George M. Martin (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "George M. Martin" in English language version.

refsWebsite

Global rank English rank

24nih.gov

4^th place

19doi.org

2^nd place

19worldcat.org

5^th place

9semanticscholar.org

11^th place

8^th place

6harvard.edu

18^th place

17^th place

4washington.edu

1,067^th place

749^th place

1umh.de

low place

1nature.com

234^th place

397^th place

1umich.edu

459^th place

360^th place

1handle.net

102^nd place

76^th place

1ellison-med-fn.org

low place

1geron.org

low place

1alz.org

low place

1businesswire.com

615^th place

407^th place

alz.org

aaic.alz.org

"AAIC Lifetime Achievement Awards | Alzheimer's Association". AAIC. Retrieved 2023-08-27.

businesswire.com

"The 22nd Longevity Prize of the Fondation IPSEN is Awarded to Andrzej Bartke". www.businesswire.com. 2017-07-24. Retrieved 2023-08-28.

doi.org

Rabinovitch, Peter S; Disteche, Christine; Kaeberlein, Matt; Martin, Kelsey C; Monnat, Raymond J; Oshima, Junko; Promislow, Daniel (2023-01-04). "In Memory of George M. Martin". The Journals of Gerontology: Series A. 78 (4): 619–620. doi:10.1093/gerona/glac257. ISSN 1079-5006. PMID 36609876.
Austad, Steven N. (2023-06-01). "George M. Martin: tribute and personal remembrance". GeroScience. 45 (3): 2085–2086. doi:10.1007/s11357-023-00747-z. ISSN 2509-2723. PMC 10400482. PMID 36745353.
McALISTER, R.; Martin, G. M.; Benditt, E. P. (June 1961). "Evidence for Multiple Cæruloplasmin Components in Human Serum". Nature. 190 (4779): 927–929. Bibcode:1961Natur.190..927M. doi:10.1038/190927b0. ISSN 1476-4687. PMID 13773713. S2CID 4251125.
Martin, G. M.; Tuan, A. (October 1966). "A definitive cloning technique for human fibroblast cultures". Proceedings of the Society for Experimental Biology and Medicine. 123 (1): 138–140. doi:10.3181/00379727-123-31423. ISSN 0037-9727. PMID 5924411. S2CID 34390842.
Martin, G. M.; Sprague, C.; Bryant, J. S. (1967-05-06). "Mitotic nondisjunction in cultivated human cells". Nature. 214 (5088): 612–613. Bibcode:1967Natur.214..612M. doi:10.1038/214612a0. ISSN 0028-0836. PMID 4226946. S2CID 4155643.
Schellenberg, G. D.; Bird, T. D.; Wijsman, E. M.; Orr, H. T.; Anderson, L.; Nemens, E.; White, J. A.; Bonnycastle, L.; Weber, J. L.; Alonso, M. E. (1992-10-23). "Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14". Science. 258 (5082): 668–671. Bibcode:1992Sci...258..668S. doi:10.1126/science.1411576. ISSN 0036-8075. PMID 1411576.
Schellenberg GD, Deeb SS, Boehnke M, et al. (April 1987). "Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type". Journal of Neurogenetics. 4 (2–3): 97–108. doi:10.3109/01677068709102337. PMID 2885403.
Guo, Q.; Furukawa, K.; Sopher, B. L.; Pham, D. G.; Xie, J.; Robinson, N.; Martin, G. M.; Mattson, M. P. (1996-12-20). "Alzheimer's PS-1 mutation perturbs calcium homeostasis and sensitizes PC12 cells to death induced by amyloid beta-peptide". NeuroReport. 8 (1): 379–383. doi:10.1097/00001756-199612200-00074. ISSN 0959-4965. PMID 9051814. S2CID 11404496.
Oshima J, Yu CE, Boehnke M, et al. (September 1994). "Integrated mapping analysis of the Werner syndrome region of chromosome 8" (PDF). Genomics. 23 (1): 100–13. doi:10.1006/geno.1994.1464. hdl:2027.42/31345. PMID 7829057.
