Hiromichi Ishikawa
Ichikawa, Japan
Last Updated: 09/26/2026
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Found 11 publications
Comparison of Productivity and Fecal Microbiotas of Sows in Commercial Farms.
Journal: Microorganisms
Published: August 31, 2020
Mutation of GALNTL5 gene identified in patients diagnosed with asthenozoospermia.
Journal: Human fertility (Cambridge, England)
Published: January 11, 2019
STX2 is a causative gene for nonobstructive azoospermia.
Journal: Human mutation
Published: December 18, 2017
Obstructive azoospermia caused by low ligation of varicocele: A case report.
Journal: Systems biology in reproductive medicine
Published: August 04, 2017
Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations.
Journal: Andrology
Published: October 24, 2016
Microhomology-mediated microduplication in the y chromosomal azoospermia factor a region in a male with mild asthenozoospermia.
Journal: Cytogenetic and genome research
Published: January 26, 2015
Copy-number variations in Y-chromosomal azoospermia factor regions identified by multiplex ligation-dependent probe amplification.
Journal: Journal of human genetics
Published: October 08, 2014
Follicle-stimulating hormone enhances recovery from low-dose doxorubicin-induced spermatogenic disorders in mice.
Journal: Journal of assisted reproduction and genetics
Published: October 04, 2014
A heterozygous mutation of GALNTL5 affects male infertility with impairment of sperm motility.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: January 09, 2014
STAT5 Orchestrates Local Epigenetic Changes for Chromatin Accessibility and Rearrangements by Direct Binding to the TCRγ Locus.
Journal: Journal of immunology (Baltimore, Md. : 1950)
Published: September 13, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026