トリプレットリピート病 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "トリプレットリピート病" in Japanese language version.

refsWebsite

Global rank Japanese rank

4^th place

24^th place

2^nd place

6^th place

18^th place

107^th place

1sciencedirect.com

149^th place

558^th place

doi.org (Global: 2^nd place; Japanese: 6^th place)

“Trinucleotide repeat disorders”. Annual Review of Neuroscience 30 (1): 575–621. (2007). doi:10.1146/annurev.neuro.29.051605.113042. PMID 17417937.
“Proteins Containing Expanded Polyglutamine Tracts and Neurodegenerative Disease”. Biochemistry 56 (9): 1199–1217. (March 2017). doi:10.1021/acs.biochem.6b00936. PMC 5727916. PMID 28170216.
“Wide range of reduced penetrance alleles in spinal and bulbar muscular atrophy: a model-based approach”. Journal of Medical Genetics 58 (6): 385–391. (June 2021). doi:10.1136/jmedgenet-2020-106963. PMID 32571900.
“Microsatellite Expansion Diseases: Repeat Toxicity Found in Translation”. Neuron 93 (2): 249–251. (January 2017). doi:10.1016/j.neuron.2017.01.001. PMID 28103472.
“GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome”. American Journal of Human Genetics 104 (1): 35–44. (January 2019). doi:10.1016/j.ajhg.2018.11.005. PMC 6323552. PMID 30554721.
“Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats in PPP2R2B”. Brain 140 (1): 27–36. (January 2017). doi:10.1093/brain/aww269. PMID 27864267.
“Chapter 34 - Spinocerebellar ataxia type 12” (英語). Handbook of Clinical Neurology. Ataxic Disorders. 103. Elsevier. (2012-01-01). pp. 535–547. doi:10.1016/b978-0-444-51892-7.00034-6. ISBN 9780444518927. PMID 21827912 2022年12月7日閲覧。
“Proteins Containing Expanded Polyglutamine Tracts and Neurodegenerative Disease”. Biochemistry 56 (9): 1199–1217. (March 2017). doi:10.1021/acs.biochem.6b00936. PMC 5727916. PMID 28170216.
“Polyglutamine (PolyQ) diseases: genetics to treatments”. Cell Transplantation 23 (4–5): 441–458. (May 2014). doi:10.3727/096368914X678454. PMID 24816443.
“Neurodegenerative disease: RNA repeats put a freeze on cells”. Nature 546 (7657): 215–216. (June 2017). Bibcode: 2017Natur.546..215S. doi:10.1038/nature22503. PMID 28562583.
“Huntington's disease”. Lancet 369 (9557): 218–228. (January 2007). doi:10.1016/S0140-6736(07)60111-1. PMID 17240289.
“Expandable DNA repeats and human disease”. Nature 447 (7147): 932–940. (June 2007). Bibcode: 2007Natur.447..932M. doi:10.1038/nature05977. PMID 17581576.
“Repeat instability during DNA repair: Insights from model systems”. Critical Reviews in Biochemistry and Molecular Biology 50 (2): 142–167. (2015). doi:10.3109/10409238.2014.999192. PMC 4454471. PMID 25608779.
“Analysis of strand slippage in DNA polymerase expansions of CAG/CTG triplet repeats associated with neurodegenerative disease”. The Journal of Biological Chemistry 273 (9): 5204–5210. (February 1998). doi:10.1074/jbc.273.9.5204. PMID 9478975.
“New insights into repeat instability: role of RNA•DNA hybrids”. RNA Biology 7 (5): 551–558. (2010). doi:10.4161/rna.7.5.12745. PMC 3073251. PMID 20729633.
“DNA slip-outs cause RNA polymerase II arrest in vitro: potential implications for genetic instability”. Nucleic Acids Research 39 (17): 7444–7454. (September 2011). doi:10.1093/nar/gkr429. PMC 3177194. PMID 21666257.

harvard.edu (Global: 18^th place; Japanese: 107^th place)

ui.adsabs.harvard.edu

“Neurodegenerative disease: RNA repeats put a freeze on cells”. Nature 546 (7657): 215–216. (June 2017). Bibcode: 2017Natur.546..215S. doi:10.1038/nature22503. PMID 28562583.
“Expandable DNA repeats and human disease”. Nature 447 (7147): 932–940. (June 2007). Bibcode: 2007Natur.447..932M. doi:10.1038/nature05977. PMID 17581576.

