Σύνδρομο Βέρνερ (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Σύνδρομο Βέρνερ" in Greek language version.

refsWebsite

Global rank Greek rank

8nih.gov

4^th place

7doi.org

2^nd place

3^rd place

6worldcat.org

5^th place

8^th place

2nature.com

234^th place

207^th place

1whonamedit.com

2,888^th place

3,435^th place

1sciencemag.org

857^th place

568^th place

1medlineplus.gov

1,581^st place

474^th place

doi.org

dx.doi.org

Norbnop, Phatchara; Srichomthong, Chalurmpon; Suphapeetiporn, Kanya; Shotelersuk, Vorasuk (2014-08). «ZRS 406A>G mutation in patients with tibial hypoplasia, polydactyly and triphalangeal first fingers» (στα αγγλικά). Journal of Human Genetics 59 (8): 467–470. doi:10.1038/jhg.2014.50. ISSN 1435-232X. https://www.nature.com/articles/jhg201450.
Gray, Matthew D.; Shen, Jiang-Cheng; Kamath-Loeb, Ashwini S.; Blank, A.; Sopher, Bryce L.; Martin, George M.; Oshima, Junko; Loeb, Lawrence A. (1997-09). «The Werner syndrome protein is a DNA helicase» (στα αγγλικά). Nature Genetics 17 (1): 100–103. doi:10.1038/ng0997-100. ISSN 1546-1718. https://www.nature.com/articles/ng0997-100.
Hasty, Paul; Campisi, Judith; Hoeijmakers, Jan; Steeg, Harry van; Vijg, Jan (2003-02-28). «Aging and Genome Maintenance: Lessons from the Mouse?» (στα αγγλικά). Science 299 (5611): 1355–1359. doi:10.1126/science.1079161. ISSN 0036-8075. PMID 12610296. https://science.sciencemag.org/content/299/5611/1355.
Masala, Maria Vittoria; Scapaticci, S.; Olivieri, Carla; Pirodda, Cesare; Montesu, Maria Antonietta; Cuccuru, Maria Antonietta; Pruneddu, Sara; Danesino, Cesare και άλλοι. (2007-05). «Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster». European journal of dermatology: EJD 17 (3): 213–216. doi:10.1684/ejd.2007.0155. ISSN 1167-1122. PMID 17478382. https://pubmed.ncbi.nlm.nih.gov/17478382/.
Navarro, Claire L.; Cau, Pierre; Lévy, Nicolas (2006-10-15). «Molecular bases of progeroid syndromes». Human Molecular Genetics 15 Spec No 2: R151–161. doi:10.1093/hmg/ddl214. ISSN 0964-6906. PMID 16987878. https://pubmed.ncbi.nlm.nih.gov/16987878/.
Epstein, C. J.; Martin, G. M.; Schultz, A. L.; Motulsky, A. G. (1966-05). «Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process». Medicine 45 (3): 177–221. doi:10.1097/00005792-196605000-00001. ISSN 0025-7974. PMID 5327241. https://pubmed.ncbi.nlm.nih.gov/5327241/.

doi.org

Werner, Otto (1985). Salk, Darrell, επιμ. Werner’s Syndrome and Human Aging. Advances in Experimental Medicine and Biology. Boston, MA: Springer US. σελίδες 1–14. ISBN 978-1-4684-7853-2.

medlineplus.gov

«Werner syndrome: MedlinePlus Genetics». medlineplus.gov (στα Αγγλικά). Ανακτήθηκε στις 30 Μαρτίου 2021.

nature.com

Norbnop, Phatchara; Srichomthong, Chalurmpon; Suphapeetiporn, Kanya; Shotelersuk, Vorasuk (2014-08). «ZRS 406A>G mutation in patients with tibial hypoplasia, polydactyly and triphalangeal first fingers» (στα αγγλικά). Journal of Human Genetics 59 (8): 467–470. doi:10.1038/jhg.2014.50. ISSN 1435-232X. https://www.nature.com/articles/jhg201450.
Gray, Matthew D.; Shen, Jiang-Cheng; Kamath-Loeb, Ashwini S.; Blank, A.; Sopher, Bryce L.; Martin, George M.; Oshima, Junko; Loeb, Lawrence A. (1997-09). «The Werner syndrome protein is a DNA helicase» (στα αγγλικά). Nature Genetics 17 (1): 100–103. doi:10.1038/ng0997-100. ISSN 1546-1718. https://www.nature.com/articles/ng0997-100.

