82 related articles for article (PubMed ID: 11113879)
1. Mitochondrial DNA 'common' deletion in Hürthle cell lesions of the thyroid.
Máximo V; Sobrinho-Simões M
J Pathol; 2000 Dec; 192(4):561-2. PubMed ID: 11113879
[No Abstract] [Full Text] [Related]
2. Re: Lohrer,H.D., Hieber,L. and Zitzelsberger,H. (2002) Differential mutation frequency in mitochondrial DNA from thyroid tumours. Carcinogenesis, 23, 1577-1582.
Lima J; Máximo V; Soares P; Williams D; Bogdanova T; Thomas GA; Sobrinho-Simões M
Carcinogenesis; 2003 Jun; 24(6):1155. PubMed ID: 12807747
[No Abstract] [Full Text] [Related]
3. Mitochondrial DNA alterations in thyroid cancer.
Tong BC; Ha PK; Dhir K; Xing M; Westra WH; Sidransky D; Califano JA
J Surg Oncol; 2003 Mar; 82(3):170-3. PubMed ID: 12619060
[TBL] [Abstract][Full Text] [Related]
4. [Mutation of mitochondrial DNA 4977 bp deletion in laryngeal squamous cell cancer].
Han YC; Kong WJ; Zhang S; Wang YJ; Wang Y; Chen X
Ai Zheng; 2004 Nov; 23(11):1297-301. PubMed ID: 15522177
[TBL] [Abstract][Full Text] [Related]
5. Core I gene is overexpressed in Hürthle and non-Hürthle cell microfollicular adenomas and follicular carcinomas of the thyroid.
Máximo V; Preto A; Crespo A; Rocha AS; Machado JC; Soares P; Sobrinho-Simões M
BMC Cancer; 2004 Mar; 4():12. PubMed ID: 15043758
[TBL] [Abstract][Full Text] [Related]
6. Heteroplasmic mutation of mitochondrial DNA D-loop and 4977-bp deletion in human cancer cells during mitochondrial DNA depletion.
Lee HC; Hsu LS; Yin PH; Lee LM; Chi CW
Mitochondrion; 2007; 7(1-2):157-63. PubMed ID: 17280876
[TBL] [Abstract][Full Text] [Related]
7. High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell lines.
Abu-Amero KK; Alzahrani AS; Zou M; Shi Y
Oncogene; 2005 Feb; 24(8):1455-60. PubMed ID: 15608681
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial A135149 mutation without MELAS but in association with papillary thyroid carcinoma.
Abu-Amero K; Zou M; Shi Y
Clin Genet; 2004 Dec; 66(6):569-70. PubMed ID: 15521990
[No Abstract] [Full Text] [Related]
9. Large deletions in mitochondrial DNA in radiation-associated human thyroid tumors.
Rogounovitch TI; Saenko VA; Shimizu-Yoshida Y; Abrosimov AY; Lushnikov EF; Roumiantsev PO; Ohtsuru A; Namba H; Tsyb AF; Yamashita S
Cancer Res; 2002 Dec; 62(23):7031-41. PubMed ID: 12460924
[TBL] [Abstract][Full Text] [Related]
10. Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.
Bonora E; Porcelli AM; Gasparre G; Biondi A; Ghelli A; Carelli V; Baracca A; Tallini G; Martinuzzi A; Lenaz G; Rugolo M; Romeo G
Cancer Res; 2006 Jun; 66(12):6087-96. PubMed ID: 16778181
[TBL] [Abstract][Full Text] [Related]
11. Development of a quantitative PCR (TaqMan) assay for relative mitochondrial DNA copy number and the common mitochondrial DNA deletion in the rat.
Nicklas JA; Brooks EM; Hunter TC; Single R; Branda RF
Environ Mol Mutagen; 2004; 44(4):313-20. PubMed ID: 15476199
[TBL] [Abstract][Full Text] [Related]
12. Somatic mitochondrial DNA mutations in human chromophobe renal cell carcinomas.
Nagy A; Wilhelm M; Sükösd F; Ljungberg B; Kovacs G
Genes Chromosomes Cancer; 2002 Nov; 35(3):256-60. PubMed ID: 12353267
[TBL] [Abstract][Full Text] [Related]
13. Mitochondrial DNA mutations in human disease.
Greaves LC; Taylor RW
IUBMB Life; 2006 Mar; 58(3):143-51. PubMed ID: 16766381
[TBL] [Abstract][Full Text] [Related]
14. Aneuploidy in oncocytic lesions of the thyroid gland: diffuse accumulation of mitochondria within the cell is associated with trisomy 7 and progressive numerical chromosomal alterations.
Dettori T; Frau DV; Lai ML; Mariotti S; Uccheddu A; Daniele GM; Tallini G; Faa G; Vanni R
Genes Chromosomes Cancer; 2003 Sep; 38(1):22-31. PubMed ID: 12874783
[TBL] [Abstract][Full Text] [Related]
15. Tumoral cell mtDNA approximately 8.9 kb deletion is more common than other deletions in gastric cancer.
Kamalidehghan B; Houshmand M; Panahi MS; Abbaszadegan MR; Ismail P; Shiroudi MB
Arch Med Res; 2006 Oct; 37(7):848-53. PubMed ID: 16971224
[TBL] [Abstract][Full Text] [Related]
16. Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome.
Abu-Amero KK; Alzahrani AS; Zou M; Shi Y
Oncogene; 2006 Feb; 25(5):677-84. PubMed ID: 16205644
[TBL] [Abstract][Full Text] [Related]
17. Genetic mutations in thyroid carcinoma.
Taccaliti A; Boscaro M
Minerva Endocrinol; 2009 Mar; 34(1):11-28. PubMed ID: 19209125
[TBL] [Abstract][Full Text] [Related]
18. Control region mutations and the 'common deletion' are frequent in the mitochondrial DNA of patients with esophageal squamous cell carcinoma.
Abnet CC; Huppi K; Carrera A; Armistead D; McKenney K; Hu N; Tang ZZ; Taylor PR; Dawsey SM
BMC Cancer; 2004 Jul; 4():30. PubMed ID: 15230979
[TBL] [Abstract][Full Text] [Related]
19. [Changes in copy number and deletion development of mitochondrial DNA in blood cells from breast cancer patients during radiochemotherapy].
Malakhova LV; Antipova VN; Guliaeva NA; Bezlepkin VG; Gaziev AI
Vopr Onkol; 2006; 52(4):398-403. PubMed ID: 17024810
[TBL] [Abstract][Full Text] [Related]
20. Large-scale mitochondrial DNA deletion mutations and nuclear genome instability in human breast cancer.
Zhu W; Qin W; Sauter ER
Cancer Detect Prev; 2004; 28(2):119-26. PubMed ID: 15068836
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]