Matsuo M - Search Results

1

Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation: analysis of the X-inactivation patterns.

Matsuo M, Muroya K, Nanao K, Hasegawa Y, Terasaki H, Kosaki K, Ogata T. Matsuo M, et al. Am J Med Genet. 2000 Apr 10;91(4):267-72. Am J Med Genet. 2000. PMID: 10766981 Review.

2

Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature.

Matsuo M, Muroya K, Kosaki K, Ishii T, Fukushima Y, Anzo M, Ogata T. Matsuo M, et al. Am J Med Genet. 1999 Sep 3;86(1):44-50. Am J Med Genet. 1999. PMID: 10440827 Review.

3

Clinical and molecular studies in 15 females with ring X chromosomes: implications for r(X) formation and mental development.

Matsuo M, Muroya K, Adachi M, Tachibana K, Asakura Y, Nakagomi Y, Hanaki K, Yokoya S, Yoshizawa A, Igarashi Y, Hanew K, Matsuo N, Ogata T. Matsuo M, et al. Among authors: matsuo n. Hum Genet. 2000 Nov;107(5):433-9. doi: 10.1007/s004390000377. Hum Genet. 2000. PMID: 11140940

4

47,XXX male: A clinical and molecular study.

Ogata T, Matsuo M, Muroya K, Koyama Y, Fukutani K. Ogata T, et al. Among authors: matsuo m. Am J Med Genet. 2001 Feb 1;98(4):353-6. doi: 10.1002/1096-8628(20010201)98:4<353::aid-ajmg1110>3.0.co;2-d. Am J Med Genet. 2001. PMID: 11170081 Review.

5

Female carriers of Xp22.3 deletion including MRX locus.

Muroya K, Kosho T, Ogata T, Matsuo M. Muroya K, et al. Among authors: matsuo m. Am J Med Genet. 1999 Jun 4;84(4):384-5. Am J Med Genet. 1999. PMID: 10340659 No abstract available.

6

Membrane stabilizing effect of vitamin E: existence of a hydrogen bond between alpha-tocopherol and phospholipids in bilayer liposomes.

Urano S, Kitahara M, Kato Y, Hasegawa Y, Matsuo M. Urano S, et al. Among authors: matsuo m. J Nutr Sci Vitaminol (Tokyo). 1990 Dec;36(6):513-9. doi: 10.3177/jnsv.36.513. J Nutr Sci Vitaminol (Tokyo). 1990. PMID: 2097323

7

Vitamin E: inhibition of retinol-induced hemolysis and membrane-stabilizing behavior.

Urano S, Inomori Y, Sugawara T, Kato Y, Kitahara M, Hasegawa Y, Matsuo M, Mukai K. Urano S, et al. Among authors: matsuo m. J Biol Chem. 1992 Sep 15;267(26):18365-70. J Biol Chem. 1992. PMID: 1526978 Free article.

8

Amplification of ten deletion-rich exons of the dystrophin gene by polymerase chain reaction shows deletions in 36 of 90 Japanese families with Duchenne muscular dystrophy.

Kitoh Y, Matsuo M, Nishio H, Takumi T, Nakajima T, Masumura T, Koga J, Nakamura H. Kitoh Y, et al. Among authors: matsuo m. Am J Med Genet. 1992 Feb 15;42(4):453-7. doi: 10.1002/ajmg.1320420408. Am J Med Genet. 1992. PMID: 1609827

9

In vitro splicing analysis showed that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G-->A mutations in introns of the dystrophin gene.

Habara Y, Takeshima Y, Awano H, Okizuka Y, Zhang Z, Saiki K, Yagi M, Matsuo M. Habara Y, et al. Among authors: matsuo m. J Med Genet. 2009 Aug;46(8):542-7. doi: 10.1136/jmg.2008.061259. Epub 2008 Nov 10. J Med Genet. 2009. PMID: 19001018

10

Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.

Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M. Nozu K, et al. Among authors: matsuo m. J Med Genet. 2008 Mar;45(3):182-6. doi: 10.1136/jmg.2007.052944. J Med Genet. 2008. PMID: 18310267

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