Mori M - Search Results

1

Diagnosis and molecular basis of mitochondrial respiratory chain disorders: exome sequencing for disease gene identification.

Ohtake A, Murayama K, Mori M, Harashima H, Yamazaki T, Tamaru S, Yamashita Y, Kishita Y, Nakachi Y, Kohda M, Tokuzawa Y, Mizuno Y, Moriyama Y, Kato H, Okazaki Y. Ohtake A, et al. Among authors: mori m. Biochim Biophys Acta. 2014 Apr;1840(4):1355-9. doi: 10.1016/j.bbagen.2014.01.025. Epub 2014 Jan 24. Biochim Biophys Acta. 2014. PMID: 24462578 Free article. Review.

2

Cloning and sequence analysis of a full length cDNA encoding human mitochondrial 3-oxoacyl-CoA thiolase.

Abe H, Ohtake A, Yamamoto S, Satoh Y, Takayanagi M, Amaya Y, Takiguchi M, Sakuraba H, Suzuki Y, Mori M, et al. Abe H, et al. Among authors: mori m. Biochim Biophys Acta. 1993 Nov 16;1216(2):304-6. doi: 10.1016/0167-4781(93)90160-f. Biochim Biophys Acta. 1993. PMID: 8241273

3

[Molecular genetics of urea cycle diseases].

Ohtake A, Mori M. Ohtake A, et al. Among authors: mori m. Seikagaku. 1990 Sep;62(9):1170-7. Seikagaku. 1990. PMID: 2258657 Japanese. No abstract available.

4

Visualization of mitochondria with green fluorescent protein in cultured fibroblasts from patients with mitochondrial diseases.

Kanazawa M, Yano M, Namchai C, Yamamoto S, Ohtake A, Takayanagi M, Mori M, Niimi H. Kanazawa M, et al. Among authors: mori m. Biochem Biophys Res Commun. 1997 Oct 20;239(2):580-4. doi: 10.1006/bbrc.1997.7448. Biochem Biophys Res Commun. 1997. PMID: 9344874

5

Molecular cloning and sequence analysis of the cDNA for human mitochondrial short-chain enoyl-CoA hydratase.

Kanazawa M, Ohtake A, Abe H, Yamamoto S, Satoh Y, Takayanagi M, Niimi H, Mori M, Hashimoto T. Kanazawa M, et al. Among authors: mori m. Enzyme Protein. 1993;47(1):9-13. doi: 10.1159/000468650. Enzyme Protein. 1993. PMID: 8012501

6

Expression analysis of two mutant human ornithine transcarbamylases in COS-7 cells.

Kogo T, Satoh Y, Kanazawa M, Yamamoto S, Takayanagi M, Ohtake A, Mori M, Niimi H. Kogo T, et al. Among authors: mori m. J Hum Genet. 1998;43(1):54-8. doi: 10.1007/s100380050037. J Hum Genet. 1998. PMID: 9609999

7

Molecular aspects of urea cycle enzymes and related disorders.

Mori M, Takiguchi M, Haraguchi Y, Matsuda I, Ohtake A, Takayanagi M. Mori M, et al. Enzyme. 1987;38(1-4):220-6. doi: 10.1159/000469208. Enzyme. 1987. PMID: 2894303

8

[Carbamyl phosphate synthetase I deficiency].

Ohtake A, Mori M. Ohtake A, et al. Among authors: mori m. Tanpakushitsu Kakusan Koso. 1988 Apr;33(5):497-9. Tanpakushitsu Kakusan Koso. 1988. PMID: 3270854 Japanese. No abstract available.

9

Y55D mutation in ornithine transcarbamylase associated with late-onset hyperammonemia in a male.

Nishiyori A, Yoshino M, Tananari Y, Matsuura T, Hoshide R, Mastuda I, Mori M, Kato H. Nishiyori A, et al. Among authors: mori m. Hum Mutat. 1998;Suppl 1:S131-3. doi: 10.1002/humu.1380110144. Hum Mutat. 1998. PMID: 9452065 No abstract available.

10

Identification of myelodysplastic syndrome-specific genes by DNA microarray analysis with purified hematopoietic stem cell fraction.

Miyazato A, Ueno S, Ohmine K, Ueda M, Yoshida K, Yamashita Y, Kaneko T, Mori M, Kirito K, Toshima M, Nakamura Y, Saito K, Kano Y, Furusawa S, Ozawa K, Mano H. Miyazato A, et al. Among authors: mori m. Blood. 2001 Jul 15;98(2):422-7. doi: 10.1182/blood.v98.2.422. Blood. 2001. PMID: 11435312 Free article.

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