Yu, C. E.; Oshima, J.; Fu, Y. H.; Wijsman, E. M.; Hisama, F.; Alisch, R.; Matthews, S.; Nakura, J.; Miki, T.; Ouais, S.; Martin, G. M.; Mulligan, J.; Schellenberg, G. D. (1996-04-12). "Positional cloning of the Werner's syndrome gene". Science. 272 (5259): 258–262. Bibcode:1996Sci...272..258Y. doi:10.1126/science.272.5259.258. ISSN 0036-8075. PMID 8602509. S2CID 18172607.
Gray, M. D.; Shen, J. C.; Kamath-Loeb, A. S.; Blank, A.; Sopher, B. L.; Martin, G. M.; Oshima, J.; Loeb, L. A. (September 1997). "The Werner syndrome protein is a DNA helicase". Nature Genetics. 17 (1): 100–103. doi:10.1038/ng0997-100. ISSN 1061-4036. PMID 9288107. S2CID 20587915.
Balajee, A. S.; Machwe, A.; May, A.; Gray, M. D.; Oshima, J.; Martin, G. M.; Nehlin, J. O.; Brosh, R.; Orren, D. K.; Bohr, V. A. (August 1999). "The Werner syndrome protein is involved in RNA polymerase II transcription". Molecular Biology of the Cell. 10 (8): 2655–2668. doi:10.1091/mbc.10.8.2655. ISSN 1059-1524. PMC 25497. PMID 10436020.
Martin, G. M.; Sprague, C. A. (1972-12-23). "Clonal senescence and atherosclerosis". Lancet. 2 (7791): 1370–1371. doi:10.1016/s0140-6736(72)92819-x. ISSN 0140-6736. PMID 4118240.
Martin, G.; Ogburn, C.; Sprague, C. (1975). "Senescence and Vascular Disease". Explorations in Aging. Advances in Experimental Medicine and Biology. Vol. 61. pp. 163–193. doi:10.1007/978-1-4615-9032-3_9. ISBN 978-1-4615-9034-7. ISSN 0065-2598. PMID 810006.
Hoehn, H.; Bryant, E. M.; Johnston, P.; Norwood, T. H.; Martin, G. M. (1975-12-18). "Non-selective isolation, stability and longevity of hybrids between normal human somatic cells". Nature. 258 (5536): 608–610. Bibcode:1975Natur.258..608H. doi:10.1038/258608a0. ISSN 0028-0836. PMID 1207734. S2CID 11467452.
Norwood, T. H.; Pendergrass, W. R.; Sprague, C. A.; Martin, G. M. (June 1974). "Dominance of the senescent phenotype in heterokaryons between replicative and post-replicative human fibroblast-like cells". Proceedings of the National Academy of Sciences of the United States of America. 71 (6): 2231–2235. Bibcode:1974PNAS...71.2231N. doi:10.1073/pnas.71.6.2231. ISSN 0027-8424. PMC 388425. PMID 4366757.
Martin, G. M.; Ogburn, C. E.; Colgin, L. M.; Gown, A. M.; Edland, S. D.; Monnat, R. J. (February 1996). "Somatic mutations are frequent and increase with age in human kidney epithelial cells". Human Molecular Genetics. 5 (2): 215–221. doi:10.1093/hmg/5.2.215. ISSN 0964-6906. PMID 8824877.
Guo, Q.; Sebastian, L.; Sopher, B. L.; Miller, M. W.; Ware, C. B.; Martin, G. M.; Mattson, M. P. (March 1999). "Increased vulnerability of hippocampal neurons from presenilin-1 mutant knock-in mice to amyloid beta-peptide toxicity: central roles of superoxide production and caspase activation". Journal of Neurochemistry. 72 (3): 1019–1029. doi:10.1046/j.1471-4159.1999.0721019.x. ISSN 0022-3042. PMID 10037473. S2CID 221870765.
Martin, G. M. (1971). "Brief proposal on immortality: an interim solution". Perspectives in Biology and Medicine. 14 (2): 339. doi:10.1353/pbm.1971.0015. ISSN 0031-5982. PMID 5546258. S2CID 71120068.

