Tanji K - Search Results

1

Thymidine kinase 2 (H126N) knockin mice show the essential role of balanced deoxynucleotide pools for mitochondrial DNA maintenance.

Akman HO, Dorado B, López LC, García-Cazorla A, Vilà MR, Tanabe LM, Dauer WT, Bonilla E, Tanji K, Hirano M. Akman HO, et al. Among authors: tanji k. Hum Mol Genet. 2008 Aug 15;17(16):2433-40. doi: 10.1093/hmg/ddn143. Epub 2008 May 8. Hum Mol Genet. 2008. PMID: 18467430 Free PMC article.

2

New morphological approaches to the study of mitochondrial encephalomyopathies.

Bonilla E, Sciacco M, Tanji K, Sparaco M, Petruzzella V, Moraes CT. Bonilla E, et al. Among authors: tanji k. Brain Pathol. 1992 Apr;2(2):113-9. doi: 10.1111/j.1750-3639.1992.tb00679.x. Brain Pathol. 1992. PMID: 1341952 Review.

3

Immunologic study of vinculin in Duchenne muscular dystrophy.

Minetti C, Tanji K, Bonilla E. Minetti C, et al. Among authors: tanji k. Neurology. 1992 Sep;42(9):1751-4. doi: 10.1212/wnl.42.9.1751. Neurology. 1992. PMID: 1513465

4

Immunolocalization of heat shock proteins in ragged-red fibers of patients with mitochondrial encephalomyopathies.

Sparaco M, Rosoklija G, Tanji K, Sciacco M, Latov N, DiMauro S, Bonilla E. Sparaco M, et al. Among authors: tanji k. Neuromuscul Disord. 1993 Jan;3(1):71-6. doi: 10.1016/0960-8966(93)90044-k. Neuromuscul Disord. 1993. PMID: 8101114

5

Abnormalities in the expression of beta-spectrin in Duchenne muscular dystrophy.

Minetti C, Tanji K, Rippa PG, Morreale G, Cordone G, Bonilla E. Minetti C, et al. Among authors: tanji k. Neurology. 1994 Jun;44(6):1149-53. doi: 10.1212/wnl.44.6.1149. Neurology. 1994. PMID: 8208414

6

Dystrophinopathy in two young boys with exercise-induced cramps and myoglobinuria.

Minetti C, Tanji K, Chang HW, Medori R, Cordone G, DiMauro S, Bonilla E. Minetti C, et al. Among authors: tanji k. Eur J Pediatr. 1993 Oct;152(10):848-51. doi: 10.1007/BF02073385. Eur J Pediatr. 1993. PMID: 8223790

7

Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy.

Bohlega S, Tanji K, Santorelli FM, Hirano M, al-Jishi A, DiMauro S. Bohlega S, et al. Among authors: tanji k. Neurology. 1996 May;46(5):1329-34. doi: 10.1212/wnl.46.5.1329. Neurology. 1996. PMID: 8628476

8

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients.

Santorelli FM, Sciacco M, Tanji K, Shanske S, Vu TH, Golzi V, Griggs RC, Mendell JR, Hays AP, Bertorini TE, Pestronk A, Bonilla E, DiMauro S. Santorelli FM, et al. Among authors: tanji k. Ann Neurol. 1996 Jun;39(6):789-95. doi: 10.1002/ana.410390615. Ann Neurol. 1996. PMID: 8651651

9

Mitochondrial disorders.

DiMauro S, Tanji K. DiMauro S, et al. Among authors: tanji k. Jpn J Hum Genet. 1997 Dec;42(4):473-87. doi: 10.1007/BF02767024. Jpn J Hum Genet. 1997. PMID: 9560947 Review.

10

Ultrastructural alterations in encephalomyopathies of mitochondrial origin.

Bonilla E, Tanji K. Bonilla E, et al. Among authors: tanji k. Biofactors. 1998;7(3):231-6. doi: 10.1002/biof.5520070315. Biofactors. 1998. PMID: 9568255 Review. No abstract available.

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