Search research articles
Contact Us
Filters
Showing results (1-10 of 31) with videos related to
Page
of 4
Sort By:
Cell Reports
|
April 16, 2024
UPF1 regulates mRNA stability by sensing poorly translated coding sequences
Damir Musaev, Mario Abdelmessih, Charles E Vejnar, et al.
Biorxiv : the Preprint Server for Biology
|
May 27, 2024
Novel cell states arise in embryonic cells devoid of key reprogramming factors
Scott E Youlten, Liyun Miao, Caroline Hoppe, et al.
Cell Reports
|
October 31, 2025
In vivo differentiation of embryonic cells devoid of key reprogramming factors
Scott E Youlten, Liyun Miao, Caroline Hoppe, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2016
Extending the mutation spectrum for Galloway-Mowat syndrome to include homozygous missense mutations in the WDR73 gene
Rasim O Rosti, Esra Dikoglu, Maha S Zaki, et al.
Developmental Cell
|
June 19, 2019
Brd4 and P300 Confer Transcriptional Competency during Zygotic Genome Activation
Shun Hang Chan, Yin Tang, Liyun Miao, et al.
Journal of Medical Genetics
|
June 20, 2017
A homozygous founder mutation in <i>TRAPPC6B</i> associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features
Isaac Marin-Valencia, Gaia Novarino, Anide Johansen, et al.
American Journal of Human Genetics
|
July 9, 2016
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly
Martin W Breuss, Tipu Sultan, Kiely N James, et al.
Genome Research
|
June 23, 2019
Genome wide analysis of 3' UTR sequence elements and proteins regulating mRNA stability during maternal-to-zygotic transition in zebrafish
Charles E Vejnar, Mario Abdel Messih, Carter M Takacs, et al.
American Journal of Human Genetics
|
August 22, 2017
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia
Isaac Marin-Valencia, Andreas Gerondopoulos, Maha S Zaki, et al.
Human Molecular Genetics
|
December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability
Martin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 31) with videos related to
Sort By:
Page
of 4
Cell Reports
|
April 16, 2024
UPF1 regulates mRNA stability by sensing poorly translated coding sequences
Damir Musaev, Mario Abdelmessih, Charles E Vejnar, et al.
Biorxiv : the Preprint Server for Biology
|
May 27, 2024
Novel cell states arise in embryonic cells devoid of key reprogramming factors
Scott E Youlten, Liyun Miao, Caroline Hoppe, et al.
Cell Reports
|
October 31, 2025
In vivo differentiation of embryonic cells devoid of key reprogramming factors
Scott E Youlten, Liyun Miao, Caroline Hoppe, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2016
Extending the mutation spectrum for Galloway-Mowat syndrome to include homozygous missense mutations in the WDR73 gene
Rasim O Rosti, Esra Dikoglu, Maha S Zaki, et al.
Developmental Cell
|
June 19, 2019
Brd4 and P300 Confer Transcriptional Competency during Zygotic Genome Activation
Shun Hang Chan, Yin Tang, Liyun Miao, et al.
Journal of Medical Genetics
|
June 20, 2017
A homozygous founder mutation in <i>TRAPPC6B</i> associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features
Isaac Marin-Valencia, Gaia Novarino, Anide Johansen, et al.
American Journal of Human Genetics
|
July 9, 2016
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly
Martin W Breuss, Tipu Sultan, Kiely N James, et al.
Genome Research
|
June 23, 2019
Genome wide analysis of 3' UTR sequence elements and proteins regulating mRNA stability during maternal-to-zygotic transition in zebrafish
Charles E Vejnar, Mario Abdel Messih, Carter M Takacs, et al.
American Journal of Human Genetics
|
August 22, 2017
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia
Isaac Marin-Valencia, Andreas Gerondopoulos, Maha S Zaki, et al.
Human Molecular Genetics
|
December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability
Martin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.
Page
of 4