Citation Impact
Citing Papers
β-Catenin Controls Hair Follicle Morphogenesis and Stem Cell Differentiation in the Skin
2001 Standout
Nucleotide excision repair in the yeast Saccharomyces cerevisiae : its relationship to specialized mitotic recombination and RNA polymerase II basal transcription
1995 StandoutNobel
Microbial etiological agents of destructive periodontal diseases
1994 Standout
Reconstitution of Human DNA Repair Excision Nuclease in a Highly Defined System
1995 StandoutNobel
Connexin disorders of the skin
2005
Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy
1994
The Molecular Pathology of Progressive Symmetric Erythrokeratoderma: A Frameshift Mutation in the Loricrin Gene and Perturbations in the Cornified Cell Envelope
1997
Transfection of pseudouridine-modified mRNA encoding CPD-photolyase leads to repair of DNA damage in human keratinocytes: A new approach with future therapeutic potential
2013 StandoutNobel
Hidradenitis suppurativa: A comprehensive review
2009 Standout
A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
1998
Order of Assembly of Human DNA Repair Excision Nuclease
1999 StandoutNobel
Mismatch repair and nucleotide excision repair proteins cooperate in the recognition of DNA interstrand crosslinks
2009 StandoutNobel
Characterization of Reaction Intermediates of Human Excision Repair Nuclease
1997 StandoutNobel
The human keratins: biology and pathology
2008 Standout
Recognition and repair of the cyclobutane thymine dimer, a major cause of skin cancers, by the human excision nuclease
2003 StandoutNobel
Genes controlling nucleotide excision repair in eukaryotic cells
1993
Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancer
1994
Ubiquitin Ligase Activity of TFIIH and the Transcriptional Response to DNA Damage
2005 StandoutNobel
Purification and Characterization of the XPF-ERCC1 Complex of Human DNA Repair Excision Nuclease
1995 StandoutNobel
Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease
2001 StandoutNobel
Distinctive Integrin Expression in the Newly Forming Epidermis During Wound Healing in Humans
1993
Suppression of subgingival Actinobacillus actinomycetemcomitans in localized juvenile periodontitis by systemic tetracycline
1993
What is segmental neurofibromatosis?
1994
Nucleotide Excision Repair in Human Cells
2013 StandoutNobel
The cornified envelope: a model of cell death in the skin
2005 Standout
Codominance associated with overexpression of certain XPD mutations
2001
Human nucleotide excision repair syndromes: Molecular clues to unexpected intricacies
1994
Genome maintenance mechanisms for preventing cancer
2001 StandoutNature
Rothmund-Thomson syndrome: Review of the world literature
1992
Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome
2002
A Yeast Four-hybrid System Identifies Cdk-activating Kinase as a Regulator of the XPD Helicase, a Subunit of Transcription Factor IIH
2001
Nucleotide excision repair and human syndromes
2000
The skin: an indispensable barrier
2008 Standout
Met, metastasis, motility and more
2003 Standout
Xeroderma Pigmentosum Group C Splice Mutation Associated with Autism and Hypoglycinemia11An abstract of this manuscript was presented at the annual meeting of the Society for Investigative Dermatology in Washington, DC
1998 StandoutNobel
Nucleotide Excision Repair
2005 StandoutNobel
A summary of mutations in the UV-sensitive disorders: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy
1999
The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
2001
DNA Repair and Ultraviolet Mutagenesis in Cells From a New Patient With Xeroderma Pigmentosum Group G and Cockayne Syndrome Resemble Xeroderma Pigmentosum Cells
1996
Proteus syndrome: Diagnostic criteria, differential diagnosis, and patient evaluation
1999
Cancer of the Ovary
2004 Standout
Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy.
1996
Hereditary Ovarian Carcinoma
1992
Restoration of Nucleotide Excision Repair in a Helicase-Deficient XPD Mutant from Intragenic Suppression by a Trichothiodystrophy Mutation
2001 StandoutNobel
Mutations in XPA That Prevent Association with ERCC1 Are Defective in Nucleotide Excision Repair
1995
Quality Control by DNA Repair
1999 StandoutScienceNobel
Mechanisms of DNA Excision Repair
1994 StandoutScienceNobel
ICRP PUBLICATION 118: ICRP Statement on Tissue Reactions and Early and Late Effects of Radiation in Normal Tissues and Organs — Threshold Doses for Tissue Reactions in a Radiation Protection Context
2012 Standout
The Yeast TFB1 and SSL1 Genes, Which Encode Subunits of Transcription Factor IIH, Are Required for Nucleotide Excision Repair and RNA Polymerase II Transcription
1995 StandoutNobel
The Diagnostic Evaluation and Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2
1997 Standout
Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition.
1999
Beta4 integrin is required for hemidesmosome formation, cell adhesion and cell survival.
1996
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD ( ERCC 2) repair/transcription gene
1997
Oxidative DNA damage: mechanisms, mutation, and disease
2003 Standout
Functional complementation of xeroderma pigmentosum complementation group E by replication protein A in an in vitro system.
1996 StandoutNobel
Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.
1993
Wound Healing--Aiming for Perfect Skin Regeneration
1997 StandoutScience
ERCC4 (XPF) Encodes a Human Nucleotide Excision Repair Protein with Eukaryotic Recombination Homologs
1996 StandoutNobel
DNA Damage in the Nucleosome Core Is Refractory to Repair by Human Excision Nuclease
2000 StandoutNobel
Life cycle of connexins in health and disease
2006 Standout
Relationship of the Xeroderma Pigmentosum Group E DNA Repair Defect to the Chromatin and DNA Binding Proteins UV-DDB and Replication Protein A
1998
Xeroderma Pigmentosum Complementation Group E Protein (XPE/DDB2): Purification of Various Complexes of XPE and Analyses of Their Damaged DNA Binding and Putative DNA Repair Properties
2005 StandoutNobel
Correction of the DNA repair defect in xeroderma pigmentosum group E by injection of a DNA damage-binding protein.
1994
Recent Insights on DNA Repair: The Mechanism of Damaged Nucleotide Excision in Eukaryotes and Its Relationship to Other Cellular Processesa
1994 StandoutNobel
Molecular cloning of the human nucleotide-excision-repair gene ERCC4.
1994 StandoutNobel
De novo design of protein logic gates
2020 StandoutScienceNobel
A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy.
1993
Works of V. Nazzaro being referenced
Prenatal diagnosis of junctional epidermolysis bullosa associated with pyloric atresia.
1990
Familial occurrence of KID (keratitis, ichthyosis, deafness) syndrome
1990
Epidermolytic hyperkeratosis: generalized form in children from parents with systematized linear form
1990
Hereditary epidermolytic palmoplantar keratoderma associated with breast and ovarian cancer in a large kindred
1987
Expression of Integrins in Junctional and Dystrophic Epidermolysis Bullosa
1990
DNA repair investigations in nine Italian patients affected by trichothiodystrophy
1992
Proteus syndrome
1991
Papillon-Lefèvre Syndrome Ultrastructural Study and Successful Treatment With Acitretin
1988
Mast cell phagocytosis of melanosomes in a case of Rothmund-Thomson's congenital poikiloderma*
1987
Progressive Symmetric Erythrokeratodermia
1986
Progressive symmetric erythrokeratodermia. Histological and ultrastructural study of patient before and after treatment with etretinate
1986