Progerin (English Wikipedia)

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

refsWebsite

Global rank English rank

19nih.gov

4^th place

9doi.org

2^nd place

8worldcat.org

5^th place

2harvard.edu

18^th place

17^th place

1handle.net

102^nd place

76^th place

1semanticscholar.org

11^th place

8^th place

1sciencedaily.com

993^rd place

920^th place

doi.org

McClintock, Dayle; Gordon, Leslie B.; Djabali, Karima (2006-02-14). "Hutchinson–Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody". Proceedings of the National Academy of Sciences. 103 (7): 2154–2159. Bibcode:2006PNAS..103.2154M. doi:10.1073/pnas.0511133103. ISSN 0027-8424. PMC 1413759. PMID 16461887.
Eriksson, Maria; Brown, W. Ted; Gordon, Leslie B.; Glynn, Michael W.; Singer, Joel; Scott, Laura; Erdos, Michael R.; Robbins, Christiane M.; Moses, Tracy Y.; Berglund, Peter; Dutra, Amalia (May 2003). "Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome". Nature. 423 (6937): 293–298. Bibcode:2003Natur.423..293E. doi:10.1038/nature01629. hdl:2027.42/62684. ISSN 0028-0836. PMC 10540076. PMID 12714972. S2CID 4420150.
Scaffidi, Paola; Misteli, Tom (April 2008). "Lamin A-dependent misregulation of adult stem cells associated with accelerated ageing". Nature Cell Biology. 10 (4): 452–459. doi:10.1038/ncb1708. ISSN 1476-4679. PMC 2396576. PMID 18311132.
Noda, Asao; Mishima, Shuji; Hirai, Yuko; Hamasaki, Kanya; Landes, Reid D.; Mitani, Hiroshi; Haga, Kei; Kiyono, Tohru; Nakamura, Nori; Kodama, Yoshiaki (December 2015). "Progerin, the protein responsible for the Hutchinson-Gilford progeria syndrome, increases the unrepaired DNA damages following exposure to ionizing radiation". Genes and Environment. 37 (1): 13. doi:10.1186/s41021-015-0018-4. ISSN 1880-7062. PMC 4917958. PMID 27350809.
Komari, Celina J.; Guttman, Anne O.; Carr, Shelby R.; Trachtenberg, Taylor L.; Orloff, Elise A.; Haas, Ashley V.; Patrick, Andrew R.; Chowdhary, Sona; Waldman, Barbara C.; Waldman, Alan S. (December 2020). "Alteration of genetic recombination and double-strand break repair in human cells by progerin expression". DNA Repair. 96: 102975. doi:10.1016/j.dnarep.2020.102975. PMC 7669652. PMID 33010688.
Piekarowicz, Katarzyna; Machowska, Magdalena; Dzianisava, Volha; Rzepecki, Ryszard (February 2019). "Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment". Cells. 8 (2): 88. doi:10.3390/cells8020088. ISSN 2073-4409. PMC 6406247. PMID 30691039.
Dubik, Niina; Mai, Sabine (2020-12-09). "Lamin A/C: Function in Normal and Tumor Cells". Cancers. 12 (12): 3688. doi:10.3390/cancers12123688. ISSN 2072-6694. PMC 7764147. PMID 33316938.
Dhillon, Sohita (February 2021). "Lonafarnib: First Approval". Drugs. 81 (2): 283–289. doi:10.1007/s40265-020-01464-z. ISSN 0012-6667. PMC 7985116. PMID 33590450.
Liu, Baohua; Zhou, Zhongjun (June 2008). "Lamin A/C, laminopathies and premature ageing". Histology and Histopathology. 23 (6): 747–763. doi:10.14670/HH-23.747. ISSN 1699-5848. PMID 18366013.

