BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 33233395)

  • 1. A Novel Germline c.1267T>A
    Gierlikowski W; Skwarek-Szewczyk A; Popow M
    Genes (Basel); 2020 Nov; 11(11):. PubMed ID: 33233395
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Heterogeneity of the Clinical Presentation of the MEN1 LRG_509 c.781C>T (p.Leu261Phe) Variant Within a Three-Generation Family.
    Gilis-Januszewska A; Bogusławska A; Hasse-Lazar K; Jurecka-Lubieniecka B; Jarząb B; Sowa-Staszczak A; Opalińska M; Godlewska M; Grochowska A; Skalniak A; Hubalewska-Dydejczyk A
    Genes (Basel); 2021 Mar; 12(4):. PubMed ID: 33807230
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel Germline c.105_107dupGCT
    Stasiak M; Dedecjus M; Zawadzka-Starczewska K; Adamska E; Tomaszewska M; Lewiński A
    Genes (Basel); 2020 Aug; 11(9):. PubMed ID: 32847108
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states.
    Agarwal SK; Kester MB; Debelenko LV; Heppner C; Emmert-Buck MR; Skarulis MC; Doppman JL; Kim YS; Lubensky IA; Zhuang Z; Green JS; Guru SC; Manickam P; Olufemi SE; Liotta LA; Chandrasekharappa SC; Collins FS; Spiegel AM; Burns AL; Marx SJ
    Hum Mol Genet; 1997 Jul; 6(7):1169-75. PubMed ID: 9215689
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Germline mutation of the multiple endocrine neoplasia type 1 (MEN1) gene in a family with primary hyperparathyroidism.
    Ohye H; Sato M; Matsubara S; Miyauchi A; Imachi H; Murao K; Takahara J
    Endocr J; 1998 Dec; 45(6):719-23. PubMed ID: 10395226
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Coincidence of multiple endocrine neoplasia types 1 and 2: mutations in the RET protooncogene and MEN1 tumor suppressor gene in a family presenting with recurrent primary hyperparathyroidism.
    Frank-Raue K; Rondot S; Hoeppner W; Goretzki P; Raue F; Meng W
    J Clin Endocrinol Metab; 2005 Jul; 90(7):4063-7. PubMed ID: 15870131
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation of the MEN1 gene in a Japanese kindred with familial isolated primary hyperparathyroidism.
    Honda M; Tsukada T; Tanaka H; Maruyama K; Yamaguchi K; Obara T; Yamaji T; Ishibashi M
    Eur J Endocrinol; 2000 Feb; 142(2):138-43. PubMed ID: 10664521
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel Germline p.Gly42Val
    Koehler VF; Jungheim K; Groß U; Iacovazzo D; Mann A; Korbonits M
    Ann Clin Lab Sci; 2017 Sep; 47(5):606-610. PubMed ID: 29066490
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel 14 base-pair deletion of the MEN1 gene in a patient with recurrent primary hyperparathyroidism.
    Katai M; Sakurai A; Uchino S; Minemura K; Hashizume K; Fukushima Y
    Jpn J Clin Oncol; 2006 Jun; 36(6):395-7. PubMed ID: 16714299
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A germline c.1546dupC MEN1 mutation in an MEN1 family: A case report.
    Cho YY; Chung YJ
    Medicine (Baltimore); 2021 Jun; 100(25):e26382. PubMed ID: 34160414
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A new double substitution mutation in the MEN1 gene: a limited penetrance and a specific phenotype.
    Ullmann U; Unuane D; Velkeniers B; Lissens W; Wuyts W; Bonduelle M
    Eur J Hum Genet; 2013 Jun; 21(6):695-7. PubMed ID: 23188049
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multiple endocrine neoplasia type 1 associated with a new germline Men1 mutation in a family with atypical tumor phenotype.
    Perakakis N; Flohr F; Kayser G; Thomusch O; Parsons L; Billmann F; von Dobschuetz E; Rondot S; Seufert J; Laubner K
    Hormones (Athens); 2016; 15(1):113-7. PubMed ID: 26732163
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial isolated hyperparathyroidism caused by single adenoma: a distinct entity different from multiple endocrine neoplasia.
    Watanabe T; Tsukamoto F; Shimizu T; Sugimoto T; Taguchi T; Nishisho I; Nakazawa H; Shiba E; Shishiba Y; Takai S
    Endocr J; 1998 Oct; 45(5):637-46. PubMed ID: 10395244
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A family of MEN1 with a novel germline missense mutation and benign polymorphisms.
    Miyauchi A; Sato M; Matsubara S; Ohye H; Kihara M; Matsusaka K; Nishitani A; Takahara J
    Endocr J; 1998 Dec; 45(6):753-9. PubMed ID: 10395230
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and genetic features of patients with multiple endocrine tumors who have neither family history nor MEN1 germline mutations.
    Sakurai A; Katai M; Yumita W; Minemura K; Hashizume K
    Endocrine; 2004 Feb; 23(1):45-9. PubMed ID: 15034196
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.
    Pannett AA; Kennedy AM; Turner JJ; Forbes SA; Cavaco BM; Bassett JH; Cianferotti L; Harding B; Shine B; Flinter F; Maidment CG; Trembath R; Thakker RV
    Clin Endocrinol (Oxf); 2003 May; 58(5):639-46. PubMed ID: 12699448
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism.
    Cetani F; Pardi E; Giovannetti A; Vignali E; Borsari S; Golia F; Cianferotti L; Viacava P; Miccoli P; Gasperi M; Pinchera A; Marcocci C
    Clin Endocrinol (Oxf); 2002 Apr; 56(4):457-64. PubMed ID: 11966738
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Germline mutations of the MEN1 gene in Korean families with multiple endocrine neoplasia type 1 (MEN1) or MEN1-related disorders.
    Park JH; Kim IJ; Kang HC; Lee SH; Shin Y; Kim KH; Lim SB; Kang SB; Lee K; Kim SY; Lee MS; Lee MK; Park JH; Moon SD; Park JG
    Clin Genet; 2003 Jul; 64(1):48-53. PubMed ID: 12791038
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel intronic mutation of MEN1 gene causing familial isolated primary hyperparathyroidism.
    Carrasco CA; González AA; Carvajal CA; Campusano C; Oestreicher E; Arteaga E; Wohllk N; Fardella CE
    J Clin Endocrinol Metab; 2004 Aug; 89(8):4124-9. PubMed ID: 15292357
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MEN1 c.825‑1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report.
    Ning Z; Wang O; Meng X; Xing X; Xia W; Jiang Y; Li M; Xu Y
    Mol Med Rep; 2015 Oct; 12(4):6152-6. PubMed ID: 26239674
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.