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1. From premature gray hair to helicase--Werner syndrome
: implications for aging and cancer
by Goto, Makoto and Miller, Robert W and Nihon Gan Gakkai
2001, Gann monograph on cancer research, ISBN 9783805571586, Volume no. 49., x, 168
Werner's syndrome
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2. Full Text Oxidative stress, mitochondrial abnormalities and antioxidant defense in Ataxia-telangiectasia, Bloom syndrome and Nijmegen breakage syndrome
by Maciejczyk, Mateusz and Mikoluc, Bozena and Pietrucha, Barbara and Heropolitanska - Pliszka, Edyta and Pac, Malgorzata and Motkowski, Radosław and Car, Halina
Redox Biology, ISSN 2213-2317, 04/2017, Volume 11, Issue C, pp. 375 - 383
Rare pleiotropic genetic disorders, Ataxia-telangiectasia (A-T), Bloom syndrome (BS) and Nijmegen breakage syndrome (NBS) are characterised by... 
Antioxidants | Oxidative stress | Nijmegen breakage syndrome (NBS) | Oxidative damage | Bloom syndrome (BS) | Ataxia-telangiectasia (A-T) | CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DNA-DAMAGE | DOUBLE-STRAND BREAKS | FIBROBLAST-CULTURES | DEFECTIVE RESPONSE | GENE | PRODUCT | RESISTANCE | ATM ACTIVATION | DYSFUNCTION | Bloom Syndrome - pathology | Nijmegen Breakage Syndrome - pathology | NADPH Oxidase 4 - genetics | Reactive Oxygen Species - metabolism | Signal Transduction | Humans | Nijmegen Breakage Syndrome - metabolism | Gene Expression Regulation | Oxidative Stress - genetics | Bloom Syndrome - metabolism | Ataxia Telangiectasia - metabolism | Mitochondria - metabolism | Bloom Syndrome - genetics | Mitochondria - pathology | Lipoproteins, LDL - genetics | Nijmegen Breakage Syndrome - genetics | NADPH Oxidase 4 - metabolism | Poly(ADP-ribose) Polymerases - metabolism | Poly(ADP-ribose) Polymerases - genetics | Ataxia Telangiectasia - pathology | DNA Repair | Ataxia Telangiectasia - genetics | Lipoproteins, LDL - metabolism | DNA Damage
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3. Full Text Human RECQ helicases: Roles in DNA metabolism, mutagenesis and cancer biology
by Monnat, Raymond J
Seminars in Cancer Biology, ISSN 1044-579X, 2010, Volume 20, Issue 5, pp. 329 - 339
Abstract Helicases use the energy of ATP hydrolysis to separate double-stranded nucleic acids to facilitate essential processes such as replication,... 
Hematology, Oncology and Palliative Medicine | Cancer predisposition syndrome | Rothmund–Thomson syndrome | Telomeres | Bloom syndrome | DNA replication | Cancer chemotherapy | Premature aging syndrome | Homologous recombination | Werner syndrome | RECQ helicases | Genetic instability | DNA repair | Rothmund-Thomson syndrome | SYNDROME GENE-PRODUCT | BLOOMS-SYNDROME HELICASE | GENOMIC INSTABILITY | WRN HELICASE | DAMAGE RESPONSE | BASE EXCISION-REPAIR | ONCOLOGY | ROTHMUND-THOMSON-SYNDROME | S-PHASE | WERNER-SYNDROME PROTEIN | Genomic Instability | RecQ Helicases - metabolism | Humans | DNA Replication | RecQ Helicases - genetics | Bloom Syndrome - genetics | DNA - metabolism | Telomere | DNA - genetics | Rothmund-Thomson Syndrome - genetics | Mutagenesis | Neoplasms - genetics | DNA Repair | Werner Syndrome - genetics | Mutation | Physiological aspects | Care and treatment | Genetic aspects | DNA | Cancer
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4. Molecular mechanisms of Werner's syndrome
by Lebel, Michel, 1967
2004, Medical intelligence unit, ISBN 0306482339, 156
Werner Syndrome | DNA Helicases | physiopathology | Werner's syndrome | genetics | Genetic aspects | Molecular aspects
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5. Genetic skin diseases predisposing to basal cell carcinoma
by Castori, Marco and Morrone, Aldo and Kanitakis, Jean and Grammatico, Paola
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
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6. Full Text RecQ helicases: caretakers of the genome
by Hickson, Ian D
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
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7. Full Text The involvement of human RECQL4 in DNA double-strand break repair
by Singh, Dharmendra Kumar and Karmakar, Parimal and Aamann, Maria and Schurman, Shepherd H and May, Alfred and Croteau, Deborah L and Burks, Lynnette and Plon, Sharon E and Bohr, Vilhelm A
Aging Cell, ISSN 1474-9718, 06/2010, Volume 9, Issue 3, pp. 358 - 371
Summary Rothmund-Thomson syndrome (RTS) is an autosomal recessive hereditary disorder associated with mutation in RECQL4 gene, a member of the human RecQ... 
