H Luthman - JoVE Visualize

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European Journal of Endocrinology|June 28, 2000

Characterisation of novel missense mutations in the GH receptor gene causing severe growth retardationB Enberg, H Luthman, K Segnestam, et al.

Diabetologia|January 1, 1993

DNA polymorphisms in the human tyrosine hydroxylase/insulin/insulin-like growth factor II chromosomal region in relation to glucose and insulin responsesM Sten-Linder, A Wedell, L Iselius, et al.

Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|August 23, 2002

Analysis of association and linkage for the interleukin-4 and interleukin-4 receptor b;alpha; regions in Swedish atopic dermatitis familiesC Söderhäll, M Bradley, I Kockum, et al.

Genomics|March 1, 1992

Contiguous localization of the genes encoding human insulin-like growth factor binding proteins 1 (IGBP1) and 3 (IGBP3) on chromosome 7E Ehrenborg, C Larsson, I Stern, et al.

Human Genetics|August 21, 2001

Linkage and association to candidate regions in Swedish atopic dermatitis familiesC Söderhäll, M Bradley, I Kockum, et al.

Diabetes|December 2, 1999

Pathophysiological and genetic characterization of the major diabetes locus in GK ratsJ Galli, H Fakhrai-Rad, A Kamel, et al.

Acta Dermato-Venereologica|January 22, 2002

The Wiskott-Aldrich syndrome gene as a candidate gene for atopic dermatitisM Bradley, C Söderhäll, C F Wahlgren, et al.

Human Genetics|May 1, 1992

Localization of the human insulin-like growth-factor-binding protein 4 gene to chromosomal region 17q12-21.1S Bajalica, S V Allander, E Ehrenborg, et al.

Diabetes|November 28, 2001

Phenotyping of individual pancreatic islets locates genetic defects in stimulus secretion coupling to Niddm1i within the major diabetes locus in GK ratsJ M Lin, H Ortsäter, H Fakhrai-Rad, et al.

Journal of Immunology (Baltimore, Md. : 1950)|February 11, 1999

A conformation-dependent epitope in Addison's disease and other endocrinological autoimmune diseases maps to a carboxyl-terminal functional domain of human steroid 21-hydroxylaseA Nikoshkov, A Falorni, S Lajic, et al.

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Showing results (41-50 of 83) with videos related to

Sort By:

Pageof 9

European Journal of Endocrinology|June 28, 2000

Characterisation of novel missense mutations in the GH receptor gene causing severe growth retardationB Enberg, H Luthman, K Segnestam, et al.

Diabetologia|January 1, 1993

DNA polymorphisms in the human tyrosine hydroxylase/insulin/insulin-like growth factor II chromosomal region in relation to glucose and insulin responsesM Sten-Linder, A Wedell, L Iselius, et al.

Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|August 23, 2002

Analysis of association and linkage for the interleukin-4 and interleukin-4 receptor b;alpha; regions in Swedish atopic dermatitis familiesC Söderhäll, M Bradley, I Kockum, et al.

Genomics|March 1, 1992

Contiguous localization of the genes encoding human insulin-like growth factor binding proteins 1 (IGBP1) and 3 (IGBP3) on chromosome 7E Ehrenborg, C Larsson, I Stern, et al.

Human Genetics|August 21, 2001

Linkage and association to candidate regions in Swedish atopic dermatitis familiesC Söderhäll, M Bradley, I Kockum, et al.

Diabetes|December 2, 1999

Pathophysiological and genetic characterization of the major diabetes locus in GK ratsJ Galli, H Fakhrai-Rad, A Kamel, et al.

Acta Dermato-Venereologica|January 22, 2002

The Wiskott-Aldrich syndrome gene as a candidate gene for atopic dermatitisM Bradley, C Söderhäll, C F Wahlgren, et al.

Human Genetics|May 1, 1992

Localization of the human insulin-like growth-factor-binding protein 4 gene to chromosomal region 17q12-21.1S Bajalica, S V Allander, E Ehrenborg, et al.

Diabetes|November 28, 2001

Phenotyping of individual pancreatic islets locates genetic defects in stimulus secretion coupling to Niddm1i within the major diabetes locus in GK ratsJ M Lin, H Ortsäter, H Fakhrai-Rad, et al.

Journal of Immunology (Baltimore, Md. : 1950)|February 11, 1999

A conformation-dependent epitope in Addison's disease and other endocrinological autoimmune diseases maps to a carboxyl-terminal functional domain of human steroid 21-hydroxylaseA Nikoshkov, A Falorni, S Lajic, et al.

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