ellison-med-fn.org

"EMF: Bio". www.ellison-med-fn.org. Retrieved 2023-08-27.

geron.org

"Awardees". www.geron.org. Retrieved 2023-08-27.

handle.net

hdl.handle.net

Oshima J, Yu CE, Boehnke M, et al. (September 1994). "Integrated mapping analysis of the Werner syndrome region of chromosome 8" (PDF). Genomics. 23 (1): 100–13. doi:10.1006/geno.1994.1464. hdl:2027.42/31345. PMID 7829057.

harvard.edu

ui.adsabs.harvard.edu

McALISTER, R.; Martin, G. M.; Benditt, E. P. (June 1961). "Evidence for Multiple Cæruloplasmin Components in Human Serum". Nature. 190 (4779): 927–929. Bibcode:1961Natur.190..927M. doi:10.1038/190927b0. ISSN 1476-4687. PMID 13773713. S2CID 4251125.
Martin, G. M.; Sprague, C.; Bryant, J. S. (1967-05-06). "Mitotic nondisjunction in cultivated human cells". Nature. 214 (5088): 612–613. Bibcode:1967Natur.214..612M. doi:10.1038/214612a0. ISSN 0028-0836. PMID 4226946. S2CID 4155643.
Schellenberg, G. D.; Bird, T. D.; Wijsman, E. M.; Orr, H. T.; Anderson, L.; Nemens, E.; White, J. A.; Bonnycastle, L.; Weber, J. L.; Alonso, M. E. (1992-10-23). "Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14". Science. 258 (5082): 668–671. Bibcode:1992Sci...258..668S. doi:10.1126/science.1411576. ISSN 0036-8075. PMID 1411576.
Yu, C. E.; Oshima, J.; Fu, Y. H.; Wijsman, E. M.; Hisama, F.; Alisch, R.; Matthews, S.; Nakura, J.; Miki, T.; Ouais, S.; Martin, G. M.; Mulligan, J.; Schellenberg, G. D. (1996-04-12). "Positional cloning of the Werner's syndrome gene". Science. 272 (5259): 258–262. Bibcode:1996Sci...272..258Y. doi:10.1126/science.272.5259.258. ISSN 0036-8075. PMID 8602509. S2CID 18172607.
Hoehn, H.; Bryant, E. M.; Johnston, P.; Norwood, T. H.; Martin, G. M. (1975-12-18). "Non-selective isolation, stability and longevity of hybrids between normal human somatic cells". Nature. 258 (5536): 608–610. Bibcode:1975Natur.258..608H. doi:10.1038/258608a0. ISSN 0028-0836. PMID 1207734. S2CID 11467452.
Norwood, T. H.; Pendergrass, W. R.; Sprague, C. A.; Martin, G. M. (June 1974). "Dominance of the senescent phenotype in heterokaryons between replicative and post-replicative human fibroblast-like cells". Proceedings of the National Academy of Sciences of the United States of America. 71 (6): 2231–2235. Bibcode:1974PNAS...71.2231N. doi:10.1073/pnas.71.6.2231. ISSN 0027-8424. PMC 388425. PMID 4366757.

nature.com

McALISTER, R.; Martin, G. M.; Benditt, E. P. (June 1961). "Evidence for Multiple Cæruloplasmin Components in Human Serum". Nature. 190 (4779): 927–929. Bibcode:1961Natur.190..927M. doi:10.1038/190927b0. ISSN 1476-4687. PMID 13773713. S2CID 4251125.

