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American Journal of Medical Genetics. Part A
|
March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants
Pagna Sok, Aniko Sabo, Lynn M Almli, et al.
Blood
|
May 1, 2020
Human erythroleukemia genetics and transcriptomes identify master transcription factors as functional disease drivers
Alexandre Fagnan, Frederik Otzen Bagger, Maria-Riera Piqué-Borràs, et al.
Blood
|
May 6, 2020
The EMT modulator SNAI1 contributes to AML pathogenesis via its interaction with LSD1
Catherine L Carmichael, Jueqiong Wang, Thao Nguyen, et al.
Nature Genetics
|
March 31, 2019
Genomic subtyping and therapeutic targeting of acute erythroleukemia
Ilaria Iacobucci, Ji Wen, Manja Meggendorfer, et al.
Blood
|
July 11, 2024
Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
Jiarna R Zerella, Claire C Homan, Peer Arts, et al.
Blood Advances
|
March 26, 2020
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Anna L Brown, Peer Arts, Catherine L Carmichael, et al.
Genetics in Medicine Open
|
September 30, 2024
Regulatory elements in <i>SEM1-DLX5-DLX6</i> (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits
Paola Nicoletti, Samreen Zafer, Lital Matok, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 29, 2020
Machine learning uncovers the most robust self-report predictors of relationship quality across 43 longitudinal couples studies
Samantha Joel, Paul W Eastwick, Colleen J Allison, et al.
Page
of 55
Search research articles
Search
Showing results (541-550 of 548) with videos related to
Sort By:
Page
of 55
You have reached the last page of results.
This site can display upto 548 results.
American Journal of Medical Genetics. Part A
|
March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants
Pagna Sok, Aniko Sabo, Lynn M Almli, et al.
Blood
|
May 1, 2020
Human erythroleukemia genetics and transcriptomes identify master transcription factors as functional disease drivers
Alexandre Fagnan, Frederik Otzen Bagger, Maria-Riera Piqué-Borràs, et al.
Blood
|
May 6, 2020
The EMT modulator SNAI1 contributes to AML pathogenesis via its interaction with LSD1
Catherine L Carmichael, Jueqiong Wang, Thao Nguyen, et al.
Nature Genetics
|
March 31, 2019
Genomic subtyping and therapeutic targeting of acute erythroleukemia
Ilaria Iacobucci, Ji Wen, Manja Meggendorfer, et al.
Blood
|
July 11, 2024
Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
Jiarna R Zerella, Claire C Homan, Peer Arts, et al.
Blood Advances
|
March 26, 2020
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Anna L Brown, Peer Arts, Catherine L Carmichael, et al.
Genetics in Medicine Open
|
September 30, 2024
Regulatory elements in <i>SEM1-DLX5-DLX6</i> (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits
Paola Nicoletti, Samreen Zafer, Lital Matok, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 29, 2020
Machine learning uncovers the most robust self-report predictors of relationship quality across 43 longitudinal couples studies
Samantha Joel, Paul W Eastwick, Colleen J Allison, et al.
Page
of 55