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Journal Abstract Search

213 related items for PubMed ID: 17088905

  • 21. Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion.
    Pradella LM, Zuntini R, Magini P, Ceccarelli C, Neri I, Cerasoli S, Graziano C, Gasparre G, Turchetti D.
    J Med Genet; 2011 Nov; 48(11):779-82. PubMed ID: 21926107
    [Abstract] [Full Text] [Related]

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  • 23. The channel-forming Sym1 protein is transported by the TIM23 complex in a presequence-independent manner.
    Reinhold R, Krüger V, Meinecke M, Schulz C, Schmidt B, Grunau SD, Guiard B, Wiedemann N, van der Laan M, Wagner R, Rehling P, Dudek J.
    Mol Cell Biol; 2012 Dec; 32(24):5009-21. PubMed ID: 23045398
    [Abstract] [Full Text] [Related]

  • 24. NOP53 as A Candidate Modifier Locus for Familial Non-Medullary Thyroid Cancer.
    Orois A, Gara SK, Mora M, Halperin I, Martínez S, Alfayate R, Kebebew E, Oriola J.
    Genes (Basel); 2019 Nov 07; 10(11):. PubMed ID: 31703244
    [Abstract] [Full Text] [Related]

  • 25. Death-associated protein 3 is overexpressed in human thyroid oncocytic tumours.
    Jacques C, Fontaine JF, Franc B, Mirebeau-Prunier D, Triau S, Savagner F, Malthiery Y.
    Br J Cancer; 2009 Jul 07; 101(1):132-8. PubMed ID: 19536094
    [Abstract] [Full Text] [Related]

  • 26. A comprehensive analysis of MNG1, TCO1, fPTC, PTEN, TSHR, and TRKA in familial nonmedullary thyroid cancer: confirmation of linkage to TCO1.
    Bevan S, Pal T, Greenberg CR, Green H, Wixey J, Bignell G, Narod SA, Foulkes WD, Stratton MR, Houlston RS.
    J Clin Endocrinol Metab; 2001 Aug 07; 86(8):3701-4. PubMed ID: 11502798
    [Abstract] [Full Text] [Related]

  • 27. Penetrance of a rare familial mutation predisposing to papillary thyroid cancer.
    Saporito D, Brock P, Hampel H, Sipos J, Fernandez S, Liyanarachchi S, de la Chapelle A, Nagy R.
    Fam Cancer; 2018 Jul 07; 17(3):431-434. PubMed ID: 29027612
    [Abstract] [Full Text] [Related]

  • 28. Frequent chromosomal DNA unbalance in thyroid oncocytic (Hürthle cell) neoplasms detected by comparative genomic hybridization.
    Tallini G, Hsueh A, Liu S, Garcia-Rostan G, Speicher MR, Ward DC.
    Lab Invest; 1999 May 07; 79(5):547-55. PubMed ID: 10334566
    [Abstract] [Full Text] [Related]

  • 29. RET rearrangements in archival oxyphilic thyroid tumors: new insights in tumorigenesis and classification of Hürthle cell carcinomas?
    Musholt PB, Imkamp F, von Wasielewski R, Schmid KW, Musholt TJ.
    Surgery; 2003 Dec 07; 134(6):881-9; discussion 889. PubMed ID: 14668719
    [Abstract] [Full Text] [Related]

  • 30. Causative role for defective expression of mitochondria-eating protein in accumulation of mitochondria in thyroid oncocytic cell tumors.
    Mussazhanova Z, Shimamura M, Kurashige T, Ito M, Nakashima M, Nagayama Y.
    Cancer Sci; 2020 Aug 07; 111(8):2814-2823. PubMed ID: 32458504
    [Abstract] [Full Text] [Related]

  • 31. A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma.
    Pigny P, Bauters C, Wemeau JL, Houcke ML, Crepin M, Caron P, Giraud S, Calender A, Buisine MP, Kerckaert JP, Porchet N.
    J Clin Endocrinol Metab; 1999 May 07; 84(5):1700-4. PubMed ID: 10323403
    [Abstract] [Full Text] [Related]

  • 32. A mutation screening of oncogenes, tumor suppressor gene TP53 and nuclear encoded mitochondrial complex I genes in oncocytic thyroid tumors.
    Evangelisti C, de Biase D, Kurelac I, Ceccarelli C, Prokisch H, Meitinger T, Caria P, Vanni R, Romeo G, Tallini G, Gasparre G, Bonora E.
    BMC Cancer; 2015 Mar 21; 15():157. PubMed ID: 25880213
    [Abstract] [Full Text] [Related]

  • 33. Identification of Rare Variants Predisposing to Thyroid Cancer.
    Wang Y, Liyanarachchi S, Miller KE, Nieminen TT, Comiskey DF, Li W, Brock P, Symer DE, Akagi K, DeLap KE, He H, Koboldt DC, de la Chapelle A.
    Thyroid; 2019 Jul 21; 29(7):946-955. PubMed ID: 30957677
    [Abstract] [Full Text] [Related]

  • 34. Characterization of mammalian translocase of inner mitochondrial membrane (Tim44) isolated from diabetic newborn mouse kidney.
    Wada J, Kanwar YS.
    Proc Natl Acad Sci U S A; 1998 Jan 06; 95(1):144-9. PubMed ID: 9419343
    [Abstract] [Full Text] [Related]

  • 35. 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 15; 66(12):6087-96. PubMed ID: 16778181
    [Abstract] [Full Text] [Related]

  • 36. Novel germline RET mutation segregating with papillary thyroid carcinomas.
    Rey JM, Brouillet JP, Fonteneau-Allaire J, Boneu A, Bastié D, Maudelonde T, Pujol P.
    Genes Chromosomes Cancer; 2001 Dec 15; 32(4):390-1. PubMed ID: 11746981
    [Abstract] [Full Text] [Related]

  • 37. Distinct loci on chromosome 1q21 and 6q22 predispose to familial nonmedullary thyroid cancer: a SNP array-based linkage analysis of 38 families.
    Suh I, Filetti S, Vriens MR, Guerrero MA, Tumino S, Wong M, Shen WT, Kebebew E, Duh QY, Clark OH.
    Surgery; 2009 Dec 15; 146(6):1073-80. PubMed ID: 19958934
    [Abstract] [Full Text] [Related]

  • 38. Familial non-medullary thyroid cancer: unraveling the genetic maze.
    Peiling Yang S, Ngeow J.
    Endocr Relat Cancer; 2016 Dec 15; 23(12):R577-R595. PubMed ID: 27807061
    [Abstract] [Full Text] [Related]

  • 39. Molecular features of thyroid oncocytic tumors.
    Gasparre G, Bonora E, Tallini G, Romeo G.
    Mol Cell Endocrinol; 2010 May 28; 321(1):67-76. PubMed ID: 20184940
    [Abstract] [Full Text] [Related]

  • 40. Identification of a KEAP1 germline mutation in a family with multinodular goitre.
    Teshiba R, Tajiri T, Sumitomo K, Masumoto K, Taguchi T, Yamamoto K.
    PLoS One; 2013 May 28; 8(5):e65141. PubMed ID: 23724128
    [Abstract] [Full Text] [Related]

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