Peripheral myelin protein 22 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Peripheral myelin protein 22" in English language version.

refsWebsite

Global rank English rank

17nih.gov

4^th place

10doi.org

2^nd place

5semanticscholar.org

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2ensembl.org

1,626^th place

1,007^th place

1harvard.edu

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doi.org

Watila MM, Balarabe SA (August 2015). "Molecular and clinical features of inherited neuropathies due to PMP22 duplication". Journal of the Neurological Sciences. 355 (1–2): 18–24. doi:10.1016/j.jns.2015.05.037. PMID 26076881. S2CID 40080925.
Li J, Parker B, Martyn C, Natarajan C, Guo J (April 2013). "The PMP22 gene and its related diseases". Molecular Neurobiology. 47 (2): 673–698. doi:10.1007/s12035-012-8370-x. PMC 3594637. PMID 23224996.
Dickson KM, Bergeron JJ, Shames I, Colby J, Nguyen DT, Chevet E, et al. (July 2002). "Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseases". Proceedings of the National Academy of Sciences of the United States of America. 99 (15): 9852–9857. Bibcode:2002PNAS...99.9852D. doi:10.1073/pnas.152621799. PMC 125041. PMID 12119418.
Zhang N, Zhu HP, Huang W, Wen X, Xie X, Jiang X, et al. (October 2022). "Unraveling the structures, functions and mechanisms of epithelial membrane protein family in human cancers". Experimental Hematology & Oncology. 11 (1): 69. doi:10.1186/s40164-022-00321-x. PMC 9552464. PMID 36217151.
Nelis E, Haites N, Van Broeckhoven C (1999). "Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies". Human Mutation. 13 (1): 11–28. doi:10.1002/(SICI)1098-1004(1999)13:1<11::AID-HUMU2>3.0.CO;2-A. PMID 9888385. S2CID 31130790.
Brennan KM, Bai Y, Shy ME (June 2015). "Demyelinating CMT--what's known, what's new and what's in store?". Neuroscience Letters. 596: 14–26. doi:10.1016/j.neulet.2015.01.059. PMID 25625223. S2CID 23911870.
Al-Thihli K, Rudkin T, Carson N, Poulin C, Melançon S, Der Kaloustian VM (September 2008). "Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype". American Journal of Medical Genetics. Part A. 146A (18): 2412–2416. doi:10.1002/ajmg.a.32456. PMID 18698610. S2CID 205309846.
Berger P, Young P, Suter U (March 2002). "Molecular cell biology of Charcot-Marie-Tooth disease". Neurogenetics. 4 (1): 1–15. doi:10.1007/s10048-002-0130-z. PMID 12030326. S2CID 25129077.
Pantera H, Shy ME, Svaren J (January 2020). "Regulating PMP22 expression as a dosage sensitive neuropathy gene". Brain Research. 1726: 146491. doi:10.1016/j.brainres.2019.146491. PMC 7006452. PMID 31586623.
D'Urso D, Ehrhardt P, Müller HW (May 1999). "Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin". The Journal of Neuroscience. 19 (9). Society for Neuroscience: 3396–3403. doi:10.1523/JNEUROSCI.19-09-03396.1999. PMC 6782240. PMID 10212299.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000109099 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000018217 – Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

Dickson KM, Bergeron JJ, Shames I, Colby J, Nguyen DT, Chevet E, et al. (July 2002). "Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseases". Proceedings of the National Academy of Sciences of the United States of America. 99 (15): 9852–9857. Bibcode:2002PNAS...99.9852D. doi:10.1073/pnas.152621799. PMC 125041. PMID 12119418.

