Bin T Teh
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Explore the profile of Bin T Teh including associated specialties, affiliations and a list of published articles.
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61
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2423
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Recent Articles
1.
Sripa B, Seubwai W, Vaeteewoottacharn K, Sawanyawisuth K, Silsirivanit A, Kaewkong W, et al.
Hum Cell
. 2020 Mar;
33(3):695-708.
PMID: 32207095
Three cholangiocarcinoma (CCA) cell line-formerly named, M156, M213 and M214 have been intensively used with discrepancy of their tumor origins. They were assumed to be originated from three different donors...
2.
Ng A, Poon S, Huang M, Lim J, Boot A, Yu W, et al.
Sci Transl Med
. 2017 Oct;
9(412).
PMID: 29046434
Many traditional pharmacopeias include and related plants, which contain nephrotoxins and mutagens in the form of aristolochic acids and similar compounds (collectively, AA). AA is implicated in multiple cancer types,...
3.
Wong M, Ng C, Kuick C, Aw S, Rajasegaran V, Lim J, et al.
Histopathology
. 2017 Aug;
72(2):320-329.
PMID: 28833375
Aims: Clear cell sarcoma of the kidney (CCSK) is a rare paediatric renal malignant tumour. The majority of CCSKs have internal tandem duplications (ITDs) of the BCOR gene, whereas a...
4.
Droscha C, Diegel C, Ethen N, Burgers T, McDonald M, Maupin K, et al.
Bone
. 2017 Apr;
98:68-78.
PMID: 28384511
Inactivating mutations that lead to loss of heterozygosity within the HRPT2/Cdc73 gene are directly linked to the development of primary hyperparathyroidism, parathyroid adenomas, and ossifying fibromas of the jaw (HPT-JT)....
5.
Pandya C, Uzilov A, Bellizzi J, Lau C, Moe A, Strahl M, et al.
JCI Insight
. 2017 Mar;
2(6):e92061.
PMID: 28352668
Parathyroid carcinoma (PC) is an extremely rare malignancy lacking effective therapeutic intervention. We generated and analyzed whole-exome sequencing data from 17 patients to identify somatic and germline genetic alterations. A...
6.
Walline H, Goudsmit C, McHugh J, Tang A, Owen J, Teh B, et al.
Head Neck
. 2017 Feb;
39(5):840-852.
PMID: 28236344
Background: Human papillomavirus (HPV)-positive oropharyngeal cancer is generally associated with excellent response to therapy, but some HPV-positive tumors progress despite aggressive therapy. The purpose of this study was to evaluate...
7.
Benusiglio P, Couve S, Gilbert-Dussardier B, Deveaux S, Le Jeune H, Da Costa M, et al.
J Med Genet
. 2015 Apr;
52(6):426-30.
PMID: 25911086
Background: Many cases of familial renal cell carcinoma (RCC) remain unexplained by mutations in the known predisposing genes or shared environmental factors. There are therefore additional, still unidentified genes involved...
8.
Yu W, McPherson J, Stevenson M, van Eijk R, Heng H, Newey P, et al.
J Clin Endocrinol Metab
. 2014 Nov;
100(2):E360-4.
PMID: 25387265
Context: Cell division cycle 73 (CDC73), encoding the protein parafibromin, is the most prevalent mutated gene in familial and sporadic parathyroid carcinoma (PC). Objective: To identify additional genetic abnormalities in...
9.
Tretiakova M, Zynger D, Luan C, Andeen N, Finn L, Kocherginsky M, et al.
Virchows Arch
. 2014 Nov;
466(1):67-76.
PMID: 25366870
Glypican 3 (GPC3), a heparan sulfate proteoglycan, plays a role in cell growth and differentiation. Mutations of the GPC3 gene are responsible for Simpson-Golabi-Behmel syndrome, which is characterized by anomalies...
10.
Malouf G, Su X, Yao H, Gao J, Xiong L, He Q, et al.
Clin Cancer Res
. 2014 Jun;
20(15):4129-40.
PMID: 24899691
Purpose: MITF/TFE translocation renal cell carcinoma (TRCC) is a rare subtype of kidney cancer. Its incidence and the genome-wide characterization of its genetic origin have not been fully elucidated. Experimental...