BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Head and neck cancer AND SDHAF2, ENSG00000167985, C11orf79, FLJ20487, 54949
30 results:

  • 1. Hypothesis: Why Different Types of SDH Gene Variants Cause Divergent Tumor Phenotypes.
    Bayley JP; Devilee P
    Genes (Basel); 2022 Jun; 13(6):. PubMed ID: 35741787
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. head and neck Paragangliomas-A Genetic Overview.
    Majewska A; Budny B; Ziemnicka K; Ruchała M; Wierzbicka M
    Int J Mol Sci; 2020 Oct; 21(20):. PubMed ID: 33081307
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  • 3. The Changing Paradigm of head and neck Paragangliomas: What Every Otolaryngologist Needs to Know.
    Cass ND; Schopper MA; Lubin JA; Fishbein L; Gubbels SP
    Ann Otol Rhinol Laryngol; 2020 Nov; 129(11):1135-1143. PubMed ID: 32486832
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  • 4. SDHx gene detection and clinical Phenotypic analysis of multiple paraganglioma in the head and neck.
    Ding Y; Feng Y; Wells M; Huang Z; Chen X
    Laryngoscope; 2019 Feb; 129(2):E67-E71. PubMed ID: 30484866
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  • 5. A novel succinate dehydrogenase subunit B germline variant associated with head and neck paraganglioma in a Dutch kindred: A family-based study.
    de Vos B; Rijken JA; Adank MA; Hoksbergen AWJ; Bayley JP; Leemans CR; Hensen EF
    Clin Otolaryngol; 2018 Jun; 43(3):841-845. PubMed ID: 29292578
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  • 6. PHEOCHROMOCYTOMA: A GENETIC and DIAGNOSTIC UPDATE.
    Mercado-Asis LB; Wolf KI; Jochmanova I; Taïeb D
    Endocr Pract; 2018 Jan; 24(1):78-90. PubMed ID: 29144820
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  • 7. Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and sdhaf2 for Gene-Informed Prevention.
    Bausch B; Schiavi F; Ni Y; Welander J; Patocs A; Ngeow J; Wellner U; Malinoc A; Taschin E; Barbon G; Lanza V; Söderkvist P; Stenman A; Larsson C; Svahn F; Chen JL; Marquard J; Fraenkel M; Walter MA; Peczkowska M; Prejbisz A; Jarzab B; Hasse-Lazar K; Petersenn S; Moeller LC; Meyer A; Reisch N; Trupka A; Brase C; Galiano M; Preuss SF; Kwok P; Lendvai N; Berisha G; Makay Ö; Boedeker CC; Weryha G; Racz K; Januszewicz A; Walz MK; Gimm O; Opocher G; Eng C; Neumann HPH;
    JAMA Oncol; 2017 Sep; 3(9):1204-1212. PubMed ID: 28384794
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  • 8. Loss of maternal chromosome 11 is a signature event in sdhaf2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas.
    Hoekstra AS; Hensen EF; Jordanova ES; Korpershoek E; van der Horst-Schrivers AN; Cornelisse C; Corssmit EP; Hes FJ; Jansen JC; Kunst HP; Timmers HJ; Bateman A; Eccles D; Bovée JV; Devilee P; Bayley JP
    Oncotarget; 2017 Feb; 8(9):14525-14536. PubMed ID: 28099933
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  • 9. Hypoxia-Inducible Factor 2α Mutation-Related Paragangliomas Classify as Discrete Pseudohypoxic Subcluster.
    Fliedner SM; Shankavaram U; Marzouca G; Elkahloun A; Jochmanova I; Daerr R; Linehan WM; Timmers H; Tischler AS; Papaspyrou K; Brieger J; de Krijger R; Breza J; Eisenhofer G; Zhuang Z; Lehnert H; Pacak K
    Neoplasia; 2016 Sep; 18(9):567-76. PubMed ID: 27659016
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  • 10. Germline mutations and genotype-phenotype associations in head and neck paraganglioma patients with negative family history in China.
    Zhu WD; Wang ZY; Chai YC; Wang XW; Chen DY; Wu H
    Eur J Med Genet; 2015 Sep; 58(9):433-8. PubMed ID: 26096992
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  • 11. Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysis.
    Bugalho MJ; Silva AL; Domingues R
    Fam Cancer; 2015 Dec; 14(4):603-7. PubMed ID: 26071763
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. Low penetrance of paraganglioma and pheochromocytoma in an extended kindred with a germline SDHB exon 3 deletion.
    Rijken JA; Niemeijer ND; Corssmit EP; Jonker MA; Leemans CR; Menko FH; Hensen EF
    Clin Genet; 2016 Jan; 89(1):128-32. PubMed ID: 25827221
    [TBL] [Abstract] [Full Text] [Related]  

