Yoshida A - Search Results

1

Molecular defect of a phosphoglycerate kinase variant (PGK-Matsue) associated with hemolytic anemia: Leu----Pro substitution caused by T/A----C/G transition in exon 3.

Maeda M, Yoshida A. Maeda M, et al. Among authors: yoshida a. Blood. 1991 Mar 15;77(6):1348-52. Blood. 1991. PMID: 2001457 Free article.

2

Molecular abnormalities of a phosphoglycerate kinase variant generated by spontaneous mutation.

Maeda M, Bawle EV, Kulkarni R, Beutler E, Yoshida A. Maeda M, et al. Among authors: yoshida a. Blood. 1992 May 15;79(10):2759-62. Blood. 1992. PMID: 1586722 Free article.

3

Molecular abnormalities of a human glucose-6-phosphate dehydrogenase variant associated with undetectable enzyme activity and immunologically cross-reacting material.

Maeda M, Constantoulakis P, Chen CS, Stamatoyannopoulos G, Yoshida A. Maeda M, et al. Among authors: yoshida a. Am J Hum Genet. 1992 Aug;51(2):386-95. Am J Hum Genet. 1992. PMID: 1353664 Free PMC article.

4

Molecular abnormality of a phosphoglycerate kinase variant (PGK-Alabama).

Yoshida A, Twele TW, Davé V, Beutler E. Yoshida A, et al. Blood Cells Mol Dis. 1995;21(3):179-81. doi: 10.1006/bcmd.1995.0020. Blood Cells Mol Dis. 1995. PMID: 8673469

5

Hematologically important mutations: molecular abnormalities of phosphoglycerate kinase.

Yoshida A. Yoshida A. Blood Cells Mol Dis. 1996;22(3):265-7. doi: 10.1006/bcmd.1996.0108. Blood Cells Mol Dis. 1996. PMID: 9075577 No abstract available.

6

Retarded and aberrant splicings caused by single exon mutation in a phosphoglycerate kinase variant.

Ookawara T, Davé V, Willems P, Martin JJ, de Barsy T, Matthys E, Yoshida A. Ookawara T, et al. Among authors: yoshida a. Arch Biochem Biophys. 1996 Mar 1;327(1):35-40. doi: 10.1006/abbi.1996.0089. Arch Biochem Biophys. 1996. PMID: 8615693

7

A single nucleotide base transition is the basis of the common human glucose-6-phosphate dehydrogenase variant A (+).

Takizawa T, Yoneyama Y, Miwa S, Yoshida A. Takizawa T, et al. Among authors: yoshida a. Genomics. 1987 Nov;1(3):228-31. doi: 10.1016/0888-7543(87)90048-6. Genomics. 1987. PMID: 3446582

The X-chromosome-linked glucose-6-phosphate dehydrogenase (G6PD) A(+) is a common variant found in about 20% of blacks. The amino acid substitution of Asp in the variant G6PD A(+) for Asn in the normal G6PD B(+) was previously found (A. ...By screening …

The X-chromosome-linked glucose-6-phosphate dehydrogenase (G6PD) A(+) is a common variant found in about 20% of blacks. The am …

8

Mutations associated with Sjögren-Larsson syndrome.

Tsukamoto N, Chang C, Yoshida A. Tsukamoto N, et al. Among authors: yoshida a. Ann Hum Genet. 1997 May;61(Pt 3):235-42. doi: 10.1046/j.1469-1809.1997.6130235.x. Ann Hum Genet. 1997. PMID: 9250352

9

The use of enzymopathic human red cells in the study of malarial parasite glucose metabolism.

Roth E Jr, Joulin V, Miwa S, Yoshida A, Akatsuka J, Cohen-Solal M, Rosa R. Roth E Jr, et al. Among authors: yoshida a. Blood. 1988 May;71(5):1408-13. Blood. 1988. PMID: 2833958 Free article.

10

Molecular defect of a phosphoglycerate kinase variant associated with haemolytic anaemia and neurological disorders in a large kindred.

Turner G, Fletcher J, Elber J, Yanagawa Y, Davé V, Yoshida A. Turner G, et al. Among authors: yoshida a. Br J Haematol. 1995 Sep;91(1):60-5. doi: 10.1111/j.1365-2141.1995.tb05245.x. Br J Haematol. 1995. PMID: 7577653

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

4,255 results

Search Page