Modulation of Splicing Events in Histone Deacetylase 3 by Various Extracellular and Signal Transduction Pathways

Por Gray, S. G., Iglesias, A. H., Teh, B. T., Dangond, F.
Publicado no Gene Expr (2018)

The performance of CGH array for the detection of cryptic constitutional chromosome imbalances

Por Schoumans, J, Anderlid, B, Blennow, E, Teh, B, Nordenskjold, M
Publicado em 2004

Familial adult renal neoplasia

Por Takahashi, M, Kahnoski, R, Gross, D, Nicol, D, Teh, B
Publicado em 2002

MET mutation and familial gastric cancer

Por Chen, J, Kearns, S, Porter, T, Richards, F, Maher, E, Teh, B
Publicado em 2001

Alterations of the Birt-Hogg-Dubé gene (BHD) in sporadic colorectal tumours

Por Kahnoski, K, Khoo, S, Nassif, N, Chen, J, Lobo, G, Segelov, E, Teh, B
Publicado em 2003

Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13.

Por Teh, B T, Silburn, P, Lindblad, K, Betz, R, Boyle, R, Schalling, M, Larsson, C
Publicado em 1995

Topoisomerase IIα in Wilms' tumour: gene alterations and immunoexpression

Por Tretiakova, M, Turkyilmaz, M, Grushko, T, Kocherginsky, M, Rubin, C, Teh, B, Yang, X J
Publicado em 2006

Clonal loss of INT-2 alleles in sporadic and familial pancreatic endocrine tumours.

Por Teh, B. T., Hayward, N. K., Wilkinson, S., Woods, G. M., Cameron, D., Shepherd, J. J.
Publicado em 1990

cDNA microarray analysis assists in diagnosis of malignant intrarenal pheochromocytoma originally masquerading as a renal cell carcinoma

Por Takahashi, M, Yang, X, McWhinney, S, Sano, N, Eng, C, Kagawa, S, Teh, B, Kanayama, H
Publicado em 2005

Genetic studies of thymic carcinoids in multiple endocrine neoplasia type 1.

Por Teh, B T, Hayward, N K, Walters, M K, Shepherd, J J, Wilkinson, S, Nordenskjold, M, Larsson, C
Publicado em 1994

Identification of MEN1 gene mutations in families with MEN 1 and related disorders

Por Bergman, L, Teh, B, Cardinal, J, Palmer, J, Walters, M, Shepherd, J, Cameron, D, Hayward, N
Publicado em 2000

Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours

Por Bergman, L, Boothroyd, C, Palmer, J, Grimmond, S, Walters, M, Teh, B, Shepherd, J, Hartley, L, Hayward, N
Publicado em 2000

Gene and protein expression markers of response to combined antiangiogenic and epidermal growth factor targeted therapy in renal cell carcinoma

Por Tsavachidou-Fenner, D., Tannir, N., Tamboli, P., Liu, W., Petillo, D., Teh, B., Mills, G. B., Jonasch, E.
Publicado em 2010

Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms.

Por Larsson, C, Shepherd, J, Nakamura, Y, Blomberg, C, Weber, G, Werelius, B, Hayward, N, Teh, B, Tokino, T, Seizinger, B
Publicado em 1992

Population-based comparison of prognostic factors in invasive micropapillary and invasive ductal carcinoma of the breast

Por Chen, A C, Paulino, A C, Schwartz, M R, Rodriguez, A A, Bass, B L, Chang, J C, Teh, B S
Publicado em 2014

Association of a novel constitutional translocation t(1q;3q) with familial renal cell carcinoma

Por Kanayama, H., Lui, W., Takahashi, M., Naroda, T., Kedra, D., Wong, F. K., Kuroki, Y., Nakahori, Y., Larsson, C., Kagawa, S., Teh, B. T.
Publicado em 2001

Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinoma

Por Morris, M R, Gentle, D, Abdulrahman, M, Clarke, N, Brown, M, Kishida, T, Yao, M, Teh, B T, Latif, F, Maher, E R
Publicado em 2008

Using process mapping to identify barriers to effective management of sepsis in a cancer hospital: lessons for successful implementation of a whole hospital pathway

Por Thursky, K, Haeusler, G, Teh, B, Comodo, D, Dean, N, Brown, C, Willis, J, Morris, K, Lingaratnam, S, Slavin, M, Worth, L
Publicado no Crit Care (2014)

A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors.

Por Teh, B T, Esapa, C T, Houlston, R, Grandell, U, Farnebo, F, Nordenskjöld, M, Pearce, C J, Carmichael, D, Larsson, C, Harris, P E
Publicado em 1998

Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one family

Por TEH, B, LINBLAD, K, NORD, B, KYTOLA, S, SCHALLING, M, LARSSON, C, RAPLEY, E, BIGGS, P, HUDDART, R, STRATTON, M, HII, S, NICOL, D
Publicado em 1999