PubRank

G Zambruno

Author PubWeight™ 74.75‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Involvement of the mismatch repair system in temozolomide-induced apoptosis. Mol Pharmacol 1998 1.83
2 The control of epidermal stem cells (holoclones) in the treatment of massive full-thickness burns with autologous keratinocytes cultured on fibrin. Transplantation 1999 1.67
3 Management of bullous pemphigoid: the European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology. Br J Dermatol 2015 1.55
4 Human melanoma cells secrete and respond to placenta growth factor and vascular endothelial growth factor. J Invest Dermatol 2000 1.41
5 A truncating mutation in the laminin-332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migration. Br J Dermatol 2014 1.40
6 Distinctive integrin expression in the newly forming epidermis during wound healing in humans. J Invest Dermatol 1993 1.39
7 A homozygous mutation in the integrin alpha6 gene in junctional epidermolysis bullosa with pyloric atresia. J Clin Invest 1997 1.35
8 Fine mapping of the PSORS4 psoriasis susceptibility region on chromosome 1q21. J Invest Dermatol 2001 1.28
9 Adenovirus-mediated VEGF(165) gene transfer enhances wound healing by promoting angiogenesis in CD1 diabetic mice. Gene Ther 2002 1.26
10 The role of CSA in the response to oxidative DNA damage in human cells. Oncogene 2007 1.25
11 Spatial discontinuities in human immunodeficiency virus type 1 quasispecies derived from epidermal Langerhans cells of a patient with AIDS and evidence for double infection. J Virol 1994 1.18
12 Congenital self-healing histiocytosis (Hashimoto-Pritzker). An ultrastructural and immunohistochemical study. Cancer 1988 1.07
13 Corrective gene transfer of keratinocytes from patients with junctional epidermolysis bullosa restores assembly of hemidesmosomes in reconstructed epithelia. Gene Ther 1998 1.07
14 Quality of life in patients with epidermolysis bullosa. Br J Dermatol 2009 1.04
15 Direct detection of HIV-1 RNA in epidermal Langerhans cells of HIV-infected patients. J Acquir Immune Defic Syndr 1993 1.02
16 Placenta growth factor is induced in human keratinocytes during wound healing. J Invest Dermatol 2000 0.99
17 Quantitation by competitive PCR of HIV-1 proviral DNA in epidermal Langerhans cells of HIV-infected patients. J Acquir Immune Defic Syndr 1994 0.96
18 Granulocyte/macrophage colony-stimulating factor treatment of human chronic ulcers promotes angiogenesis associated with de novo vascular endothelial growth factor transcription in the ulcer bed. Br J Dermatol 2006 0.96
19 Role of integrins in cell adhesion and polarity in normal keratinocytes and human skin pathologies. J Dermatol 1994 0.96
20 Immunohistochemical study of normal skin of HIV-1-infected patients shows no evidence of infection of epidermal Langerhans cells by HIV. AIDS Res Hum Retroviruses 1989 0.94
21 Apoptosis and efficient repair of DNA damage protect human keratinocytes against UVB. Cell Death Differ 2003 0.93
22 Corrective transduction of human epidermal stem cells in laminin-5-dependent junctional epidermolysis bullosa. Hum Gene Ther 1998 0.93
23 Expression of an estrogen receptor-associated protein (p29) in epithelial tumors of the skin. J Cutan Pathol 1989 0.93
24 Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosis. Cell Death Dis 2012 0.91
25 New type of epidermal nevus syndrome. Dermatology 2000 0.91
26 Involucrin expression in keratinization disorders of the skin--a preliminary study. Br J Dermatol 1987 0.90
27 Binding properties, cell delivery, and gene transfer of adenoviral penton base displaying bacteriophage. Virology 2001 0.89
28 Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10. Br J Dermatol 2010 0.89
29 In vitro infection of human epidermal Langerhans' cells with HIV-1. Immunology 1995 0.89
30 Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibility. Hum Genet 1999 0.88
31 Association of piebaldism and neurofibromatosis type 1 in a girl. Pediatr Dermatol 2002 0.88
32 Induction of senescence pathways in Kindler syndrome primary keratinocytes. Br J Dermatol 2013 0.87
33 Compound heterozygosity for an out-of-frame deletion and a splice site mutation in the LAMB3 gene causes nonlethal junctional epidermolysis bullosa. Biochem Biophys Res Commun 1998 0.86
34 Expression of B7 costimulatory molecule in cultured human epidermal Langerhans cells is regulated at the mRNA level. J Invest Dermatol 1994 0.86
35 Toward epidermal stem cell-mediated ex vivo gene therapy of junctional epidermolysis bullosa. Hum Gene Ther 2000 0.85
36 Beta 1 and beta 3 integrin upregulation in rapidly progressive glomerulonephritis. Nephrol Dial Transplant 1995 0.85
37 The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutation. Br J Dermatol 2010 0.84
