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Results: 1 to 20 of 197

Similar articles for PubMed (Select 19480934)

1.

Somatic mitochondrial mutations in pilocytic astrocytoma.

Lueth M, Wronski L, Giese A, Kirschner-Schwabe R, Pietsch T, von Deimling A, Henze G, Kurtz A, Driever PH.

Cancer Genet Cytogenet. 2009 Jul;192(1):30-5. doi: 10.1016/j.cancergencyto.2009.03.002.

PMID:
19480934
2.

Simultaneous DNA and RNA Mapping of Somatic Mitochondrial Mutations across Diverse Human Cancers.

Stewart JB, Alaei-Mahabadi B, Sabarinathan R, Samuelsson T, Gorodkin J, Gustafsson CM, Larsson E.

PLoS Genet. 2015 Jun 30;11(6):e1005333. doi: 10.1371/journal.pgen.1005333. eCollection 2015 Jun.

3.

A somatic T15091C mutation in the Cytb gene of mouse mitochondrial DNA dominantly induces respiration defects.

Hayashi C, Takibuchi G, Shimizu A, Mito T, Ishikawa K, Nakada K, Hayashi JI.

Biochem Biophys Res Commun. 2015 Jun 10. pii: S0006-291X(15)30104-2. doi: 10.1016/j.bbrc.2015.06.052. [Epub ahead of print]

PMID:
26072375
4.

Deciphering the spectrum of somatic mutations in the entire mitochondrial DNA genome.

Chen XZ, Fang Y, Shi YH, Cui JH, Li LY, Xu YC, Ling B.

Genet Mol Res. 2015 Apr 30;14(2):4331-7. doi: 10.4238/2015.April.30.5.

5.

Novel mutations in cholangiocarcinoma with low frequencies revealed by whole mitochondrial genome sequencing.

Muisuk K, Silsirivanit A, Imtawil K, Bunthot S, Pukhem A, Pairojkul C, Wongkham S, Wongkham C.

Asian Pac J Cancer Prev. 2015;16(5):1737-42.

6.

Identification and functional prediction of mitochondrial complex III and IV mutations associated with glioblastoma.

Lloyd RE, Keatley K, Littlewood DT, Meunier B, Holt WV, An Q, Higgins SC, Polyzoidis S, Stephenson KF, Ashkan K, Fillmore HL, Pilkington GJ, McGeehan JE.

Neuro Oncol. 2015 Jul;17(7):942-52. doi: 10.1093/neuonc/nov020. Epub 2015 Mar 2.

7.

Capture of somatic mtDNA point mutations with severe effects on oxidative phosphorylation in synaptosome cybrid clones from human brain.

McKenzie M, Chiotis M, Hroudová J, Lopez Sanchez MI, Lim SC, Cook MJ, McKelvie P, Cotton RG, Murphy M, St John JC, Trounce IA.

Hum Mutat. 2014 Dec;35(12):1476-84. doi: 10.1002/humu.22694.

PMID:
25219341
8.

Germ-line and somatic DICER1 mutations in pineoblastoma.

de Kock L, Sabbaghian N, Druker H, Weber E, Hamel N, Miller S, Choong CS, Gottardo NG, Kees UR, Rednam SP, van Hest LP, Jongmans MC, Jhangiani S, Lupski JR, Zacharin M, Bouron-Dal Soglio D, Huang A, Priest JR, Perry A, Mueller S, Albrecht S, Malkin D, Grundy RG, Foulkes WD.

Acta Neuropathol. 2014 Oct;128(4):583-95. doi: 10.1007/s00401-014-1318-7. Epub 2014 Jul 15.

9.

Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma.

Fontebasso AM, Papillon-Cavanagh S, Schwartzentruber J, Nikbakht H, Gerges N, Fiset PO, Bechet D, Faury D, De Jay N, Ramkissoon LA, Corcoran A, Jones DT, Sturm D, Johann P, Tomita T, Goldman S, Nagib M, Bendel A, Goumnerova L, Bowers DC, Leonard JR, Rubin JB, Alden T, Browd S, Geyer JR, Leary S, Jallo G, Cohen K, Gupta N, Prados MD, Carret AS, Ellezam B, Crevier L, Klekner A, Bognar L, Hauser P, Garami M, Myseros J, Dong Z, Siegel PM, Malkin H, Ligon AH, Albrecht S, Pfister SM, Ligon KL, Majewski J, Jabado N, Kieran MW.

Nat Genet. 2014 May;46(5):462-6. doi: 10.1038/ng.2950. Epub 2014 Apr 6.

10.

Adult pilocytic astrocytomas: clinical features and molecular analysis.

Theeler BJ, Ellezam B, Sadighi ZS, Mehta V, Tran MD, Adesina AM, Bruner JM, Puduvalli VK.

