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Cell
|
July 18, 2015
Integrative Analyses of Human Reprogramming Reveal Dynamic Nature of Induced Pluripotency
Davide Cacchiarelli, Cole Trapnell, Michael J Ziller, et al.
Orphanet Journal of Rare Diseases
|
January 25, 2025
Combined biochemical profiling and DNA sequencing in the expanded newborn screening for inherited metabolic diseases: the experience in an Italian reference center
Simona Fecarotta, Lorenzo Vaccaro, Alessandra Verde, et al.
Cell Stem Cell
|
April 7, 2018
A CLK3-HMGA2 Alternative Splicing Axis Impacts Human Hematopoietic Stem Cell Molecular Identity throughout Development
Marcella Cesana, Michael H Guo, Davide Cacchiarelli, et al.
Nature
|
July 8, 2016
Multiple mechanisms disrupt the let-7 microRNA family in neuroblastoma
John T Powers, Kaloyan M Tsanov, Daniel S Pearson, et al.
Journal of Human Genetics
|
April 30, 2025
Variant sub-tiering, disease-gene associations and strictness of clinical criteria improves the interpretation of variants of uncertain significance in hereditary cardiomyopathies and rhythm disorders
Marco Castori, Sandra Mastroianno, Andrea Fontana, et al.
The EMBO Journal
|
July 28, 2020
MiT/TFE factors control ER-phagy via transcriptional regulation of FAM134B
Laura Cinque, Chiara De Leonibus, Maria Iavazzo, et al.
Nature Communications
|
April 30, 2024
A case of T-cell acute lymphoblastic leukemia in retroviral gene therapy for ADA-SCID
Daniela Cesana, Maria Pia Cicalese, Andrea Calabria, et al.
Biorxiv : the Preprint Server for Biology
|
January 23, 2024
Polygenic risk for schizophrenia converges on alternative polyadenylation as molecular mechanism underlying synaptic impairment
Florian J Raabe, Anna Hausruckinger, Miriam Gagliardi, et al.
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Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Cell
|
July 18, 2015
Integrative Analyses of Human Reprogramming Reveal Dynamic Nature of Induced Pluripotency
Davide Cacchiarelli, Cole Trapnell, Michael J Ziller, et al.
Orphanet Journal of Rare Diseases
|
January 25, 2025
Combined biochemical profiling and DNA sequencing in the expanded newborn screening for inherited metabolic diseases: the experience in an Italian reference center
Simona Fecarotta, Lorenzo Vaccaro, Alessandra Verde, et al.
Cell Stem Cell
|
April 7, 2018
A CLK3-HMGA2 Alternative Splicing Axis Impacts Human Hematopoietic Stem Cell Molecular Identity throughout Development
Marcella Cesana, Michael H Guo, Davide Cacchiarelli, et al.
Nature
|
July 8, 2016
Multiple mechanisms disrupt the let-7 microRNA family in neuroblastoma
John T Powers, Kaloyan M Tsanov, Daniel S Pearson, et al.
Journal of Human Genetics
|
April 30, 2025
Variant sub-tiering, disease-gene associations and strictness of clinical criteria improves the interpretation of variants of uncertain significance in hereditary cardiomyopathies and rhythm disorders
Marco Castori, Sandra Mastroianno, Andrea Fontana, et al.
The EMBO Journal
|
July 28, 2020
MiT/TFE factors control ER-phagy via transcriptional regulation of FAM134B
Laura Cinque, Chiara De Leonibus, Maria Iavazzo, et al.
Nature Communications
|
April 30, 2024
A case of T-cell acute lymphoblastic leukemia in retroviral gene therapy for ADA-SCID
Daniela Cesana, Maria Pia Cicalese, Andrea Calabria, et al.
Biorxiv : the Preprint Server for Biology
|
January 23, 2024
Polygenic risk for schizophrenia converges on alternative polyadenylation as molecular mechanism underlying synaptic impairment
Florian J Raabe, Anna Hausruckinger, Miriam Gagliardi, et al.
Page
of 3