nih.gov

pubmed.ncbi.nlm.nih.gov

Rabinovitch, Peter S; Disteche, Christine; Kaeberlein, Matt; Martin, Kelsey C; Monnat, Raymond J; Oshima, Junko; Promislow, Daniel (2023-01-04). "In Memory of George M. Martin". The Journals of Gerontology: Series A. 78 (4): 619–620. doi:10.1093/gerona/glac257. ISSN 1079-5006. PMID 36609876.
Austad, Steven N. (2023-06-01). "George M. Martin: tribute and personal remembrance". GeroScience. 45 (3): 2085–2086. doi:10.1007/s11357-023-00747-z. ISSN 2509-2723. PMC 10400482. PMID 36745353.
McALISTER, R.; Martin, G. M.; Benditt, E. P. (June 1961). "Evidence for Multiple Cæruloplasmin Components in Human Serum". Nature. 190 (4779): 927–929. Bibcode:1961Natur.190..927M. doi:10.1038/190927b0. ISSN 1476-4687. PMID 13773713. S2CID 4251125.
Martin, G. M.; Derr, M. A.; Benditt, E. P. (March 1964). "Ceruloplasmins of Several Animal Species. Comparison of Electrophoretic Mobilities and Substrate Specificity". Laboratory Investigation; A Journal of Technical Methods and Pathology. 13: 282–287. ISSN 0023-6837. PMID 14127032.
Martin, G. M.; Tuan, A. (October 1966). "A definitive cloning technique for human fibroblast cultures". Proceedings of the Society for Experimental Biology and Medicine. 123 (1): 138–140. doi:10.3181/00379727-123-31423. ISSN 0037-9727. PMID 5924411. S2CID 34390842.
Martin, G. M.; Sprague, C.; Bryant, J. S. (1967-05-06). "Mitotic nondisjunction in cultivated human cells". Nature. 214 (5088): 612–613. Bibcode:1967Natur.214..612M. doi:10.1038/214612a0. ISSN 0028-0836. PMID 4226946. S2CID 4155643.
Martin, G. M.; Sprague, C. A.; Epstein, C. J. (July 1970). "Replicative life-span of cultivated human cells. Effects of donor's age, tissue, and genotype". Laboratory Investigation; A Journal of Technical Methods and Pathology. 23 (1): 86–92. ISSN 0023-6837. PMID 5431223.
Schellenberg, G. D.; Bird, T. D.; Wijsman, E. M.; Orr, H. T.; Anderson, L.; Nemens, E.; White, J. A.; Bonnycastle, L.; Weber, J. L.; Alonso, M. E. (1992-10-23). "Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14". Science. 258 (5082): 668–671. Bibcode:1992Sci...258..668S. doi:10.1126/science.1411576. ISSN 0036-8075. PMID 1411576.
Schellenberg GD, Deeb SS, Boehnke M, et al. (April 1987). "Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type". Journal of Neurogenetics. 4 (2–3): 97–108. doi:10.3109/01677068709102337. PMID 2885403.
Guo, Q.; Furukawa, K.; Sopher, B. L.; Pham, D. G.; Xie, J.; Robinson, N.; Martin, G. M.; Mattson, M. P. (1996-12-20). "Alzheimer's PS-1 mutation perturbs calcium homeostasis and sensitizes PC12 cells to death induced by amyloid beta-peptide". NeuroReport. 8 (1): 379–383. doi:10.1097/00001756-199612200-00074. ISSN 0959-4965. PMID 9051814. S2CID 11404496.
Oshima J, Yu CE, Boehnke M, et al. (September 1994). "Integrated mapping analysis of the Werner syndrome region of chromosome 8" (PDF). Genomics. 23 (1): 100–13. doi:10.1006/geno.1994.1464. hdl:2027.42/31345. PMID 7829057.
