BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 9345104)

  • 21. Overview of thyroid physiology: an essential for understanding familial euthyroid multinodular goiter.
    Martinez JH; Palermo C; González FF; Laboy I
    Bol Asoc Med P R; 2013; 105(2):68-71. PubMed ID: 23882995
    [TBL] [Abstract][Full Text] [Related]  

  • 22. An InDel in Phospholipase-C-B-1 Is Linked with Euthyroid Multinodular Goiter.
    Bakhsh AD; Ladas I; Hamshere ML; Bullock M; Kirov G; Zhang L; Taylor PN; Gregory JW; Scott-Coombes D; Völzke H; Teumer A; Mantripragada K; Williams ED; Clifton-Bligh RJ; Williams NM; Ludgate ME
    Thyroid; 2018 Jul; 28(7):891-901. PubMed ID: 29897006
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The 14q restless legs syndrome locus in the French Canadian population.
    Levchenko A; Montplaisir JY; Dubé MP; Riviere JB; St-Onge J; Turecki G; Xiong L; Thibodeau P; Desautels A; Verlaan DJ; Rouleau GA
    Ann Neurol; 2004 Jun; 55(6):887-91. PubMed ID: 15174026
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma.
    Bonora E; Rizzato C; Diquigiovanni C; Oudot-Mellakh T; Campa D; Vargiolu M; Guedj M; ; McKay JD; Romeo G; Canzian F; Lesueur F
    Int J Cancer; 2014 May; 134(9):2098-107. PubMed ID: 24127282
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Polymorphisms in the TSHR (thyrotropin receptor) gene on chromosome 14q31 are not associated with mental retardation in the iodine-deficient areas of China.
    Guo TW; Zhang FC; Gao JJ; Bian L; Gao XC; Ma J; Yang M; Ji Q; Duan SW; Zheng ZJ; Li RL; Feng GY; St Clair D; He L
    Neurosci Lett; 2005 Jul 1-8; 382(1-2):179-84. PubMed ID: 15911145
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Papillary thyroid carcinoma associated with papillary renal neoplasia: genetic linkage analysis of a distinct heritable tumor syndrome.
    Malchoff CD; Sarfarazi M; Tendler B; Forouhar F; Whalen G; Joshi V; Arnold A; Malchoff DM
    J Clin Endocrinol Metab; 2000 May; 85(5):1758-64. PubMed ID: 10843148
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer.
    McKay JD; Thompson D; Lesueur F; Stankov K; Pastore A; Watfah C; Strolz S; Riccabona G; Moncayo R; Romeo G; Goldgar DE
    J Med Genet; 2004 Jun; 41(6):407-12. PubMed ID: 15173224
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.
    Gispert S; Santos N; Damen R; Voit T; Schulz J; Klockgether T; Orozco G; Kreuz F; Weissenbach J; Auburger G
    Am J Hum Genet; 1995 Jan; 56(1):183-7. PubMed ID: 7825576
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The association between multinodular goiter and thyroid cancer.
    Verburg FA; Reiners C
    Minerva Endocrinol; 2010 Sep; 35(3):187-92. PubMed ID: 20938421
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Lack of reported mutations in a Japanese case of toxic multinodular goiter.
    Hanamitsu M; Takeuchi E; Kitanishi T; Sakurai H; Tanaka H; Kitano H
    ORL J Otorhinolaryngol Relat Spec; 2002; 64(4):275-7. PubMed ID: 12232474
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Activating thyrotropin receptor mutations in histologically heterogeneous hyperfunctioning nodules of multinodular goiter.
    Tonacchera M; Vitti P; Agretti P; Giulianetti B; Mazzi B; Cavaliere R; Ceccarini G; Fiore E; Viacava P; Naccarato A; Pinchera A; Chiovato L
    Thyroid; 1998 Jul; 8(7):559-64. PubMed ID: 9709907
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Two autonomous nodules of a patient with multinodular goiter harbor different activating mutations of the thyrotropin receptor gene.
    Duprez L; Hermans J; Van Sande J; Dumont JE; Vassart G; Parma J
    J Clin Endocrinol Metab; 1997 Jan; 82(1):306-8. PubMed ID: 8989278
    [No Abstract]   [Full Text] [Related]  

  • 34. Increased risk for nonmedullary thyroid cancer in the first degree relatives of prevalent cases of nonmedullary thyroid cancer: a hospital-based study.
    Pal T; Vogl FD; Chappuis PO; Tsang R; Brierley J; Renard H; Sanders K; Kantemiroff T; Bagha S; Goldgar DE; Narod SA; Foulkes WD
    J Clin Endocrinol Metab; 2001 Nov; 86(11):5307-12. PubMed ID: 11701697
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
    Scott WK; Gaskell PC; Lennon F; Wolpert CM; Menold MM; Aylsworth AS; Warner C; Farrell CD; Boustany RM; Albright SG; Boyd E; Kingston HM; Cumming WJ; Vance JM; Pericak-Vance MA
    Neurogenetics; 1997 Sep; 1(2):95-102. PubMed ID: 10732810
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q.
    Stevanin G; Sousa PS; Cancel G; Dürr A; Dubourg O; Nicholson GA; Weissenbach J; Jardim E; Agid Y; Cassa E
    Neurobiol Dis; 1994 Nov; 1(1-2):79-82. PubMed ID: 9216989
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification of a new candidate locus for uric acid nephrolithiasis.
    Ombra MN; Forabosco P; Casula S; Angius A; Maestrale G; Petretto E; Casu G; Colussi G; Usai E; Melis P; Pirastu M
    Am J Hum Genet; 2001 May; 68(5):1119-29. PubMed ID: 11309680
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A new form of familial multi-nodular goitre with progression to differentiated thyroid cancer.
    Bakhsh A; Kirov G; Gregory JW; Williams ED; Ludgate M
    Endocr Relat Cancer; 2006 Jun; 13(2):475-83. PubMed ID: 16728575
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Familial papillary (nonmedullary) thyroid carcinoma].
    Gärtner R
    Dtsch Med Wochenschr; 2012 Jul; 137(28-29):1474. PubMed ID: 22760408
    [No Abstract]   [Full Text] [Related]  

  • 40. Familial papillary thyroid carcinoma is genetically distinct from familial adenomatous polyposis coli.
    Malchoff CD; Sarfarazi M; Tendler B; Forouhar F; Whalen G; Malchoff DM
    Thyroid; 1999 Mar; 9(3):247-52. PubMed ID: 10211600
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.