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Showing results (411-420 of 469) with videos related to

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Nature Communications|August 17, 2023
C16orf72/HAPSTR1/TAPR1 functions with BRCA1/Senataxin to modulate replication-associated R-loops and confer resistance to PARP disruptionAbhishek Bharadwaj Sharma, Muhammad Khairul Ramlee, Joel Kosmin, et al.
Blood|January 29, 2011
Global gene expression analysis of human erythroid progenitorsAlison T Merryweather-Clarke, Ann Atzberger, Shamit Soneji, et al.
Biochimica Et Biophysica Acta|September 27, 2000
Localization, expression and genomic structure of the gene encoding the human serine protease testisinJ D Hooper, N Bowen, H Marshall, et al.
Nature Communications|September 23, 2018
A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactionsJill M Brown, Nigel A Roberts, Bryony Graham, et al.
Nature|June 10, 2021
Defining genome architecture at base-pair resolutionPeng Hua, Mohsin Badat, Lars L P Hanssen, et al.
Blood|January 21, 2014
Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expressionVip Viprakasit, Supachai Ekwattanakit, Suchada Riolueang, et al.
Science (New York, N.Y.)|May 27, 2006
A regulatory SNP causes a human genetic disease by creating a new transcriptional promoterMarco De Gobbi, Vip Viprakasit, Jim R Hughes, et al.
Haematologica|May 30, 2013
Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type IChristian Babbs, Nigel A Roberts, Luis Sanchez-Pulido, et al.
Nature Communications|July 2, 2026
CDIN1-Codanin-1 complex defective in congenital dyserythropoietic anaemia type I is an RNA nucleaseSanja Brolih, Hafiz Saqib Ali, Caroline Scott, et al.
The EMBO Journal|November 8, 2011
An interspecies analysis reveals a key role for unmethylated CpG dinucleotides in vertebrate Polycomb complex recruitmentMagnus D Lynch, Andrew J H Smith, Marco De Gobbi, et al.
Pageof 47

Showing results (411-420 of 469) with videos related to

Sort By:
Pageof 47
Nature Communications|August 17, 2023
C16orf72/HAPSTR1/TAPR1 functions with BRCA1/Senataxin to modulate replication-associated R-loops and confer resistance to PARP disruptionAbhishek Bharadwaj Sharma, Muhammad Khairul Ramlee, Joel Kosmin, et al.
Blood|January 29, 2011
Global gene expression analysis of human erythroid progenitorsAlison T Merryweather-Clarke, Ann Atzberger, Shamit Soneji, et al.
Biochimica Et Biophysica Acta|September 27, 2000
Localization, expression and genomic structure of the gene encoding the human serine protease testisinJ D Hooper, N Bowen, H Marshall, et al.
Nature Communications|September 23, 2018
A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactionsJill M Brown, Nigel A Roberts, Bryony Graham, et al.
Nature|June 10, 2021
Defining genome architecture at base-pair resolutionPeng Hua, Mohsin Badat, Lars L P Hanssen, et al.
Blood|January 21, 2014
Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expressionVip Viprakasit, Supachai Ekwattanakit, Suchada Riolueang, et al.
Science (New York, N.Y.)|May 27, 2006
A regulatory SNP causes a human genetic disease by creating a new transcriptional promoterMarco De Gobbi, Vip Viprakasit, Jim R Hughes, et al.
Haematologica|May 30, 2013
Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type IChristian Babbs, Nigel A Roberts, Luis Sanchez-Pulido, et al.
Nature Communications|July 2, 2026
CDIN1-Codanin-1 complex defective in congenital dyserythropoietic anaemia type I is an RNA nucleaseSanja Brolih, Hafiz Saqib Ali, Caroline Scott, et al.
The EMBO Journal|November 8, 2011
An interspecies analysis reveals a key role for unmethylated CpG dinucleotides in vertebrate Polycomb complex recruitmentMagnus D Lynch, Andrew J H Smith, Marco De Gobbi, et al.
Pageof 47