ファンコーニ貧血 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ファンコーニ貧血" in Japanese language version.

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16nih.gov

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11doi.org

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2elsevier.com

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2sciencemag.org

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1orpha.net

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1nejm.org

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1whonamedit.com

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1wikipedia.org

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1medscape.com

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1urologyjournal.us

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1worldcat.org

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1sciencedirect.com

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558^th place

1genesdev.org

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doi.org

Schwartz, Robert S.; d'Andrea, Alan D. (May 2010). “Susceptibility pathways in Fanconi's anemia and breast cancer”. N. Engl. J. Med. 362 (20): 1909–1919. doi:10.1056/NEJMra0809889. PMC 3069698. PMID 20484397.
Kutler DI, Auerbach AD (2004). “Fanconi anemia in Ashkenazi Jews”. Fam. Cancer 3 (3–4): 241–248. doi:10.1007/s10689-004-9565-8. PMID 15516848.
Verlinsky Y, Rechitsky S, Schoolcraft W, Strom C, Kuliev A (2001). “, Preimplantation diagnosis for Fanconi anemia combined with HLA matching”. JAMA 285 (24): 3130–3133. doi:10.1001/jama.285.24.3130. PMID 11427142.
Zhang X, Li J, Sejas DP, Pang Q (2005). “Hypoxia-reoxygenation induces premature senescence in FA bone marrow hematopoietic cells”. Blood 106 (1): 75–85. doi:10.1182/blood-2004-08-3033. PMID 15769896.
Deans AJ, West SC (December 2009). “FANCM connects the genome instability disorders Bloom's Syndrome and Fanconi Anemia”. Mol. Cell 36 (6): 943–53. doi:10.1016/j.molcel.2009.12.006. PMID 20064461.
Vandenberg CJ, Gergely F, Ong CY et al. (2003). “BRCA1-independent ubiquitination of FANCD2”. Mol. Cell 12 (1): 247–254. doi:10.1016/S1097-2765(03)00281-8. PMID 12887909.
Garcia-Higuera I, Taniguchi T, Ganesan S et al. (2001). “Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway”. Mol. Cell 7 (2): 249–262. doi:10.1016/S1097-2765(01)00173-3. PMID 11239454.
Cortez D, Wang Y, Qin J, Elledge SJ (1999). “Requirement of ATM-dependent phosphorylation of brca1 in the DNA damage response to double-strand breaks”. Science 286 (5442): 1162–1166. doi:10.1126/science.286.5442.1162. PMID 10550055.
Howlett NG, Taniguchi T, Olson S et al. (2002). “Biallelic inactivation of BRCA2 in Fanconi anemia”. Science 297 (5581): 606–609. doi:10.1126/science.1073834. PMID 12065746.
Connor F, Bertwistle D, Mee PJ et al. (1997). “Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation”. Nat. Genet. 17 (4): 423–430. doi:10.1038/ng1297-423. PMID 9398843.
de Winter JP, Waisfisz Q, Rooimans MA et al. (1998). “The Fanconi anaemia group G gene FANCG is identical with XRCC9”. Nat. Genet. 20 (3): 281–283. doi:10.1038/3093. PMID 9806548.

elsevier.com

linkinghub.elsevier.com

genesdev.org

Wang Y, Cortez D, Yazdi P, Neff N, Elledge SJ, Qin J (2000). “BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures”. Genes Dev. 14 (8): 927–39. PMC 316544. PMID 10783165.

medscape.com

emedicine.medscape.com

Fanconi Anemia Treatment & Management: Approach Considerations, Supportive Care, Hematopoietic Stem Cell Transplantation and Androgen Therapy. (2022-07-08).

nejm.org

content.nejm.org

Schwartz, Robert S.; d'Andrea, Alan D. (May 2010). “Susceptibility pathways in Fanconi's anemia and breast cancer”. N. Engl. J. Med. 362 (20): 1909–1919. doi:10.1056/NEJMra0809889. PMC 3069698. PMID 20484397.

