T. Barber

发表

The Genomic Landscapes of Human Breast and Colorectal Cancers

A. Sparks, G. Parmigiani, J. Ptak, 2007, Science.

The Consensus Coding Sequences of Human Breast and Colorectal Cancers

G. Parmigiani, J. Ptak, L. Wood, 2006, Science.

Identification of target genes regulated by PAX3 and PAX3-FKHR in embryogenesis and alveolar rhabdomyosarcoma.

Oana A. Tomescu, S. Ruben, T. Barber, 2002, Genomics.

Negative regulation of the serine/threonine kinase B-Raf by Akt.

T. Barber, K. Guan, C. Figueroa, 2000, The Journal of biological chemistry.

Genome-wide survey of recurrent HBV integration in hepatocellular carcinoma

Angela M. Liu, Yingrui Li, Chunsheng Zhang, 2012, Nature Genetics.

Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers

G. Parmigiani, K. Kinzler, B. Vogelstein, 2008, Proceedings of the National Academy of Sciences.

A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1.

T. Barber, T. Friedman, R. Morell, 1993, Human molecular genetics.

Whole-genome sequencing of asian lung cancers: second-hand smoke unlikely to be responsible for higher incidence of lung cancer among Asian never-smokers.

B. Peters, Geoffrey B. Nilsen, P. Ng, 2014, Cancer research.

PAX3 gene structure, alternative splicing and evolution.

T. Barber, T. Friedman, M. C. Barber, 1999, Gene.

Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2.

W. Miller, D. W. Anderson, J. Touchman, 1999, Genomics.

Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.

J. Lupski, T. Barber, T. Friedman, 1998, American journal of human genetics.

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17

J. Weber, T. Barber, T. Friedman, 1995, Nature Genetics.

Breast and Colorectal Cancers The Consensus Coding Sequences of Human

G. Parmigiani, J. Ptak, L. Wood, 2007 .

Somatic mutations of EGFR in colorectal cancers and glioblastomas.

K. Kinzler, B. Vogelstein, V. Velculescu, 2004, The New England journal of medicine.

Somatic Mutations in CCK2R Alter Receptor Activity that Promote Oncogenic Phenotypes

K. Kinzler, B. Vogelstein, V. Velculescu, 2012, Molecular Cancer Research.

TEM8 Interacts with the Cleaved C5 Domain of Collagen α3(VI)

K. Kinzler, B. Vogelstein, S. Seaman, 2004, Cancer Research.

Whole-genome sequencing identifies recurrent mutations in hepatocellular carcinoma

Lin Li, Shibing Deng, Hongyue Dai, 2013, Genome research.

Response to Comments on "The Consensus Coding Sequences of Human Breast and Colorectal Cancers"

Giovanni Parmigiani, Victor E. Velculescu, Bert Vogelstein, 2007, Science.

Somatic Mutations in GRM1 in Cancer Alter Metabotropic Glutamate Receptor 1 Intracellular Localization and Signaling

T. Barber, S. Ferguson, Melinda D Willard, 2013, Molecular Pharmacology.

Mutations in two short noncoding mononucleotide repeats in most microsatellite-unstable colorectal cancers.

Rainer Lehtonen, Bert Vogelstein, Jukka-Pekka Mecklin, 2005, Cancer research.

TEM8 interacts with the cleaved C5 domain of collagen alpha 3(VI).

K. Kinzler, B. Vogelstein, S. Seaman, 2004, Cancer research.

Whole-genome sequencing of asian lung cancers: second-hand smoke unlikely to be responsible for higher incidence of lung cancer among Asian never-smokers.

B. Peters, Geoffrey B. Nilsen, P. Ng, 2014, Cancer research.

Genome-wide survey of recurrent HBV integration in hepatocellular carcinoma

Angela M. Liu, Chunsheng Zhang, Yujie Hu, 2012, Nature Genetics.

Somatic Mutations in GRM1 in Cancer Alter Metabotropic Glutamate Receptor 1 Intracellular Localization and Signaling

T. Barber, S. Ferguson, Melinda D Willard, 2013, Molecular Pharmacology.