Wada Y - Search Results

1

MYRF haploinsufficiency causes 46,XY and 46,XX disorders of sex development: bioinformatics consideration.

Hamanaka K, Takata A, Uchiyama Y, Miyatake S, Miyake N, Mitsuhashi S, Iwama K, Fujita A, Imagawa E, Alkanaq AN, Koshimizu E, Azuma Y, Nakashima M, Mizuguchi T, Saitsu H, Wada Y, Minami S, Katoh-Fukui Y, Masunaga Y, Fukami M, Hasegawa T, Ogata T, Matsumoto N. Hamanaka K, et al. Among authors: wada y. Hum Mol Genet. 2019 Jul 15;28(14):2319-2329. doi: 10.1093/hmg/ddz066. Hum Mol Genet. 2019. PMID: 30985895

2

CXorf6 is a causative gene for hypospadias.

Fukami M, Wada Y, Miyabayashi K, Nishino I, Hasegawa T, Nordenskjöld A, Camerino G, Kretz C, Buj-Bello A, Laporte J, Yamada G, Morohashi K, Ogata T. Fukami M, et al. Among authors: wada y. Nat Genet. 2006 Dec;38(12):1369-71. doi: 10.1038/ng1900. Epub 2006 Nov 5. Nat Genet. 2006. PMID: 17086185

3

Association of severe micropenis with Gly146Ala polymorphism in the gene for steroidogenic factor-1.

Wada Y, Okada M, Hasegawa T, Ogata T. Wada Y, et al. Endocr J. 2005 Aug;52(4):445-8. doi: 10.1507/endocrj.52.445. Endocr J. 2005. PMID: 16127213 Free article.

4

Association of cryptorchidism with Gly146Ala polymorphism in the gene for steroidogenic factor-1.

Wada Y, Okada M, Fukami M, Sasagawa I, Ogata T. Wada Y, et al. Fertil Steril. 2006 Mar;85(3):787-90. doi: 10.1016/j.fertnstert.2005.09.016. Fertil Steril. 2006. PMID: 16500365 Free article.

5

MAMLD1 (CXorf6) is a New Gene for Hypospadias.

Ogata T, Fukami M, Wada Y. Ogata T, et al. Among authors: wada y. Clin Pediatr Endocrinol. 2008;17(4):87-93. doi: 10.1297/cpe.17.87. Epub 2008 Nov 8. Clin Pediatr Endocrinol. 2008. PMID: 24790369 Free PMC article. Review.

6

Novel Splice Site Mutation in MAMLD1 in a Patient with Hypospadias.

Igarashi M, Wada Y, Kojima Y, Miyado M, Nakamura M, Muroya K, Mizuno K, Hayashi Y, Nonomura K, Kohri K, Ogata T, Fukami M. Igarashi M, et al. Among authors: wada y. Sex Dev. 2015;9(3):130-5. doi: 10.1159/000380842. Epub 2015 Mar 31. Sex Dev. 2015. PMID: 25833151

7

Mutation and polymorphism analyses of INSL3 and LGR8/GREAT in 62 Japanese patients with cryptorchidism.

Yamazawa K, Wada Y, Sasagawa I, Aoki K, Ueoka K, Ogata T. Yamazawa K, et al. Among authors: wada y. Horm Res. 2007;67(2):73-6. doi: 10.1159/000096089. Epub 2006 Oct 6. Horm Res. 2007. PMID: 17028442

8

Mastermind-like domain-containing 1 (MAMLD1 or CXorf6) transactivates the Hes3 promoter, augments testosterone production, and contains the SF1 target sequence.

Fukami M, Wada Y, Okada M, Kato F, Katsumata N, Baba T, Morohashi K, Laporte J, Kitagawa M, Ogata T. Fukami M, et al. Among authors: wada y. J Biol Chem. 2008 Feb 29;283(9):5525-32. doi: 10.1074/jbc.M703289200. Epub 2007 Dec 27. J Biol Chem. 2008. PMID: 18162467 Free article.

9

Mutation analysis of SOX9 and single copy number variant analysis of the upstream region in eight patients with campomelic dysplasia and acampomelic campomelic dysplasia.

Wada Y, Nishimura G, Nagai T, Sawai H, Yoshikata M, Miyagawa S, Hanita T, Sato S, Hasegawa T, Ishikawa S, Ogata T. Wada Y, et al. Am J Med Genet A. 2009 Dec;149A(12):2882-5. doi: 10.1002/ajmg.a.33107. Am J Med Genet A. 2009. PMID: 19921652 No abstract available.

10

Premature ovarian failure and androgen receptor gene CAG repeat lengths weighted by X chromosome inactivation patterns.

Sugawa F, Wada Y, Maruyama T, Uchida H, Ishizuka B, Ogata T. Sugawa F, et al. Among authors: wada y. Fertil Steril. 2009 Feb;91(2):649-52. doi: 10.1016/j.fertnstert.2007.11.085. Epub 2008 Feb 20. Fertil Steril. 2009. PMID: 18281036 Free article.

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