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Publications by Kiyoto Kurima

A Noncoding Point Mutation of Zeb1 Causes Multiple Developmental Malformations and Obesity in Twirler Mice

Molecular Biology

Cancer Research

English

Cysteine Substitution Reveals the Pore-Forming Region of TMC1 in Hair Cell Sensory Transduction Channels

Biophysical Journal

English

Related publications

Multiple Causes of Human Kidney Malformations

Archives of Disease in Childhood

English

A Point Mutation in the Gene for Asparagine-Linked Glycosylation 10B (Alg10b) Causes Nonsyndromic Hearing Impairment in Mice (Mus Musculus)

Multidisciplinary

English

Embryonic Exposure to 2,2′,3,5′,6‐pentachlorobiphenyl (PCB‐95) Causes Developmental Malformations in Zebrafish

Environmental Toxicology and Chemistry

Environmental Chemistry

English

A Point Mutation in Sec61 1 Leads to Diabetes and Hepatosteatosis in Mice

Internal Medicine

English

Gα11 Mutation in Mice Causes Hypocalcemia Rectifiable by Calcilytic Therapy

English

Loss of P53 Sensitizes Mice With a Mutation in Ccm1 (KRIT1) to Development of Cerebral Vascular Malformations

American Journal of Pathology

Forensic Medicine

English

HomozygousDNAH1frameshift Mutation Causes Multiple Morphological Anomalies of the Sperm Flagella in Chinese

Clinical Genetics

English

A Founder Mutation in the Ashkenazi Jewish Population Affecting Messenger RNA Splicing of the CCM2 Gene Causes Cerebral Cavernous Malformations

Genetics in Medicine

English

Targeted Inactivation of Copper Transporter Atp7b in Hepatocytes Causes Liver Steatosis and Obesity in Mice

American Journal of Physiology - Gastrointestinal and Liver Physiology

Gastroenterology

English