nih.gov

pubmed.ncbi.nlm.nih.gov

Watila MM, Balarabe SA (August 2015). "Molecular and clinical features of inherited neuropathies due to PMP22 duplication". Journal of the Neurological Sciences. 355 (1–2): 18–24. doi:10.1016/j.jns.2015.05.037. PMID 26076881. S2CID 40080925.
Li J, Parker B, Martyn C, Natarajan C, Guo J (April 2013). "The PMP22 gene and its related diseases". Molecular Neurobiology. 47 (2): 673–698. doi:10.1007/s12035-012-8370-x. PMC 3594637. PMID 23224996.
Dickson KM, Bergeron JJ, Shames I, Colby J, Nguyen DT, Chevet E, et al. (July 2002). "Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseases". Proceedings of the National Academy of Sciences of the United States of America. 99 (15): 9852–9857. Bibcode:2002PNAS...99.9852D. doi:10.1073/pnas.152621799. PMC 125041. PMID 12119418.
Zhang N, Zhu HP, Huang W, Wen X, Xie X, Jiang X, et al. (October 2022). "Unraveling the structures, functions and mechanisms of epithelial membrane protein family in human cancers". Experimental Hematology & Oncology. 11 (1): 69. doi:10.1186/s40164-022-00321-x. PMC 9552464. PMID 36217151.
Nelis E, Haites N, Van Broeckhoven C (1999). "Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies". Human Mutation. 13 (1): 11–28. doi:10.1002/(SICI)1098-1004(1999)13:1<11::AID-HUMU2>3.0.CO;2-A. PMID 9888385. S2CID 31130790.
Brennan KM, Bai Y, Shy ME (June 2015). "Demyelinating CMT--what's known, what's new and what's in store?". Neuroscience Letters. 596: 14–26. doi:10.1016/j.neulet.2015.01.059. PMID 25625223. S2CID 23911870.
Al-Thihli K, Rudkin T, Carson N, Poulin C, Melançon S, Der Kaloustian VM (September 2008). "Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype". American Journal of Medical Genetics. Part A. 146A (18): 2412–2416. doi:10.1002/ajmg.a.32456. PMID 18698610. S2CID 205309846.
Berger P, Young P, Suter U (March 2002). "Molecular cell biology of Charcot-Marie-Tooth disease". Neurogenetics. 4 (1): 1–15. doi:10.1007/s10048-002-0130-z. PMID 12030326. S2CID 25129077.
Pantera H, Shy ME, Svaren J (January 2020). "Regulating PMP22 expression as a dosage sensitive neuropathy gene". Brain Research. 1726: 146491. doi:10.1016/j.brainres.2019.146491. PMC 7006452. PMID 31586623.
D'Urso D, Ehrhardt P, Müller HW (May 1999). "Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin". The Journal of Neuroscience. 19 (9). Society for Neuroscience: 3396–3403. doi:10.1523/JNEUROSCI.19-09-03396.1999. PMC 6782240. PMID 10212299.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Li J, Parker B, Martyn C, Natarajan C, Guo J (April 2013). "The PMP22 gene and its related diseases". Molecular Neurobiology. 47 (2): 673–698. doi:10.1007/s12035-012-8370-x. PMC 3594637. PMID 23224996.
Dickson KM, Bergeron JJ, Shames I, Colby J, Nguyen DT, Chevet E, et al. (July 2002). "Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseases". Proceedings of the National Academy of Sciences of the United States of America. 99 (15): 9852–9857. Bibcode:2002PNAS...99.9852D. doi:10.1073/pnas.152621799. PMC 125041. PMID 12119418.
Zhang N, Zhu HP, Huang W, Wen X, Xie X, Jiang X, et al. (October 2022). "Unraveling the structures, functions and mechanisms of epithelial membrane protein family in human cancers". Experimental Hematology & Oncology. 11 (1): 69. doi:10.1186/s40164-022-00321-x. PMC 9552464. PMID 36217151.
Pantera H, Shy ME, Svaren J (January 2020). "Regulating PMP22 expression as a dosage sensitive neuropathy gene". Brain Research. 1726: 146491. doi:10.1016/j.brainres.2019.146491. PMC 7006452. PMID 31586623.
D'Urso D, Ehrhardt P, Müller HW (May 1999). "Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin". The Journal of Neuroscience. 19 (9). Society for Neuroscience: 3396–3403. doi:10.1523/JNEUROSCI.19-09-03396.1999. PMC 6782240. PMID 10212299.

semanticscholar.org

api.semanticscholar.org

Watila MM, Balarabe SA (August 2015). "Molecular and clinical features of inherited neuropathies due to PMP22 duplication". Journal of the Neurological Sciences. 355 (1–2): 18–24. doi:10.1016/j.jns.2015.05.037. PMID 26076881. S2CID 40080925.
Nelis E, Haites N, Van Broeckhoven C (1999). "Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies". Human Mutation. 13 (1): 11–28. doi:10.1002/(SICI)1098-1004(1999)13:1<11::AID-HUMU2>3.0.CO;2-A. PMID 9888385. S2CID 31130790.
Brennan KM, Bai Y, Shy ME (June 2015). "Demyelinating CMT--what's known, what's new and what's in store?". Neuroscience Letters. 596: 14–26. doi:10.1016/j.neulet.2015.01.059. PMID 25625223. S2CID 23911870.
Al-Thihli K, Rudkin T, Carson N, Poulin C, Melançon S, Der Kaloustian VM (September 2008). "Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype". American Journal of Medical Genetics. Part A. 146A (18): 2412–2416. doi:10.1002/ajmg.a.32456. PMID 18698610. S2CID 205309846.
Berger P, Young P, Suter U (March 2002). "Molecular cell biology of Charcot-Marie-Tooth disease". Neurogenetics. 4 (1): 1–15. doi:10.1007/s10048-002-0130-z. PMID 12030326. S2CID 25129077.