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Michalle Soudack

Showing results (51-60 of 56) with videos related to

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Pediatric Research|March 5, 2022
Treatment of severe Kaposiform lymphangiomatosis positive for NRAS mutation by MEK inhibitionGuy Chowers, Gadi Abebe-Campino, Hana Golan, et al.
Journal of the American Society of Nephrology : JASN|March 23, 2013
Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signalingAsaf Vivante, Michal Mark-Danieli, Miriam Davidovits, et al.
Scientific Reports|June 9, 2017
The first Neanderthal remains from an open-air Middle Palaeolithic site in the LevantElla Been, Erella Hovers, Ravid Ekshtain, et al.
Molecular Genetics and Metabolism|August 26, 2019
Cerebral and portal vein thrombosis, macrocephaly and atypical absence seizures in Glycosylphosphatidyl inositol deficiency due to a PIGM promoter mutationBen Pode-Shakked, Gali Heimer, Thierry Vilboux, et al.
The Journal of Experimental Medicine|July 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defectsAmos J Simon, Atar Lev, Yong Zhang, et al.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Pediatric Research|March 5, 2022
Treatment of severe Kaposiform lymphangiomatosis positive for NRAS mutation by MEK inhibitionGuy Chowers, Gadi Abebe-Campino, Hana Golan, et al.
Journal of the American Society of Nephrology : JASN|March 23, 2013
Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signalingAsaf Vivante, Michal Mark-Danieli, Miriam Davidovits, et al.
Scientific Reports|June 9, 2017
The first Neanderthal remains from an open-air Middle Palaeolithic site in the LevantElla Been, Erella Hovers, Ravid Ekshtain, et al.
Molecular Genetics and Metabolism|August 26, 2019
Cerebral and portal vein thrombosis, macrocephaly and atypical absence seizures in Glycosylphosphatidyl inositol deficiency due to a PIGM promoter mutationBen Pode-Shakked, Gali Heimer, Thierry Vilboux, et al.
The Journal of Experimental Medicine|July 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defectsAmos J Simon, Atar Lev, Yong Zhang, et al.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Pageof 6