Satokata I - Search Results

1

Erythrocyte Na/K flux ratio in relation to sodium intake and a family history of essential hypertension in normotensive children.

Uchiyama M, Satokata I. Uchiyama M, et al. Among authors: satokata i. J Hum Hypertens. 1993 Feb;7(1):47-51. J Hum Hypertens. 1993. PMID: 8383770

2

Two novel splicing mutations in the XPA gene in patients with group A xeroderma pigmentosum.

Satokata I, Uchiyama M, Tanaka K. Satokata I, et al. Hum Mol Genet. 1995 Oct;4(10):1993-4. doi: 10.1093/hmg/4.10.1993. Hum Mol Genet. 1995. PMID: 8595429 No abstract available.

3

[A close relationship between the renal potassium regulation and the maximum binding of ouabain to erythrocytes].

Uchiyama M, Hayakawa H, Satokata I, Sakai K. Uchiyama M, et al. Among authors: satokata i. Nihon Jinzo Gakkai Shi. 1991 Feb;33(2):125-30. Nihon Jinzo Gakkai Shi. 1991. PMID: 2051638 Japanese.

4

[Mice carrying null mutations of the homeotic genes Hoxa10 and Msx1].

Satokata I, Uchiyama M. Satokata I, et al. Tanpakushitsu Kakusan Koso. 1995 Oct;40(14):2134-43. Tanpakushitsu Kakusan Koso. 1995. PMID: 8532869 Review. Japanese. No abstract available.

5

[Erythrocyte sodium transport in children with pseudohypoaldosteronism].

Uchiyama M, Gomi T, Satokata I, Sakai K. Uchiyama M, et al. Among authors: satokata i. Rinsho Byori. 1988 Jun;36(6):685-8. Rinsho Byori. 1988. PMID: 3210317 Japanese. No abstract available.

6

Plasma atrial natriuretic peptide in congenital heart disease.

Uchiyama M, Satokata I, Aikawa T, Sakai K. Uchiyama M, et al. Among authors: satokata i. Acta Paediatr Scand. 1987 Jul;76(4):669-70. doi: 10.1111/j.1651-2227.1987.tb10541.x. Acta Paediatr Scand. 1987. PMID: 2957889 No abstract available.

7

[Age-related changes in atrial natriuretic polypeptide in childhood].

Satokata I, Uchiyama M, Aikawa T, Hara R, Sakai K. Satokata I, et al. Rinsho Byori. 1987 Oct;35(10):1159-62. Rinsho Byori. 1987. PMID: 2963923 Japanese. No abstract available.

8

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation.

Satokata I, Ma L, Ohshima H, Bei M, Woo I, Nishizawa K, Maeda T, Takano Y, Uchiyama M, Heaney S, Peters H, Tang Z, Maxson R, Maas R. Satokata I, et al. Nat Genet. 2000 Apr;24(4):391-5. doi: 10.1038/74231. Nat Genet. 2000. PMID: 10742104

9

Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease.

Yoshida A, Morisaki H, Nakaji M, Kitano M, Kim KS, Sagawa K, Ishikawa S, Satokata I, Mitani Y, Kato H, Hamaoka K, Echigo S, Shiraishi I, Morisaki T. Yoshida A, et al. Among authors: satokata i. J Hum Genet. 2016 Feb;61(2):157-62. doi: 10.1038/jhg.2015.126. Epub 2015 Oct 22. J Hum Genet. 2016. PMID: 26490186

10

Molecular basis of group A xeroderma pigmentosum: a missense mutation and two deletions located in a zinc finger consensus sequence of the XPAC gene.

Satokata I, Tanaka K, Okada Y. Satokata I, et al. Hum Genet. 1992 Mar;88(6):603-7. doi: 10.1007/BF02265282. Hum Genet. 1992. PMID: 1339397

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

34 results

Search Page

Filters