조로증 (Korean Wikipedia)

Analysis of information sources in references of the Wikipedia article "조로증" in Korean language version.

refsWebsite

Global rank Korean rank

6doi.org

2^nd place

3^rd place

6nih.gov

4^th place

1web.archive.org

1^st place

1jbc.org

4,455^th place

1,231^st place

1biologists.org

3,870^th place

1,743^rd place

1oxfordjournals.org

1,389^th place

550^th place

1elsevier.com

610^th place

351^st place

biologists.org

jcs.biologists.org

Manju K, Muralikrishna B, Parnaik VK (July 2006). “Expression of disease-causing lamin A mutants impairs the formation of DNA repair foci”. 《J. Cell. Sci.》 119 (Pt 13): 2704–14. doi:10.1242/jcs.03009. PMID 16772334. CS1 관리 - 여러 이름 (링크)

doi.org

dx.doi.org

Biton S, Dar I, Mittelman L, Pereg Y, Barzilai A, Shiloh Y (June 2006). “Nuclear ataxia-telangiectasia mutated (ATM) mediates the cellular response to DNA double strand breaks in human neuron-like cells”. 《J. Biol. Chem.》 281 (25): 17482–91. doi:10.1074/jbc.M601895200. PMID 16627474. 2009년 4월 25일에 원본 문서에서 보존된 문서. 2015년 11월 10일에 확인함. CS1 관리 - 여러 이름 (링크)
Manju K, Muralikrishna B, Parnaik VK (July 2006). “Expression of disease-causing lamin A mutants impairs the formation of DNA repair foci”. 《J. Cell. Sci.》 119 (Pt 13): 2704–14. doi:10.1242/jcs.03009. PMID 16772334. CS1 관리 - 여러 이름 (링크)
Scaffidi P, Misteli T (May 2006). “Lamin A-dependent nuclear defects in human aging”. 《Science》 312 (5776): 1059–63. doi:10.1126/science.1127168. PMC 1855250. PMID 16645051.
Brosh RM, Bohr VA (2007). “Human premature aging, DNA repair and RecQ helicases”. 《Nucleic Acids Res.》 35 (22): 7527–44. doi:10.1093/nar/gkm1008. PMC 2190726. PMID 18006573.
Kitao S, Shimamoto A, Goto M, 외. (May 1999). “Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome”. 《Nat. Genet.》 22 (1): 82–4. doi:10.1038/8788. PMID 10319867.
Kleijer WJ, Laugel V, Berneburg M, 외. (May 2008). “Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy”. 《DNA Repair (Amst.)》 7 (5): 744–50. doi:10.1016/j.dnarep.2008.01.014. PMID 18329345.

elsevier.com

linkinghub.elsevier.com

Kleijer WJ, Laugel V, Berneburg M, 외. (May 2008). “Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy”. 《DNA Repair (Amst.)》 7 (5): 744–50. doi:10.1016/j.dnarep.2008.01.014. PMID 18329345.

jbc.org

Biton S, Dar I, Mittelman L, Pereg Y, Barzilai A, Shiloh Y (June 2006). “Nuclear ataxia-telangiectasia mutated (ATM) mediates the cellular response to DNA double strand breaks in human neuron-like cells”. 《J. Biol. Chem.》 281 (25): 17482–91. doi:10.1074/jbc.M601895200. PMID 16627474. 2009년 4월 25일에 원본 문서에서 보존된 문서. 2015년 11월 10일에 확인함. CS1 관리 - 여러 이름 (링크)

nih.gov

ncbi.nlm.nih.gov

Biton S, Dar I, Mittelman L, Pereg Y, Barzilai A, Shiloh Y (June 2006). “Nuclear ataxia-telangiectasia mutated (ATM) mediates the cellular response to DNA double strand breaks in human neuron-like cells”. 《J. Biol. Chem.》 281 (25): 17482–91. doi:10.1074/jbc.M601895200. PMID 16627474. 2009년 4월 25일에 원본 문서에서 보존된 문서. 2015년 11월 10일에 확인함. CS1 관리 - 여러 이름 (링크)
Manju K, Muralikrishna B, Parnaik VK (July 2006). “Expression of disease-causing lamin A mutants impairs the formation of DNA repair foci”. 《J. Cell. Sci.》 119 (Pt 13): 2704–14. doi:10.1242/jcs.03009. PMID 16772334. CS1 관리 - 여러 이름 (링크)
Scaffidi P, Misteli T (May 2006). “Lamin A-dependent nuclear defects in human aging”. 《Science》 312 (5776): 1059–63. doi:10.1126/science.1127168. PMC 1855250. PMID 16645051.
Brosh RM, Bohr VA (2007). “Human premature aging, DNA repair and RecQ helicases”. 《Nucleic Acids Res.》 35 (22): 7527–44. doi:10.1093/nar/gkm1008. PMC 2190726. PMID 18006573.
Kitao S, Shimamoto A, Goto M, 외. (May 1999). “Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome”. 《Nat. Genet.》 22 (1): 82–4. doi:10.1038/8788. PMID 10319867.
Kleijer WJ, Laugel V, Berneburg M, 외. (May 2008). “Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy”. 《DNA Repair (Amst.)》 7 (5): 744–50. doi:10.1016/j.dnarep.2008.01.014. PMID 18329345.

oxfordjournals.org

nar.oxfordjournals.org

Brosh RM, Bohr VA (2007). “Human premature aging, DNA repair and RecQ helicases”. 《Nucleic Acids Res.》 35 (22): 7527–44. doi:10.1093/nar/gkm1008. PMC 2190726. PMID 18006573.

web.archive.org

Biton S, Dar I, Mittelman L, Pereg Y, Barzilai A, Shiloh Y (June 2006). “Nuclear ataxia-telangiectasia mutated (ATM) mediates the cellular response to DNA double strand breaks in human neuron-like cells”. 《J. Biol. Chem.》 281 (25): 17482–91. doi:10.1074/jbc.M601895200. PMID 16627474. 2009년 4월 25일에 원본 문서에서 보존된 문서. 2015년 11월 10일에 확인함. CS1 관리 - 여러 이름 (링크)