Neuro Oncol. 2014 Jun;16(6):841-7. doi: 10.1093/neuonc/not246. Epub 2014 Jan 26.

11.

Mutational patterns in the breast cancer mitochondrial genome, with clinical correlates.

McMahon S, LaFramboise T.

Carcinogenesis. 2014 May;35(5):1046-54. doi: 10.1093/carcin/bgu012. Epub 2014 Jan 18.

12.

Mitochondrial Cytochrome c Oxidase subunit 1 Sequence Variation in Prostate Cancer.

Scott TA, Arnold R, Petros JA.

Scientifica (Cairo). 2012;2012:701810.

13.

Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma.

Jones DT, Hutter B, Jäger N, Korshunov A, Kool M, Warnatz HJ, Zichner T, Lambert SR, Ryzhova M, Quang DA, Fontebasso AM, Stütz AM, Hutter S, Zuckermann M, Sturm D, Gronych J, Lasitschka B, Schmidt S, Seker-Cin H, Witt H, Sultan M, Ralser M, Northcott PA, Hovestadt V, Bender S, Pfaff E, Stark S, Faury D, Schwartzentruber J, Majewski J, Weber UD, Zapatka M, Raeder B, Schlesner M, Worth CL, Bartholomae CC, von Kalle C, Imbusch CD, Radomski S, Lawerenz C, van Sluis P, Koster J, Volckmann R, Versteeg R, Lehrach H, Monoranu C, Winkler B, Unterberg A, Herold-Mende C, Milde T, Kulozik AE, Ebinger M, Schuhmann MU, Cho YJ, Pomeroy SL, von Deimling A, Witt O, Taylor MD, Wolf S, Karajannis MA, Eberhart CG, Scheurlen W, Hasselblatt M, Ligon KL, Kieran MW, Korbel JO, Yaspo ML, Brors B, Felsberg J, Reifenberger G, Collins VP, Jabado N, Eils R, Lichter P, Pfister SM; International Cancer Genome Consortium PedBrain Tumor Project.

Nat Genet. 2013 Aug;45(8):927-32. doi: 10.1038/ng.2682. Epub 2013 Jun 30.

14.

Somatic mitochondrial DNA mutations in Chinese patients with osteosarcoma.

Yu M, Wan Y, Zou Q.

Int J Exp Pathol. 2013 Apr;94(2):126-32. doi: 10.1111/iep.12015. Epub 2013 Feb 27.

15.

H3F3A K27M mutation in pediatric CNS tumors: a marker for diffuse high-grade astrocytomas.

Gielen GH, Gessi M, Hammes J, Kramm CM, Waha A, Pietsch T.

Am J Clin Pathol. 2013 Mar;139(3):345-9. doi: 10.1309/AJCPABOHBC33FVMO.

16.

Somatic mutations of the mitochondrial genome in Chinese patients with Ewing sarcoma.

Yu M, Wan Y, Zou Q.

Hum Pathol. 2013 Jul;44(7):1350-6. doi: 10.1016/j.humpath.2012.11.004. Epub 2013 Jan 31.

PMID:
23375644
17.

Part II. Mitochondrial mutational status of high nitric oxide adapted cell line BT-20 (BT-20-HNO) as it relates to human primary breast tumors.

De Vitto H, Mendonça BS, Elseth KM, Vesper BJ, Portari EA, Gallo CV, Paradise WA, Rumjanek FD, Radosevich JA.

Tumour Biol. 2013 Feb;34(1):337-47. doi: 10.1007/s13277-012-0555-4. Epub 2012 Dec 14.

PMID:
23238816
18.

Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma.

Gutmann DH, McLellan MD, Hussain I, Wallis JW, Fulton LL, Fulton RS, Magrini V, Demeter R, Wylie T, Kandoth C, Leonard JR, Guha A, Miller CA, Ding L, Mardis ER.

Genome Res. 2013 Mar;23(3):431-9. doi: 10.1101/gr.142604.112. Epub 2012 Dec 5.

19.

[Roles of mitochondrial DNA somatic mutations in the pathogenesis of benign breast disease: a perspective from whole genome study].

Yang Y, Mei S, He JD, Guo XJ, Che YH, Zhang Y, Li L.

Zhonghua Yi Xue Za Zhi. 2012 Sep 11;92(34):2394-7. Chinese.

PMID:
23158660
20.

Mitochondrial genome variations in advanced stage endometriosis: a study in South Indian population.

Govatati S, Tipirisetti NR, Perugu S, Kodati VL, Deenadayal M, Satti V, Bhanoori M, Shivaji S.

PLoS One. 2012;7(7):e40668. doi: 10.1371/journal.pone.0040668. Epub 2012 Jul 17.

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