Terms: = Bone cancer AND TERT, EST2, Q8NG46, Q8N6C3, Q2XS35, O14783, O14746, 7015, hEST2, TCS1, TRT, TP2 AND Diagnosis
29 results:
1. Adult granulosa cell tumor of the testis with malignant tendency: A case report with genetic analysis using high-throughput sequencing.
Deng L; Zeng J; Qiu JF; Yang LH; Ma J
Medicine (Baltimore); 2023 Aug; 102(32):e34523. PubMed ID: 37565864
[TBL] [Abstract] [Full Text] [Related]
2. Report of Consensus Panel 3 from the 11th International workshop on Waldenström's Macroglobulinemia: Recommendations for molecular diagnosis in Waldenström's Macroglobulinemia.
Garcia-Sanz R; Varettoni M; Jiménez C; Ferrero S; Poulain S; San-Miguel JF; Guerrera ML; Drandi D; Bagratuni T; McMaster M; Roccaro AM; Roos-Weil D; Leiba M; Li Y; Qiu L; Hou J; De Larrea CF; Castillo JJ; Dimopoulos M; Owen RG; Treon SP; Hunter ZR
Semin Hematol; 2023 Mar; 60(2):90-96. PubMed ID: 37099028
[TBL] [Abstract] [Full Text] [Related]
3. [Differential diagnostic between hepatocellular carcinoma and hepatoid carcinoma with bone metastasis revelation: What tools can be used?].
Neyrand S; Bringuier PP; Benzerdjeb N; Hervieu V; Fenouil T
Ann Pathol; 2023 Sep; 43(5):407-411. PubMed ID: 36822899
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4. Combined analysis of PHOX2B at two time points and its value for further risk stratification in high-risk neuroblastoma.
Yue Z; Gao C; Xing T; Zhao W; Duan C; Wang X; Jin M; Su Y
Pediatr Blood Cancer; 2023 May; 70(5):e30261. PubMed ID: 36815592
[TBL] [Abstract] [Full Text] [Related]
5. Pan-cancer analysis of tert and Validation in Osteosarcoma Cell Lines.
Xie L; Yin W; Tang F; He M
Biochem Biophys Res Commun; 2023 Jan; 639():106-116. PubMed ID: 36476950
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6. Thyroid carcinoma metastases to central nervous system and vertebrae.
Kleinschmidt-DeMasters B; Marshall C
Folia Neuropathol; 2022; 60(3):292-300. PubMed ID: 36382481
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7. JAK2V617F variant allele frequency, non-driver mutations, single-nucleotide variants and polycythemia vera outcome.
Kanduła Z; Janowski M; Więckowska B; Paczkowska E; Lewandowski K
J Cancer Res Clin Oncol; 2023 Jul; 149(8):4789-4803. PubMed ID: 36242602
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8. Prospective longitudinal evaluation of treatment-related toxicity and health-related quality of life during the first year of treatment for pediatric acute lymphoblastic leukemia.
Schilstra CE; McCleary K; Fardell JE; Donoghoe MW; McCormack E; Kotecha RS; Lourenco RA; Ramachandran S; Cockcroft R; Conyers R; Cross S; Dalla-Pozza L; Downie P; Revesz T; Osborn M; Alvaro F; Wakefield CE; Marshall GM; Mateos MK; Trahair TN
BMC Cancer; 2022 Sep; 22(1):985. PubMed ID: 36109702
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9. Non-Iodine-Avid Disease Is Highly Prevalent in Distant Metastatic Differentiated Thyroid cancer With Papillary Histology.
Soe MH; Chiang JM; Flavell RR; Khanafshar E; Mendoza L; Kang H; Liu C
J Clin Endocrinol Metab; 2022 Jul; 107(8):e3206-e3216. PubMed ID: 35556126
[TBL] [Abstract] [Full Text] [Related]
10. Functional interaction between compound heterozygous tert mutations causes severe telomere biology disorder.
Niaz A; Truong J; Manoleras A; Fox LC; Blombery P; Vasireddy RS; Pickett HA; Curtin JA; Barbaro PM; Rodgers J; Roy J; Riley LG; Holien JK; Cohen SB; Bryan TM
Blood Adv; 2022 Jun; 6(12):3779-3791. PubMed ID: 35477117
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11. Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes.