RTS | Bloom syndrome | BLM | RecQ helicase | WRN | Premature aging | Rothmund-Thomson syndrome | Werner syndrome | Double-strand break repair | SYNDROME PROTEIN | WERNER-SYNDROME | MAMMALIAN-CELLS | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | GENOTOXIC AGENTS | REPLICATION | ROTHMUND-THOMSON-SYNDROME | BLOOM-SYNDROME | MUTATIONS | ASSOCIATION | GENE-PRODUCT | DNA - genetics | Rothmund-Thomson Syndrome - genetics | Cell Line | RecQ Helicases - metabolism | DNA Repair | Humans | DNA - metabolism | Histones - metabolism | Rothmund-Thomson Syndrome - metabolism | Cell Survival - radiation effects | DNA Breaks, Double-Stranded | Rothmund-Thomson Syndrome - pathology | Proteins | Gerontology | Genetic disorders | DNA | Genetic research | Automated teller machines | Universities and colleges | Double strand break repair | Rothmund-Thomson syndrome (RTS) | Werner syndrome (WRN) | Bloom syndrome (BLM)
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8. Full Text Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions
by Oshima, Junko and Sidorova, Julia M and Monnat, Raymond J
Ageing Research Reviews, ISSN 1568-1637, 2016, Volume 33, pp. 105 - 114
Abstract Werner syndrome (WS) is a prototypical segmental progeroid syndrome characterized by multiple features consistent with accelerated aging. It is caused... 
Neurology | Internal Medicine | Human | Werner syndrome | Progeroid syndrome | Genomic instability | BLM RECQ HELICASES | SYNDROME FIBROBLASTS | TELOMERE RECOMBINATION | DOUBLE-STRAND BREAKS | SYNDROME PROTEIN | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | PLURIPOTENT STEM-CELLS | DNA-POLYMERASE DELTA | REPLICATION FORK PROGRESSION | WRN-DEFICIENT | HOMOLOGOUS RECOMBINATION | Werner Syndrome - metabolism | DNA Repair | Humans | Werner Syndrome - genetics | DNA Replication | Aging, Premature - genetics | Werner Syndrome Helicase - genetics | Mutation | Exodeoxyribonucleases | Aging, Premature - metabolism | Werner Syndrome - diagnosis | Werner Syndrome - physiopathology | Telomeres | Genetic transcription | Health aspects | Genomics | Genes
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9. Full Text Familial skin cancer syndromes Increased risk of nonmelanotic skin cancers and extracutaneous tumors
by Jaju, Prajakta D and Ransohoff, Katherine J and Tang, Jean Y and Sarin, Kavita Y
Journal of the American Academy of Dermatology, ISSN 0190-9622, 03/2016, Volume 74, Issue 3, pp. 437 - 451
Nonmelanoma skin cancers (NMSCs) represent the most common malignancies worldwide, with reported incidence rising each year. Both cutaneous squamous cell... 
Muir-Torre syndrome | Bloom syndrome | dyskeratosis congenita | Gorlin syndrome | genetic testing | nonmelanoma skin cancer | Rothmund-Thomson syndrome | oculocutaneous albinism | Werner syndrome | ADENOSINE-DEAMINASE | MICROSATELLITE INSTABILITY | DERMATOFIBROSARCOMA PROTUBERANS | EPIDERMOLYSIS-BULLOSA | DERMATOLOGY | HEALING SQUAMOUS EPITHELIOMA | DUPRE-CHRISTOL SYNDROME | SCLEROATROPHIC SYNDROME | BASAL-CELL CARCINOMA | Rothmunde-Thomson syndrome | FERGUSON-SMITH | Muire-Torre syndrome | AUTOSOMAL-DOMINANT | Carcinoma, Basal Cell - therapy | Skin Neoplasms - therapy | Carcinoma, Squamous Cell - epidemiology | Humans | Carcinoma, Squamous Cell - therapy | Neoplastic Syndromes, Hereditary - diagnosis | Risk | Carcinoma, Basal Cell - epidemiology | Skin Neoplasms - epidemiology | Carcinoma, Basal Cell - diagnosis | Carcinoma, Squamous Cell - diagnosis | Neoplastic Syndromes, Hereditary - epidemiology | Skin Neoplasms - diagnosis | Skin Neoplasms - genetics | Neoplastic Syndromes, Hereditary - therapy | Decision Trees
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10. Full Text Accelerated epigenetic aging in Werner syndrome
by Maierhofer, Anna and Flunkert, Julia and Oshima, Junko and Martin, George M and Haaf, Thomas and Horvath, Steve
Aging, ISSN 1945-4589, 2017, Volume 9, Issue 4, pp. 1143 - 1152
Individuals suffering from Werner syndrome (WS) exhibit many clinical signs of accelerated aging. While the underlying constitutional mutation leads to... 