Yu, C. E.; Oshima, J.; Fu, Y. H.; Wijsman, E. M.; Hisama, F.; Alisch, R.; Matthews, S.; Nakura, J.; Miki, T.; Ouais, S.; Martin, G. M.; Mulligan, J.; Schellenberg, G. D. (1996-04-12). "Positional cloning of the Werner's syndrome gene". Science. 272 (5259): 258–262. Bibcode:1996Sci...272..258Y. doi:10.1126/science.272.5259.258. ISSN 0036-8075. PMID 8602509. S2CID 18172607.
Gray, M. D.; Shen, J. C.; Kamath-Loeb, A. S.; Blank, A.; Sopher, B. L.; Martin, G. M.; Oshima, J.; Loeb, L. A. (September 1997). "The Werner syndrome protein is a DNA helicase". Nature Genetics. 17 (1): 100–103. doi:10.1038/ng0997-100. ISSN 1061-4036. PMID 9288107. S2CID 20587915.
Balajee, A. S.; Machwe, A.; May, A.; Gray, M. D.; Oshima, J.; Martin, G. M.; Nehlin, J. O.; Brosh, R.; Orren, D. K.; Bohr, V. A. (August 1999). "The Werner syndrome protein is involved in RNA polymerase II transcription". Molecular Biology of the Cell. 10 (8): 2655–2668. doi:10.1091/mbc.10.8.2655. ISSN 1059-1524. PMC 25497. PMID 10436020.
Martin, G. M.; Sprague, C. A. (1972-12-23). "Clonal senescence and atherosclerosis". Lancet. 2 (7791): 1370–1371. doi:10.1016/s0140-6736(72)92819-x. ISSN 0140-6736. PMID 4118240.
Martin, G.; Ogburn, C.; Sprague, C. (1975). "Senescence and Vascular Disease". Explorations in Aging. Advances in Experimental Medicine and Biology. Vol. 61. pp. 163–193. doi:10.1007/978-1-4615-9032-3_9. ISBN 978-1-4615-9034-7. ISSN 0065-2598. PMID 810006.
Hoehn, H.; Bryant, E. M.; Johnston, P.; Norwood, T. H.; Martin, G. M. (1975-12-18). "Non-selective isolation, stability and longevity of hybrids between normal human somatic cells". Nature. 258 (5536): 608–610. Bibcode:1975Natur.258..608H. doi:10.1038/258608a0. ISSN 0028-0836. PMID 1207734. S2CID 11467452.
Norwood, T. H.; Pendergrass, W. R.; Sprague, C. A.; Martin, G. M. (June 1974). "Dominance of the senescent phenotype in heterokaryons between replicative and post-replicative human fibroblast-like cells". Proceedings of the National Academy of Sciences of the United States of America. 71 (6): 2231–2235. Bibcode:1974PNAS...71.2231N. doi:10.1073/pnas.71.6.2231. ISSN 0027-8424. PMC 388425. PMID 4366757.
Martin, G. M.; Ogburn, C. E.; Colgin, L. M.; Gown, A. M.; Edland, S. D.; Monnat, R. J. (February 1996). "Somatic mutations are frequent and increase with age in human kidney epithelial cells". Human Molecular Genetics. 5 (2): 215–221. doi:10.1093/hmg/5.2.215. ISSN 0964-6906. PMID 8824877.
Guo, Q.; Sebastian, L.; Sopher, B. L.; Miller, M. W.; Ware, C. B.; Martin, G. M.; Mattson, M. P. (March 1999). "Increased vulnerability of hippocampal neurons from presenilin-1 mutant knock-in mice to amyloid beta-peptide toxicity: central roles of superoxide production and caspase activation". Journal of Neurochemistry. 72 (3): 1019–1029. doi:10.1046/j.1471-4159.1999.0721019.x. ISSN 0022-3042. PMID 10037473. S2CID 221870765.
Martin, G. M. (1971). "Brief proposal on immortality: an interim solution". Perspectives in Biology and Medicine. 14 (2): 339. doi:10.1353/pbm.1971.0015. ISSN 0031-5982. PMID 5546258. S2CID 71120068.

