Mate-Pair Sequencing as a Powerful Clinical Tool for the Characterization of Cancers with a DNA Viral Etiology

Por Gao, Ge, Smith, David I.
Publicado no Viruses (2015)

WWOX, large common fragile site genes, and cancer

Por Gao, Ge, Smith, David I
Publicado no Exp Biol Med (Maywood) (2015)

Next-generation sequencing: a transformative tool for vaccinology

Por Dhiman, Neelam, Smith, David I, Poland, Gregory A
Publicado em 2009

Human TopBP1 Ensures Genome Integrity during Normal S Phase

Por Kim, Ja-Eun, McAvoy, Sarah A., Smith, David I., Chen, Junjie
Publicado em 2005

Prognostic Significance of Decreased Expression of Six Large Common Fragile Site Genes in Oropharyngeal Squamous Cell Carcinomas

Por Gao, Ge, Kasperbauer, Jan L., Tombers, Nicole M., Cornell, Melissa D., Smith, David I.
Publicado no Transl Oncol (2014)

Exon Skipping in IVD RNA Processing in Isovaleric Acidemia Caused by Point Mutations in the Coding Region of the IVD Gene

Por Vockley, Jerry, Rogan, Peter K., Anderson, Bambi D., Willard, Jan, Seelan, Ratnam S., Smith, David I., Liu, Wanguo
Publicado em 2000

Concurrent Human Papillomavirus-Positive Squamous Cell Carcinoma of the Oropharynx in a Married Couple

Por Brobst, Tyler D., García, Joaquín J., Price, Katharine A., Gao, Ge, Smith, David I., Price, Daniel L.
Publicado no Case Rep Otolaryngol (2016)

Third Type of Plasmid Conferring Gentamicin Resistance in Pseudomonas aeruginosa

Por Smith, David I., Lus, R. Gomez, Calvo, M. C. Rubio, Datta, Naomi, Jacob, A. E., