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BMC Genomics
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April 17, 2015
Different distribution of histone modifications in genes with unidirectional and bidirectional transcription and a role of CTCF and cohesin in directing transcription
Susanne Bornelöv, Jan Komorowski, Claes Wadelius
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms
|
June 25, 2021
Polymorphisms rs55710213 and rs56334587 regulate SCD1 expression by modulating HNF4A binding
Gang Pan, Marco Cavalli, Claes Wadelius
Biodata Mining
|
August 17, 2010
SICTIN: Rapid footprinting of massively parallel sequencing data
Stefan Enroth, Robin Andersson, Claes Wadelius, et al.
Plos One
|
January 14, 2012
Combinations of histone modifications mark exon inclusion levels
Stefan Enroth, Susanne Bornelöv, Claes Wadelius, et al.
Ophthalmic Genetics
|
July 16, 2005
Analysis of rare variants and common haplotypes in the optineurin gene in Swedish glaucoma cases
Mattias Jansson, Claes Wadelius, Tayebeh Rezaie, et al.
Lipids in Health and Disease
|
January 29, 2016
Looking beyond GWAS: allele-specific transcription factor binding drives the association of GALNT2 to HDL-C plasma levels
Marco Cavalli, Gang Pan, Helena Nord, et al.
Molecular Vision
|
March 26, 2003
Evaluation of the Oculomedin gene in the etiology of primary open angle and exfoliative glaucoma
Mattias Jansson, Lidija Tomic, Lill-Inger Larsson, et al.
Acta Ophthalmologica
|
April 27, 2013
Best vitelliform macular dystrophy in a Swedish family: genetic analysis and a seven-year follow-up of photodynamic treatment of a young boy with choroidal neovascularization
Christina I Frennesson, Claes Wadelius, Sven Erik G Nilsson
Molecular Vision
|
November 17, 2005
The promoter of inducible nitric oxide synthase implicated in glaucoma based on genetic analysis and nuclear factor binding
Mehdi Motallebipour, Alvaro Rada-Iglesias, Mattias Jansson, et al.
Nucleic Acids Research
|
May 20, 2009
Identification of candidate regulatory SNPs by combination of transcription-factor-binding site prediction, SNP genotyping and haploChIP
Adam Ameur, Alvaro Rada-Iglesias, Jan Komorowski, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 80) with videos related to
Sort By:
Page
of 8
BMC Genomics
|
April 17, 2015
Different distribution of histone modifications in genes with unidirectional and bidirectional transcription and a role of CTCF and cohesin in directing transcription
Susanne Bornelöv, Jan Komorowski, Claes Wadelius
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms
|
June 25, 2021
Polymorphisms rs55710213 and rs56334587 regulate SCD1 expression by modulating HNF4A binding
Gang Pan, Marco Cavalli, Claes Wadelius
Biodata Mining
|
August 17, 2010
SICTIN: Rapid footprinting of massively parallel sequencing data
Stefan Enroth, Robin Andersson, Claes Wadelius, et al.
Plos One
|
January 14, 2012
Combinations of histone modifications mark exon inclusion levels
Stefan Enroth, Susanne Bornelöv, Claes Wadelius, et al.
Ophthalmic Genetics
|
July 16, 2005
Analysis of rare variants and common haplotypes in the optineurin gene in Swedish glaucoma cases
Mattias Jansson, Claes Wadelius, Tayebeh Rezaie, et al.
Lipids in Health and Disease
|
January 29, 2016
Looking beyond GWAS: allele-specific transcription factor binding drives the association of GALNT2 to HDL-C plasma levels
Marco Cavalli, Gang Pan, Helena Nord, et al.
Molecular Vision
|
March 26, 2003
Evaluation of the Oculomedin gene in the etiology of primary open angle and exfoliative glaucoma
Mattias Jansson, Lidija Tomic, Lill-Inger Larsson, et al.
Acta Ophthalmologica
|
April 27, 2013
Best vitelliform macular dystrophy in a Swedish family: genetic analysis and a seven-year follow-up of photodynamic treatment of a young boy with choroidal neovascularization
Christina I Frennesson, Claes Wadelius, Sven Erik G Nilsson
Molecular Vision
|
November 17, 2005
The promoter of inducible nitric oxide synthase implicated in glaucoma based on genetic analysis and nuclear factor binding
Mehdi Motallebipour, Alvaro Rada-Iglesias, Mattias Jansson, et al.
Nucleic Acids Research
|
May 20, 2009
Identification of candidate regulatory SNPs by combination of transcription-factor-binding site prediction, SNP genotyping and haploChIP
Adam Ameur, Alvaro Rada-Iglesias, Jan Komorowski, et al.
Page
of 8