RRM2B (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "RRM2B" in Japanese language version.

refsWebsite

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18nih.gov

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24^th place

10doi.org

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2ensembl.org

1,626^th place

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2wikipedia.org

low place

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

“A ribonucleotide reductase gene involved in a p53-dependent cell-cycle checkpoint for DNA damage”. Nature 404 (6773): 42–9. (March 2000). doi:10.1038/35003506. PMID 10716435.
“A ribonucleotide reductase gene is a transcriptional target of p53 and p73”. Oncogene 19 (37): 4283–9. (August 2000). doi:10.1038/sj.onc.1203774. PMID 10980602.
“Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion”. Nature Genetics 39 (6): 776–80. (June 2007). doi:10.1038/ng2040. PMID 17486094.
“Defects in mitochondrial DNA replication and human disease”. Critical Reviews in Biochemistry and Molecular Biology 47 (1): 64–74. (2012). doi:10.3109/10409238.2011.632763. PMC 3244805. PMID 22176657.
“ATM-mediated serine 72 phosphorylation stabilizes ribonucleotide reductase small subunit p53R2 protein against MDM2 to DNA damage”. Proceedings of the National Academy of Sciences of the United States of America 105 (47): 18519–24. (November 2008). doi:10.1073/pnas.0803313105. PMC 2587585. PMID 19015526.
“A novel mutation of the RRM2B gene in an infant with early fatal encephalomyopathy, central hypomyelination, and tubulopathy”. Molecular Genetics and Metabolism 98 (3): 300–4. (November 2009). doi:10.1016/j.ymgme.2009.06.012. PMID 19616983.
“Novel RRM2B Mutation and Severe Mitochondrial DNA Depletion: Report of 2 Cases and Review of the Literature”. Neuropediatrics. (May 2017). doi:10.1055/s-0037-1601867. PMID 28482374.
“Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism”. PloS One 11 (8): e0156738. (2016). doi:10.1371/journal.pone.0156738. PMID 27483465.
“Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia”. Genome Biology 12 (9): R92. (September 2011). doi:10.1186/gb-2011-12-9-r92. PMC 3308055. PMID 21951382.
“Gene expression analysis for predicting gemcitabine resistance in human cholangiocarcinoma”. Journal of Hepato-Biliary-Pancreatic Sciences 18 (5): 700–11. (September 2011). doi:10.1007/s00534-011-0376-7. PMID 21451941.

ensembl.org (Global: 1,626^th place; Japanese: 2,625^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000048392 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000022292 - Ensembl, May 2017

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

pubmed.ncbi.nlm.nih.gov

“A ribonucleotide reductase gene involved in a p53-dependent cell-cycle checkpoint for DNA damage”. Nature 404 (6773): 42–9. (March 2000). doi:10.1038/35003506. PMID 10716435.
“A ribonucleotide reductase gene is a transcriptional target of p53 and p73”. Oncogene 19 (37): 4283–9. (August 2000). doi:10.1038/sj.onc.1203774. PMID 10980602.
“Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion”. Nature Genetics 39 (6): 776–80. (June 2007). doi:10.1038/ng2040. PMID 17486094.
“Defects in mitochondrial DNA replication and human disease”. Critical Reviews in Biochemistry and Molecular Biology 47 (1): 64–74. (2012). doi:10.3109/10409238.2011.632763. PMC 3244805. PMID 22176657.
“ATM-mediated serine 72 phosphorylation stabilizes ribonucleotide reductase small subunit p53R2 protein against MDM2 to DNA damage”. Proceedings of the National Academy of Sciences of the United States of America 105 (47): 18519–24. (November 2008). doi:10.1073/pnas.0803313105. PMC 2587585. PMID 19015526.
“A novel mutation of the RRM2B gene in an infant with early fatal encephalomyopathy, central hypomyelination, and tubulopathy”. Molecular Genetics and Metabolism 98 (3): 300–4. (November 2009). doi:10.1016/j.ymgme.2009.06.012. PMID 19616983.
“Novel RRM2B Mutation and Severe Mitochondrial DNA Depletion: Report of 2 Cases and Review of the Literature”. Neuropediatrics. (May 2017). doi:10.1055/s-0037-1601867. PMID 28482374.
“Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism”. PloS One 11 (8): e0156738. (2016). doi:10.1371/journal.pone.0156738. PMID 27483465.
“Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia”. Genome Biology 12 (9): R92. (September 2011). doi:10.1186/gb-2011-12-9-r92. PMC 3308055. PMID 21951382.
“Gene expression analysis for predicting gemcitabine resistance in human cholangiocarcinoma”. Journal of Hepato-Biliary-Pancreatic Sciences 18 (5): 700–11. (September 2011). doi:10.1007/s00534-011-0376-7. PMID 21451941.

wikipedia.org (Global: low place; Japanese: low place)

en.wikipedia.org

GRCh38: Ensembl release 89: ENSG00000048392 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000022292 - Ensembl, May 2017

RRM2B (Japanese Wikipedia)

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

ensembl.org (Global: 1,626th place; Japanese: 2,625th place)

May2017.archive.ensembl.org

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

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

pmc.ncbi.nlm.nih.gov

ghr.nlm.nih.gov

wikipedia.org (Global: low place; Japanese: low place)

en.wikipedia.org

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

ensembl.org (Global: 1,626^th place; Japanese: 2,625^th place)

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