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Jacek Majewski

Showing results (101-110 of 333) with videos related to

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Przeglad Lekarski|February 24, 2005
[Atrial fibrillation in a long-term follow-up after mitral valve replacement]Jacek Majewski, Maria Sniezek-Maciejewska, Jerzy Sadowski, et al.
Plos One|July 6, 2019
Loss of function mutation of Eftud2, the gene responsible for mandibulofacial dysostosis with microcephaly (MFDM), leads to pre-implantation arrest in mouseMarie-Claude Beauchamp, Anissa Djedid, Kevin Daupin, et al.
Pediatrics|January 16, 2013
Iron refractory iron deficiency anemia: presentation with hyperferritinemia and response to oral iron therapyDong-Anh Khuong-Quang, Jeremy Schwartzentruber, Mark Westerman, et al.
European Journal of Human Genetics : EJHG|November 6, 2014
Meconium ileus in a Lebanese family secondary to mutations in the GUCY2C geneAmanda Smith, Dennis E Bulman, Claire Goldsmith, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2021
Depletion of H3K36me2 recapitulates epigenomic and phenotypic changes induced by the H3.3K36M oncohistone mutationKartik N Rajagopalan, Xiao Chen, Daniel N Weinberg, et al.
Arthritis Research & Therapy|June 2, 2011
Cis-regulation of IRF5 expression is unable to fully account for systemic lupus erythematosus association: analysis of multiple experiments with lymphoblastoid cell linesElisa Alonso-Perez, Marian Suarez-Gestal, Manuel Calaza, et al.
Ophthalmic Genetics|July 16, 2005
HEMICENTIN-1 (FIBULIN-6) and the 1q31 AMD locus in the context of complex disease: review and perspectiveDennis W Schultz, Richard G Weleber, Gus Lawrence, et al.
American Journal of Human Genetics|January 2, 2003
Cold-induced sweating syndrome is caused by mutations in the CRLF1 genePer M Knappskog, Jacek Majewski, Avi Livneh, et al.
Molecular Cell|March 20, 2012
The Sam68 STAR RNA-binding protein regulates mTOR alternative splicing during adipogenesisMarc-Étienne Huot, Gillian Vogel, Amber Zabarauskas, et al.
Scientific Reports|July 19, 2022
Identification of FAT3 as a new candidate gene for adolescent idiopathic scoliosisDina Nada, Cédric Julien, Simon Papillon-Cavanagh, et al.
Pageof 34

Showing results (101-110 of 333) with videos related to

Sort By:
Pageof 34
Przeglad Lekarski|February 24, 2005
[Atrial fibrillation in a long-term follow-up after mitral valve replacement]Jacek Majewski, Maria Sniezek-Maciejewska, Jerzy Sadowski, et al.
Plos One|July 6, 2019
Loss of function mutation of Eftud2, the gene responsible for mandibulofacial dysostosis with microcephaly (MFDM), leads to pre-implantation arrest in mouseMarie-Claude Beauchamp, Anissa Djedid, Kevin Daupin, et al.
Pediatrics|January 16, 2013
Iron refractory iron deficiency anemia: presentation with hyperferritinemia and response to oral iron therapyDong-Anh Khuong-Quang, Jeremy Schwartzentruber, Mark Westerman, et al.
European Journal of Human Genetics : EJHG|November 6, 2014
Meconium ileus in a Lebanese family secondary to mutations in the GUCY2C geneAmanda Smith, Dennis E Bulman, Claire Goldsmith, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2021
Depletion of H3K36me2 recapitulates epigenomic and phenotypic changes induced by the H3.3K36M oncohistone mutationKartik N Rajagopalan, Xiao Chen, Daniel N Weinberg, et al.
Arthritis Research & Therapy|June 2, 2011
Cis-regulation of IRF5 expression is unable to fully account for systemic lupus erythematosus association: analysis of multiple experiments with lymphoblastoid cell linesElisa Alonso-Perez, Marian Suarez-Gestal, Manuel Calaza, et al.
Ophthalmic Genetics|July 16, 2005
HEMICENTIN-1 (FIBULIN-6) and the 1q31 AMD locus in the context of complex disease: review and perspectiveDennis W Schultz, Richard G Weleber, Gus Lawrence, et al.
American Journal of Human Genetics|January 2, 2003
Cold-induced sweating syndrome is caused by mutations in the CRLF1 genePer M Knappskog, Jacek Majewski, Avi Livneh, et al.
Molecular Cell|March 20, 2012
The Sam68 STAR RNA-binding protein regulates mTOR alternative splicing during adipogenesisMarc-Étienne Huot, Gillian Vogel, Amber Zabarauskas, et al.
Scientific Reports|July 19, 2022
Identification of FAT3 as a new candidate gene for adolescent idiopathic scoliosisDina Nada, Cédric Julien, Simon Papillon-Cavanagh, et al.
Pageof 34