Xeroderma pigmentosum (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Xeroderma pigmentosum" in English language version.

refsWebsite

Global rank English rank

21nih.gov

4^th place

14doi.org

2^nd place

4web.archive.org

1^st place

4books.google.com

3^rd place

3semanticscholar.org

11^th place

8^th place

1dermnetnz.org

7,563^rd place

5,361^st place

1myriad.com

low place

1rarediseases.org

5,181^st place

3,260^th place

1harvard.edu

18^th place

17^th place

1handle.net

102^nd place

76^th place

1indiatoday.in

94^th place

66^th place

1clinuvel.com

low place

1fda.gov

447^th place

338^th place

1scenesse.com

low place

1jamanetwork.com

2,650^th place

3,409^th place

1baltimoresun.com

453^rd place

267^th place

1latimes.com

22^nd place

19^th place

1variety.com

13^th place

12^th place

1capradio.org

low place

1deankoontz.com

low place

1pbs.org

198^th place

154^th place

1abqjournal.com

2,906^th place

1,720^th place

1peoplesworld.org

low place

9,498^th place

1vov.vn

3,364^th place

low place

abqjournal.com

Ziff D. "Hiding From the Sun". The Albuquerque Journal. Retrieved 2018-06-29.

baltimoresun.com

digitaledition.baltimoresun.com

Walsh, Katie (23 March 2018). "No spark in sick teen romance - Baltimore Sun". Baltimore Sun. Tribune New Service. Retrieved 2018-07-08.

books.google.com

Ahmad S, Hanaoka F (2008). Molecular Mechanisms of Xeroderma Pigmentosum. Springer Science & Business Media. p. 17. ISBN 9780387095998.
Griffiths C, Barker J, Bleiker T, Chalmers R, Creamer D (2016). Rook's Textbook of Dermatology, 4 Volume Set. John Wiley & Sons. ISBN 9781118441190.
Salway JG (2011). Medical Biochemistry at a Glance. John Wiley & Sons. p. 313. ISBN 9781118292402.
Almeida, Craig A.; Barry, Sheila A. (2011-08-26). Cancer: Basic Science and Clinical Aspects. John Wiley & Sons. ISBN 9781444357394.

capradio.org

2017 Interview, capradio.org, 2017.

clinuvel.com

"SCENESSE® (afamelanotide 16mg) – Welcome to CLINUVEL". Archived from the original on 2020-10-20. Retrieved 2020-09-24.

deankoontz.com

"Frequently Asked Questions". Dean Koontz. Archived from the original on 24 August 2018. Retrieved 24 August 2018.

dermnetnz.org

"Xeroderma pigmentosum". dermnetnz.org. Retrieved 25 February 2020.

