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A proline-90 residue unique to SUMO-4 prevents maturation and sumoylation

Biochemical and biophysical research communications, 2005-11, Vol.337 (2), p.517-520

2005

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Pro-453 to ser mutation in CYP21 is associated with nonclassic steroid 21-hydroxylase deficiency

Molecular endocrinology (Baltimore, Md.), 1992-08, Vol.6 (8), p.1211-1215

1992

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Nonclassic adrenal hyperplasia : current concepts

The journal of clinical endocrinology and metabolism, 1994-04, Vol.78 (4), p.810-815

1994

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Salt-wasting congenital adrenal hyperplasia : detection and characterization of mutations in the steroid 21-hydroxylase gene, CYP21, using the polymerase chain reaction

The journal of clinical endocrinology and metabolism, 1992-03, Vol.74 (3), p.553-558

1992

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Association of a CAG/CAA repeat sequence in the TBP gene with type I diabetes

Biochemical and biophysical research communications, 2004-10, Vol.323 (3), p.865-869

2004

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Genetics of diabetes in Nauru: effects of foreign admixture, HLA antigens and the insulin-gene-linked polymorphism

Diabetologia, 1983-07, Vol.25 (1), p.13-17

1983

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Oligonucleotide probes for HLA-DQA and DQB genes define susceptibility to type 1 (insulin-dependent) diabetes mellitus

Diabetologia, 1988-10, Vol.31 (10), p.751-757

1988

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Molecular Genetics of 21-Hydroxylase Deficient Late-Onset Adrenal Hyperplasia

Seminars in reproductive medicine, 1993-11, Vol.11 (4), p.347-352

1993

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Characterization of three HLA-DR beta genes isolated from an HLA-DR 3/4 insulin-dependent diabetic patient

Immunogenetics (New York), 1986-07, Vol.24 (1), p.41-46

1986

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Hairy leukemic cells which hyperexpress Ii do not demonstrate Ii genome alterations by restriction endonuclease analysis

American journal of hematology, 1987-07, Vol.25 (3), p.285-289

1987

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Association of polar amino acids at position 26 of the HLA-DQB1 first domain with the anticentromere autoantibody response in systemic sclerosis (Scleroderma)

The Journal of clinical investigation, 1992-04, Vol.89 (4), p.1208-1213

1992

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DNA insertion sequences near the insulin gene are not associated with maturity-onset diabetes of young people

Diabetologia, 1983-07, Vol.25 (1), p.18-20

1983

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Insulin-gene flanking sequences, diabetes mellitus and atherosclerosis: a review

Diabetologia, 1985-08, Vol.28 (8), p.556-564

1985

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Clinical review 56: Nonclassic adrenal hyperplasia: current concepts

The journal of clinical endocrinology and metabolism, 1994-04, Vol.78 (4), p.810-815

1994

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Direct analysis of CYP21B genes in 21-hydroxylase deficiency using polymerase chain reaction amplification

Molecular endocrinology (Baltimore, Md.), 1990, Vol.4 (1), p.125-131

1990

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Diabetes mellitus, atherosclerosis, and the 5′ flanking polymorphism of the human insulin gene

Journal of inherited metabolic disease, 1986-03, Vol.9 (S1), p.98-110

1986

Volltextzugriff (PDF)

Analysis of a 1963-bp polymorphic region flanking the human insulin gene

Gene, 1984-12, Vol.32 (3), p.475-479

1984

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Gestational diabetes mellitus is associated with HLA-DQ beta-chain DNA endonuclease fragments

Diabetes research (Edinburgh, Scotland), 1987-11, Vol.6 (3), p.109

1987

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New approaches to therapy and diagnosis of diabetes

Diabetologia, 1982-02, Vol.22 (2), p.61-67

1982

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Clinical review 56: Nonclassic adrenal hyperplasia: current concepts

The journal of clinical endocrinology and metabolism, 1994-04, Vol.78 (4), p.810-815

1994

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Linkage analyses in type I diabetes mellitus using CASPAR, a software and statistical program for conditional analysis of polygenic diseases

Human heredity, 1997-07, Vol.47 (4), p.211-222

1997

Volltextzugriff (PDF)

Identification of an HLA-DQ beta-chain related genomic sequence associated with insulin-dependent diabetes

Biomedica biochimica acta, 1985, Vol.44 (1), p.33

1985

Volltextzugriff (PDF)

Pro-453 to Ser mutation in CYP21 is associated with nonclassic steroid 21-hydroxylase deficiency

Molecular endocrinology (Baltimore, Md.), 1992-08, Vol.6 (8), p.1211-1215

1992

Volltextzugriff (PDF)

Salt-wasting congenital adrenal hyperplasia: detection and characterization of mutations in the steroid 21-hydroxylase gene, CYP21, using the polymerase chain reaction

The journal of clinical endocrinology and metabolism, 1992-03, Vol.74 (3), p.553-558

1992

Volltextzugriff (PDF)

Noninstrumental Determination of Silver in Fixing Baths — an Extension

Journal of the SMPTE, 1968-08, Vol.77 (8), p.809-810

1968

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A proline-90 residue unique to SUMO-4 prevents maturation and sumoylation

Pro-453 to ser mutation in CYP21 is associated with nonclassic steroid 21-hydroxylase deficiency

Nonclassic adrenal hyperplasia : current concepts

Salt-wasting congenital adrenal hyperplasia : detection and characterization of mutations in the steroid 21-hydroxylase gene, CYP21, using the polymerase chain reaction

Association of a CAG/CAA repeat sequence in the TBP gene with type I diabetes

Genetics of diabetes in Nauru: effects of foreign admixture, HLA antigens and the insulin-gene-linked polymorphism

Oligonucleotide probes for HLA-DQA and DQB genes define susceptibility to type 1 (insulin-dependent) diabetes mellitus

Molecular Genetics of 21-Hydroxylase Deficient Late-Onset Adrenal Hyperplasia

Characterization of three HLA-DR beta genes isolated from an HLA-DR 3/4 insulin-dependent diabetic patient

Hairy leukemic cells which hyperexpress Ii do not demonstrate Ii genome alterations by restriction endonuclease analysis

Association of polar amino acids at position 26 of the HLA-DQB1 first domain with the anticentromere autoantibody response in systemic sclerosis (Scleroderma)

DNA insertion sequences near the insulin gene are not associated with maturity-onset diabetes of young people

Insulin-gene flanking sequences, diabetes mellitus and atherosclerosis: a review

Clinical review 56: Nonclassic adrenal hyperplasia: current concepts

Direct analysis of CYP21B genes in 21-hydroxylase deficiency using polymerase chain reaction amplification

Diabetes mellitus, atherosclerosis, and the 5′ flanking polymorphism of the human insulin gene

Analysis of a 1963-bp polymorphic region flanking the human insulin gene

Gestational diabetes mellitus is associated with HLA-DQ beta-chain DNA endonuclease fragments

New approaches to therapy and diagnosis of diabetes

Clinical review 56: Nonclassic adrenal hyperplasia: current concepts

Linkage analyses in type I diabetes mellitus using CASPAR, a software and statistical program for conditional analysis of polygenic diseases

Identification of an HLA-DQ beta-chain related genomic sequence associated with insulin-dependent diabetes

Pro-453 to Ser mutation in CYP21 is associated with nonclassic steroid 21-hydroxylase deficiency

Salt-wasting congenital adrenal hyperplasia: detection and characterization of mutations in the steroid 21-hydroxylase gene, CYP21, using the polymerase chain reaction

Noninstrumental Determination of Silver in Fixing Baths — an Extension

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