ncbi.nlm.nih.gov

Austad, Steven N. (2023-06-01). "George M. Martin: tribute and personal remembrance". GeroScience. 45 (3): 2085–2086. doi:10.1007/s11357-023-00747-z. ISSN 2509-2723. PMC 10400482. PMID 36745353.
Balajee, A. S.; Machwe, A.; May, A.; Gray, M. D.; Oshima, J.; Martin, G. M.; Nehlin, J. O.; Brosh, R.; Orren, D. K.; Bohr, V. A. (August 1999). "The Werner syndrome protein is involved in RNA polymerase II transcription". Molecular Biology of the Cell. 10 (8): 2655–2668. doi:10.1091/mbc.10.8.2655. ISSN 1059-1524. PMC 25497. PMID 10436020.
Norwood, T. H.; Pendergrass, W. R.; Sprague, C. A.; Martin, G. M. (June 1974). "Dominance of the senescent phenotype in heterokaryons between replicative and post-replicative human fibroblast-like cells". Proceedings of the National Academy of Sciences of the United States of America. 71 (6): 2231–2235. Bibcode:1974PNAS...71.2231N. doi:10.1073/pnas.71.6.2231. ISSN 0027-8424. PMC 388425. PMID 4366757.

semanticscholar.org

api.semanticscholar.org

McALISTER, R.; Martin, G. M.; Benditt, E. P. (June 1961). "Evidence for Multiple Cæruloplasmin Components in Human Serum". Nature. 190 (4779): 927–929. Bibcode:1961Natur.190..927M. doi:10.1038/190927b0. ISSN 1476-4687. PMID 13773713. S2CID 4251125.
Martin, G. M.; Tuan, A. (October 1966). "A definitive cloning technique for human fibroblast cultures". Proceedings of the Society for Experimental Biology and Medicine. 123 (1): 138–140. doi:10.3181/00379727-123-31423. ISSN 0037-9727. PMID 5924411. S2CID 34390842.
Martin, G. M.; Sprague, C.; Bryant, J. S. (1967-05-06). "Mitotic nondisjunction in cultivated human cells". Nature. 214 (5088): 612–613. Bibcode:1967Natur.214..612M. doi:10.1038/214612a0. ISSN 0028-0836. PMID 4226946. S2CID 4155643.
Guo, Q.; Furukawa, K.; Sopher, B. L.; Pham, D. G.; Xie, J.; Robinson, N.; Martin, G. M.; Mattson, M. P. (1996-12-20). "Alzheimer's PS-1 mutation perturbs calcium homeostasis and sensitizes PC12 cells to death induced by amyloid beta-peptide". NeuroReport. 8 (1): 379–383. doi:10.1097/00001756-199612200-00074. ISSN 0959-4965. PMID 9051814. S2CID 11404496.
Yu, C. E.; Oshima, J.; Fu, Y. H.; Wijsman, E. M.; Hisama, F.; Alisch, R.; Matthews, S.; Nakura, J.; Miki, T.; Ouais, S.; Martin, G. M.; Mulligan, J.; Schellenberg, G. D. (1996-04-12). "Positional cloning of the Werner's syndrome gene". Science. 272 (5259): 258–262. Bibcode:1996Sci...272..258Y. doi:10.1126/science.272.5259.258. ISSN 0036-8075. PMID 8602509. S2CID 18172607.
Gray, M. D.; Shen, J. C.; Kamath-Loeb, A. S.; Blank, A.; Sopher, B. L.; Martin, G. M.; Oshima, J.; Loeb, L. A. (September 1997). "The Werner syndrome protein is a DNA helicase". Nature Genetics. 17 (1): 100–103. doi:10.1038/ng0997-100. ISSN 1061-4036. PMID 9288107. S2CID 20587915.
Hoehn, H.; Bryant, E. M.; Johnston, P.; Norwood, T. H.; Martin, G. M. (1975-12-18). "Non-selective isolation, stability and longevity of hybrids between normal human somatic cells". Nature. 258 (5536): 608–610. Bibcode:1975Natur.258..608H. doi:10.1038/258608a0. ISSN 0028-0836. PMID 1207734. S2CID 11467452.
Guo, Q.; Sebastian, L.; Sopher, B. L.; Miller, M. W.; Ware, C. B.; Martin, G. M.; Mattson, M. P. (March 1999). "Increased vulnerability of hippocampal neurons from presenilin-1 mutant knock-in mice to amyloid beta-peptide toxicity: central roles of superoxide production and caspase activation". Journal of Neurochemistry. 72 (3): 1019–1029. doi:10.1046/j.1471-4159.1999.0721019.x. ISSN 0022-3042. PMID 10037473. S2CID 221870765.
Martin, G. M. (1971). "Brief proposal on immortality: an interim solution". Perspectives in Biology and Medicine. 14 (2): 339. doi:10.1353/pbm.1971.0015. ISSN 0031-5982. PMID 5546258. S2CID 71120068.

umh.de

Martin, George (2019-04-08). "George M. Martin, M.D. Curriculum Vita" (PDF). Retrieved 2023-08-27.

