Aya K - Search Results

1

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

Liu L, Aya K, Tanaka H, Shimizu J, Ito S, Seino Y. Liu L, et al. Among authors: aya k. Acta Med Okayama. 2001 Jun;55(3):161-5. doi: 10.18926/AMO/32022. Acta Med Okayama. 2001. PMID: 11434428

2

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

Kobayashi M, Tanaka H, Tsuzuki K, Tsuyuki M, Igaki H, Ichinose Y, Aya K, Nishioka N, Seino Y. Kobayashi M, et al. Among authors: aya k. J Clin Endocrinol Metab. 1997 Aug;82(8):2716-9. doi: 10.1210/jcem.82.8.4135. J Clin Endocrinol Metab. 1997. PMID: 9253359

3

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

Aya K, Tanaka H, Ichinose Y, Kobayashi M, Seino Y. Aya K, et al. Kidney Int. 1999 May;55(5):1696-703. doi: 10.1046/j.1523-1755.1999.00417.x. Kidney Int. 1999. PMID: 10231431

4

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

Aya K, Tanaka H, Seino Y. Aya K, et al. Kidney Int. 2000 Feb;57(2):401-4. doi: 10.1046/j.1523-1755.2000.00859.x. Kidney Int. 2000. PMID: 10652016

5

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

Kinuta K, Tanaka H, Moriwake T, Aya K, Kato S, Seino Y. Kinuta K, et al. Among authors: aya k. Endocrinology. 2000 Apr;141(4):1317-24. doi: 10.1210/endo.141.4.7403. Endocrinology. 2000. PMID: 10746634

6

A missense mutation in the nephrin gene impairs membrane targeting.

Shimizu J, Tanaka H, Aya K, Ito S, Sado Y, Seino Y. Shimizu J, et al. Among authors: aya k. Am J Kidney Dis. 2002 Oct;40(4):697-703. doi: 10.1053/ajkd.2002.35676. Am J Kidney Dis. 2002. PMID: 12324903

7

NPHS1 gene mutation in Japanese patients with congenital nephrotic syndrome.

Aya K, Shimizu J, Ohtomo Y, Satomura K, Suzuki H, Yan K, Sado Y, Morishima T, Tanaka H. Aya K, et al. Nephrol Dial Transplant. 2009 Aug;24(8):2411-4. doi: 10.1093/ndt/gfp122. Epub 2009 Mar 25. Nephrol Dial Transplant. 2009. PMID: 19321760

8

Functional analysis of NPHS1 mutations in Japanese patients.

Miyai T, Aya K, Takaiwa M, Yan K, Sado Y, Tanaka H, Morishima T. Miyai T, et al. Among authors: aya k. Histol Histopathol. 2014 Feb;29(2):279-84. doi: 10.14670/HH-29.279. Epub 2013 Oct 21. Histol Histopathol. 2014. PMID: 24142548

9

A novel homozygous mutation of the EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis.

Aochi S, Nakanishi G, Suzuki N, Setsu N, Suzuki D, Aya K, Iwatsuki K. Aochi S, et al. Among authors: aya k. Br J Dermatol. 2007 Dec;157(6):1265-6. doi: 10.1111/j.1365-2133.2007.08206.x. Epub 2007 Oct 4. Br J Dermatol. 2007. PMID: 17916203 No abstract available.

10

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

Takaiwa M, Aya K, Miyai T, Hasegawa K, Yokoyama M, Kondo Y, Kodani N, Seino Y, Tanaka H, Morishima T. Takaiwa M, et al. Among authors: aya k. Bone. 2010 Aug;47(2):256-62. Bone. 2010. PMID: 20641162

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