DNA methylation | Epigenetics | Epigenetic clock | Werner syndrome | Progeria | DNA METHYLATION AGE | BIOLOGICAL AGE | epigenetics | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | progeria | ALL-CAUSE MORTALITY | DISEASE | CEREBELLUM | COHORT | CLOCK | T-CELLS | epigenetic clock | TELOMERE LENGTH | BLOOD | Epigenesis, Genetic | Humans | Middle Aged | Male | Aging, Premature - genetics | Sex Characteristics | Blood Cell Count | CD8-Positive T-Lymphocytes | DNA Methylation | Werner Syndrome - genetics | Aged, 80 and over | Aging | Biomarkers | Lymphocyte Count | Adult | Female | Aged | DNA Damage | Blood Cells - ultrastructure | Index Medicus
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11. Full Text The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease
by Campisi, Judith and Gray, Matthew D and Mian, I. Saira and Huang, Shurong and Li, Baomin and Oshima, Junko
Nature Genetics, ISSN 1061-4036, 10/1998, Volume 20, Issue 2, pp. 114 - 116
CELLS | WERNER-SYNDROME | HELICASE | INVITRO | DISEASE | GENETICS & HEREDITY | DNA Helicases - metabolism | RecQ Helicases | Electrophoresis, Polyacrylamide Gel | Humans | Werner Syndrome - genetics | Werner Syndrome Helicase | Exodeoxyribonucleases - metabolism | DNA - metabolism | Exodeoxyribonuclease V | Werner Syndrome - enzymology | DNA Helicases - genetics
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12. Full Text LMNA mutations in atypical Werner's syndrome
by Chen, Lishan and Lee, Lin and Kudlow, Brian A and Dos Santos, Heloisa G and Sletvold, Olav and Shafeghati, Yousef and Botha, Eleanor G and Garg, Abhimanyu and Hanson, Nancy B and Martin, George M and Mian, I Saira and Kennedy, Brian K and Oshima, Junko
The Lancet, ISSN 0140-6736, 08/2003, Volume 362, Issue 9382, pp. 440 - 445
Werner's syndrome is a progeroid syndrome caused by mutations at the helicase locus. Some features of this disorder are also present in laminopathies caused by... 
ORGANIZATION | NUCLEAR-ENVELOPE | MEDICINE, GENERAL & INTERNAL | PROTEIN | FAMILIAL PARTIAL LIPODYSTROPHY | ENCODING LAMIN A/C | DISEASE | DREIFUSS MUSCULAR-DYSTROPHY | GENE-EXPRESSION | HUTCHINSON-GILFORD PROGERIA | MISSENSE MUTATIONS | Werner Syndrome - classification | Humans | RNA, Messenger - genetics | Werner Syndrome Helicase | Cells, Cultured | Exons - genetics | Male | Mutation - genetics | Reverse Transcriptase Polymerase Chain Reaction | Mutation, Missense - genetics | RecQ Helicases | DNA Mutational Analysis | Pedigree | Werner Syndrome - genetics | Adolescent | Lamin Type A - genetics | Fibroblasts | Female | Registries | Exodeoxyribonucleases | Nuclear Proteins - genetics | Child | DNA Helicases - genetics | Werner Syndrome - diagnosis | Physiological aspects | Genetic aspects | Genetic disorders | Diagnosis | Werner syndrome | Gene mutations | Medical disorders | Patients | Mutation | Laboratories | Exons | mRNA | Lamins | Nuclei | Muscular dystrophy | Gene sequencing | DNA helicase | Proteins | Osteoporosis | Missense mutation | Atherosclerosis | Age | Deoxyribonucleic acid--DNA | Phenotypes | Cloning | Insulin | Molecular chains | Heterozygosity | Polymerase chain reaction | Studies | Werner's syndrome | Morphology | Skin | Diabetes
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13. Full Text A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging
by Zhang, Weiqi and Li, Jingyi and Suzuki, Keiichiro and Qu, Jing and Wang, Ping and Zhou, Junzhi and Liu, Xiaomeng and Ren, Ruotong and Xu, Xiuling and Ocampo, Alejandro and Yuan, Tingting and Yang, Jiping and Li, Ying and Shi, Liang and Guan, Dee and Pan, Huize and Duan, Shunlei and Ding, Zhichao and Li, Mo and Yi, Fei and Bai, Ruijun and Wang, Yayu and Chen, Chang and Yang, Fuquan and Li, Xiaoyu and Wang, Zimei and Aizawa, Emi and Goebl, April and Soligalla, Rupa Devi and Reddy, Pradeep and Esteban, Concepcion Rodriguez and Tang, Fuchou and Liu, Guang-Hui and Belmonte, Juan Carlos Izpisua
Science, ISSN 0036-8075, 06/2015, Volume 348, Issue 6239, pp. 1160 - 1163
Werner syndrome (WS) is a premature aging disorder caused by WRN protein deficiency. Here, we report on the generation of a human WS model in human embryonic... 
DEFECTS | COMPLEX | WRN | GENE | IPSCS | MULTIDISCIPLINARY SCIENCES | DISEASE | Physiological aspects | Aging | Chromatin | Werner syndrome | Health aspects | Stem cells | Proteins | Genetic disorders | Cellular | Alterations | Disorders | Determinants | Maintenance | Anchoring
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