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Ann Maguire

Showing results (51-60 of 57) with videos related to

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Molecular Genetics and Metabolism|December 31, 2023
A novel iPSC model reveals selective vulnerability of neurons in multiple sulfatase deficiencyVi Pham, Livia Sertori Finoti, Margaret M Cassidy, et al.
Stem Cell Reports|August 30, 2024
Tropomyosin 1 deficiency facilitates cell state transitions and enhances hemogenic endothelial cell specification during hematopoiesisMadison B Wilken, Gennadiy Fonar, Rong Qiu, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
High density SNP array and reanalysis of genome sequencing uncovers CNVs associated with neurodevelopmental disorders in KOLF2.1J iPSCsCarolina Gracia-Diaz, Jonathan E Perdomo, Munir E Khan, et al.
Blood Advances|February 9, 2021
Restoring RUNX1 deficiency in RUNX1 familial platelet disorder by inhibiting its degradationMichelle C Krutein, Matthew R Hart, Donovan J Anderson, et al.
Cell Genomics|May 2, 2024
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of FAIM2Sheridan H Littleton, Khanh B Trang, Christina M Volpe, et al.
Journal of General Internal Medicine|January 25, 2008
Part-time physicians...prevalent, connected, and satisfiedHilit F Mechaber, Rachel B Levine, Linda Baier Manwell, et al.
Haematologica|December 28, 2023
LNK/<i>SH2B3</i> as a novel driver in juvenile myelomonocytic leukemiaAstrid Wintering, Anna Hecht, Julia Meyer, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Molecular Genetics and Metabolism|December 31, 2023
A novel iPSC model reveals selective vulnerability of neurons in multiple sulfatase deficiencyVi Pham, Livia Sertori Finoti, Margaret M Cassidy, et al.
Stem Cell Reports|August 30, 2024
Tropomyosin 1 deficiency facilitates cell state transitions and enhances hemogenic endothelial cell specification during hematopoiesisMadison B Wilken, Gennadiy Fonar, Rong Qiu, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
High density SNP array and reanalysis of genome sequencing uncovers CNVs associated with neurodevelopmental disorders in KOLF2.1J iPSCsCarolina Gracia-Diaz, Jonathan E Perdomo, Munir E Khan, et al.
Blood Advances|February 9, 2021
Restoring RUNX1 deficiency in RUNX1 familial platelet disorder by inhibiting its degradationMichelle C Krutein, Matthew R Hart, Donovan J Anderson, et al.
Cell Genomics|May 2, 2024
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of FAIM2Sheridan H Littleton, Khanh B Trang, Christina M Volpe, et al.
Journal of General Internal Medicine|January 25, 2008
Part-time physicians...prevalent, connected, and satisfiedHilit F Mechaber, Rachel B Levine, Linda Baier Manwell, et al.
Haematologica|December 28, 2023
LNK/<i>SH2B3</i> as a novel driver in juvenile myelomonocytic leukemiaAstrid Wintering, Anna Hecht, Julia Meyer, et al.
Pageof 6