Genomic structure of the human unconventional myosin VI gene

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1979 • 22,482 citations

A simple salting out procedure for extracting DNA from human nucleated cells

1988 • 20,341 citations

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.

1989 • 3,707 citations

Large-Scale Identification, Mapping, and Genotyping of Single-Nucleotide Polymorphisms in the Human Genome

1998 • 2,163 citations

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1997 • 1,435 citations

Defective myosin VIIA gene responsible for Usher syndrome type IB

1995 • 1,051 citations

Genetic Epidemiology of Hearing Impairment

1991 • 941 citations

A new bacteriophage P1–derived vector for the propagation of large human DNA fragments

1994 • 857 citations

A type VII myosin encoded by the mouse deafness gene shaker-1

1995 • 674 citations

Myosin VI is an actin-based motor that moves backwards

1999 • 664 citations

A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones

1990 • 650 citations

Unconventional Myosins in Cell Movement, Membrane Traffic, and Signal Transduction

1998 • 649 citations

Unconventional Myosins in Inner-Ear Sensory Epithelia

1997 • 531 citations

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

1995 • 507 citations

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1997 • 455 citations

Association of Unconventional Myosin MYO15 Mutations with Human Nonsyndromic Deafness DFNB3

1998 • 429 citations

Correction of Deafness in shaker-2 Mice by an Unconventional Myosin in a BAC Transgene

1998 • 410 citations

Nonsyndromic Deafness DFNA1 Associated with Mutation of a Human Homolog of the Drosophila Gene diaphanous

1997 • 409 citations

Unconventional Myosins

1995 • 362 citations

Mutation in Transcription Factor POU4F3 Associated with Inherited Progressive Hearing Loss in Humans

1998 • 338 citations

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

1998 • 325 citations

Transplacental Uptake of Glucose Is Decreased in Embryonic Lethal Connexin26-deficient Mice

1998 • 280 citations

Role of Myosin VI in the Differentiation of Cochlear Hair Cells

1999 • 261 citations

The Localization of Myosin VI at the Golgi Complex and Leading Edge of Fibroblasts and Its Phosphorylation and Recruitment into Membrane Ruffles of A431 Cells after Growth Factor Stimulation

1998 • 198 citations

Vectorette PCR: a novel approach to genomic walking.

1991 • 186 citations

Protein kinase CK2

1997 • 169 citations

Genomic Organization of the ATM Gene

1996 • 167 citations

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

2000 • 154 citations

The Usher syndromes

1999 • 148 citations

Unconventional myosins and the genetics of hearing loss

1999 • 118 citations

The Usher syndromes

1999 • 112 citations

Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice

1997 • 104 citations

Two Nonmuscle Myosin II Heavy Chain Isoforms Expressed in Rabbit Brains: Filament Forming Properties, the Effects of Phosphorylation by Protein Kinase C and Casein Kinase II, and Location of the Phosphorylation Sites

1998 • 102 citations

Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).

1998 • 23 citations

Characterization of isoform diversity in smooth muscle myosin heavy chains

1994 • 22 citations