Published in Arch Dermatol on November 01, 2012
Multifocal capillary malformations in an older, asymptomatic child with a novel RASA1 mutation. Clin Exp Dermatol (2015) 0.75
De novo mutations of SETBP1 cause Schinzel-Giedion syndrome. Nat Genet (2010) 5.72
Migration matters: regulatory T-cell compartmentalization determines suppressive activity in vivo. Blood (2005) 2.55
Managing comorbid disease in patients with psoriasis. BMJ (2010) 1.89
KINK-1, a novel small-molecule inhibitor of IKKbeta, and the susceptibility of melanoma cells to antitumoral treatment. J Natl Cancer Inst (2008) 1.72
Deadly allies: the fatal interplay between platelets and metastasizing cancer cells. Blood (2010) 1.67
Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population. Eur J Hum Genet (2005) 1.62
Brain-derived neurotrophic factor (BDNF) gene polymorphisms shape cortical plasticity in humans. Brain Stimul (2010) 1.57
Inactivation of insulin-like factor 6 disrupts the progression of spermatogenesis at late meiotic prophase. Endocrinology (2009) 1.52
Xeroderma pigmentosum-variant patients from America, Europe, and Asia. J Invest Dermatol (2008) 1.46
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. Genet Med (2009) 1.38
Monocytes/macrophages prevent healing defects and left ventricular thrombus formation after myocardial infarction. FASEB J (2012) 1.31
Imiquimod, a topical immune response modifier, in the treatment of cutaneous metastases of malignant melanoma. Dermatology (2002) 1.31
Pathways of proliferation and antiapoptosis driven in breast cancer stem cells by stem cell protein piwil2. Cancer Res (2010) 1.26
Tumor-selective induction of apoptosis and the small-molecule immune response modifier imiquimod. J Natl Cancer Inst (2003) 1.25
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance. Hum Mol Genet (2014) 1.25
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum. Eur J Hum Genet (2011) 1.20
A role for caspase-1 in heart failure. Circ Res (2007) 1.13
8-methoxypsoralen plus ultraviolet A therapy acts via inhibition of the IL-23/Th17 axis and induction of Foxp3+ regulatory T cells involving CTLA4 signaling in a psoriasis-like skin disorder. J Immunol (2010) 1.13
Comparative study of human-induced pluripotent stem cells derived from bone marrow cells, hair keratinocytes, and skin fibroblasts. Eur Heart J (2012) 1.10
Junctional adhesion molecules (JAM)-B and -C contribute to leukocyte extravasation to the skin and mediate cutaneous inflammation. J Invest Dermatol (2005) 1.10
The antitumoral mode of action of imiquimod and other imidazoquinolines. Curr Med Chem (2007) 1.09
Functional evaluation of paraplegin mutations by a yeast complementation assay. Hum Mutat (2010) 1.09
P-selectin: a common therapeutic target for cardiovascular disorders, inflammation and tumour metastasis. Expert Opin Ther Targets (2007) 1.06
Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors. Hum Mol Genet (2013) 1.03
Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly. Acta Neuropathol Commun (2014) 0.99
Selection of patients for long-term surveillance with digital dermoscopy by assessment of melanoma risk factors. Arch Dermatol (2010) 0.99
Involvement of IL-9 in Th17-associated inflammation and angiogenesis of psoriasis. PLoS One (2013) 0.99
Anaphylaxis to iodinated contrast material: nonallergic hypersensitivity or IgE-mediated allergy? AJR Am J Roentgenol (2008) 0.98
Reliability of diagnosis of melanoma in situ. Lancet (2002) 0.96
NF-kappaB inhibition through proteasome inhibition or IKKbeta blockade increases the susceptibility of melanoma cells to cytostatic treatment through distinct pathways. J Invest Dermatol (2009) 0.95
Dendritic epidermal T cells (DETC) are diminished in integrin alphaE(CD103)-deficient mice. J Invest Dermatol (2002) 0.94
Damage-induced DNA replication stalling relies on MAPK-activated protein kinase 2 activity. Proc Natl Acad Sci U S A (2013) 0.94