nih.gov

ncbi.nlm.nih.gov

Hasty, Paul; Campisi, Judith; Hoeijmakers, Jan; Steeg, Harry van; Vijg, Jan (2003-02-28). «Aging and Genome Maintenance: Lessons from the Mouse?» (στα αγγλικά). Science 299 (5611): 1355–1359. doi:10.1126/science.1079161. ISSN 0036-8075. PMID 12610296. https://science.sciencemag.org/content/299/5611/1355.
Masala, Maria Vittoria; Scapaticci, S.; Olivieri, Carla; Pirodda, Cesare; Montesu, Maria Antonietta; Cuccuru, Maria Antonietta; Pruneddu, Sara; Danesino, Cesare και άλλοι. (2007-05). «Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster». European journal of dermatology: EJD 17 (3): 213–216. doi:10.1684/ejd.2007.0155. ISSN 1167-1122. PMID 17478382. https://pubmed.ncbi.nlm.nih.gov/17478382/.
Navarro, Claire L.; Cau, Pierre; Lévy, Nicolas (2006-10-15). «Molecular bases of progeroid syndromes». Human Molecular Genetics 15 Spec No 2: R151–161. doi:10.1093/hmg/ddl214. ISSN 0964-6906. PMID 16987878. https://pubmed.ncbi.nlm.nih.gov/16987878/.
Epstein, C. J.; Martin, G. M.; Schultz, A. L.; Motulsky, A. G. (1966-05). «Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process». Medicine 45 (3): 177–221. doi:10.1097/00005792-196605000-00001. ISSN 0025-7974. PMID 5327241. https://pubmed.ncbi.nlm.nih.gov/5327241/.
Oshima, Junko· Martin, George M. (1993). Adam, Margaret P., επιμ. GeneReviews®. Seattle (WA): University of Washington, Seattle.

pubmed.ncbi.nlm.nih.gov

Masala, Maria Vittoria; Scapaticci, S.; Olivieri, Carla; Pirodda, Cesare; Montesu, Maria Antonietta; Cuccuru, Maria Antonietta; Pruneddu, Sara; Danesino, Cesare και άλλοι. (2007-05). «Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster». European journal of dermatology: EJD 17 (3): 213–216. doi:10.1684/ejd.2007.0155. ISSN 1167-1122. PMID 17478382. https://pubmed.ncbi.nlm.nih.gov/17478382/.
Navarro, Claire L.; Cau, Pierre; Lévy, Nicolas (2006-10-15). «Molecular bases of progeroid syndromes». Human Molecular Genetics 15 Spec No 2: R151–161. doi:10.1093/hmg/ddl214. ISSN 0964-6906. PMID 16987878. https://pubmed.ncbi.nlm.nih.gov/16987878/.
Epstein, C. J.; Martin, G. M.; Schultz, A. L.; Motulsky, A. G. (1966-05). «Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process». Medicine 45 (3): 177–221. doi:10.1097/00005792-196605000-00001. ISSN 0025-7974. PMID 5327241. https://pubmed.ncbi.nlm.nih.gov/5327241/.

sciencemag.org

science.sciencemag.org

Hasty, Paul; Campisi, Judith; Hoeijmakers, Jan; Steeg, Harry van; Vijg, Jan (2003-02-28). «Aging and Genome Maintenance: Lessons from the Mouse?» (στα αγγλικά). Science 299 (5611): 1355–1359. doi:10.1126/science.1079161. ISSN 0036-8075. PMID 12610296. https://science.sciencemag.org/content/299/5611/1355.

whonamedit.com

«Werner's syndrome». www.whonamedit.com. Ανακτήθηκε στις 30 Μαρτίου 2021.

worldcat.org

Norbnop, Phatchara; Srichomthong, Chalurmpon; Suphapeetiporn, Kanya; Shotelersuk, Vorasuk (2014-08). «ZRS 406A>G mutation in patients with tibial hypoplasia, polydactyly and triphalangeal first fingers» (στα αγγλικά). Journal of Human Genetics 59 (8): 467–470. doi:10.1038/jhg.2014.50. ISSN 1435-232X. https://www.nature.com/articles/jhg201450.
Gray, Matthew D.; Shen, Jiang-Cheng; Kamath-Loeb, Ashwini S.; Blank, A.; Sopher, Bryce L.; Martin, George M.; Oshima, Junko; Loeb, Lawrence A. (1997-09). «The Werner syndrome protein is a DNA helicase» (στα αγγλικά). Nature Genetics 17 (1): 100–103. doi:10.1038/ng0997-100. ISSN 1546-1718. https://www.nature.com/articles/ng0997-100.
Hasty, Paul; Campisi, Judith; Hoeijmakers, Jan; Steeg, Harry van; Vijg, Jan (2003-02-28). «Aging and Genome Maintenance: Lessons from the Mouse?» (στα αγγλικά). Science 299 (5611): 1355–1359. doi:10.1126/science.1079161. ISSN 0036-8075. PMID 12610296. https://science.sciencemag.org/content/299/5611/1355.
Masala, Maria Vittoria; Scapaticci, S.; Olivieri, Carla; Pirodda, Cesare; Montesu, Maria Antonietta; Cuccuru, Maria Antonietta; Pruneddu, Sara; Danesino, Cesare και άλλοι. (2007-05). «Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster». European journal of dermatology: EJD 17 (3): 213–216. doi:10.1684/ejd.2007.0155. ISSN 1167-1122. PMID 17478382. https://pubmed.ncbi.nlm.nih.gov/17478382/.
Navarro, Claire L.; Cau, Pierre; Lévy, Nicolas (2006-10-15). «Molecular bases of progeroid syndromes». Human Molecular Genetics 15 Spec No 2: R151–161. doi:10.1093/hmg/ddl214. ISSN 0964-6906. PMID 16987878. https://pubmed.ncbi.nlm.nih.gov/16987878/.
Epstein, C. J.; Martin, G. M.; Schultz, A. L.; Motulsky, A. G. (1966-05). «Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process». Medicine 45 (3): 177–221. doi:10.1097/00005792-196605000-00001. ISSN 0025-7974. PMID 5327241. https://pubmed.ncbi.nlm.nih.gov/5327241/.