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Publications by Kiyoshi Hayasaka

De Novo Mutations in GNAO1, Encoding a Gαo Subunit of Heterotrimeric G Proteins, Cause Epileptic Encephalopathy

American Journal of Human Genetics
Genetics
2013English

A Mutation of COX6A1 Causes a Recessive Axonal or Mixed Form of Charcot-Marie-Tooth Disease

American Journal of Human Genetics
Genetics
2014English

Phenotypic Variability in a Family With Townes–Brocks Syndrome

Journal of Human Genetics
Genetics
2010English

Unique Food-Entrained Circadian Rhythm in Cysteine414-Alanine Mutant mCRY1 Transgenic Mice

Sleep and Biological Rhythms
NeurologyPhysiological PsychologyNeuropsychologyPhysiology
2016English

Electroweak Physics From Belle

2010English

Small Heat Shock Protein 27 Mutation in a Japanese Patient With Distal Hereditary Motor Neuropathy

Journal of Human Genetics
Genetics
2005English

The GARS Gene Is Rarely Mutated in Japanese Patients With Charcot–Marie–Tooth Neuropathy

Journal of Human Genetics
Genetics
2009English

Nonketotic Hyperglycinemia: Two Patients With Primary Defects of P-Protein and T-Protein, Respectively, in the Glycine Cleavage System

Pediatric Research
Child HealthPediatricsPerinatology
1983English

Neonatal Hyperbilirubinemia in Japanese Neonates: Analysis of the Heme Oxygenase-1 Gene and Fetal Hemoglobin Composition in Cord Blood

Pediatric Research
Child HealthPediatricsPerinatology
2003English

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