  • 13. A registry-based study of thyroid paraganglioma: histological and genetic characteristics.
    von Dobschuetz E; Leijon H; Schalin-Jäntti C; Schiavi F; Brauckhoff M; Peczkowska M; Spiazzi G; Demattè S; Cecchini ME; Sartorato P; Krajewska J; Hasse-Lazar K; Roszkowska-Purska K; Taschin E; Malinoc A; Akslen LA; Arola J; Lange D; Fassina A; Pennelli G; Barbareschi M; Luettges J; Prejbisz A; Januszewicz A; Strate T; Bausch B; Castinetti F; Jarzab B; Opocher G; Eng C; Neumann HP
    Endocr Relat Cancer; 2015 Apr; 22(2):191-204. PubMed ID: 25595276
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. Sinonasal paraganglioma with long-delayed recurrence and metastases: genetic and imaging findings.
    Michel J; Taïeb D; Jolibert M; Torrents J; Wassef M; Morange I; Essamet W; Barlier A; Dessi P; Fakhry N
    J Clin Endocrinol Metab; 2013 Nov; 98(11):4262-6. PubMed ID: 24030938
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  • 15. Genetics of hereditary head and neck paragangliomas.
    Boedeker CC; Hensen EF; Neumann HP; Maier W; van Nederveen FH; Suárez C; Kunst HP; Rodrigo JP; Takes RP; Pellitteri PK; Rinaldo A; Ferlito A
    Head Neck; 2014 Jun; 36(6):907-16. PubMed ID: 23913591
    [TBL] [Abstract] [Full Text] [Related]  

  • 16. A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma.
    Rattenberry E; Vialard L; Yeung A; Bair H; McKay K; Jafri M; Canham N; Cole TR; Denes J; Hodgson SV; Irving R; Izatt L; Korbonits M; Kumar AV; Lalloo F; Morrison PJ; Woodward ER; Macdonald F; Wallis Y; Maher ER
    J Clin Endocrinol Metab; 2013 Jul; 98(7):E1248-56. PubMed ID: 23666964
    [TBL] [Abstract] [Full Text] [Related]  

  • 17. Genetic studies in a coexistence of acromegaly, pheochromocytoma, gastrointestinal stromal tumor (GIST) and thyroid follicular adenoma.
    Boguszewski CL; Fighera TM; Bornschein A; Marques FM; Dénes J; Rattenbery E; Maher ER; Stals K; Ellard S; Korbonits M
    Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):507-12. PubMed ID: 23295290
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  • 18. The genetics of paragangliomas.
    Burnichon N; Abermil N; Buffet A; Favier J; Gimenez-Roqueplo AP
    Eur Ann Otorhinolaryngol Head Neck Dis; 2012 Dec; 129(6):315-8. PubMed ID: 23078982
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  • 19. Identification of a signaling axis HIF-1α/microRNA-210/ISCU independent of SDH mutation that defines a subgroup of head and neck paragangliomas.
    Merlo A; de Quiros SB; Secades P; Zambrano I; Balbín M; Astudillo A; Scola B; Arístegui M; Suarez C; Chiara MD
    J Clin Endocrinol Metab; 2012 Nov; 97(11):E2194-200. PubMed ID: 22977270
    [TBL] [Abstract] [Full Text] [Related]  

  • 20. head and neck paragangliomas: clinical and molecular genetic classification.
    Offergeld C; Brase C; Yaremchuk S; Mader I; Rischke HC; Gläsker S; Schmid KW; Wiech T; Preuss SF; Suárez C; Kopeć T; Patocs A; Wohllk N; Malekpour M; Boedeker CC; Neumann HP
    Clinics (Sao Paulo); 2012; 67 Suppl 1(Suppl 1):19-28. PubMed ID: 22584701
    [TBL] [Abstract] [Full Text] [Related]  


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