Nata M - Search Results

1

Complete XY gonadal dysgenesis and aspects of the SRYgenotype and gonadal tumor formation.

Uehara S, Hashiyada M, Sato K, Nata M, Funato T, Okamura K. Uehara S, et al. Among authors: nata m. J Hum Genet. 2002;47(6):279-84. doi: 10.1007/s100380200040. J Hum Genet. 2002. PMID: 12111377

2

CpG dinucleotide methylation patterns in the human androgen receptor gene and X-chromosome inactivation in peripheral blood leukocytes of phenotypically normal women.

Sato K, Hashiyada M, Uehara S, Nata M, Okamura K. Sato K, et al. Among authors: nata m. J Hum Genet. 2003;48(7):374-9. doi: 10.1007/s10038-003-0040-4. Epub 2003 Jul 1. J Hum Genet. 2003. PMID: 12838396

3

Complete androgen insensitivity in a 47,XXY patient with uniparental disomy for the X chromosome.

Uehara S, Tamura M, Nata M, Kanetake J, Hashiyada M, Terada Y, Yaegashi N, Funato T, Yajima A. Uehara S, et al. Among authors: nata m. Am J Med Genet. 1999 Sep 10;86(2):107-11. doi: 10.1002/(sici)1096-8628(19990910)86:2<107::aid-ajmg3>3.0.co;2-4. Am J Med Genet. 1999. PMID: 10449642

4

X chromosome inactivation patterns in 45,X/46,XX mosaics.

Uehara S, Sato K, Hashiyada M, Obara Y, Matsuzaki S, Nata M, Okamura K. Uehara S, et al. Among authors: nata m. J Hum Genet. 2001;46(3):126-31. doi: 10.1007/s100380170099. J Hum Genet. 2001. PMID: 11310579

5

X-chromosome inactivation in the human trophoblast of early pregnancy.

Uehara S, Tamura M, Nata M, Ji G, Yaegashi N, Okamura K, Yajima A. Uehara S, et al. Among authors: nata m. J Hum Genet. 2000;45(3):119-26. doi: 10.1007/s100380050197. J Hum Genet. 2000. PMID: 10807535

6

Isochromosome consisting of terminal short arm and proximal long arm X in a girl with short stature.

Uehara S, Hanew K, Harada N, Yamamori S, Nata M, Niikawa N, Okamura K. Uehara S, et al. Among authors: nata m. Am J Med Genet. 2001 Mar 15;99(3):196-9. doi: 10.1002/1096-8628(20010315)99:3<196::aid-ajmg1157>3.0.co;2-a. Am J Med Genet. 2001. PMID: 11241489

7

Molecular biologic analyses of tetragametic chimerism in a true hermaphrodite with 46,XX/46,XY.

Uehara S, Nata M, Nagae M, Sagisaka K, Okamura K, Yajima A. Uehara S, et al. Among authors: nata m. Fertil Steril. 1995 Jan;63(1):189-92. doi: 10.1016/s0015-0282(16)57317-8. Fertil Steril. 1995. PMID: 7805911 Free article.

8

A Turner syndrome woman with a ring X chromosome [45,X/46,X,r(X)(p22.3q27)] whose child also had a ring X chromosome.

Uehara S, Nata M, Obara Y, Niinuma T, Funato T, Yajima A. Uehara S, et al. Among authors: nata m. Fertil Steril. 1997 Mar;67(3):576-9. doi: 10.1016/s0015-0282(97)80091-x. Fertil Steril. 1997. PMID: 9091352 Free article.

9

Polymorphism of 17 STRs by multiplex analysis in Japanese population.

Hashiyada M, Itakura Y, Nagashima T, Nata M, Funayama M. Hashiyada M, et al. Among authors: nata m. Forensic Sci Int. 2003 May 5;133(3):250-3. doi: 10.1016/s0379-0738(03)00075-6. Forensic Sci Int. 2003. PMID: 12787660

10

12 Y-chromosomal STR haplotypes in Japanese.

Hashiyada M, Nagashima T, Itakura Y, Sakai J, Kanawaku Y, Kanetake J, Nata M, Funayama M. Hashiyada M, et al. Among authors: nata m. Forensic Sci Int. 2006 May 10;158(2-3):204-12. doi: 10.1016/j.forsciint.2005.04.035. Epub 2005 Jun 13. Forensic Sci Int. 2006. PMID: 15955651

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