K. Ohkubo

Mitochondrial gene mutations in the tRNA(Leu(UUR)) region and diabetes: prevalence and clinical phenotypes in Japan.

K. Ohkubo, A. Yamano, M. Nagashima, 2001, Clinical chemistry.

Novel subtype of congenital partial lipodystrophy with mandibular hypoplasia, sensorineural deafness and short stature of unknown genetic origin

K. Ohkubo, Kunihisa Kobayashi, Y. Tajiri, 2017, Journal of diabetes investigation.

Definitive diagnosis of mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome caused by a recurrent de novo mutation in the POLD1 gene.

H. Maegawa, A. Kashiwagi, T. Kaname, 2018, Endocrine journal.

Inhibitory Effect of the α1-Antitrypsin Pittsburgh Type-Mutant (α1-PIM/R) on Proinsulin Processing in the Regulated Secretory Pathway of the Pancreatic β-Cell Line MIN6

J. Miyazaki, Y. Ikehara, K. Ohkubo, 2003 .

Genotypes of the pancreatic β‐cell K‐ATP channel and clinical phenotypes of Japanese patients with persistent hyperinsulinaemic hypoglycaemia of infancy

N. Okamoto, S. Suita, T. Taguchi, 2005, Clinical endocrinology.

Clinical application of the different cross-reactivities of anti-insulin antibodies to insulin lispro to evaluate endogenous insulin secretion.

Y. Akehi, K. Ohkubo, A. Matsunaga, 2013, Clinica chimica acta; international journal of clinical chemistry.

Inhibitory effect of the alpha1-antitrypsin Pittsburgh type-mutant (alpha1-PIM/R) on proinsulin processing in the regulated secretory pathway of the pancreatic beta-cell line MIN6.

J. Miyazaki, Y. Ikehara, K. Ohkubo, 2003, Endocrine journal.

A novel mutation of CLCNKB in a Japanese patient of Gitelman-like phenotype with diuretic insensitivity to thiazide administration

T. Yanase, A. Maeyama, K. Ohkubo, 2014, Meta gene.

Mutations in the sulfonylurea receptor gene in relation to the long-term outcome of persistent hyperinsulinemic hypoglycemia of infancy.

S. Suita, T. Taguchi, K. Ohkubo, 2002, Journal of Pediatric Surgery.