handle.net

hdl.handle.net

Eriksson, Maria; Brown, W. Ted; Gordon, Leslie B.; Glynn, Michael W.; Singer, Joel; Scott, Laura; Erdos, Michael R.; Robbins, Christiane M.; Moses, Tracy Y.; Berglund, Peter; Dutra, Amalia (May 2003). "Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome". Nature. 423 (6937): 293–298. Bibcode:2003Natur.423..293E. doi:10.1038/nature01629. hdl:2027.42/62684. ISSN 0028-0836. PMC 10540076. PMID 12714972. S2CID 4420150.

harvard.edu

ui.adsabs.harvard.edu

McClintock, Dayle; Gordon, Leslie B.; Djabali, Karima (2006-02-14). "Hutchinson–Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody". Proceedings of the National Academy of Sciences. 103 (7): 2154–2159. Bibcode:2006PNAS..103.2154M. doi:10.1073/pnas.0511133103. ISSN 0027-8424. PMC 1413759. PMID 16461887.
Eriksson, Maria; Brown, W. Ted; Gordon, Leslie B.; Glynn, Michael W.; Singer, Joel; Scott, Laura; Erdos, Michael R.; Robbins, Christiane M.; Moses, Tracy Y.; Berglund, Peter; Dutra, Amalia (May 2003). "Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome". Nature. 423 (6937): 293–298. Bibcode:2003Natur.423..293E. doi:10.1038/nature01629. hdl:2027.42/62684. ISSN 0028-0836. PMC 10540076. PMID 12714972. S2CID 4420150.

nih.gov

pubmed.ncbi.nlm.nih.gov

McClintock, Dayle; Gordon, Leslie B.; Djabali, Karima (2006-02-14). "Hutchinson–Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody". Proceedings of the National Academy of Sciences. 103 (7): 2154–2159. Bibcode:2006PNAS..103.2154M. doi:10.1073/pnas.0511133103. ISSN 0027-8424. PMC 1413759. PMID 16461887.
Eriksson, Maria; Brown, W. Ted; Gordon, Leslie B.; Glynn, Michael W.; Singer, Joel; Scott, Laura; Erdos, Michael R.; Robbins, Christiane M.; Moses, Tracy Y.; Berglund, Peter; Dutra, Amalia (May 2003). "Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome". Nature. 423 (6937): 293–298. Bibcode:2003Natur.423..293E. doi:10.1038/nature01629. hdl:2027.42/62684. ISSN 0028-0836. PMC 10540076. PMID 12714972. S2CID 4420150.
Gordon, Leslie B.; Brown, W. Ted; Collins, Francis S. (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "Hutchinson-Gilford Progeria Syndrome", GeneReviews®, Seattle (WA): University of Washington, Seattle, PMID 20301300, retrieved 2022-04-26
Scaffidi, Paola; Misteli, Tom (April 2008). "Lamin A-dependent misregulation of adult stem cells associated with accelerated ageing". Nature Cell Biology. 10 (4): 452–459. doi:10.1038/ncb1708. ISSN 1476-4679. PMC 2396576. PMID 18311132.
Noda, Asao; Mishima, Shuji; Hirai, Yuko; Hamasaki, Kanya; Landes, Reid D.; Mitani, Hiroshi; Haga, Kei; Kiyono, Tohru; Nakamura, Nori; Kodama, Yoshiaki (December 2015). "Progerin, the protein responsible for the Hutchinson-Gilford progeria syndrome, increases the unrepaired DNA damages following exposure to ionizing radiation". Genes and Environment. 37 (1): 13. doi:10.1186/s41021-015-0018-4. ISSN 1880-7062. PMC 4917958. PMID 27350809.
Komari, Celina J.; Guttman, Anne O.; Carr, Shelby R.; Trachtenberg, Taylor L.; Orloff, Elise A.; Haas, Ashley V.; Patrick, Andrew R.; Chowdhary, Sona; Waldman, Barbara C.; Waldman, Alan S. (December 2020). "Alteration of genetic recombination and double-strand break repair in human cells by progerin expression". DNA Repair. 96: 102975. doi:10.1016/j.dnarep.2020.102975. PMC 7669652. PMID 33010688.
Piekarowicz, Katarzyna; Machowska, Magdalena; Dzianisava, Volha; Rzepecki, Ryszard (February 2019). "Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment". Cells. 8 (2): 88. doi:10.3390/cells8020088. ISSN 2073-4409. PMC 6406247. PMID 30691039.
Dubik, Niina; Mai, Sabine (2020-12-09). "Lamin A/C: Function in Normal and Tumor Cells". Cancers. 12 (12): 3688. doi:10.3390/cancers12123688. ISSN 2072-6694. PMC 7764147. PMID 33316938.
Dhillon, Sohita (February 2021). "Lonafarnib: First Approval". Drugs. 81 (2): 283–289. doi:10.1007/s40265-020-01464-z. ISSN 0012-6667. PMC 7985116. PMID 33590450.
Liu, Baohua; Zhou, Zhongjun (June 2008). "Lamin A/C, laminopathies and premature ageing". Histology and Histopathology. 23 (6): 747–763. doi:10.14670/HH-23.747. ISSN 1699-5848. PMID 18366013.

