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Vitiligo pathogenesis: autoimmune disease, genetic defect, excessive reactive oxygen species, calcium imbalance, or what else?

Experimental dermatology, 2008-02, Vol.17 (2), p.139-140

2008

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Development of a 3D human in vitro skin co-culture model for detecting irritants in real-time

Biotechnology and bioengineering, 2010-08, Vol.106 (5), p.794-803

2010

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Radiation-induced melanoma-associated leucoderma, systemic antimelanoma immunity and disease-free survival in a patient with advanced-stage melanoma: a case report and immunological analysis

British journal of dermatology (1951), 2013-04, Vol.168 (4), p.733-738

2013

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Demonstration of autoantibodies against tyrosine hydroxylase in patients with alopecia areata

British journal of dermatology (1951), 2011-12, Vol.165 (6), p.1236-1243

2011

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The angiotensin-converting enzyme gene insertion/deletion polymorphism in Indian patients with vitiligo: a case-control study and meta-analysis

British journal of dermatology (1951), 2013-06, Vol.168 (6), p.1195-1204

2013

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Epitopes, avidity and IgG subclasses of tyrosine hydroxylase autoantibodies in vitiligo and alopecia areata patients

British journal of dermatology (1951), 2012-07, Vol.167 (1), p.17-28

2012

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Tumour necrosis factor-α antagonists as therapies for vitiligo

British journal of dermatology (1951), 2015-09, Vol.173 (3), p.635-635

Kemp, E.H.

2015

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The CC genotype of the ERCC1 C118T single-nucleotide polymorphism impacts positively on the efficacy of narrowband ultraviolet B therapy for vitiligo

British journal of dermatology (1951), 2015-08, Vol.173 (2), p.324-325

Kemp, E.H.

2015

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Association between the angiotensin-converting enzyme gene insertion/deletion polymorphism and susceptibility to systemic lupus erythematosus in an Indian population

Scandinavian journal of rheumatology, 2015-09, Vol.44 (5), p.425-427

2015

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A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase ( ) confers susceptibility to generalised vitiligo

Genes and immunity, 2005-10, Vol.6 (7), p.584-587

2005

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Antithyroid hormone autoantibodies in vitiligo

British journal of dermatology (1951), 2014-10, Vol.171 (4), p.690-690

Kemp, E.H.

2014

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Programmed death 1 expressing regulatory T cells in vitiligo

British journal of dermatology (1951), 2015-04, Vol.172 (4), p.847-848

Kemp, E.H.

2015

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Melanoma cell migration is upregulated by tumour necrosis factor-α and suppressed by α-melanocyte-stimulating hormone

British journal of cancer, 2004-04, Vol.90 (7), p.1457-1463

2004

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Alemtuzumab-induced halo naevus-like hypopigmentation - new insights into secondary skin autoimmunity in response to an immune cell-depleting antibody

Journal of the European Academy of Dermatology and Venereology, 2021-01, Vol.35 (1), p.e28

2021

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Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease

The journal of clinical endocrinology and metabolism, 2000-02, Vol.85 (2), p.688-691

2000

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Localization of GerAA and GerAC Germination Proteins in the Bacillus subtilis Spore

Journal of Bacteriology, 2001-07, Vol.183 (14), p.4317-4322

2001

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A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients

Clinical endocrinology (Oxford), 1998-11, Vol.49 (5), p.609-613

1998

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Autoantibodies to tyrosinase-related protein-1 detected in the sera of vitiligo patients using a quantitative radiobinding assay

British journal of dermatology (1951), 1998-11, Vol.139 (5), p.798-805

1998

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Vitiligo pathogenesis: autoimmune disease, genetic defect, excessive reactive oxygen species, calcium imbalance, or what else?

