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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
November 9, 2005
[Molecular diagnostics in diabetes mellitus]
Lise Bjørkhaug, Stefan Johansson, Helge Raeder, et al.
BMC Genomics
|
November 23, 2012
Limitations and possibilities of low cell number ChIP-seq
Gregor D Gilfillan, Timothy Hughes, Ying Sheng, et al.
European Journal of Human Genetics : EJHG
|
February 28, 2008
Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease
Beate Skinningsrud, Eystein S Husebye, Kristina Gervin, et al.
Pigment Cell Research
|
January 15, 2005
CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases
Anne Blomhoff, E Helen Kemp, David J Gawkrodger, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 3, 2008
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency
Beate Skinningsrud, Eystein S Husebye, Simon H Pearce, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 9, 2004
Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease
Anne Blomhoff, Benedicte A Lie, Anne G Myhre, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 12, 2002
Autoimmune adrenocortical failure in Norway autoantibodies and human leukocyte antigen class II associations related to clinical features
Anne Grethe Myhre, Dag E Undlien, Kristian Løvås, et al.
Plos Genetics
|
February 1, 2012
DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes
Kristina Gervin, Magnus D Vigeland, Morten Mattingsdal, et al.
Genome Research
|
September 28, 2011
Extensive variation and low heritability of DNA methylation identified in a twin study
Kristina Gervin, Martin Hammerø, Hanne E Akselsen, et al.
Human Immunology
|
June 23, 2007
Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease
Benedicte A Lie, Marte K Viken, Hanne E Akselsen, et al.
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Search research articles
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Showing results (11-20 of 44) with videos related to
Sort By:
Page
of 5
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
November 9, 2005
[Molecular diagnostics in diabetes mellitus]
Lise Bjørkhaug, Stefan Johansson, Helge Raeder, et al.
BMC Genomics
|
November 23, 2012
Limitations and possibilities of low cell number ChIP-seq
Gregor D Gilfillan, Timothy Hughes, Ying Sheng, et al.
European Journal of Human Genetics : EJHG
|
February 28, 2008
Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease
Beate Skinningsrud, Eystein S Husebye, Kristina Gervin, et al.
Pigment Cell Research
|
January 15, 2005
CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases
Anne Blomhoff, E Helen Kemp, David J Gawkrodger, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 3, 2008
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency
Beate Skinningsrud, Eystein S Husebye, Simon H Pearce, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 9, 2004
Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease
Anne Blomhoff, Benedicte A Lie, Anne G Myhre, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 12, 2002
Autoimmune adrenocortical failure in Norway autoantibodies and human leukocyte antigen class II associations related to clinical features
Anne Grethe Myhre, Dag E Undlien, Kristian Løvås, et al.
Plos Genetics
|
February 1, 2012
DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes
Kristina Gervin, Magnus D Vigeland, Morten Mattingsdal, et al.
Genome Research
|
September 28, 2011
Extensive variation and low heritability of DNA methylation identified in a twin study
Kristina Gervin, Martin Hammerø, Hanne E Akselsen, et al.
Human Immunology
|
June 23, 2007
Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease
Benedicte A Lie, Marte K Viken, Hanne E Akselsen, et al.
Page
of 5