NHLRC1: Difference between revisions
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*{{Cite journal | vauthors=Gentry MS, Worby CA, Dixon JE |title=Insights into Lafora disease: malin is an E3 ubiquitin ligase that ubiquitinates and promotes the degradation of laforin. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=102 |issue= 24 |pages= 8501–6 |year= 2005 |pmid= 15930137 |doi= 10.1073/pnas.0503285102 | pmc=1150849 }} | *{{Cite journal | vauthors=Gentry MS, Worby CA, Dixon JE |title=Insights into Lafora disease: malin is an E3 ubiquitin ligase that ubiquitinates and promotes the degradation of laforin. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=102 |issue= 24 |pages= 8501–6 |year= 2005 |pmid= 15930137 |doi= 10.1073/pnas.0503285102 | pmc=1150849 }} | ||
*{{Cite journal |vauthors=Lohi H, Ianzano L, Zhao XC, etal |title=Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy. |journal=Hum. Mol. Genet. |volume=14 |issue= 18 |pages= 2727–36 |year= 2006 |pmid= 16115820 |doi= 10.1093/hmg/ddi306 }} | *{{Cite journal |vauthors=Lohi H, Ianzano L, Zhao XC, etal |title=Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy. |journal=Hum. Mol. Genet. |volume=14 |issue= 18 |pages= 2727–36 |year= 2006 |pmid= 16115820 |doi= 10.1093/hmg/ddi306 }} | ||
*{{Cite journal |vauthors=Singh S, Sethi I, Francheschetti S, etal |title=Novel NHLRC1 mutations and genotype-phenotype correlations in patients with Lafora's progressive myoclonic epilepsy. |journal=J. Med. Genet. |volume=43 |issue= 9 |pages= e48 |year= 2007 |pmid= 16950819 |doi= 10.1136/jmg.2005.039479 }} | *{{Cite journal |vauthors=Singh S, Sethi I, Francheschetti S, etal |title=Novel NHLRC1 mutations and genotype-phenotype correlations in patients with Lafora's progressive myoclonic epilepsy. |journal=J. Med. Genet. |volume=43 |issue= 9 |pages= e48 |year= 2007 |pmid= 16950819 |doi= 10.1136/jmg.2005.039479 |pmc=2564581 }} | ||
*{{Cite journal | vauthors=Mittal S, Dubey D, Yamakawa K, Ganesh S |title=Lafora disease proteins malin and laforin are recruited to aggresomes in response to proteasomal impairment. |journal=Hum. Mol. Genet. |volume=16 |issue= 7 |pages= 753–62 |year= 2007 |pmid= 17337485 |doi= 10.1093/hmg/ddm006 }} | *{{Cite journal | vauthors=Mittal S, Dubey D, Yamakawa K, Ganesh S |title=Lafora disease proteins malin and laforin are recruited to aggresomes in response to proteasomal impairment. |journal=Hum. Mol. Genet. |volume=16 |issue= 7 |pages= 753–62 |year= 2007 |pmid= 17337485 |doi= 10.1093/hmg/ddm006 }} | ||
}} | }} | ||
Latest revision as of 10:07, 16 May 2018
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NHL repeat-containing protein 1 is a protein that in humans is encoded by the NHLRC1 gene.[1][2]
See also
References
- ↑ Chan EM, Young EJ, Ianzano L, Munteanu I, Zhao X, Christopoulos CC, Avanzini G, Elia M, Ackerley CA, Jovic NJ, Bohlega S, Andermann E, Rouleau GA, Delgado-Escueta AV, Minassian BA, Scherer SW (Sep 2003). "Mutations in NHLRC1 cause progressive myoclonus epilepsy". Nat Genet. 35 (2): 125–7. doi:10.1038/ng1238. PMID 12958597.
- ↑ "Entrez Gene: NHLRC1 NHL repeat containing 1".
External links
Further reading
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6". Nature. 425 (6960): 805–11. doi:10.1038/nature02055. PMID 14574404.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Gómez-Abad C, Gómez-Garre P, Gutiérrez-Delicado E, et al. (2006). "Lafora disease due to EPM2B mutations: a clinical and genetic study". Neurology. 64 (6): 982–6. doi:10.1212/01.WNL.0000154519.10805.F7. PMID 15781812.
- Gentry MS, Worby CA, Dixon JE (2005). "Insights into Lafora disease: malin is an E3 ubiquitin ligase that ubiquitinates and promotes the degradation of laforin". Proc. Natl. Acad. Sci. U.S.A. 102 (24): 8501–6. doi:10.1073/pnas.0503285102. PMC 1150849. PMID 15930137.
- Lohi H, Ianzano L, Zhao XC, et al. (2006). "Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy". Hum. Mol. Genet. 14 (18): 2727–36. doi:10.1093/hmg/ddi306. PMID 16115820.
- Singh S, Sethi I, Francheschetti S, et al. (2007). "Novel NHLRC1 mutations and genotype-phenotype correlations in patients with Lafora's progressive myoclonic epilepsy". J. Med. Genet. 43 (9): e48. doi:10.1136/jmg.2005.039479. PMC 2564581. PMID 16950819.
- Mittal S, Dubey D, Yamakawa K, Ganesh S (2007). "Lafora disease proteins malin and laforin are recruited to aggresomes in response to proteasomal impairment". Hum. Mol. Genet. 16 (7): 753–62. doi:10.1093/hmg/ddm006. PMID 17337485.
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