Ménière's disease is associated with single nucleotide polymorphisms in the human potassium channel genes, KCNE1 and KCNE3
about
Deep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitusGenetics of vestibular disorders: pathophysiological insightsFunctional significance of K+ channel β-subunit KCNE3 in auditory neuronsPolymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian populationPotassium channel gene mutations rarely cause atrial fibrillationLocalization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.The genetics of Ménière's disease.Genetic disorders of the vestibular system.Genetics of recurrent vertigo and vestibular disordersPolymorphisms in genes involved in oxidative stress response in patients with sudden sensorineural hearing loss and Ménière's disease in a Japanese population.KCNE1 and KCNE3: The yin and yang of voltage-gated K(+) channel regulationRegulation of ENaC-mediated sodium transport by glucocorticoids in Reissner's membrane epitheliumSequence variants in host cell factor C1 are associated with Ménière's disease.An Examination of KCNE1 Mutations and Common Variants in Chronic Tinnitus.A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies.Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis.The aetiopathologies of Ménière's disease: a contemporary review.Genetics of ion homeostasis in Ménière's Disease.Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease.Association between polymorphisms in genes encoding methylenetetrahydrofolate reductase and the risk of Ménière's disease.Association of interleukin-1 gene polymorphisms with sudden sensorineural hearing loss and Ménière's disease.Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association.Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings.
P2860
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P2860
Ménière's disease is associated with single nucleotide polymorphisms in the human potassium channel genes, KCNE1 and KCNE3
description
2005 nî lūn-bûn
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2005 թուականին հրատարակուած գիտական յօդուած
@hyw
2005 թվականին հրատարակված գիտական հոդված
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2005年の論文
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2005年論文
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2005年論文
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2005年論文
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2005年論文
@zh-mo
2005年論文
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2005年论文
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name
Ménière's disease is associate ...... channel genes, KCNE1 and KCNE3
@ast
Ménière's disease is associate ...... channel genes, KCNE1 and KCNE3
@en
Ménière's disease is associate ...... channel genes, KCNE1 and KCNE3
@nl
type
label
Ménière's disease is associate ...... channel genes, KCNE1 and KCNE3
@ast
Ménière's disease is associate ...... channel genes, KCNE1 and KCNE3
@en
Ménière's disease is associate ...... channel genes, KCNE1 and KCNE3
@nl
prefLabel
Ménière's disease is associate ...... channel genes, KCNE1 and KCNE3
@ast
Ménière's disease is associate ...... channel genes, KCNE1 and KCNE3
@en
Ménière's disease is associate ...... channel genes, KCNE1 and KCNE3
@nl
P2093
P2860
P3181
P356
P1433
P1476
Ménière's disease is associate ...... channel genes, KCNE1 and KCNE3
@en
P2093
Hiroshi Hibino
Katsumi Doi
Naoki Matsushiro
Tadashi Kitahara
Takashi Sato
Takeshi Kubo
Toshihiro Kuramasu
P2860
P304
P3181
P356
10.1159/000089410
P407
P50
P577
2005-01-01T00:00:00Z