K. Aya

发表

Vitamin D is an important factor in estrogen biosynthesis of both female and male gonads.

T. Moriwake, H. Tanaka, Y. Seino, 2000, Endocrinology.

A Glanzmann’s mutation in β3 integrin specifically impairs osteoclast function

D. Ory, R. Faccio, S. Teitelbaum, 2001 .

Late-onset Lymphedema and Protein-losing Enteropathy with Noonan Syndrome

Hiroyuki Tanaka, T. Morishima, Hidehiko Maruyama, 2009, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

The Association with Dietary Patterns and Risk of Anemia in Japanese Elderly

K. Aya, I. Eri, 2020 .

Long-term outcome of childhood-onset complicated nephrotic syndrome after a multicenter, double-blind, randomized, placebo-controlled trial of rituximab

K. Nakanishi, S. Ito, T. Morimoto, 2017, Pediatric Nephrology.

Fibroblast growth factor 23 concentrations in healthy term infants during the early postpartum period.

Hiroyuki Tanaka, Y. Seino, T. Morishima, 2010, Bone.

NF-(kappa)B-inducing kinase controls lymphocyte and osteoclast activities in inflammatory arthritis.

H. Kitaura, O. Kanagawa, Muhammad A Alhawagri, 2005, The Journal of clinical investigation.

Marrow Stromal Cells and Osteoclast Precursors Differentially Contribute to TNF-α-Induced Osteoclastogenesis In Vivo1

Matthew J. Silva, Shi Wei, S. Takeshita, 2004, The Journal of Immunology.

Induced Osteoclastogenesis In Vivo α Precursors Differentially Contribute to TNF-Marrow Stromal Cells and Osteoclast

Matthew J. Silva, Shi Wei, S. Takeshita, 2004 .

Expression of parathyroid hormone-related peptide messenger ribonucleic acid in developing kidney.

H. Tanaka, Y. Seino, M. Kobayashi, 1999, Kidney international.

Expression of parathyroid-related peptide mRNA in the kidney

K. Aya, 1997 .

Expression of PTHrP mRNA in kidney.

Y. Seino, Hiroyuki Tanaka, K. Aya, 1997 .

Nephrin is an important component of the barrier system in the testis.

H. Tanaka, Y. Seino, L. Liu, 2001, Acta medica Okayama.

Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial

R. Mori, Y. Ohashi, K. Nakanishi, 2014, The Lancet.

A missense mutation in the nephrin gene impairs membrane targeting.

Hiroyuki Tanaka, Y. Sado, Y. Seino, 2002, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type.

Hiroyuki Tanaka, H. Tanaka, Y. Seino, 2000, Kidney international.

A cross-sectional nationwide survey of congenital and infantile nephrotic syndrome in Japan

K. Iijima, T. Kaneko, K. Ishikura, 2020, BMC Nephrology.

NPHS1 gene mutation in Japanese patients with congenital nephrotic syndrome.

K. Yan, Hiroyuki Tanaka, Y. Sado, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

NF-κB–inducing kinase controls lymphocyte and osteoclast activities in inflammatory arthritis

Osami Kanagawa, Deborah V. Novack, H. Kitaura, 2005 .

A Glanzmann's mutation in beta 3 integrin specifically impairs osteoclast function.

D. Ory, R. Faccio, S. Teitelbaum, 2001, The Journal of clinical investigation.

Two novel missense mutations in calcium-sensing receptor gene associated with neonatal severe hyperparathyroidism.

H. Tanaka, Y. Seino, M. Kobayashi, 1997, The Journal of clinical endocrinology and metabolism.

Functional analysis of NPHS 1 mutations in Japanese 1 patients 2 3

K. Yan, Hiroyuki Tanaka, Y. Sado, 2013 .

NPHS 1 gene mutation in Japanese patients with congenital nephrotic syndrome

K. Yan, Hiroyuki Tanaka, Y. Sado, 2009 .

Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial

R. Mori, Y. Ohashi, K. Nakanishi, 2014, The Lancet.