doi.org

Halpern J, Hopping B, Brostoff JM (October 2008). "Photosensitivity, corneal scarring and developmental delay: Xeroderma Pigmentosum in a tropical country". Cases Journal. 1 (1): 254. doi:10.1186/1757-1626-1-254. PMC 2577106. PMID 18937855.
Lehmann AR, McGibbon D, Stefanini M (November 2011). "Xeroderma pigmentosum". Orphanet Journal of Rare Diseases. 6: 70. doi:10.1186/1750-1172-6-70. PMC 3221642. PMID 22044607.
Brooks PJ (July 2008). "The 8,5'-cyclopurine-2'-deoxynucleosides: candidate neurodegenerative DNA lesions in xeroderma pigmentosum, and unique probes of transcription and nucleotide excision repair". DNA Repair. 7 (7): 1168–79. doi:10.1016/j.dnarep.2008.03.016. PMC 2797313. PMID 18495558.
Daya-Grosjean L, Sarasin A (April 2005). "The role of UV induced lesions in skin carcinogenesis: an overview of oncogene and tumor suppressor gene modifications in xeroderma pigmentosum skin tumors". Mutation Research. 571 (1–2): 43–56. Bibcode:2005MRFMM.571...43D. doi:10.1016/j.mrfmmm.2004.11.013. PMID 15748637.
Sugitani N, Sivley RM, Perry KE, Capra JA, Chazin WJ (August 2016). "XPA: A key scaffold for human nucleotide excision repair". DNA Repair. 44: 123–135. doi:10.1016/j.dnarep.2016.05.018. PMC 4958585. PMID 27247238.
Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, Emmert S, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH (November 2006). "Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome". Human Mutation. 27 (11): 1092–103. doi:10.1002/humu.20392. PMID 16947863. S2CID 22852219.
Sugasawa K, Ng JM, Masutani C, Iwai S, van der Spek PJ, Eker AP, Hanaoka F, Bootsma D, Hoeijmakers JH (August 1998). "Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair". Molecular Cell. 2 (2): 223–32. doi:10.1016/s1097-2765(00)80132-x. PMID 9734359.
Andressoo JO, Hoeijmakers JH, Mitchell JR (December 2006). "Nucleotide excision repair disorders and the balance between cancer and aging". Cell Cycle. 5 (24): 2886–8. doi:10.4161/cc.5.24.3565. PMID 17172862. S2CID 43682426.
van de Ven M, Andressoo JO, van der Horst GT, Hoeijmakers JH, Mitchell JR (November 2012). "Effects of compound heterozygosity at the Xpd locus on cancer and ageing in mouse models". DNA Repair. 11 (11): 874–83. doi:10.1016/j.dnarep.2012.08.003. PMID 23046824.
Iovine B, Iannella ML, Bevilacqua MA (December 2011). "Damage-specific DNA binding protein 1 (DDB1): a protein with a wide range of functions". The International Journal of Biochemistry & Cell Biology. 43 (12): 1664–7. doi:10.1016/j.biocel.2011.09.001. PMID 21959250.
Sijbers AM, de Laat WL, Ariza RR, Biggerstaff M, Wei YF, Moggs JG, Carter KC, Shell BK, Evans E, de Jong MC, Rademakers S, de Rooij J, Jaspers NG, Hoeijmakers JH, Wood RD (September 1996). "Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease". Cell. 86 (5): 811–22. doi:10.1016/s0092-8674(00)80155-5. hdl:1765/3110. PMID 8797827. S2CID 12957716.
Barnhoorn S, Uittenboogaard LM, Jaarsma D, Vermeij WP, Tresini M, Weymaere M, Menoni H, Brandt RM, de Waard MC, Botter SM, Sarker AH, Jaspers NG, van der Horst GT, Cooper PK, Hoeijmakers JH, van der Pluijm I (October 2014). "Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency". PLOS Genetics. 10 (10): e1004686. doi:10.1371/journal.pgen.1004686. PMC 4191938. PMID 25299392.
Kraemer, Kenneth H. (1 February 1987). "Xeroderma Pigmentosum". Archives of Dermatology. 123 (2): 241. doi:10.1001/archderm.1987.01660260111026. Retrieved 21 June 2020.
Kraemer KH, DiGiovanna JJ (March 2015). "Forty years of research on xeroderma pigmentosum at the US National Institutes of Health". Photochemistry and Photobiology. 91 (2): 452–9. doi:10.1111/php.12345. PMC 4355260. PMID 25220021.

fda.gov

Commissioner, Office of the (2020-03-24). "FDA approves first treatment to increase pain-free light exposure in patients with a rare disorder". FDA. Retrieved 2020-09-24.^{[dead link]}

handle.net

hdl.handle.net

Sijbers AM, de Laat WL, Ariza RR, Biggerstaff M, Wei YF, Moggs JG, Carter KC, Shell BK, Evans E, de Jong MC, Rademakers S, de Rooij J, Jaspers NG, Hoeijmakers JH, Wood RD (September 1996). "Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease". Cell. 86 (5): 811–22. doi:10.1016/s0092-8674(00)80155-5. hdl:1765/3110. PMID 8797827. S2CID 12957716.

harvard.edu

ui.adsabs.harvard.edu

Daya-Grosjean L, Sarasin A (April 2005). "The role of UV induced lesions in skin carcinogenesis: an overview of oncogene and tumor suppressor gene modifications in xeroderma pigmentosum skin tumors". Mutation Research. 571 (1–2): 43–56. Bibcode:2005MRFMM.571...43D. doi:10.1016/j.mrfmmm.2004.11.013. PMID 15748637.

indiatoday.in

"Xeroderma pigmentosum". India Today. September 24, 2014. Retrieved 2020-07-05.

jamanetwork.com

Kraemer, Kenneth H. (1 February 1987). "Xeroderma Pigmentosum". Archives of Dermatology. 123 (2): 241. doi:10.1001/archderm.1987.01660260111026. Retrieved 21 June 2020.

latimes.com

Holder K (1994-05-01). "Family in Twilight for Sun-Sensitive Girls : Health: Two daughters have a rare genetic intolerance that leaves victims vulnerable to skin cancers, blindness and neurological damage after exposure to sunlight". Associated Press. Retrieved 2017-09-14.

myriad.com

"Not found". Archived from the original on 2022-10-26. Retrieved 2023-03-06.

