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Publications by Lynne M. Coluccio

Myo1c Mutations Associated With Hearing Loss Cause Defects in the Interaction With Nucleotide and Actin

Cellular and Molecular Life Sciences

Molecular Neuroscience

Molecular Medicine

Molecular Biology

English

Truncation of a Mammalian Myosin I Results in Loss of Ca2+-Sensitive Motility

Journal of Biological Chemistry

Molecular Biology

English

Related publications

Recessive Mutations of TMC1 Associated With Moderate to Severe Hearing Loss

Molecular Neuroscience

English

Noncoding Mutations of HGF Are Associated With Nonsyndromic Hearing Loss, DFNB39

American Journal of Human Genetics

English

Pathogenic Polyglutamine Proteins Cause Dendrite Defects Associated With Specific Actin Cytoskeletal Alterations in Drosophila

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Independent Mutations in MouseVangl2That Cause Neural Tube Defects inLooptailMice Impair Interaction With Members of theDishevelledFamily

Journal of Biological Chemistry

Molecular Biology

English

Novel PTPRQ Mutations Identified in Three Congenital Hearing Loss Patients With Various Types of Hearing Loss

Annals of Otology, Rhinology and Laryngology

Otorhinolaryngology

English

Single-Nucleotide Polymorphisms in XPO5 Are Associated With Noise-Induced Hearing Loss in a Chinese Population

Biochemistry Research International

English

Biallelic Mutations in LRRC56, Encoding a Protein Associated With Intraflagellar Transport, Cause Mucociliary Clearance and Laterality Defects

American Journal of Human Genetics

English

Modiolar Dehiscence Associated With Sensorineural Hearing Loss

Otology and Neurotology

Otorhinolaryngology

Sensory Systems

English

GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss

Revista Romana de Medicina de Laborator

English