Published in Hautarzt on October 01, 2007
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Transgenic expression of the chemokine receptor encoded by human herpesvirus 8 induces an angioproliferative disease resembling Kaposi's sarcoma. J Exp Med (2000) 2.21
Two novel IL-1 family members, IL-1 delta and IL-1 epsilon, function as an antagonist and agonist of NF-kappa B activation through the orphan IL-1 receptor-related protein 2. J Immunol (2001) 2.03
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Very early cytological and DNA-cytometric diagnosis of in situ carcinoma in an immunosuppressed liver transplant recipient. J Oral Pathol Med (2006) 1.49
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Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss. Br J Dermatol (2012) 1.44
Fatal hepatic failure with liposomal doxorubicin. Lancet (1993) 1.41
Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia. Hum Mol Genet (1998) 1.34
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Obtaining interpretable fuzzy classification rules from medical data. Artif Intell Med (1999) 1.24
A gene for universal congenital alopecia maps to chromosome 8p21-22. Am J Hum Genet (1998) 1.23
Methylation of SOCS-3 and SOCS-1 in the carcinogenesis of Barrett's adenocarcinoma. Gut (2007) 1.22
Role of integrin alphaE(CD103)beta7 for tissue-specific epidermal localization of CD8+ T lymphocytes. J Invest Dermatol (2001) 1.20
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Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patients. Genes Chromosomes Cancer (1999) 1.08
Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes. Hum Mutat (1997) 1.07
[Accumulation of tattoo pigment in sentinel lymph nodes]. Hautarzt (2009) 1.05
The BH3-only member Noxa causes apoptosis in melanoma cells by multiple pathways. Oncogene (2008) 1.01
Decline of infectious skin manifestations in the era of highly active antiretroviral therapy. AIDS (2000) 1.00
Uptake and trafficking of DNA in keratinocytes: evidence for DNA-binding proteins. Gene Ther (2004) 1.00
MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma. Oncogenesis (2012) 1.00
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A novel missense mutation in the DNA mismatch repair gene hMLH1 present among East Asians but not among Europeans. Hum Hered (1998) 0.99
[Metastatic Crohn disease. Atypical manifestation]. Hautarzt (2010) 0.98
Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness. Br J Dermatol (2011) 0.97
Enantioselective high-performance liquid chromatography assay of (+)R- and (-)S-alpha-lipoic acid in human plasma. Chirality (1997) 0.97
Differential chemokine expression in chronic GVHD of the conjunctiva. Bone Marrow Transplant (2010) 0.96
MSH6 mutation in Muir-Torre syndrome: could this be a rare finding? Br J Dermatol (2007) 0.96
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Agonists of proteinase-activated receptor-2 modulate human neutrophil cytokine secretion, expression of cell adhesion molecules, and migration within 3-D collagen lattices. J Leukoc Biol (2004) 0.95
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Repeated epicutaneous exposures to ovalbumin progressively induce atopic dermatitis-like skin lesions in mice. Clin Exp Allergy (2007) 0.93
Topical tacrolimus for pyoderma gangrenosum. Lancet (1998) 0.92
The TRAF1/C5 locus confers risk for familial and severe alopecia areata. Br J Dermatol (2009) 0.92
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3. Am J Hum Genet (2000) 0.92
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Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic study. Am J Dermatopathol (1999) 0.90
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The history of photography in dermatology. Milestones from the roots to the 20th century. Arch Dermatol (1996) 0.89
The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata. Br J Dermatol (2007) 0.88
Investigation of selected cytokine genes suggests that IL2RA and the TNF/LTA locus are risk factors for severe alopecia areata. Br J Dermatol (2012) 0.88
Loss of the PLA2G2A gene in a sporadic colorectal tumor of a patient with a PLA2G2A germline mutation and absence of PLA2G2A germline alterations in patients with FAP. Hum Genet (1997) 0.87