ncbi.nlm.nih.gov

McClintock, Dayle; Gordon, Leslie B.; Djabali, Karima (2006-02-14). "Hutchinson–Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody". Proceedings of the National Academy of Sciences. 103 (7): 2154–2159. Bibcode:2006PNAS..103.2154M. doi:10.1073/pnas.0511133103. ISSN 0027-8424. PMC 1413759. PMID 16461887.
Eriksson, Maria; Brown, W. Ted; Gordon, Leslie B.; Glynn, Michael W.; Singer, Joel; Scott, Laura; Erdos, Michael R.; Robbins, Christiane M.; Moses, Tracy Y.; Berglund, Peter; Dutra, Amalia (May 2003). "Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome". Nature. 423 (6937): 293–298. Bibcode:2003Natur.423..293E. doi:10.1038/nature01629. hdl:2027.42/62684. ISSN 0028-0836. PMC 10540076. PMID 12714972. S2CID 4420150.
Gordon, Leslie B.; Brown, W. Ted; Collins, Francis S. (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "Hutchinson-Gilford Progeria Syndrome", GeneReviews®, Seattle (WA): University of Washington, Seattle, PMID 20301300, retrieved 2022-04-26
Scaffidi, Paola; Misteli, Tom (April 2008). "Lamin A-dependent misregulation of adult stem cells associated with accelerated ageing". Nature Cell Biology. 10 (4): 452–459. doi:10.1038/ncb1708. ISSN 1476-4679. PMC 2396576. PMID 18311132.
Noda, Asao; Mishima, Shuji; Hirai, Yuko; Hamasaki, Kanya; Landes, Reid D.; Mitani, Hiroshi; Haga, Kei; Kiyono, Tohru; Nakamura, Nori; Kodama, Yoshiaki (December 2015). "Progerin, the protein responsible for the Hutchinson-Gilford progeria syndrome, increases the unrepaired DNA damages following exposure to ionizing radiation". Genes and Environment. 37 (1): 13. doi:10.1186/s41021-015-0018-4. ISSN 1880-7062. PMC 4917958. PMID 27350809.
Komari, Celina J.; Guttman, Anne O.; Carr, Shelby R.; Trachtenberg, Taylor L.; Orloff, Elise A.; Haas, Ashley V.; Patrick, Andrew R.; Chowdhary, Sona; Waldman, Barbara C.; Waldman, Alan S. (December 2020). "Alteration of genetic recombination and double-strand break repair in human cells by progerin expression". DNA Repair. 96: 102975. doi:10.1016/j.dnarep.2020.102975. PMC 7669652. PMID 33010688.
Piekarowicz, Katarzyna; Machowska, Magdalena; Dzianisava, Volha; Rzepecki, Ryszard (February 2019). "Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment". Cells. 8 (2): 88. doi:10.3390/cells8020088. ISSN 2073-4409. PMC 6406247. PMID 30691039.
Dubik, Niina; Mai, Sabine (2020-12-09). "Lamin A/C: Function in Normal and Tumor Cells". Cancers. 12 (12): 3688. doi:10.3390/cancers12123688. ISSN 2072-6694. PMC 7764147. PMID 33316938.
Dhillon, Sohita (February 2021). "Lonafarnib: First Approval". Drugs. 81 (2): 283–289. doi:10.1007/s40265-020-01464-z. ISSN 0012-6667. PMC 7985116. PMID 33590450.

