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

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1996 • 1,746 citations

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1997 • 878 citations

An Efficient Algorithm for Spectral Analysis of Heart Rate Variability

1986 • 826 citations

Mutations in the hminK gene cause long QT syndrome and suppress lKs function

1997 • 763 citations

Beat-to-Beat QT Interval Variability

1997 • 609 citations

A constitutively open potassium channel formed by KCNQ1 and KCNE3

2000 • 481 citations

Inner Ear Defects Induced by Null Mutationof the isk Gene

1996 • 395 citations

An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome

1996 • 390 citations

A minK–HERG complex regulates the cardiac potassium current IKr

1997 • 376 citations

Loss of imprinting of a paternally expressed transcript, with antisense orientation to K _V LQT1, occurs frequently in Beckwith–Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

1999 • 360 citations

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements

1997 • 354 citations

Targeted disruption of the murine Na+/H+ exchanger isoform 2 gene causes reduced viability of gastric parietal cells and loss of net acid secretion.

1998 • 249 citations

Developmental Changes in the Delayed Rectifier K ⁺ Channels in Mouse Heart

1996 • 227 citations

In Vivo Cardiac Electrophysiology Studies in the Mouse

1996 • 226 citations

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 • 222 citations

Developmental Changes in Ionic Channel Activity in the Embryonic Murine Heart

1996 • 209 citations

Replacement by Homologous Recombination of the minK Gene With lacZ Reveals Restriction of minK Expression to the Mouse Cardiac Conduction System

1999 • 188 citations

Hypertrophic gastropathy in Helicobacter felis-infected wild-type C57BL/6 mice and p53 hemizygous transgenic mice

1996 • 180 citations

Projections from the ventral cochlear nucleus to the dorsal cochlear nucleus in rats

1997 • 142 citations

Low Frequency of p57KIP2 Mutation in Beckwith-Wiedemann Syndrome

1997 • 141 citations

Electrophysiological properties of neonatal mouse cardiac myocytes in primary culture.

1994 • 139 citations

Gastric H+, K+-adenosine triphosphatase β subunit is required for normal function, development, and membrane structure of mouse parietal cells

1999 • 138 citations

Detection of the SYT-SSX chimeric RNA of synovial sarcoma in paraffin-embedded tissue and its application in problematic cases.

1998 • 118 citations

Olfactory Neuroblastoma is Not Related to the Ewing Family of Tumors

1998 • 113 citations

Imprinting of mouse Kvlqt1 is developmentally regulated

1998 • 98 citations

Anti-minK Antisense Decreases the Amplitude of the Rapidly Activating Cardiac Delayed Rectifier K ⁺ Current

1995 • 89 citations

Pathways of processing of the gastrin precursor in rat antral mucosa.

1995 • 63 citations

Overexpression of transforming growth factor-α alters differentiation of gastric cell lineages

1996 • 63 citations

Otopathology in a case of multichannel cochlear implantation

1994 • 53 citations

AdultKCNE1-Knockout Mice Exhibit a Mild Cardiac Cellular Phenotype

1998 • 45 citations

Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5.

1998 • 44 citations

Strain-Dependent Developmental Relaxation of Imprinting of an Endogenous Mouse Gene, Kvlqt1

1998 • 37 citations

Identification and characteristics of delayed rectifier K+ current in fetal mouse ventricular myocytes

1996 • 35 citations

Loss of Imprinting in Human Cancer

1994 • 24 citations