BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Kidney tumors AND CDC73, HRPT2, 79577, ENSG00000134371, HPT-JT, Q6P1J9, FLJ23316, C1orf28 AND Diagnosis
17 results:

  • 1. Insights into Hyperparathyroidism-Jaw Tumour Syndrome: From Endocrine Acumen to the Spectrum of
    Gheorghe AM; Sima OC; Florescu AF; Ciuche A; Nistor C; Sandru F; Carsote M
    Int J Mol Sci; 2024 Feb; 25(4):. PubMed ID: 38396977
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. Brown tumor due to primary hyperparathyroidism in a familial case: a case report.
    Diao Z; Zhang J; Zhao J; Sun W; Pu Z
    BMC Endocr Disord; 2023 Oct; 23(1):214. PubMed ID: 37807045
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. Rare duplication of the cdc73 gene and atypical hyperparathyroidism-jaw tumor syndrome: A case report and review of the literature.
    Garrigues G; Batisse-Lignier M; Uhrhammer N; Privat M; Ponelle-Chachuat F; Kelly A; Gay-Bellile M; Viala S; Bidet Y; Bignon YJ; Cavaillé M
    Mol Genet Genomic Med; 2023 May; 11(5):e2133. PubMed ID: 36639964
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. A two-generation hyperparathyroidism-jaw tumor (hpt-jt) syndrome family: clinical presentations, pathological characteristics and genetic analysis: a case report.
    Yang D; Zheng J; Tang F; He Q; Huang H; Zhou P
    Diagn Pathol; 2022 Sep; 17(1):71. PubMed ID: 36153594
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. Familial kidney Cancer: Implications of New Syndromes and Molecular Insights.
    Carlo MI; Hakimi AA; Stewart GD; Bratslavsky G; Brugarolas J; Chen YB; Linehan WM; Maher ER; Merino MJ; Offit K; Reuter VE; Shuch B; Coleman JA
    Eur Urol; 2019 Dec; 76(6):754-764. PubMed ID: 31326218
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. Familial and Hereditary Forms of Primary Hyperparathyroidism.
    Cetani F; Saponaro F; Borsari S; Marcocci C
    Front Horm Res; 2019; 51():40-51. PubMed ID: 30641519
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Parathyroid carcinoma.
    Salcuni AS; Cetani F; Guarnieri V; Nicastro V; Romagnoli E; de Martino D; Scillitani A; Cole DEC
    Best Pract Res Clin Endocrinol Metab; 2018 Dec; 32(6):877-889. PubMed ID: 30551989
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. cdc73 Germline Mutation in a Family With Mixed Epithelial and Stromal tumors.
    Vocke CD; Ricketts CJ; Ball MW; Schmidt LS; Metwalli AR; Middelton LA; Killian JK; Khan J; Meltzer PS; Simonds WF; Merino MJ; Linehan WM
    Urology; 2019 Feb; 124():91-97. PubMed ID: 30452964
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. Morphological clues to the appropriate recognition of hereditary renal neoplasms.
    Moch H; Ohashi R; Gandhi JS; Amin MB
    Semin Diagn Pathol; 2018 May; 35(3):184-192. PubMed ID: 29454577
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. Endocrine neoplasms in familial syndromes of hyperparathyroidism.
    Li Y; Simonds WF
    Endocr Relat Cancer; 2016 Jun; 23(6):R229-47. PubMed ID: 27207564
    [TBL] [Abstract] [Full Text] [Related]  

  • 11. [cdc73 gene mutation and parafibromin expression status of parathyroid carcinoma in Chinese].
    Kong J; Wang O; Nie M; Shi J; Jiang Y; Li M; Xia WB; Meng XW; Xing XP
    Zhonghua Yi Xue Za Zhi; 2013 Nov; 93(42):3364-8. PubMed ID: 24418033
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. Frequent large germline hrpt2 deletions in a French National cohort of patients with primary hyperparathyroidism.
    Bricaire L; Odou MF; Cardot-Bauters C; Delemer B; North MO; Salenave S; Vezzosi D; Kuhn JM; Murat A; Caron P; Sadoul JL; Silve C; Chanson P; Barlier A; Clauser E; Porchet N; Groussin L;
    J Clin Endocrinol Metab; 2013 Feb; 98(2):E403-8. PubMed ID: 23293331
    [TBL] [Abstract] [Full Text] [Related]  

  • 13. Hyperparathyroidism-jaw tumor syndrome.
    Kutcher MR; Rigby MH; Bullock M; Trites J; Taylor SM; Hart RD
    Head Neck; 2013 Jun; 35(6):E175-7. PubMed ID: 22302605
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. Parathyroid cancer.
    Sharretts JM; Kebebew E; Simonds WF
    Semin Oncol; 2010 Dec; 37(6):580-90. PubMed ID: 21167377
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. Rapid mutation screening for hrpt2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.
    Howell VM; Cardinal JW; Richardson AL; Gimm O; Robinson BG; Marsh DJ
    J Mol Diagn; 2006 Nov; 8(5):559-66. PubMed ID: 17065424
    [TBL] [Abstract] [Full Text] [Related]  

  • 16. Parathyroid carcinoma.
    Mittendorf EA; McHenry CR
    J Surg Oncol; 2005 Mar; 89(3):136-42. PubMed ID: 15719375
    [TBL] [Abstract] [Full Text] [Related]  

  • 17. Hyperparathyroidism in hereditary syndromes: special expressions and special managements.
    Marx SJ; Simonds WF; Agarwal SK; Burns AL; Weinstein LS; Cochran C; Skarulis MC; Spiegel AM; Libutti SK; Alexander HR; Chen CC; Chang R; Chandrasekharappa SC; Collins FS
    J Bone Miner Res; 2002 Nov; 17 Suppl 2():N37-43. PubMed ID: 12412776
    [TBL] [Abstract] [Full Text] [Related]  


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