sciencedaily.com

"Anti-cancer Drugs May Hold Promise For Premature Aging Disorder". ScienceDaily. Retrieved 2022-04-26.

semanticscholar.org

api.semanticscholar.org

Eriksson, Maria; Brown, W. Ted; Gordon, Leslie B.; Glynn, Michael W.; Singer, Joel; Scott, Laura; Erdos, Michael R.; Robbins, Christiane M.; Moses, Tracy Y.; Berglund, Peter; Dutra, Amalia (May 2003). "Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome". Nature. 423 (6937): 293–298. Bibcode:2003Natur.423..293E. doi:10.1038/nature01629. hdl:2027.42/62684. ISSN 0028-0836. PMC 10540076. PMID 12714972. S2CID 4420150.

worldcat.org

search.worldcat.org

McClintock, Dayle; Gordon, Leslie B.; Djabali, Karima (2006-02-14). "Hutchinson–Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody". Proceedings of the National Academy of Sciences. 103 (7): 2154–2159. Bibcode:2006PNAS..103.2154M. doi:10.1073/pnas.0511133103. ISSN 0027-8424. PMC 1413759. PMID 16461887.
Eriksson, Maria; Brown, W. Ted; Gordon, Leslie B.; Glynn, Michael W.; Singer, Joel; Scott, Laura; Erdos, Michael R.; Robbins, Christiane M.; Moses, Tracy Y.; Berglund, Peter; Dutra, Amalia (May 2003). "Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome". Nature. 423 (6937): 293–298. Bibcode:2003Natur.423..293E. doi:10.1038/nature01629. hdl:2027.42/62684. ISSN 0028-0836. PMC 10540076. PMID 12714972. S2CID 4420150.
Scaffidi, Paola; Misteli, Tom (April 2008). "Lamin A-dependent misregulation of adult stem cells associated with accelerated ageing". Nature Cell Biology. 10 (4): 452–459. doi:10.1038/ncb1708. ISSN 1476-4679. PMC 2396576. PMID 18311132.
Noda, Asao; Mishima, Shuji; Hirai, Yuko; Hamasaki, Kanya; Landes, Reid D.; Mitani, Hiroshi; Haga, Kei; Kiyono, Tohru; Nakamura, Nori; Kodama, Yoshiaki (December 2015). "Progerin, the protein responsible for the Hutchinson-Gilford progeria syndrome, increases the unrepaired DNA damages following exposure to ionizing radiation". Genes and Environment. 37 (1): 13. doi:10.1186/s41021-015-0018-4. ISSN 1880-7062. PMC 4917958. PMID 27350809.
Piekarowicz, Katarzyna; Machowska, Magdalena; Dzianisava, Volha; Rzepecki, Ryszard (February 2019). "Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment". Cells. 8 (2): 88. doi:10.3390/cells8020088. ISSN 2073-4409. PMC 6406247. PMID 30691039.
Dubik, Niina; Mai, Sabine (2020-12-09). "Lamin A/C: Function in Normal and Tumor Cells". Cancers. 12 (12): 3688. doi:10.3390/cancers12123688. ISSN 2072-6694. PMC 7764147. PMID 33316938.
Dhillon, Sohita (February 2021). "Lonafarnib: First Approval". Drugs. 81 (2): 283–289. doi:10.1007/s40265-020-01464-z. ISSN 0012-6667. PMC 7985116. PMID 33590450.
Liu, Baohua; Zhou, Zhongjun (June 2008). "Lamin A/C, laminopathies and premature ageing". Histology and Histopathology. 23 (6): 747–763. doi:10.14670/HH-23.747. ISSN 1699-5848. PMID 18366013.