Experimental dermatology, 2008-02, Vol.17 (2), p.139-160

2008

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Autoantibodies in vitiligo patients are not directed to the melanocyte differentiation antigen MelanA/MART1

Clinical and experimental immunology, 2002-09, Vol.129 (3), p.527-532

2002

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Analysis of a microsatellite polymorphism of the cytotoxic T-lymphocyte antigen-4 gene in patients with vitiligo

British journal of dermatology (1951), 1999-01, Vol.140 (1), p.73-78

1999

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Molecular mapping of epitopes on melanocyte‐specific protein Pmel17 which are recognized by autoantibodies in patients with vitiligo

Clinical and experimental immunology, 2001-06, Vol.124 (3), p.509-515

2001

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Vitiligo patients from India (Mumbai) show differences in clinical, demographic and autoantibody profiles compared to patients in western countries

Journal of the European Academy of Dermatology and Venereology, 2013-03, Vol.27 (3), p.279-286

2013

Volltextzugriff (PDF)

Graves' Disease, Hypoparathyroidism, Systemic Lupus Erythematosus, Alopecia, and Angioedema: Autoimmune Polyglandular Syndrome Variant or Coincidence?

International journal of immunopathology and pharmacology, 2013-01, Vol.26 (1), p.217-222

2013

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HLA-G does not have a pathophysiological role in Graves’ disease

Journal of clinical pathology, 2003-06, Vol.56 (6), p.475-477

2003

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Vitiligo pathogenesis: autoimmune disease, genetic defect, excessive reactive oxygen species, calcium imbalance, or what else?

Development of a 3D human in vitro skin co-culture model for detecting irritants in real-time

Radiation-induced melanoma-associated leucoderma, systemic antimelanoma immunity and disease-free survival in a patient with advanced-stage melanoma: a case report and immunological analysis

Demonstration of autoantibodies against tyrosine hydroxylase in patients with alopecia areata

The angiotensin-converting enzyme gene insertion/deletion polymorphism in Indian patients with vitiligo: a case-control study and meta-analysis

Epitopes, avidity and IgG subclasses of tyrosine hydroxylase autoantibodies in vitiligo and alopecia areata patients

Tumour necrosis factor-α antagonists as therapies for vitiligo

The CC genotype of the ERCC1 C118T single-nucleotide polymorphism impacts positively on the efficacy of narrowband ultraviolet B therapy for vitiligo

Association between the angiotensin-converting enzyme gene insertion/deletion polymorphism and susceptibility to systemic lupus erythematosus in an Indian population

A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase ( ) confers susceptibility to generalised vitiligo

Antithyroid hormone autoantibodies in vitiligo

Programmed death 1 expressing regulatory T cells in vitiligo

Melanoma cell migration is upregulated by tumour necrosis factor-α and suppressed by α-melanocyte-stimulating hormone

Alemtuzumab-induced halo naevus-like hypopigmentation - new insights into secondary skin autoimmunity in response to an immune cell-depleting antibody

Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease

Localization of GerAA and GerAC Germination Proteins in the Bacillus subtilis Spore

A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients

Autoantibodies to tyrosinase-related protein-1 detected in the sera of vitiligo patients using a quantitative radiobinding assay

Vitiligo pathogenesis: autoimmune disease, genetic defect, excessive reactive oxygen species, calcium imbalance, or what else?

Autoantibodies in vitiligo patients are not directed to the melanocyte differentiation antigen MelanA/MART1

Analysis of a microsatellite polymorphism of the cytotoxic T-lymphocyte antigen-4 gene in patients with vitiligo

Molecular mapping of epitopes on melanocyte‐specific protein Pmel17 which are recognized by autoantibodies in patients with vitiligo

Vitiligo patients from India (Mumbai) show differences in clinical, demographic and autoantibody profiles compared to patients in western countries

Graves' Disease, Hypoparathyroidism, Systemic Lupus Erythematosus, Alopecia, and Angioedema: Autoimmune Polyglandular Syndrome Variant or Coincidence?

HLA-G does not have a pathophysiological role in Graves’ disease

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