nih.gov

pubmed.ncbi.nlm.nih.gov

Halpern J, Hopping B, Brostoff JM (October 2008). "Photosensitivity, corneal scarring and developmental delay: Xeroderma Pigmentosum in a tropical country". Cases Journal. 1 (1): 254. doi:10.1186/1757-1626-1-254. PMC 2577106. PMID 18937855.
Lehmann AR, McGibbon D, Stefanini M (November 2011). "Xeroderma pigmentosum". Orphanet Journal of Rare Diseases. 6: 70. doi:10.1186/1750-1172-6-70. PMC 3221642. PMID 22044607.
Brooks PJ (July 2008). "The 8,5'-cyclopurine-2'-deoxynucleosides: candidate neurodegenerative DNA lesions in xeroderma pigmentosum, and unique probes of transcription and nucleotide excision repair". DNA Repair. 7 (7): 1168–79. doi:10.1016/j.dnarep.2008.03.016. PMC 2797313. PMID 18495558.
Daya-Grosjean L, Sarasin A (April 2005). "The role of UV induced lesions in skin carcinogenesis: an overview of oncogene and tumor suppressor gene modifications in xeroderma pigmentosum skin tumors". Mutation Research. 571 (1–2): 43–56. Bibcode:2005MRFMM.571...43D. doi:10.1016/j.mrfmmm.2004.11.013. PMID 15748637.
Sugitani N, Sivley RM, Perry KE, Capra JA, Chazin WJ (August 2016). "XPA: A key scaffold for human nucleotide excision repair". DNA Repair. 44: 123–135. doi:10.1016/j.dnarep.2016.05.018. PMC 4958585. PMID 27247238.
Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, Emmert S, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH (November 2006). "Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome". Human Mutation. 27 (11): 1092–103. doi:10.1002/humu.20392. PMID 16947863. S2CID 22852219.
Sugasawa K, Ng JM, Masutani C, Iwai S, van der Spek PJ, Eker AP, Hanaoka F, Bootsma D, Hoeijmakers JH (August 1998). "Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair". Molecular Cell. 2 (2): 223–32. doi:10.1016/s1097-2765(00)80132-x. PMID 9734359.
Andressoo JO, Hoeijmakers JH, Mitchell JR (December 2006). "Nucleotide excision repair disorders and the balance between cancer and aging". Cell Cycle. 5 (24): 2886–8. doi:10.4161/cc.5.24.3565. PMID 17172862. S2CID 43682426.
van de Ven M, Andressoo JO, van der Horst GT, Hoeijmakers JH, Mitchell JR (November 2012). "Effects of compound heterozygosity at the Xpd locus on cancer and ageing in mouse models". DNA Repair. 11 (11): 874–83. doi:10.1016/j.dnarep.2012.08.003. PMID 23046824.
Iovine B, Iannella ML, Bevilacqua MA (December 2011). "Damage-specific DNA binding protein 1 (DDB1): a protein with a wide range of functions". The International Journal of Biochemistry & Cell Biology. 43 (12): 1664–7. doi:10.1016/j.biocel.2011.09.001. PMID 21959250.
Sijbers AM, de Laat WL, Ariza RR, Biggerstaff M, Wei YF, Moggs JG, Carter KC, Shell BK, Evans E, de Jong MC, Rademakers S, de Rooij J, Jaspers NG, Hoeijmakers JH, Wood RD (September 1996). "Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease". Cell. 86 (5): 811–22. doi:10.1016/s0092-8674(00)80155-5. hdl:1765/3110. PMID 8797827. S2CID 12957716.
Barnhoorn S, Uittenboogaard LM, Jaarsma D, Vermeij WP, Tresini M, Weymaere M, Menoni H, Brandt RM, de Waard MC, Botter SM, Sarker AH, Jaspers NG, van der Horst GT, Cooper PK, Hoeijmakers JH, van der Pluijm I (October 2014). "Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency". PLOS Genetics. 10 (10): e1004686. doi:10.1371/journal.pgen.1004686. PMC 4191938. PMID 25299392.
Kraemer KH, DiGiovanna JJ (March 2015). "Forty years of research on xeroderma pigmentosum at the US National Institutes of Health". Photochemistry and Photobiology. 91 (2): 452–9. doi:10.1111/php.12345. PMC 4355260. PMID 25220021.

