Shigeharu Wakana
Kobe, 6500047, Japan
Last Updated: 09/26/2026
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Found 70 publications
Mammalian genome research resources available from the National BioResource Project in Japan.
Journal: Mammalian genome : official journal of the International Mammalian Genome Society
Published: July 16, 2024
An inherited life-threatening arrhythmia model established by screening randomly mutagenized mice.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 15, 2024
Loss of CAPS2/Cadps2 leads to exocrine pancreatic cell injury and intracellular accumulation of secretory granules in mice.
Journal: Frontiers in molecular biosciences
Published: September 09, 2022
An old model with new insights: endogenous retroviruses drive the evolvement toward ASD susceptibility and hijack transcription machinery during development.
Journal: Molecular psychiatry
Published: June 20, 2022
A novel ENU-induced Cpox mutation causes microcytic hypochromic anemia in mice.
Journal: Experimental animals
Published: May 08, 2022
Deficiency of protocadherin 9 leads to reduction in positive emotional behaviour.
Journal: Scientific reports
Published: April 16, 2022
Establishment of mouse line showing inducible priapism-like phenotypes.
Journal: Reproductive medicine and biology
Published: March 29, 2022
Characterization of single nucleotide polymorphisms for a forward genetics approach using genetic crosses in C57BL/6 and BALB/c substrains of mice.
Journal: Experimental animals
Published: January 04, 2022
Deletion of Jdp2 enhances Slc7a11 expression in Atoh-1 positive cerebellum granule cell progenitors in vivo.
Journal: Stem cell research & therapy
Published: February 23, 2021
Impact of endogenous melatonin on rhythmic behaviors, reproduction, and survival revealed in melatonin-proficient C57BL/6J congenic mice.
Journal: Journal of pineal research
Published: February 13, 2021
Methodology and theoretical basis of forward genetic screening for sleep/wakefulness in mice.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: July 25, 2019
Pathogenic POGZ mutation causes impaired cortical development and reversible autism-like phenotypes.
Pathogenic POGZ mutation causes impaired cortical development and reversible autism-like phenotypes.
Journal: Nature communications
Published: July 05, 2019
Last Updated: 09/26/2026