Tanaka Y - Search Results

1

Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations.

Nakamura S, Miyado M, Saito K, Katsumi M, Nakamura A, Kobori Y, Tanaka Y, Ishikawa H, Yoshida A, Okada H, Hata K, Nakabayashi K, Okamura K, Ogata H, Matsubara Y, Ogata T, Nakai H, Fukami M. Nakamura S, et al. Among authors: tanaka y. Andrology. 2017 Jul;5(4):824-831. doi: 10.1111/andr.12378. Andrology. 2017. PMID: 28718531 Free article.

2

Copy-number variations in Y-chromosomal azoospermia factor regions identified by multiplex ligation-dependent probe amplification.

Saito K, Miyado M, Kobori Y, Tanaka Y, Ishikawa H, Yoshida A, Katsumi M, Saito H, Kubota T, Okada H, Ogata T, Fukami M. Saito K, et al. Among authors: tanaka y. J Hum Genet. 2015 Mar;60(3):127-31. doi: 10.1038/jhg.2014.115. Epub 2015 Jan 8. J Hum Genet. 2015. PMID: 25566757

3

Microhomology-mediated microduplication in the y chromosomal azoospermia factor a region in a male with mild asthenozoospermia.

Katsumi M, Ishikawa H, Tanaka Y, Saito K, Kobori Y, Okada H, Saito H, Nakabayashi K, Matsubara Y, Ogata T, Fukami M, Miyado M. Katsumi M, et al. Among authors: tanaka y. Cytogenet Genome Res. 2014;144(4):285-9. doi: 10.1159/000377649. Epub 2015 Mar 6. Cytogenet Genome Res. 2014. PMID: 25765000

4

STX2 is a causative gene for nonobstructive azoospermia.

Nakamura S, Kobori Y, Ueda Y, Tanaka Y, Ishikawa H, Yoshida A, Katsumi M, Saito K, Nakamura A, Ogata T, Okada H, Nakai H, Miyado M, Fukami M. Nakamura S, et al. Among authors: tanaka y. Hum Mutat. 2018 Jun;39(6):830-833. doi: 10.1002/humu.23423. Epub 2018 Apr 10. Hum Mutat. 2018. PMID: 29570232

5

Germline-Derived Gain-of-Function Variants of Gsα-Coding GNAS Gene Identified in Nephrogenic Syndrome of Inappropriate Antidiuresis.

Miyado M, Fukami M, Takada S, Terao M, Nakabayashi K, Hata K, Matsubara Y, Tanaka Y, Sasaki G, Nagasaki K, Shiina M, Ogata K, Masunaga Y, Saitsu H, Ogata T. Miyado M, et al. Among authors: tanaka y. J Am Soc Nephrol. 2019 May;30(5):877-889. doi: 10.1681/ASN.2018121268. Epub 2019 Apr 8. J Am Soc Nephrol. 2019. PMID: 30962325 Free PMC article.

6

Identification of chromosome 15q26 terminal deletion with telomere sequences and its bearing on genotype-phenotype analysis.

Dateki S, Fukami M, Tanaka Y, Sasaki G, Moriuchi H, Ogata T. Dateki S, et al. Among authors: tanaka y. Endocr J. 2011;58(3):155-9. doi: 10.1507/endocrj.k10e-251. Epub 2011 Jan 14. Endocr J. 2011. PMID: 21242650 Free article.

7

Impaired urinary water excretion in a three-generation family.

Tanaka Y, Sugita K, Saito T, Muroya K, Ishikawa SE, Awazu M, Ogata T. Tanaka Y, et al. Pediatr Nephrol. 2001 Oct;16(10):820-2. doi: 10.1007/s004670100663. Pediatr Nephrol. 2001. PMID: 11605790

8

Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome.

Yoshida R, Hasegawa T, Hasegawa Y, Nagai T, Kinoshita E, Tanaka Y, Kanegane H, Ohyama K, Onishi T, Hanew K, Okuyama T, Horikawa R, Tanaka T, Ogata T. Yoshida R, et al. Among authors: tanaka t, tanaka y. J Clin Endocrinol Metab. 2004 Jul;89(7):3359-64. doi: 10.1210/jc.2003-032091. J Clin Endocrinol Metab. 2004. PMID: 15240615

9

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.

Kagami M, Sekita Y, Nishimura G, Irie M, Kato F, Okada M, Yamamori S, Kishimoto H, Nakayama M, Tanaka Y, Matsuoka K, Takahashi T, Noguchi M, Tanaka Y, Masumoto K, Utsunomiya T, Kouzan H, Komatsu Y, Ohashi H, Kurosawa K, Kosaki K, Ferguson-Smith AC, Ishino F, Ogata T. Kagami M, et al. Among authors: tanaka y. Nat Genet. 2008 Feb;40(2):237-42. doi: 10.1038/ng.2007.56. Epub 2008 Jan 6. Nat Genet. 2008. PMID: 18176563

10

High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndrome.

Fujii K, Ishikawa S, Uchikawa H, Komura D, Shapero MH, Shen F, Hung J, Arai H, Tanaka Y, Sasaki K, Kohno Y, Yamada M, Jones KW, Aburatani H, Miyashita T. Fujii K, et al. Among authors: tanaka y. Hum Genet. 2007 Dec;122(5):459-66. doi: 10.1007/s00439-007-0419-y. Epub 2007 Aug 17. Hum Genet. 2007. PMID: 17703323

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