Successful Nd:YAG laser therapy for hair removal in the oral cavity after plastic reconstruction using hairy donor sites. Dermatology (2013) 0.93
Imiquimod, a Toll-like receptor-7 agonist, induces perforin in cytotoxic T lymphocytes in vitro. Mol Immunol (2004) 0.93
Platelet-activating factor blockade inhibits the T-helper type 17 cell pathway and suppresses psoriasis-like skin disease in K5.hTGF-β1 transgenic mice. Am J Pathol (2011) 0.92
FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish. Am J Hum Genet (2011) 0.92
Melanoma arising in segmental nevus spilus: detection by sequential digital dermatoscopy. J Am Acad Dermatol (2009) 0.92
Methotrexate-induced toxic epidermal necrolysis-like skin toxicity. Eur J Dermatol (2007) 0.91
The small heat shock protein ODF1/HSPB10 is essential for tight linkage of sperm head to tail and male fertility in mice. Mol Cell Biol (2011) 0.90
Integrin alpha E(CD103)beta 7 influences cellular shape and motility in a ligand-dependent fashion. Blood (2008) 0.90
Tumor necrosis factor antagonists in the therapy of psoriasis. Clin Dermatol (2008) 0.90
Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2. J Pediatr (2009) 0.90
The dark side of beauty: acne fulminans induced by anabolic steroids in a male bodybuilder. Arch Dermatol (2012) 0.89
Inhibition of platelet GPIb alpha and promotion of melanoma metastasis. J Invest Dermatol (2009) 0.89
Skin cancer in organ transplant recipients: effects of immunosuppressive medications on DNA repair. Exp Dermatol (2012) 0.88
Interfering with leukocyte rolling--a promising therapeutic approach in inflammatory skin disorders? Trends Pharmacol Sci (2003) 0.88
Characterization of three XPG-defective patients identifies three missense mutations that impair repair and transcription. J Invest Dermatol (2013) 0.88
Aminopenicillin-induced exanthema allows treatment with certain cephalosporins or phenoxymethyl penicillin. J Antimicrob Chemother (2007) 0.88
Proteinase-activated receptor-2 (PAR2): a tumor suppressor in skin carcinogenesis. J Invest Dermatol (2007) 0.88
Successful treatment of a large hemangioma with propranolol. J Dtsch Dermatol Ges (2009) 0.87
Animal models of psoriasis. Clin Dermatol (2007) 0.87
Junctional adhesion molecule (JAM)-B supports lymphocyte rolling and adhesion through interaction with alpha4beta1 integrin. Immunology (2009) 0.87
Adhesion maturation of neutrophils on nanoscopically presented platelet glycoprotein Ibα. ACS Nano (2013) 0.87
PECAM-1 polymorphism affects monocyte adhesion to endothelial cells. Transplantation (2008) 0.86
Successful treatment of severe keratosis pilaris rubra with a 595-nm pulsed dye laser. Dermatol Surg (2009) 0.86
A 3p interstitial deletion in two monozygotic twin brothers and an 18-year-old man: further characterization and review. Am J Med Genet A (2013) 0.85
Recommendations for detection of individual risk for comorbidities in patients with psoriasis. Arch Dermatol Res (2013) 0.85
Targeting leukocyte trafficking to inflamed skin: still an attractive therapeutic approach? Exp Dermatol (2007) 0.85
Expression of gp130 in tumors and inflammatory disorders of the skin: formal proof of its identity as CD146 (MUC18, Mel-CAM). J Invest Dermatol (2005) 0.85
The complex clinical picture of side effects to anticoagulation. Med Clin North Am (2010) 0.85
Overexpression of peroxisomal testis-specific 1 protein induces germ cell apoptosis and leads to infertility in male mice. Mol Biol Cell (2011) 0.85
Development of segmental superficial actinic porokeratosis during immunosuppressive therapy for pemphigus vulgaris. Acta Derm Venereol (2010) 0.85
Impaired induction of adhesion molecule expression in immortalized endothelial cells leads to functional defects in dynamic interactions with lymphocytes. J Invest Dermatol (2007) 0.84
Neural peptidase endothelin-converting enzyme 1 regulates endothelin 1-induced pruritus. J Clin Invest (2014) 0.84
