SCN1A (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "SCN1A" in French language version.

refsWebsite

Global rank French rank

17nih.gov

4^th place

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14doi.org

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3harvard.edu

18^th place

118^th place

2ensembl.org

1,626^th place

2,018^th place

1scn1a.info

low place

1smh.com.au

132^nd place

410^th place

doi.org

dx.doi.org

« Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24 », Cytogenetics and Cell Genetics, vol. 67, n^o 3,‎ 1994, p. 178–86 (PMID 8062593, DOI 10.1159/000133818)
« Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A », Epilepsy Research, vol. 48, n^os 1-2,‎ janvier 2002, p. 15–23 (PMID 11823106, DOI 10.1016/S0920-1211(01)00313-8)
« International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels », Pharmacological Reviews, vol. 57, n^o 4,‎ décembre 2005, p. 397–409 (PMID 16382098, DOI 10.1124/pr.57.4.4)
« Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects », The Journal of Physiology, vol. 588, n^o Pt 11,‎ juin 2010, p. 1841–8 (PMID 20351042, PMCID 2901972, DOI 10.1113/jphysiol.2010.188482)
« Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation », The Journal of Neuroscience, vol. 27, n^o 22,‎ mai 2007, p. 5903–14 (PMID 17537961, PMCID 6672241, DOI 10.1523/JNEUROSCI.5270-06.2007)
« Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin », Proceedings of the National Academy of Sciences of the United States of America, vol. 102, n^o 15,‎ avril 2005, p. 5507–12 (PMID 15805193, PMCID 556232, DOI 10.1073/pnas.0407346102, Bibcode 2005PNAS..102.5507T)
« Identification of the promoter region and the 5'-untranslated exons of the human voltage-gated sodium channel Nav1.1 gene (SCN1A) and enhancement of gene expression by the 5'-untranslated exons », Journal of Neuroscience Research, vol. 86, n^o 15,‎ novembre 2008, p. 3375–81 (PMID 18655196, DOI 10.1002/jnr.21790)
« Messenger RNA coding for only the alpha subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes », Proceedings of the National Academy of Sciences of the United States of America, vol. 83, n^o 19,‎ octobre 1986, p. 7503–7 (PMID 2429308, PMCID 386747, DOI 10.1073/pnas.83.19.7503, Bibcode 1986PNAS...83.7503G)
« Primary structure of the adult human skeletal muscle voltage-dependent sodium channel », Annals of Neurology, vol. 31, n^o 2,‎ février 1992, p. 131–7 (PMID 1315496, DOI 10.1002/ana.410310203)
« Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel », Proceedings of the National Academy of Sciences of the United States of America, vol. 89, n^o 2,‎ janvier 1992, p. 554–8 (PMID 1309946, PMCID 48277, DOI 10.1073/pnas.89.2.554, Bibcode 1992PNAS...89..554G)
« Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2 », Nature Genetics, vol. 24, n^o 4,‎ avril 2000, p. 343–5 (PMID 10742094, DOI 10.1038/74159)
« Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2 », The Journal of Neuroscience, vol. 21, n^o 19,‎ octobre 2001, p. 7481–90 (PMID 11567038, PMCID 6762922, DOI 10.1523/jneurosci.21-19-07481.2001)
« Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy », Neurology, vol. 60, n^o 12,‎ juin 2003, p. 1961–7 (PMID 12821740, DOI 10.1212/01.wnl.0000069463.41870.2f)
« Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins », The Journal of Neuroscience, vol. 18, n^o 1,‎ janvier 1998, p. 128–37 (PMID 9412493, PMCID 6793384, DOI 10.1523/jneurosci.18-01-00128.1998)

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000144285 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000064329 - Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

« Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin », Proceedings of the National Academy of Sciences of the United States of America, vol. 102, n^o 15,‎ avril 2005, p. 5507–12 (PMID 15805193, PMCID 556232, DOI 10.1073/pnas.0407346102, Bibcode 2005PNAS..102.5507T)
« Messenger RNA coding for only the alpha subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes », Proceedings of the National Academy of Sciences of the United States of America, vol. 83, n^o 19,‎ octobre 1986, p. 7503–7 (PMID 2429308, PMCID 386747, DOI 10.1073/pnas.83.19.7503, Bibcode 1986PNAS...83.7503G)
« Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel », Proceedings of the National Academy of Sciences of the United States of America, vol. 89, n^o 2,‎ janvier 1992, p. 554–8 (PMID 1309946, PMCID 48277, DOI 10.1073/pnas.89.2.554, Bibcode 1992PNAS...89..554G)

nih.gov

ncbi.nlm.nih.gov

« Publications PubMed pour l'Homme », sur National Center for Biotechnology Information, U.S. National Library of Medicine
« Publications PubMed pour la Souris », sur National Center for Biotechnology Information, U.S. National Library of Medicine
« Entrez Gene: SCN1A sodium channel, voltage-gated, type I, alpha subunit »
« Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24 », Cytogenetics and Cell Genetics, vol. 67, n^o 3,‎ 1994, p. 178–86 (PMID 8062593, DOI 10.1159/000133818)
« Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A », Epilepsy Research, vol. 48, n^os 1-2,‎ janvier 2002, p. 15–23 (PMID 11823106, DOI 10.1016/S0920-1211(01)00313-8)
« International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels », Pharmacological Reviews, vol. 57, n^o 4,‎ décembre 2005, p. 397–409 (PMID 16382098, DOI 10.1124/pr.57.4.4)
« Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects », The Journal of Physiology, vol. 588, n^o Pt 11,‎ juin 2010, p. 1841–8 (PMID 20351042, PMCID 2901972, DOI 10.1113/jphysiol.2010.188482)
« Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation », The Journal of Neuroscience, vol. 27, n^o 22,‎ mai 2007, p. 5903–14 (PMID 17537961, PMCID 6672241, DOI 10.1523/JNEUROSCI.5270-06.2007)
« Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin », Proceedings of the National Academy of Sciences of the United States of America, vol. 102, n^o 15,‎ avril 2005, p. 5507–12 (PMID 15805193, PMCID 556232, DOI 10.1073/pnas.0407346102, Bibcode 2005PNAS..102.5507T)
« Identification of the promoter region and the 5'-untranslated exons of the human voltage-gated sodium channel Nav1.1 gene (SCN1A) and enhancement of gene expression by the 5'-untranslated exons », Journal of Neuroscience Research, vol. 86, n^o 15,‎ novembre 2008, p. 3375–81 (PMID 18655196, DOI 10.1002/jnr.21790)
« Messenger RNA coding for only the alpha subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes », Proceedings of the National Academy of Sciences of the United States of America, vol. 83, n^o 19,‎ octobre 1986, p. 7503–7 (PMID 2429308, PMCID 386747, DOI 10.1073/pnas.83.19.7503, Bibcode 1986PNAS...83.7503G)
« Primary structure of the adult human skeletal muscle voltage-dependent sodium channel », Annals of Neurology, vol. 31, n^o 2,‎ février 1992, p. 131–7 (PMID 1315496, DOI 10.1002/ana.410310203)
« Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel », Proceedings of the National Academy of Sciences of the United States of America, vol. 89, n^o 2,‎ janvier 1992, p. 554–8 (PMID 1309946, PMCID 48277, DOI 10.1073/pnas.89.2.554, Bibcode 1992PNAS...89..554G)
« Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2 », Nature Genetics, vol. 24, n^o 4,‎ avril 2000, p. 343–5 (PMID 10742094, DOI 10.1038/74159)
« Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2 », The Journal of Neuroscience, vol. 21, n^o 19,‎ octobre 2001, p. 7481–90 (PMID 11567038, PMCID 6762922, DOI 10.1523/jneurosci.21-19-07481.2001)
« Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy », Neurology, vol. 60, n^o 12,‎ juin 2003, p. 1961–7 (PMID 12821740, DOI 10.1212/01.wnl.0000069463.41870.2f)
« Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins », The Journal of Neuroscience, vol. 18, n^o 1,‎ janvier 1998, p. 128–37 (PMID 9412493, PMCID 6793384, DOI 10.1523/jneurosci.18-01-00128.1998)

scn1a.info

Lossin C, « SCN1A infobase » (consulté le 30 octobre 2009) : « compilation of genetic variations in the SCN1A gene that alter the expression or function of Nav1.1 »

smh.com.au

Robotham J, « Sick babies denied treatment in DNA row – », National News, Sidney Morning Herald – smh.com.au, 29 novembre 2008 (consulté le 2 janvier 2020)