Blombery P; Fox L; Ryland GL; Thompson ER; Lickiss J; McBean M; Yerneni S; Hughes D; Greenway A; Mechinaud F; Wood EM; Lieschke GJ; Szer J; Barbaro P; Roy J; Wight J; Lynch E; Martyn M; Gaff C; Ritchie D
Haematologica; 2021 Jan; 106(1):64-73. PubMed ID: 32054657
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12. Spinal solitary fibrous tumor of the neck: Next-generation sequencing-based analysis of genomic aberrations.
Ando M; Kobayashi H; Shinozaki-Ushiku A; Chikuda H; Matsubayashi Y; Yoshida M; Saito Y; Kohsaka S; Oda K; Miyagawa K; Aburatani H; Mano H; Yamasoba T
Auris Nasus Larynx; 2020 Dec; 47(6):1058-1063. PubMed ID: 31879078
[TBL] [Abstract] [Full Text] [Related]
13. Peculiar pathological, radiological and clinical features of skull-base de-differentiated chordomas. Results from a referral centre case-series and literature review.
Asioli S; Zoli M; Guaraldi F; Sollini G; Bacci A; Gibertoni D; Ricci C; Morandi L; Pasquini E; Righi A; Mazzatenta D
Histopathology; 2020 Apr; 76(5):731-739. PubMed ID: 31652338
[TBL] [Abstract] [Full Text] [Related]
14. Thyroid cancer bone Metastasis: Survival and Genomic Characteristics of a Large tertiary Care Cohort.
Kondraciuk JD; Rice SL; Zhou X; Gharzeddine K; Knezevic A; Spratt DE; Sabra M; Larson SM; Grewal RK; Osborne JR
Clin Nucl Med; 2019 Aug; 44(8):e465-e471. PubMed ID: 31274625
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15. Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders.
Trotta L; Norberg A; Taskinen M; Béziat V; Degerman S; Wartiovaara-Kautto U; Välimaa H; Jahnukainen K; Casanova JL; Seppänen M; Saarela J; Koskenvuo M; Martelius T
Orphanet J Rare Dis; 2018 Aug; 13(1):139. PubMed ID: 30115091
[TBL] [Abstract] [Full Text] [Related]
16. Induction of senescence in primary glioblastoma cells by serum and TGFβ.
Kumar R; Gont A; Perkins TJ; Hanson JEL; Lorimer IAJ
Sci Rep; 2017 May; 7(1):2156. PubMed ID: 28526854
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17. Effects of testosterone replacement therapy on hypogonadal men with osteopenia or osteoporosis: a subanalysis of a prospective randomized controlled study in Japan (EARTH study).
Shigehara K; Konaka H; Koh E; Nakashima K; Iijima M; Nohara T; Izumi K; Kitagawa Y; Kadono Y; Sugimoto K; Iwamoto T; Mizokami A; Namiki M
Aging Male; 2017 Sep; 20(3):139-145. PubMed ID: 28347184
[TBL] [Abstract] [Full Text] [Related]
18. Mucosal malignant melanoma - a clinical, oncological, pathological and genetic survey.
Mikkelsen LH; Larsen AC; von Buchwald C; Drzewiecki KT; Prause JU; Heegaard S
APMIS; 2016 Jun; 124(6):475-86. PubMed ID: 27004972
[TBL] [Abstract] [Full Text] [Related]
19. Extensive Therapies for Extraneural Metastases from Glioblastoma, as Confirmed with the OncoScan Assay.
Xu M; Wang Y; Xu J; Yao Y; Yu WX; Zhong P
World Neurosurg; 2016 Jun; 90():698.e7-698.e11. PubMed ID: 26852708
[TBL] [Abstract] [Full Text] [Related]
20. Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up.
Burris AM; Ballew BJ; Kentosh JB; Turner CE; Norton SA; ; ; Giri N; Alter BP; Nellan A; Gamper C; Hartman KR; Savage SA
Pediatr Neurol; 2016 Mar; 56():62-68.e1. PubMed ID: 26810774
[TBL] [Abstract] [Full Text] [Related]
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