nih.gov (Global: 4^th place; Japanese: 24^th place)

pubmed.ncbi.nlm.nih.gov

“Trinucleotide repeat disorders”. Annual Review of Neuroscience 30 (1): 575–621. (2007). doi:10.1146/annurev.neuro.29.051605.113042. PMID 17417937.
“Proteins Containing Expanded Polyglutamine Tracts and Neurodegenerative Disease”. Biochemistry 56 (9): 1199–1217. (March 2017). doi:10.1021/acs.biochem.6b00936. PMC 5727916. PMID 28170216.
“Wide range of reduced penetrance alleles in spinal and bulbar muscular atrophy: a model-based approach”. Journal of Medical Genetics 58 (6): 385–391. (June 2021). doi:10.1136/jmedgenet-2020-106963. PMID 32571900.
“Microsatellite Expansion Diseases: Repeat Toxicity Found in Translation”. Neuron 93 (2): 249–251. (January 2017). doi:10.1016/j.neuron.2017.01.001. PMID 28103472.
“GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome”. American Journal of Human Genetics 104 (1): 35–44. (January 2019). doi:10.1016/j.ajhg.2018.11.005. PMC 6323552. PMID 30554721.
“Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats in PPP2R2B”. Brain 140 (1): 27–36. (January 2017). doi:10.1093/brain/aww269. PMID 27864267.
“Chapter 34 - Spinocerebellar ataxia type 12” (英語). Handbook of Clinical Neurology. Ataxic Disorders. 103. Elsevier. (2012-01-01). pp. 535–547. doi:10.1016/b978-0-444-51892-7.00034-6. ISBN 9780444518927. PMID 21827912 2022年12月7日閲覧。
“Proteins Containing Expanded Polyglutamine Tracts and Neurodegenerative Disease”. Biochemistry 56 (9): 1199–1217. (March 2017). doi:10.1021/acs.biochem.6b00936. PMC 5727916. PMID 28170216.
“Polyglutamine (PolyQ) diseases: genetics to treatments”. Cell Transplantation 23 (4–5): 441–458. (May 2014). doi:10.3727/096368914X678454. PMID 24816443.
“Neurodegenerative disease: RNA repeats put a freeze on cells”. Nature 546 (7657): 215–216. (June 2017). Bibcode: 2017Natur.546..215S. doi:10.1038/nature22503. PMID 28562583.
“Huntington's disease”. Lancet 369 (9557): 218–228. (January 2007). doi:10.1016/S0140-6736(07)60111-1. PMID 17240289.
“Expandable DNA repeats and human disease”. Nature 447 (7147): 932–940. (June 2007). Bibcode: 2007Natur.447..932M. doi:10.1038/nature05977. PMID 17581576.
“Repeat instability during DNA repair: Insights from model systems”. Critical Reviews in Biochemistry and Molecular Biology 50 (2): 142–167. (2015). doi:10.3109/10409238.2014.999192. PMC 4454471. PMID 25608779.
“Analysis of strand slippage in DNA polymerase expansions of CAG/CTG triplet repeats associated with neurodegenerative disease”. The Journal of Biological Chemistry 273 (9): 5204–5210. (February 1998). doi:10.1074/jbc.273.9.5204. PMID 9478975.
“New insights into repeat instability: role of RNA•DNA hybrids”. RNA Biology 7 (5): 551–558. (2010). doi:10.4161/rna.7.5.12745. PMC 3073251. PMID 20729633.
“DNA slip-outs cause RNA polymerase II arrest in vitro: potential implications for genetic instability”. Nucleic Acids Research 39 (17): 7444–7454. (September 2011). doi:10.1093/nar/gkr429. PMC 3177194. PMID 21666257.

pmc.ncbi.nlm.nih.gov

rarediseases.info.nih.gov

“Fragile XE syndrome”. Genetic and Rare Diseases Information Center (GARD). 2012年9月14日閲覧。

sciencedirect.com (Global: 149^th place; Japanese: 558^th place)

“Chapter 34 - Spinocerebellar ataxia type 12” (英語). Handbook of Clinical Neurology. Ataxic Disorders. 103. Elsevier. (2012-01-01). pp. 535–547. doi:10.1016/b978-0-444-51892-7.00034-6. ISBN 9780444518927. PMID 21827912 2022年12月7日閲覧。