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List of works by Kentaro Katayama

A deletion in the endothelin-B receptor gene is responsible for the Waardenburg syndrome-like phenotypes of WS4 mice

scientific article published on 01 October 2006

A mutation in the nuclear pore complex gene Tmem48 causes gametogenesis defects in skeletal fusions with sterility (sks) mice

scientific journal article

A role for the Golgi matrix protein giantin in ciliogenesis through control of the localization of dynein-2.

scientific article published on 17 September 2013

Age-related pathophysiological changes in rats with unilateral renal agenesis

scientific article published on 07 February 2011

Characterization of chromosomal inversion of the mouse hairy ears (Eh) mutation associated with cleft palate

scientific article published on 01 April 2007

Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalities

scientific article published on 22 September 2009

Characterization of the skeletal fusion with sterility (sks) mouse showing axial skeleton abnormalities caused by defects of embryonic skeletal development

scientific article

Critical roles of Astrin in the mitosis of immature rat Sertoli cells

scientific article

Giantin is required for coordinated production of aggrecan, link protein and type XI collagen during chondrogenesis

scientific article published on 22 March 2018

Heparanase localization during palatogenesis in mice.

scientific article published on 12 February 2013

Homeobox family Hoxc localization during murine palate formation.

scientific article published on 31 December 2015

Insertional mutation in the Golgb1 gene is associated with osteochondrodysplasia and systemic edema in the OCD rat.

scientific article

Loss of Wwox Causes Defective Development of Cerebral Cortex with Hypomyelination in a Rat Model of Lethal Dwarfism with Epilepsy

scientific article published on 23 July 2019

Postnatal development of hypoplastic thymus in semi-lethal dwarf pet/pet males

scientific article published on 26 November 2010

Progression of renal fibrosis in congenital CKD model rats with reduced number of nephrons

scientific article published on 06 February 2017

Short-limbed dwarfism: slw is a new allele of Npr2 causing chondrodysplasia.

scientific article published on 28 August 2007

Suppressed recombination on mouse chromosome 15 defined regions of chromosomal inversions associated with koala (koa) and hairy ears (eh) mutations

scientific article published on 01 January 2008

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