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European Journal of Dermatology, ISSN 1167-1122, 05/2012, Volume 22, Issue 3, pp. 299 - 309
Basal cell carcinoma (BCC) is the commonest cancer in humans. Predisposing factors reflect common genetic variations and environmental influences in most... 
Xeroderma pigmentosum | Folliculo-sebaceus unit | Basal cell carcinoma | Gorlin syndrome | Bazex-Dupré-Christol syndrome | Epidermal nevus syndrome | epidermal nevus syndrome | EPIDERMODYSPLASIA-VERRUCIFORMIS | CARTILAGE-HAIR HYPOPLASIA | xeroderma pigmentosum | DUPRE-CHRISTOL-SYNDROME | COARSE SPARSE HAIR | Bazex-Dupre-Christol syndrome | folliculo-sebaceus unit | SCHULZ-PASSARGE SYNDROME | DERMATOLOGY | FOLLICULAR HAMARTOMA SYNDROME | XERODERMA-PIGMENTOSUM | NEVUS SEBACEUS | basal cell carcinoma | ROTHMUND-THOMSON-SYNDROME | PHAKOMATOSIS-PIGMENTOKERATOTICA | Genetic Testing | Carcinoma, Basal Cell - genetics | Xeroderma Pigmentosum - genetics | Humans | Hypotrichosis - genetics | Rothmund-Thomson Syndrome - epidemiology | Carcinoma, Basal Cell - epidemiology | Carcinoma, Skin Appendage - genetics | Skin Diseases, Genetic - genetics | Nevus, Sebaceous of Jadassohn - epidemiology | Skin Diseases, Genetic - epidemiology | Werner Syndrome - genetics | Histiocytoma, Benign Fibrous - epidemiology | Facial Dermatoses - epidemiology | Histiocytoma, Benign Fibrous - genetics | Hamartoma Syndrome, Multiple - genetics | Facial Dermatoses - genetics | Hypotrichosis - epidemiology | Comorbidity | Cyanosis - epidemiology | Cyanosis - genetics | Basal Cell Nevus Syndrome - epidemiology | Xeroderma Pigmentosum - epidemiology | DNA Replication | Skin Neoplasms - epidemiology | Werner Syndrome - epidemiology | Hamartoma Syndrome, Multiple - epidemiology | Rothmund-Thomson Syndrome - genetics | Skin Neoplasms - genetics | Carcinoma, Skin Appendage - epidemiology | Nevus, Sebaceous of Jadassohn - genetics | Basal Cell Nevus Syndrome - genetics | Mutation
Journal Article
Nature Reviews Cancer, ISSN 1474-175X, 03/2003, Volume 3, Issue 3, pp. 169 - 178
RecQ helicases are highly conserved from bacteria to man. Germline mutations in three of the five known family members in humans give rise to debilitating... 
BLOOMS-SYNDROME GENE | TOPOISOMERASE-III-ALPHA | SYNDROME DNA HELICASE | FUNCTIONAL INTERACTION | ONCOLOGY | ROTHMUND-THOMSON-SYNDROME | STALLED REPLICATION FORKS | MISMATCH REPAIR | HOLLIDAY JUNCTIONS | WERNER-SYNDROME PROTEIN | SISTER-CHROMATID EXCHANGES | Species Specificity | Humans | Rothmund-Thomson Syndrome - enzymology | Werner Syndrome Helicase | DNA Repair - physiology | DNA Repair - genetics | Escherichia coli Proteins - physiology | RecQ Helicases | Cell Transformation, Neoplastic - genetics | Werner Syndrome - genetics | DNA Helicases - genetics | Genes, Tumor Suppressor | Protein Structure, Tertiary | Adenosine Triphosphatases - deficiency | Bloom Syndrome - enzymology | DNA Helicases - chemistry | Genetic Predisposition to Disease | Mutagenesis - genetics | DNA Helicases - deficiency | Bloom Syndrome - genetics | Werner Syndrome - enzymology | Mice, Knockout | Protein Interaction Mapping | Rothmund-Thomson Syndrome - genetics | Animals | DNA Replication - physiology | Multienzyme Complexes - physiology | DNA Replication - genetics | Escherichia coli Proteins - genetics | Adenosine Triphosphatases - chemistry | Adenosine Triphosphatases - genetics | Mice | Exodeoxyribonucleases | Adenosine Triphosphatases - physiology | DNA Helicases - physiology | Gene mutations | Physiological aspects | Genetic aspects | Research | Health aspects | Helicases | Cancer
Journal Article
DNA and Cell Biology, ISSN 1044-5498, 01/2007, Volume 26, Issue 1, pp. 1 - 18
Journal Article
Cancer Letters, ISSN 0304-3835, 01/2018, Volume 413, pp. 1 - 10
Human RecQ helicases that share homology with E. coli RecQ helicase play critical roles in diverse biological activities such as DNA replication,... 
Premature aging syndromes | Aneuploidy | DNA replication | RecQ helicases | Mitotic checkpoint | Cancer | OXIDATIVE STRESS | MCM PROTEINS | SYNDROME GENE-PRODUCT | DNA-DAMAGE | RAPADILINO SYNDROME | P53 | REPAIR | ONCOLOGY | ROTHMUND-THOMSON-SYNDROME | EXPRESSION | BALLER-GEROLD-SYNDROME | Limb Deformities, Congenital - enzymology | Genomic Instability | Limb Deformities, Congenital - genetics | Cell Proliferation | RecQ Helicases - metabolism | Humans | Rothmund-Thomson Syndrome - enzymology | Craniosynostoses - enzymology | RecQ Helicases - genetics | Antineoplastic Agents - therapeutic use | DNA, Mitochondrial - genetics | Neoplasms - genetics | Cell Transformation, Neoplastic - genetics | Patella - abnormalities | Biomarkers, Tumor - metabolism | Heart Septal Defects, Atrial - genetics | Anal Canal - enzymology | Patella - enzymology | Biomarkers, Tumor - antagonists & inhibitors | Heart Septal Defects, Atrial - enzymology | Genetic Predisposition to Disease | DNA, Mitochondrial - metabolism | Craniosynostoses - genetics | Neoplasms - enzymology | DNA Replication | Radius - abnormalities | Cell Transformation, Neoplastic - metabolism | Enzyme Inhibitors - therapeutic use | Neoplasms - drug therapy | Anal Canal - abnormalities | Rothmund-Thomson Syndrome - genetics | Dwarfism - genetics | Phenotype | Radius - enzymology | RecQ Helicases - antagonists & inhibitors | DNA Repair | Dwarfism - enzymology | Biomarkers, Tumor - genetics | Mutation | Cell Transformation, Neoplastic - pathology | Neoplasms - pathology | Medical research | Genomics | Cancer cells | Medicine, Experimental | Genetic aspects | Disease susceptibility | Genetic transcription | Index Medicus
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 11/2001, Volume 29, Issue 21, pp. 4378 - 4386
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 11/2019, Volume 10, Issue 1, pp. 5284 - 18
Journal Article
The Lancet, ISSN 0140-6736, 08/2003, Volume 362, Issue 9382, pp. 440 - 445
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 02/2018, Volume 39, Issue 2, pp. 255 - 265
Journal Article
Journal Article