38 A glutamine insertion in the 1A alpha helical domain of the keratin 4 gene in a familial case of white sponge nevus. J Invest Dermatol 2000 0.84
39 Expression of the soluble vascular endothelial growth factor receptor-1 in cutaneous melanoma: role in tumour progression. Br J Dermatol 2011 0.83
40 Delayed diagnosis of dyskeratosis congenita in a 40-year-old woman with multiple head and neck squamous cell carcinomas. Br J Dermatol 2007 0.83
41 Novel mutations in the LAMC2 gene in non-Herlitz junctional epidermolysis bullosa: effects on laminin-5 assembly, secretion, and deposition. J Invest Dermatol 2001 0.83
42 Circumscribed palmo-plantar hypokeratosis: a disease of desquamation? Immunohistological study of five cases and literature review. J Eur Acad Dermatol Venereol 2011 0.83
43 Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus. Ann Hum Genet 2004 0.83
44 Compound heterozygosity for a recessive glycine substitution and a splice site mutation in the COL7A1 gene causes an unusually mild form of localized recessive dystrophic epidermolysis bullosa. J Invest Dermatol 1998 0.82
45 Beta-1 integrins in the normal human glomerular capillary wall: an immunoelectron microscopy study. Nephron 1994 0.82
46 Expression of neural-tissue markers (S-100 protein and Leu-7 antigen) by sweat gland tumors of the skin. An immunohistochemical study. J Am Acad Dermatol 1987 0.82
47 Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in the type VII collagen gene. Br J Dermatol 2002 0.82
48 Development of a novel ELISA system for detection of anti-BP180 IgG and characterization of autoantibody profile in bullous pemphigoid patients. Br J Dermatol 2004 0.82
49 Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex. Br J Dermatol 2011 0.82
50 New insights into the autoantibody-mediated mechanisms of autoimmune bullous diseases and urticaria. Clin Exp Rheumatol 2006 0.82
51 Free radical production during metabolism of organic hydroperoxides by normal human keratinocytes. J Invest Dermatol 1993 0.81
52 Eccrine syringofibroadenoma. Immunohistological study of a new case. Am J Dermatopathol 1987 0.81
53 Antibodies against sialophorin (CD43) enhance the capacity of dendritic cells to cluster and activate T lymphocytes. J Immunol 1997 0.81
54 Treatment of leg ulcers with cryopreserved allogeneic cultured epithelium. A multicenter study. Arch Dermatol 1992 0.81
55 Human epidermal basal keratinocytes express CDw29 antigens. Br J Dermatol 1989 0.81
56 Immunohistochemistry of cutaneous graft-versus-host disease after allogeneic bone marrow transplantation. J Dermatol 1991 0.80
57 Novel and recurrent mutations in the integrin beta 4 subunit gene causing lethal junctional epidermolysis bullosa with pyloric atresia. Exp Dermatol 2003 0.80
58 Cutaneous phaeohyphomycosis due to Cladosporium cladosporioides. Mycoses 1993 0.80
59 Pemphigus. S2 Guideline for diagnosis and treatment--guided by the European Dermatology Forum (EDF) in cooperation with the European Academy of Dermatology and Venereology (EADV). J Eur Acad Dermatol Venereol 2014 0.79
60 Persistent unilateral orbital and eyelid oedema as a manifestation of Melkersson-Rosenthal syndrome. J Eur Acad Dermatol Venereol 2005 0.79
61 A novel antigen of the dermal-epidermal junction defined by an anti-CD1b monoclonal antibody (NU-T2). Arch Dermatol Res 1993 0.79
62 Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum. Clin Genet 2011 0.79
63 A homozygous nonsense mutation in type XVII collagen gene (COL17A1) uncovers an alternatively spliced mRNA accounting for an unusually mild form of non-Herlitz junctional epidermolysis bullosa. J Invest Dermatol 2001 0.79
64 Trisomic rescue causing reduction to homozygosity for a novel ABCA12 mutation in harlequin ichthyosis. Clin Genet 2009 0.79
65 Very late activation-3 integrin is the dominant beta 1-integrin on the glomerular capillary wall: an immunofluorescence study in nephrotic syndrome. Nephron 1992 0.78
66 Immunity to extracellular matrix antigens is associated with ultrastructural alterations of the stroma and stratified epithelium basement membrane in the skin of Hashimotos thyroiditis patients. Int J Immunopathol Pharmacol 2006 0.78
67 Sensitivity of different assays for the serological diagnosis of epidermolysis bullosa acquisita: analysis of a cohort of 24 Italian patients. J Eur Acad Dermatol Venereol 2014 0.78
68 Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization. Clin Genet 2006 0.78
69 Antigenic thymus-epidermis relationships. Reactivity of a panel of anti-thymic cell monoclonal antibodies on human keratinocytes and Langerhans cells. Dermatologica 1987 0.78
70 Genomic organization of the human integrin beta4 gene. Mamm Genome 1997 0.78