Cutaneous side effects of inhibition of VEGF signal transduction. J Dtsch Dermatol Ges (2009) 0.84
Functional and molecular genetic analyses of nine newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes. Exp Dermatol (2013) 0.84
Cyclosporin A, but not everolimus, inhibits DNA repair mediated by calcineurin: implications for tumorigenesis under immunosuppression. Exp Dermatol (2011) 0.84
Seven-point checklist for dermatoscopy: performance during 10 years of prospective surveillance of patients at increased melanoma risk. J Am Acad Dermatol (2010) 0.84
Cyclosporin A inhibits nucleotide excision repair via downregulation of the xeroderma pigmentosum group A and G proteins, which is mediated by calcineurin inhibition. Exp Dermatol (2011) 0.84
Molecular biology of basal and squamous cell carcinomas. Adv Exp Med Biol (2014) 0.83
Downregulation of endothelial adhesion molecules by dimethylfumarate, but not monomethylfumarate, and impairment of dynamic lymphocyte-endothelial cell interactions. Exp Dermatol (2011) 0.83
Molecular genetic analysis of 16 XP-C patients from Germany: environmental factors predominately contribute to phenotype variations. Exp Dermatol (2012) 0.83
Perioral dermatitis. J Dtsch Dermatol Ges (2010) 0.82
PS3, a semisynthetic beta-1,3-glucan sulfate, diminishes contact hypersensitivity responses through inhibition of L- and P-selectin functions. J Invest Dermatol (2008) 0.82
Treatment of scabies with 5% permethrin cream: results of a German multicenter study. J Dtsch Dermatol Ges (2006) 0.82
Diminished thrombus formation and alleviation of myocardial infarction and reperfusion injury through antibody- or small-molecule-mediated inhibition of selectin-dependent platelet functions. Haematologica (2007) 0.81
Intertriginous urticaria pigmentosa. Dermatology (2005) 0.81
Halting angiogenesis by non-viral somatic gene therapy alleviates psoriasis and murine psoriasiform skin lesions. J Clin Invest (2010) 0.81
No association of vitamin D metabolism-related polymorphisms and melanoma risk as well as melanoma prognosis: a case-control study. Arch Dermatol Res (2012) 0.81
Disruption of the murine dynein light chain gene Tcte3-3 results in asthenozoospermia. Reproduction (2010) 0.81
Introduction of functional chimeric E/L-selectin by RNA electroporation to target dendritic cells from blood to lymph nodes. Cancer Immunol Immunother (2007) 0.81
Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes. Eur J Med Genet (2012) 0.80
Anaphylaxis during treatment of nausea and vomiting: IgE-mediated metoclopramide allergy. Ann Pharmacother (2006) 0.80
Enhanced T-cell activation by immature dendritic cells loaded with HSP70-expressing heat-killed melanoma cells. Exp Dermatol (2009) 0.80
Methemoglobinemia due to local anesthesia with low-dose prilocaine. Dermatol Surg (2008) 0.80
Modulating T cell functions does not alleviate chronic inflammatory skin lesions in K5.TGF beta 1 transgenic mice. Exp Dermatol (2010) 0.80
To die or not to die, that's the question--and the answer may depend on netrin-1. J Natl Cancer Inst (2009) 0.80
Molecular interactions of B-CAM (basal-cell adhesion molecule) and laminin in epithelial skin cancer. Arch Dermatol Res (2004) 0.80
Diffuse melanosis in a patient with multifocal liver and thyroid metastases of a malignant melanoma. J Dtsch Dermatol Ges (2012) 0.80
Vasoactive Therapy in Systemic Sclerosis: Real-life Therapeutic Practice in More Than 3000 Patients. J Rheumatol (2015) 0.80
Nanoscale integrin ligand patterns determine melanoma cell behavior. ACS Nano (2014) 0.79
Circular, nanostructured and biofunctionalized hydrogel microchannels for dynamic cell adhesion studies. Lab Chip (2012) 0.79
Heredity of port-wine stains: investigation of families without a RASA1 mutation. J Cosmet Laser Ther (2015) 0.79
Familial intellectual disability and autistic behavior caused by a small FMR2 gene deletion. Am J Med Genet A (2011) 0.79