메뉴 건너뛰기




Volumn 106, Issue 12, 2000, Pages 1447-1455

Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CELL HYPERPLASIA; CONTROLLED STUDY; ENDOLYMPHATIC SAC; GENE DISRUPTION; GENE FUNCTION; GENE INACTIVATION; HEARING IMPAIRMENT; HEART ELECTROPHYSIOLOGY; HISTOPATHOLOGY; MOUSE; NONHUMAN; PRIORITY JOURNAL; STOMACH MUCOSA;

EID: 0034518479     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI10897     Document Type: Article
Times cited : (264)

References (38)
  • 1
    • 9044240040 scopus 로고    scopus 로고
    • Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhyrhmias
    • (1996) Nat. Genet. , vol.12 , pp. 17-23
    • Wang, Q.1
  • 4
    • 0031054075 scopus 로고    scopus 로고
    • A novel mutation in the potassium channel gene KvLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
    • (1997) Nat. Genet. , vol.15 , pp. 186-189
    • Neyroud, N.1
  • 10
    • 0030876316 scopus 로고    scopus 로고
    • Beat-to-beat QT interval variability: Novel evidence for repolarization lability in ischemic and nonischemic dilated cardiomyopathy
    • (1997) Circulation , vol.96 , pp. 1557-1565
    • Berger, R.D.1
  • 13
    • 0031969525 scopus 로고    scopus 로고
    • Olfactory neuroblastoma is not related to the Ewing family of tumors: Absence of EWS/FLI1 gene fusion and MIC2 expression
    • (1998) Am. J. Surg. Pathol. , vol.22 , pp. 391-398
    • Argani, P.1
  • 15
    • 9044240040 scopus 로고    scopus 로고
    • Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arthythmias
    • (1996) Nat. Genet. , vol.12 , pp. 17-23
    • Wang, Q.1
  • 16
    • 0033524661 scopus 로고    scopus 로고
    • Replacement by homologous recombination of the minK gene with lacZ reveals restriction of minK expression to the mouse cardiac conduction system
    • (1999) Circ. Res. , vol.84 , pp. 146-152
    • Kupershmidt, S.1
  • 17
    • 0030461289 scopus 로고    scopus 로고
    • Inner ear defects induced by null mutation of the Isk gene
    • (1996) Neuron. , vol.17 , pp. 1251-1264
    • Vetter, D.E.1
  • 18
    • 0027174442 scopus 로고
    • Dynamics of epithelial cells in the corpus of the mouse stomach. III. Inward migration of neck cells followed by progressive transformation into zymogenic cells
    • (1993) Anat. Rec. , vol.236 , pp. 297-313
    • Karam, S.M.1    Leblond, C.P.2
  • 19
    • 0030001806 scopus 로고    scopus 로고
    • Overexpression of transforming growth factor-alpha alters differentiation of gastric cell lineages
    • (1996) Dig. Dis. Sci. , vol.41 , pp. 773-784
    • Goldenring, J.R.1
  • 20
    • 0030050183 scopus 로고    scopus 로고
    • Hypertrophic gastropathy in Helicobacter felis-infected wild-type C57BL/6 mice and p53 hemizygous transgenic mice
    • (1996) Gastroenterology , vol.110 , pp. 155-166
    • Fox, J.G.1
  • 21
    • 18144451568 scopus 로고    scopus 로고
    • Targeted disruption of the murine Na+/H+ exchanger isoform 2 gene causes reduced viability of gastric parietal cells and loss of net acid secretion
    • J. Clin. Invest. , vol.101 , pp. 1243-1253
    • Schultheis, P.J.1
  • 23
    • 0034642569 scopus 로고    scopus 로고
    • A constitutively open potassium channel formed by KCNQ1 and KCNE3
    • (2000) Nature , vol.403 , pp. 196-199
    • Schroeder, B.C.1
  • 24
    • 0028016257 scopus 로고
    • Electrophysiological properties of neonatal mouse cardiac myocytes in primary culture
    • (1994) J. Physiol. , vol.479 , pp. 265-279
    • Nuss, H.B.1    Marban, E.2
  • 25
    • 0030024562 scopus 로고    scopus 로고
    • Developmental changes in ionic channel activity in the embryonic murine heart
    • (1996) Circ. Res. , vol.78 , pp. 15-25
    • Davies, M.P.1
  • 26
  • 29
    • 0030872366 scopus 로고    scopus 로고
    • A minK-HERG complex regulates the cardiac potassium current l(Kr)
    • (1997) Nature , vol.388 , pp. 289-292
    • McDonald, T.V.1
  • 31
    • 0001053533 scopus 로고    scopus 로고
    • Atrio-venticular block and long QT in KvLQT 1 deficient transgenic mice
    • (1999) Circulation , vol.100 , pp. 351
    • Demolombe, S.1
  • 35
    • 16044364516 scopus 로고    scopus 로고
    • KIP2 is mutated in Beckwith-Wiedemann syndrome
    • (1996) Nat. Genet. , vol.14 , pp. 171-173
    • Hatada, H.1
  • 37
    • 0033609117 scopus 로고    scopus 로고
    • Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
    • (1999) Proc. Natl. Acad. Sci. USA , vol.96 , pp. 5203-5208
    • Lee, M.P.1
  • 38
    • 0032530827 scopus 로고    scopus 로고
    • Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5
    • (1998) Cancer Res. , vol.58 , pp. 4155-4159
    • Lee, M.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.