71 A founder synonymous COL7A1 mutation in three Danish families with dominant dystrophic epidermolysis bullosa pruriginosa identifies exonic regulatory sequences required for exon 87 splicing. Br J Dermatol 2011 0.78
72 A recurrent nonsense mutation occurring as a de novo event in a patient with recessive dystrophic epidermolysis bullosa. Dermatology 2011 0.77
73 Intracellular degradation of beta4 integrin in lethal junctional epidermolysis bullosa with pyloric atresia. Br J Dermatol 2004 0.77
74 Alpha-6 (CD 49f) integrin expression in genetic and acquired bullous skin diseases. A comparison of its distribution with bullous pemphigoid antigen. J Cutan Pathol 1992 0.77
75 Gene correction of integrin beta4-dependent pyloric atresia-junctional epidermolysis bullosa keratinocytes establishes a role for beta4 tyrosines 1422 and 1440 in hemidesmosome assembly. J Biol Chem 2001 0.77
76 Spleen dendritic cells exhibit altered morphology and increased allostimulatory capacity after short-term culture. Exp Dermatol 1992 0.76
77 A novel frameshift mutation in the KIND1 gene in Turkish siblings with Kindler syndrome. Br J Dermatol 2008 0.76
78 Activation of immature dendritic cells via membrane sialophorin (CD43). Adv Exp Med Biol 1997 0.76
79 Herlitz junctional epidermolysis bullosa: laminin-5 mutational profile and carrier frequency in the Italian population. Br J Dermatol 2007 0.76
80 [Successful treatment of Norwegian scabies with ivermectin in a patient with recessive dystrophic epidermolysis bullosa]. Minerva Pediatr 2004 0.76
81 Kaposi's sarcoma with primary bone lesions in an HIV-seronegative man. Br J Dermatol 1996 0.75
82 Discontinuous distribution of HIV-1 quasispecies in epidermal Langerhans cells of an AIDS patient and evidence for double infection. Adv Exp Med Biol 1995 0.75
83 Linear IgA dermatosis with IgA antibodies to type VII collagen. Br J Dermatol 1996 0.75
84 Isolated acral Darier's disease with haemorrhagic lesions in a kindred. Br J Dermatol 1996 0.75
85 Ultrastructural study of the skin in a case of juvenile ceroid-lipofuscinosis. Am J Dermatopathol 1990 0.75
86 Expression of ICAM-3/CD50 in normal and diseased skin. Br J Dermatol 1995 0.75
87 [A case of anetoderma associated with discoid type lupus erythematosus. Clinico-histologic and pathogenetic observations]. G Ital Dermatol Venereol 1986 0.75
88 Non-Herlitz junctional epidermolysis bullosa without hair involvement associated with BP180 deficiency. Dermatology 2001 0.75
89 [Double-blind comparison of a betamethasone dipropionate-iodochloroxyquinoline combination and a flumethasone pivalate-iodochloroxyquinoline combination in the therapy of steroid-sensitive dermatoses with superinfection]. G Ital Dermatol Venereol 1986 0.75
90 Involucrin expression in adnexal skin tumours. An immunohistological study. Virchows Arch A Pathol Anat Histopathol 1986 0.75
91 Characterization of the ultraviolet B and X-ray response of primary cultured epidermal cells from patients with disseminated superficial actinic porokeratosis. Br J Dermatol 2004 0.75
92 Netherton syndrome and its multifaceted defective protein LEKTI. G Ital Dermatol Venereol 2013 0.75
93 [Hashimoto-Pritzker congenital self-healing histiocytosis]. Pediatrie 1988 0.75
94 Branch point and donor splice-site COL7A1 mutations in mild recessive dystrophic epidermolysis bullosa. Br J Dermatol 2009 0.75
95 [Evaluation of the efficacy and tolerance of betamethasone dipropionate and salicylic acid in steroid-sensitive dry dermatosis]. G Ital Dermatol Venereol 1986 0.75
96 Granular-cell tumours of the skin do not express carcino-embryonic antigen. J Cutan Pathol 1986 0.75
97 The evaluation of family impact of recessive dystrophic epidermolysis bullosa using the Italian version of the Family Dermatology Life Quality Index. J Eur Acad Dermatol Venereol 2012 0.75
98 [Adhesion molecules in the skin: distribution, biological role and physiopathological implications of integrins]. G Ital Dermatol Venereol 1990 0.75
99 [Chronic urticaria. II. Follow-up of 69 patients (etiological and therapeutic study)]. G Ital Dermatol Venereol 1984 0.75
100 [Oral hairy leukoplakia in AIDS. Histologic and ultrastructural study of 8 cases]. Ann Dermatol Venereol 1990 0.75
101 GP37 expression in normal and diseased human epidermis: a marker for keratinocyte differentiation. Acta Derm Venereol 1986 0.75
102 [Prolonged preservation of venous allografts for vascular access in hemodialysis]. Acta Urol Belg 1990 0.75
103 Pemphigus vulgaris following cobalt therapy for bronchial carcinoma. Dermatologica 1989 0.75
104 180-kDa bullous pemphigoid antigen defective generalized atrophic benign epidermolysis bullosa: report of four cases with an unusually mild phenotype. Br J Dermatol 1998 0.75