Search research articles
Contact Us
Filters
Showing results (51-60 of 57) with videos related to
Page
of 6
Sort By:
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 deficiency
Vi 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 hematopoiesis
Madison 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 iPSCs
Carolina 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 degradation
Michelle 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 FAIM2
Sheridan H Littleton, Khanh B Trang, Christina M Volpe, et al.
Journal of General Internal Medicine
|
January 25, 2008
Part-time physicians...prevalent, connected, and satisfied
Hilit 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 leukemia
Astrid Wintering, Anna Hecht, Julia Meyer, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 57) with videos related to
Sort By:
Page
of 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 deficiency
Vi 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 hematopoiesis
Madison 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 iPSCs
Carolina 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 degradation
Michelle 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 FAIM2
Sheridan H Littleton, Khanh B Trang, Christina M Volpe, et al.
Journal of General Internal Medicine
|
January 25, 2008
Part-time physicians...prevalent, connected, and satisfied
Hilit 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 leukemia
Astrid Wintering, Anna Hecht, Julia Meyer, et al.
Page
of 6