nih.gov

pubmed.ncbi.nlm.nih.gov

Schwartz, Robert S.; d'Andrea, Alan D. (May 2010). “Susceptibility pathways in Fanconi's anemia and breast cancer”. N. Engl. J. Med. 362 (20): 1909–1919. doi:10.1056/NEJMra0809889. PMC 3069698. PMID 20484397.
Kutler DI, Auerbach AD (2004). “Fanconi anemia in Ashkenazi Jews”. Fam. Cancer 3 (3–4): 241–248. doi:10.1007/s10689-004-9565-8. PMID 15516848.
Verlinsky Y, Rechitsky S, Schoolcraft W, Strom C, Kuliev A (2001). “, Preimplantation diagnosis for Fanconi anemia combined with HLA matching”. JAMA 285 (24): 3130–3133. doi:10.1001/jama.285.24.3130. PMID 11427142.
Butturini, A.; Gale, R. P.; Verlander, P. C.; Adler-Brecher, B.; Gillio, A. P.; Auerbach, A. D. (1994-09-01). “Hematologic abnormalities in Fanconi anemia: an International Fanconi Anemia Registry study”. Blood 84 (5): 1650–1655. ISSN 0006-4971. PMID 8068955.
Zhang X, Li J, Sejas DP, Pang Q (2005). “Hypoxia-reoxygenation induces premature senescence in FA bone marrow hematopoietic cells”. Blood 106 (1): 75–85. doi:10.1182/blood-2004-08-3033. PMID 15769896.
Deans AJ, West SC (December 2009). “FANCM connects the genome instability disorders Bloom's Syndrome and Fanconi Anemia”. Mol. Cell 36 (6): 943–53. doi:10.1016/j.molcel.2009.12.006. PMID 20064461.
Vandenberg CJ, Gergely F, Ong CY et al. (2003). “BRCA1-independent ubiquitination of FANCD2”. Mol. Cell 12 (1): 247–254. doi:10.1016/S1097-2765(03)00281-8. PMID 12887909.
Garcia-Higuera I, Taniguchi T, Ganesan S et al. (2001). “Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway”. Mol. Cell 7 (2): 249–262. doi:10.1016/S1097-2765(01)00173-3. PMID 11239454.
Wang Y, Cortez D, Yazdi P, Neff N, Elledge SJ, Qin J (2000). “BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures”. Genes Dev. 14 (8): 927–39. PMC 316544. PMID 10783165.
Cortez D, Wang Y, Qin J, Elledge SJ (1999). “Requirement of ATM-dependent phosphorylation of brca1 in the DNA damage response to double-strand breaks”. Science 286 (5442): 1162–1166. doi:10.1126/science.286.5442.1162. PMID 10550055.
Howlett NG, Taniguchi T, Olson S et al. (2002). “Biallelic inactivation of BRCA2 in Fanconi anemia”. Science 297 (5581): 606–609. doi:10.1126/science.1073834. PMID 12065746.
Connor F, Bertwistle D, Mee PJ et al. (1997). “Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation”. Nat. Genet. 17 (4): 423–430. doi:10.1038/ng1297-423. PMID 9398843.
Auerbach AD, Rogatko A, Schroeder-Kurth TM (1989). “International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity”. Blood 73 (2): 391–6. PMID 2917181.
de Winter JP, Waisfisz Q, Rooimans MA et al. (1998). “The Fanconi anaemia group G gene FANCG is identical with XRCC9”. Nat. Genet. 20 (3): 281–283. doi:10.1038/3093. PMID 9806548.

pmc.ncbi.nlm.nih.gov

orpha.net

Fanconi's Anemia Orphanet Encyclopedia, Ethel Moustacchi, October 2003

sciencedirect.com

Deans AJ, West SC (December 2009). “FANCM connects the genome instability disorders Bloom's Syndrome and Fanconi Anemia”. Mol. Cell 36 (6): 943–53. doi:10.1016/j.molcel.2009.12.006. PMID 20064461.

sciencemag.org

urologyjournal.us

Institut Biologia Fonamental de Barcelona, "Constitutional chromosomal instability: a case with three primary and sequential cancers", USUJ 2009. Retrieved 2010-04-13

whonamedit.com

synd/61 - Who Named It?

wikipedia.org

en.wikipedia.org

synd/61 - Who Named It?

worldcat.org

search.worldcat.org

Butturini, A.; Gale, R. P.; Verlander, P. C.; Adler-Brecher, B.; Gillio, A. P.; Auerbach, A. D. (1994-09-01). “Hematologic abnormalities in Fanconi anemia: an International Fanconi Anemia Registry study”. Blood 84 (5): 1650–1655. ISSN 0006-4971. PMID 8068955.