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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
February 9, 2012
[Individual genome sequencing]
Dag E Undlien
Bioinformatics (Oxford, England)
|
April 10, 2024
shinyseg: a web application for flexible cosegregation and sensitivity analysis
Christian Carrizosa, Dag E Undlien, Magnus D Vigeland
Pediatric Diabetes
|
March 1, 2011
Does the relative risk for type 1 diabetes conferred by HLA-DQ, INS, and PTPN22 polymorphisms vary with maternal age, birth weight, or cesarean section?
Lars C Stene, Kjersti S Rønningen, Dag E Undlien, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 6, 2009
T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency
Eirik Bratland, Beate Skinningsrud, Dag E Undlien, et al.
Pediatric Diabetes
|
November 10, 2009
An inverse association between history of childhood eczema and subsequent risk of type 1 diabetes that is not likely to be explained by HLA-DQ, PTPN22, or CTLA4 polymorphisms
Lars C Stene, Kjersti S Rønningen, Marit Bjørnvold, et al.
Journal of Biomolecular Screening
|
January 28, 2009
Genome-wide linkage analysis with clustered SNP markers
Kaja K Selmer, Kristin Brandal, Ole K Olstad, et al.
Arthritis and Rheumatism
|
July 13, 2002
A gene in the telomeric HLA complex distinct from HLA-A is involved in predisposition to juvenile idiopathic arthritis
Anna Smerdel, Benedicte A Lie, Rafal Ploski, et al.
Human Immunology
|
October 3, 2003
No evidence of type 1 diabetes susceptibility genes in the region centromeric of the HLA complex
Stefan Johansson, Benedicte A Lie, Anne Cambon-Thomsen, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
March 8, 2013
Childhood lung function and the association with β2-adrenergic receptor haplotypes
Tale M Torjussen, Monica C Munthe-Kaas, Petter Mowinckel, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 24, 2009
X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene
Beate Skinningsrud, Eystein S Husebye, Gregor D Gilfillan, et al.
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of 5
Search research articles
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Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
February 9, 2012
[Individual genome sequencing]
Dag E Undlien
Bioinformatics (Oxford, England)
|
April 10, 2024
shinyseg: a web application for flexible cosegregation and sensitivity analysis
Christian Carrizosa, Dag E Undlien, Magnus D Vigeland
Pediatric Diabetes
|
March 1, 2011
Does the relative risk for type 1 diabetes conferred by HLA-DQ, INS, and PTPN22 polymorphisms vary with maternal age, birth weight, or cesarean section?
Lars C Stene, Kjersti S Rønningen, Dag E Undlien, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 6, 2009
T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency
Eirik Bratland, Beate Skinningsrud, Dag E Undlien, et al.
Pediatric Diabetes
|
November 10, 2009
An inverse association between history of childhood eczema and subsequent risk of type 1 diabetes that is not likely to be explained by HLA-DQ, PTPN22, or CTLA4 polymorphisms
Lars C Stene, Kjersti S Rønningen, Marit Bjørnvold, et al.
Journal of Biomolecular Screening
|
January 28, 2009
Genome-wide linkage analysis with clustered SNP markers
Kaja K Selmer, Kristin Brandal, Ole K Olstad, et al.
Arthritis and Rheumatism
|
July 13, 2002
A gene in the telomeric HLA complex distinct from HLA-A is involved in predisposition to juvenile idiopathic arthritis
Anna Smerdel, Benedicte A Lie, Rafal Ploski, et al.
Human Immunology
|
October 3, 2003
No evidence of type 1 diabetes susceptibility genes in the region centromeric of the HLA complex
Stefan Johansson, Benedicte A Lie, Anne Cambon-Thomsen, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
March 8, 2013
Childhood lung function and the association with β2-adrenergic receptor haplotypes
Tale M Torjussen, Monica C Munthe-Kaas, Petter Mowinckel, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 24, 2009
X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene
Beate Skinningsrud, Eystein S Husebye, Gregor D Gilfillan, et al.
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of 5