ncbi.nlm.nih.gov

Halpern J, Hopping B, Brostoff JM (October 2008). "Photosensitivity, corneal scarring and developmental delay: Xeroderma Pigmentosum in a tropical country". Cases Journal. 1 (1): 254. doi:10.1186/1757-1626-1-254. PMC 2577106. PMID 18937855.
Lehmann AR, McGibbon D, Stefanini M (November 2011). "Xeroderma pigmentosum". Orphanet Journal of Rare Diseases. 6: 70. doi:10.1186/1750-1172-6-70. PMC 3221642. PMID 22044607.
Brooks PJ (July 2008). "The 8,5'-cyclopurine-2'-deoxynucleosides: candidate neurodegenerative DNA lesions in xeroderma pigmentosum, and unique probes of transcription and nucleotide excision repair". DNA Repair. 7 (7): 1168–79. doi:10.1016/j.dnarep.2008.03.016. PMC 2797313. PMID 18495558.
Sugitani N, Sivley RM, Perry KE, Capra JA, Chazin WJ (August 2016). "XPA: A key scaffold for human nucleotide excision repair". DNA Repair. 44: 123–135. doi:10.1016/j.dnarep.2016.05.018. PMC 4958585. PMID 27247238.
Barnhoorn S, Uittenboogaard LM, Jaarsma D, Vermeij WP, Tresini M, Weymaere M, Menoni H, Brandt RM, de Waard MC, Botter SM, Sarker AH, Jaspers NG, van der Horst GT, Cooper PK, Hoeijmakers JH, van der Pluijm I (October 2014). "Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency". PLOS Genetics. 10 (10): e1004686. doi:10.1371/journal.pgen.1004686. PMC 4191938. PMID 25299392.
Kraemer KH, DiGiovanna JJ (March 2015). "Forty years of research on xeroderma pigmentosum at the US National Institutes of Health". Photochemistry and Photobiology. 91 (2): 452–9. doi:10.1111/php.12345. PMC 4355260. PMID 25220021.

ghr.nlm.nih.gov

"Xeroderma pigmentosum". Genetics Home Reference. U.S. Library of Medicine. 26 June 2018. Retrieved 28 June 2018.

rarediseases.info.nih.gov

"Xeroderma pigmentosum". Genetic and Rare Diseases Information Center (GARD). U.S. Department of Health and Human Services. 2018. Retrieved 28 June 2018.

pbs.org

"A Rare Genetic Disorder Is Stalking the Children of the Navajo Nation In POV's 'Sun Kissed,' Premiering Thursday, Oct. 18, 2012, on PBS". 7 June 2012. Archived from the original on 2018-06-29. Retrieved 2018-06-29.

peoplesworld.org

Bender A (2013-03-06). "Rare disease suddenly arises on Navajo Reservation". People's World. Retrieved 2018-06-29.

rarediseases.org

"Xeroderma Pigmentosum". NORD (National Organization for Rare Disorders). 2017. Retrieved 28 June 2018.

scenesse.com

"Scenesse (afamelanotide) for adults with a history of phototoxic reactions from EPP". SCENESSE® (Afamelanotide). Retrieved 2020-09-24.

semanticscholar.org

api.semanticscholar.org

Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, Emmert S, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH (November 2006). "Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome". Human Mutation. 27 (11): 1092–103. doi:10.1002/humu.20392. PMID 16947863. S2CID 22852219.
Andressoo JO, Hoeijmakers JH, Mitchell JR (December 2006). "Nucleotide excision repair disorders and the balance between cancer and aging". Cell Cycle. 5 (24): 2886–8. doi:10.4161/cc.5.24.3565. PMID 17172862. S2CID 43682426.
Sijbers AM, de Laat WL, Ariza RR, Biggerstaff M, Wei YF, Moggs JG, Carter KC, Shell BK, Evans E, de Jong MC, Rademakers S, de Rooij J, Jaspers NG, Hoeijmakers JH, Wood RD (September 1996). "Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease". Cell. 86 (5): 811–22. doi:10.1016/s0092-8674(00)80155-5. hdl:1765/3110. PMID 8797827. S2CID 12957716.

variety.com

Voros D (1994-04-15). "Review: 'Children of the Dark'". Variety. Retrieved 2017-09-14.

vov.vn

Khúc hát mặt trời (in Vietnamese), 7 November 2015, retrieved 2021-08-09

web.archive.org

"Not found". Archived from the original on 2022-10-26. Retrieved 2023-03-06.
"SCENESSE® (afamelanotide 16mg) – Welcome to CLINUVEL". Archived from the original on 2020-10-20. Retrieved 2020-09-24.
"Frequently Asked Questions". Dean Koontz. Archived from the original on 24 August 2018. Retrieved 24 August 2018.
"A Rare Genetic Disorder Is Stalking the Children of the Navajo Nation In POV's 'Sun Kissed,' Premiering Thursday, Oct. 18, 2012, on PBS". 7 June 2012. Archived from the original on 2018-06-29. Retrieved 2018-06-29.