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Opposing effects of high- and low-molecular weight hyaluronan on CXCL12-induced CXCR4 signaling depend on CD44. Cell Death Dis (2013) 0.87
Identification of functional genes during Fas-mediated apoptosis using a randomly fragmented cDNA library. Cell Mol Life Sci (2005) 0.87
[Hemiatrophia faciei progressiva (Parry-Romberg-syndrome) ]. Hautarzt (2006) 0.87
Structure and function of proteins of the phosphotransferase system and of 6-phospho-beta-glycosidases in gram-positive bacteria. FEMS Microbiol Rev (1993) 0.86
Gene expression in actinic keratoses: pharmacological modulation by imiquimod. Br J Dermatol (2004) 0.86
High serum IgE concentrations: association with HLA-DR and markers on chromosome 5q31 and chromosome 11q13. J Allergy Clin Immunol (1997) 0.86
Pyoderma gangrenosum: another cutaneous side-effect of sunitinib? Br J Dermatol (2008) 0.86
Viral interference during simultaneous transduction with two independent helper-free retroviral vectors. Hum Gene Ther (1996) 0.85
[Embolia cutis medicamentosa after subcutaneous injection of pegylated interferon-alpha]. Hautarzt (2005) 0.84
[Androgenetic alopecia. Current aspects of a common phenotype]. Hautarzt (2003) 0.84
Split tibialis posterior tendon transfer with concomitant distal tibial derotational osteotomy in children with cerebral palsy. J Pediatr Orthop (2001) 0.84
Topical tacrolimus for recalcitrant leg ulcer in rheumatoid arthritis. Rheumatology (Oxford) (2000) 0.84
[Rare types of vasculitis as markers of plasmocytoma]. Hautarzt (2006) 0.84
[Subungual squamous cell carcinoma. An important differential diagnosis of subungual tumors]. Hautarzt (2009) 0.84
Evidence for a polygenic contribution to androgenetic alopecia. Br J Dermatol (2013) 0.83
[Infantile hemangioma. Successful treatment with propranolol]. Hautarzt (2010) 0.83
Liposomal doxorubicin in AIDS-related Kaposi's sarcoma. Lancet (1993) 0.83
The second ECVAM workshop on phototoxicity testing. The report and recommendations of ECVAM workshop 42. Altern Lab Anim (2001) 0.83
Fine mapping of the human AR/EDA2R locus in androgenetic alopecia. Br J Dermatol (2010) 0.82
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Panniculitis due to potassium bromide. Brain Dev (1998) 0.81
Effects of streptozotocin-induced diabetes in domestic pigs with focus on the amino acid metabolism. Lab Anim (2009) 0.81
[Galli-Galli disease. Clinical and histopathological investigation using a case series of 18 patients]. Hautarzt (2011) 0.81
Calgranulin C is overexpressed in lesional psoriasis. J Invest Dermatol (2000) 0.81
Topical FK506: suppression of allergic and irritant contact dermatitis in the guinea pig. Arch Dermatol Res (1994) 0.81
Multiple eruptive myxoid dermatofibromas: report of first case and review of literature. Br J Dermatol (2007) 0.81
Acute generalized exanthematous pustulosis following a Loxosceles spider bite in Great Britain. Br J Dermatol (2009) 0.81
[Incontinentia pigmenti (Bloch-Sulzberger syndrome)]. Hautarzt (2010) 0.81
[Therapy with epidermal growth factor receptor inhibitors. Clinical spectrum of cutaneous adverse effects]. Hautarzt (2010) 0.81
Determination of retigabine and its acetyl metabolite in biological matrices by on-line solid-phase extraction (column switching) liquid chromatography with tandem mass spectrometry. J Chromatogr B Biomed Sci Appl (2000) 0.81
Metastatic colon cancer triggering an acute attack of variegate porphyria. Int J Colorectal Dis (2008) 0.81
Concentrations of the atherogenic Lp(a) are elevated in FH. Eur J Hum Genet (1998) 0.81
[Pityriasis rubra pilaris]. Hautarzt (2004) 0.80
Applications of tacrolimus for the treatment of skin disorders. Immunopharmacology (2000) 0.80
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family. Br J Dermatol (2000) 0.80
Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue. Hum Genet (1997) 0.80
A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp. Br J Dermatol (2005) 0.80
[Successful treatment of a professional tattoo with the R20 method]. Hautarzt (2014) 0.80
Topical tacrolimus for the treatment of inflammatory skin diseases. Expert Opin Pharmacother (2001) 0.80
[Trombiculiasis in humans]. Hautarzt (2008) 0.79
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach. Br J Dermatol (2002) 0.79