umich.edu

deepblue.lib.umich.edu

Oshima J, Yu CE, Boehnke M, et al. (September 1994). "Integrated mapping analysis of the Werner syndrome region of chromosome 8" (PDF). Genomics. 23 (1): 100–13. doi:10.1006/geno.1994.1464. hdl:2027.42/31345. PMID 7829057.

washington.edu

worldcat.org

search.worldcat.org

Rabinovitch, Peter S; Disteche, Christine; Kaeberlein, Matt; Martin, Kelsey C; Monnat, Raymond J; Oshima, Junko; Promislow, Daniel (2023-01-04). "In Memory of George M. Martin". The Journals of Gerontology: Series A. 78 (4): 619–620. doi:10.1093/gerona/glac257. ISSN 1079-5006. PMID 36609876.
Austad, Steven N. (2023-06-01). "George M. Martin: tribute and personal remembrance". GeroScience. 45 (3): 2085–2086. doi:10.1007/s11357-023-00747-z. ISSN 2509-2723. PMC 10400482. PMID 36745353.
McALISTER, R.; Martin, G. M.; Benditt, E. P. (June 1961). "Evidence for Multiple Cæruloplasmin Components in Human Serum". Nature. 190 (4779): 927–929. Bibcode:1961Natur.190..927M. doi:10.1038/190927b0. ISSN 1476-4687. PMID 13773713. S2CID 4251125.
Martin, G. M.; Derr, M. A.; Benditt, E. P. (March 1964). "Ceruloplasmins of Several Animal Species. Comparison of Electrophoretic Mobilities and Substrate Specificity". Laboratory Investigation; A Journal of Technical Methods and Pathology. 13: 282–287. ISSN 0023-6837. PMID 14127032.
Martin, G. M.; Tuan, A. (October 1966). "A definitive cloning technique for human fibroblast cultures". Proceedings of the Society for Experimental Biology and Medicine. 123 (1): 138–140. doi:10.3181/00379727-123-31423. ISSN 0037-9727. PMID 5924411. S2CID 34390842.
Martin, G. M.; Sprague, C.; Bryant, J. S. (1967-05-06). "Mitotic nondisjunction in cultivated human cells". Nature. 214 (5088): 612–613. Bibcode:1967Natur.214..612M. doi:10.1038/214612a0. ISSN 0028-0836. PMID 4226946. S2CID 4155643.
Martin, G. M.; Sprague, C. A.; Epstein, C. J. (July 1970). "Replicative life-span of cultivated human cells. Effects of donor's age, tissue, and genotype". Laboratory Investigation; A Journal of Technical Methods and Pathology. 23 (1): 86–92. ISSN 0023-6837. PMID 5431223.
Schellenberg, G. D.; Bird, T. D.; Wijsman, E. M.; Orr, H. T.; Anderson, L.; Nemens, E.; White, J. A.; Bonnycastle, L.; Weber, J. L.; Alonso, M. E. (1992-10-23). "Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14". Science. 258 (5082): 668–671. Bibcode:1992Sci...258..668S. doi:10.1126/science.1411576. ISSN 0036-8075. PMID 1411576.
Guo, Q.; Furukawa, K.; Sopher, B. L.; Pham, D. G.; Xie, J.; Robinson, N.; Martin, G. M.; Mattson, M. P. (1996-12-20). "Alzheimer's PS-1 mutation perturbs calcium homeostasis and sensitizes PC12 cells to death induced by amyloid beta-peptide". NeuroReport. 8 (1): 379–383. doi:10.1097/00001756-199612200-00074. ISSN 0959-4965. PMID 9051814. S2CID 11404496.
Yu, C. E.; Oshima, J.; Fu, Y. H.; Wijsman, E. M.; Hisama, F.; Alisch, R.; Matthews, S.; Nakura, J.; Miki, T.; Ouais, S.; Martin, G. M.; Mulligan, J.; Schellenberg, G. D. (1996-04-12). "Positional cloning of the Werner's syndrome gene". Science. 272 (5259): 258–262. Bibcode:1996Sci...272..258Y. doi:10.1126/science.272.5259.258. ISSN 0036-8075. PMID 8602509. S2CID 18172607.
