Pallotti F - Search Results

1

Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2.

Sue CM, Karadimas C, Checcarelli N, Tanji K, Papadopoulou LC, Pallotti F, Guo FL, Shanske S, Hirano M, De Vivo DC, Van Coster R, Kaplan P, Bonilla E, DiMauro S. Sue CM, et al. Among authors: pallotti f. Ann Neurol. 2000 May;47(5):589-95. Ann Neurol. 2000. PMID: 10805329

2

Mitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects.

DiMauro S, Tanji K, Bonilla E, Pallotti F, Schon EA. DiMauro S, et al. Among authors: pallotti f. Muscle Nerve. 2002 Nov;26(5):597-607. doi: 10.1002/mus.10194. Muscle Nerve. 2002. PMID: 12402281 Review.

3

Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging.

Pallotti F, Chen X, Bonilla E, Schon EA. Pallotti F, et al. Am J Hum Genet. 1996 Sep;59(3):591-602. Am J Hum Genet. 1996. PMID: 8751860 Free PMC article.

4

A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV.

Bruno C, Martinuzzi A, Tang Y, Andreu AL, Pallotti F, Bonilla E, Shanske S, Fu J, Sue CM, Angelini C, DiMauro S, Manfredi G. Bruno C, et al. Among authors: pallotti f. Am J Hum Genet. 1999 Sep;65(3):611-20. doi: 10.1086/302546. Am J Hum Genet. 1999. PMID: 10441567 Free PMC article.

5

Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA.

Andreu AL, Hanna MG, Reichmann H, Bruno C, Penn AS, Tanji K, Pallotti F, Iwata S, Bonilla E, Lach B, Morgan-Hughes J, DiMauro S. Andreu AL, et al. Among authors: pallotti f. N Engl J Med. 1999 Sep 30;341(14):1037-44. doi: 10.1056/NEJM199909303411404. N Engl J Med. 1999. PMID: 10502593 Free article.

6

Analysis of mtDNA deletions in muscle by in situ hybridization.

Vu TH, Tanji K, Pallotti F, Golzi V, Hirano M, DiMauro S, Bonilla E. Vu TH, et al. Among authors: pallotti f. Muscle Nerve. 2000 Jan;23(1):80-5. doi: 10.1002/(sici)1097-4598(200001)23:1<80::aid-mus10>3.0.co;2-v. Muscle Nerve. 2000. PMID: 10590409 Clinical Trial.

7

Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.

Giordano C, Pallotti F, Walker WF, Checcarelli N, Musumeci O, Santorelli F, d'Amati G, Schon EA, DiMauro S, Hirano M, Davidson MM. Giordano C, et al. Among authors: pallotti f. Biochem Biophys Res Commun. 2002 Apr 26;293(1):521-9. doi: 10.1016/S0006-291X(02)00256-5. Biochem Biophys Res Commun. 2002. PMID: 12054632

8

The fate of human sperm-derived mtDNA in somatic cells.

Manfredi G, Thyagarajan D, Papadopoulou LC, Pallotti F, Schon EA. Manfredi G, et al. Among authors: pallotti f. Am J Hum Genet. 1997 Oct;61(4):953-60. doi: 10.1086/514887. Am J Hum Genet. 1997. PMID: 9382109 Free PMC article.

9

Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations.

Pallotti F, Baracca A, Hernandez-Rosa E, Walker WF, Solaini G, Lenaz G, Melzi D'Eril GV, Dimauro S, Schon EA, Davidson MM. Pallotti F, et al. Biochem J. 2004 Dec 1;384(Pt 2):287-93. doi: 10.1042/BJ20040561. Biochem J. 2004. PMID: 15324306 Free PMC article.

10

A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck.

Pallotti F, Binelli G, Fabbri R, Valentino ML, Vicenti R, Macciocca M, Cevoli S, Baruzzi A, DiMauro S, Carelli V. Pallotti F, et al. PLoS One. 2014 May 7;9(5):e96663. doi: 10.1371/journal.pone.0096663. eCollection 2014. PLoS One. 2014. PMID: 24805791 Free PMC article.

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