski, Donald Metcalf, Lisa A Mielke, et al.
Blood|June 4, 2015
Polycomb repressive complex 2 component Suz12 is required for hematopoietic stem cell function and lymphopoiesisStanley C W Lee, Sarah Miller, Craig Hyland, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|February 12, 2021
Combined small-cell lung carcinoma revealed to be an intratumoural metastasis by genetic analysisK D Lach, M Sorin, C Huynh, et al.
Pediatric Blood & Cancer|June 29, 2019
Targeted therapy and disease monitoring in CNTRL-FGFR1-driven leukaemiaLauren M Brown, Ray C Bartolo, Nadia M Davidson, et al.
Clinical Genetics|September 1, 2017
Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathyS Perrier, L Gauquelin, M Tétreault, et al.
Pageof 13

Showing results (91-100 of 128) with videos related to

Sort By:
Pageof 13
The Journal of Experimental Medicine|March 15, 2023
Overexpression of Lmo2 initiates T-lymphoblastic leukemia via impaired thymocyte competitionHesham D Abdulla, Raed Alserihi, Christoffer Flensburg, et al.
Cancer Research|December 28, 2012
Epigenetic regulator Smchd1 functions as a tumor suppressorHuei San Leong, Kelan Chen, Yifang Hu, et al.
Blood|May 7, 2010
Opposing roles of polycomb repressive complexes in hematopoietic stem and progenitor cellsIan J Majewski, Matthew E Ritchie, Belinda Phipson, et al.
Kidney International|August 3, 2006
Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndromeP Vylet'al, M Kublová, M Kalbácová, et al.
Clinical Genetics|May 21, 2013
WDR19: an ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior-Loken syndromeR G Coussa, E A Otto, H-Y Gee, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 13, 2006
A mutation in the translation initiation codon of Gata-1 disrupts megakaryocyte maturation and causes thrombocytopeniaIan J Majewski, Donald Metcalf, Lisa A Mielke, et al.
Blood|June 4, 2015
Polycomb repressive complex 2 component Suz12 is required for hematopoietic stem cell function and lymphopoiesisStanley C W Lee, Sarah Miller, Craig Hyland, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|February 12, 2021
Combined small-cell lung carcinoma revealed to be an intratumoural metastasis by genetic analysisK D Lach, M Sorin, C Huynh, et al.
Pediatric Blood & Cancer|June 29, 2019
Targeted therapy and disease monitoring in CNTRL-FGFR1-driven leukaemiaLauren M Brown, Ray C Bartolo, Nadia M Davidson, et al.
Clinical Genetics|September 1, 2017
Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathyS Perrier, L Gauquelin, M Tétreault, et al.
Pageof 13