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

Basic local alignment search tool

1990 • 87,358 citations

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1979 • 22,482 citations

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1997 • 1,435 citations

Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness

1993 • 1,173 citations

The I.M.A.G.E. Consortium: An Integrated Molecular Analysis of Genomes and Their Expression

1996 • 1,132 citations

Defective myosin VIIA gene responsible for Usher syndrome type IB

1995 • 1,051 citations

p140mDia, a mammalian homolog of Drosophila diaphanous, is a target protein for Rho small GTPase and is a ligand for profilin

1997 • 819 citations

Bni1p, a Yeast Formin Linking Cdc42p and the Actin Cytoskeleton During Polarized Morphogenesis

1997 • 654 citations

Construction and Characterization of a Human Bacterial Artificial Chromosome Library

1996 • 459 citations

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

1997 • 455 citations

Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4

1995 • 421 citations

diaphanous is required for cytokinesis in Drosophila and shares domains of similarity with the products of the limb deformity gene

1994 • 408 citations

Rho effectors and reorganization of actin cytoskeleton

1997 • 379 citations

Actin filaments in sensory hairs of inner ear receptor cells.

1977 • 296 citations

Genes responsible for human hereditary deafness: symphony of a thousand

1996 • 276 citations

A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness

1994 • 271 citations

'Formins': proteins deduced from the alternative transcripts of the limb deformity gene

1990 • 201 citations

The gene for an inherited form of deafness maps to chromosome 5q31.

1992 • 189 citations

The three faces of profilin

1993 • 179 citations

Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations

1997 • 170 citations

Actin cytoskeleton: Are FH proteins local organizers?

1997 • 114 citations

Disruption of formin-encoding transcripts in two mutant limb deformity alleles

1990 • 110 citations

Changes in the organization of actin filaments in the stereocilia of noise-damaged lizard cochleae

1982 • 109 citations

Genetics of deafness

1996 • 46 citations

Genetic Evidence That Formins Function within the Nucleus

1996 • 39 citations

The Role of a Single Formin Isoform in the Limb and Renal Phenotypes of Limb Deformity

1997 • 39 citations

Low frequency hereditary deafness in man with childhood onset.

1981 • 39 citations

Preservation and visualization of actin-containing filaments in the apical zone of cochlear sensory cells

1982 • 36 citations

Mapping of DFN2 to Xq22

1996 • 36 citations

The Mouseformin(Fmn) Gene: Genomic Structure, Novel Exons, and Genetic Mapping

1997 • 32 citations

Formins: phosphoprotein isoforms encoded by the mouse limb deformity locus.

1993 • 28 citations

Drosophila-related expressed sequences

1997 • 23 citations