Gray, M. D.; Shen, J. C.; Kamath-Loeb, A. S.; Blank, A.; Sopher, B. L.; Martin, G. M.; Oshima, J.; Loeb, L. A. (September 1997). "The Werner syndrome protein is a DNA helicase". Nature Genetics. 17 (1): 100–103. doi:10.1038/ng0997-100. ISSN 1061-4036. PMID 9288107. S2CID 20587915.
Balajee, A. S.; Machwe, A.; May, A.; Gray, M. D.; Oshima, J.; Martin, G. M.; Nehlin, J. O.; Brosh, R.; Orren, D. K.; Bohr, V. A. (August 1999). "The Werner syndrome protein is involved in RNA polymerase II transcription". Molecular Biology of the Cell. 10 (8): 2655–2668. doi:10.1091/mbc.10.8.2655. ISSN 1059-1524. PMC 25497. PMID 10436020.
Martin, G. M.; Sprague, C. A. (1972-12-23). "Clonal senescence and atherosclerosis". Lancet. 2 (7791): 1370–1371. doi:10.1016/s0140-6736(72)92819-x. ISSN 0140-6736. PMID 4118240.
Martin, G.; Ogburn, C.; Sprague, C. (1975). "Senescence and Vascular Disease". Explorations in Aging. Advances in Experimental Medicine and Biology. Vol. 61. pp. 163–193. doi:10.1007/978-1-4615-9032-3_9. ISBN 978-1-4615-9034-7. ISSN 0065-2598. PMID 810006.
Hoehn, H.; Bryant, E. M.; Johnston, P.; Norwood, T. H.; Martin, G. M. (1975-12-18). "Non-selective isolation, stability and longevity of hybrids between normal human somatic cells". Nature. 258 (5536): 608–610. Bibcode:1975Natur.258..608H. doi:10.1038/258608a0. ISSN 0028-0836. PMID 1207734. S2CID 11467452.
Norwood, T. H.; Pendergrass, W. R.; Sprague, C. A.; Martin, G. M. (June 1974). "Dominance of the senescent phenotype in heterokaryons between replicative and post-replicative human fibroblast-like cells". Proceedings of the National Academy of Sciences of the United States of America. 71 (6): 2231–2235. Bibcode:1974PNAS...71.2231N. doi:10.1073/pnas.71.6.2231. ISSN 0027-8424. PMC 388425. PMID 4366757.
Martin, G. M.; Ogburn, C. E.; Colgin, L. M.; Gown, A. M.; Edland, S. D.; Monnat, R. J. (February 1996). "Somatic mutations are frequent and increase with age in human kidney epithelial cells". Human Molecular Genetics. 5 (2): 215–221. doi:10.1093/hmg/5.2.215. ISSN 0964-6906. PMID 8824877.
Guo, Q.; Sebastian, L.; Sopher, B. L.; Miller, M. W.; Ware, C. B.; Martin, G. M.; Mattson, M. P. (March 1999). "Increased vulnerability of hippocampal neurons from presenilin-1 mutant knock-in mice to amyloid beta-peptide toxicity: central roles of superoxide production and caspase activation". Journal of Neurochemistry. 72 (3): 1019–1029. doi:10.1046/j.1471-4159.1999.0721019.x. ISSN 0022-3042. PMID 10037473. S2CID 221870765.
Martin, G. M. (1971). "Brief proposal on immortality: an interim solution". Perspectives in Biology and Medicine. 14 (2): 339. doi:10.1353/pbm.1971.0015. ISSN 0031-5982. PMID 5546258. S2CID 71120068.

George M. Martin (English Wikipedia)

alz.org

aaic.alz.org

businesswire.com

doi.org

ellison-med-fn.org

geron.org

handle.net

hdl.handle.net

harvard.edu

ui.adsabs.harvard.edu

nature.com

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

umh.de

umich.edu

deepblue.lib.umich.edu

washington.edu

depts.washington.edu

pathology.washington.edu

mstp.washington.edu

worldcat.org

search.worldcat.org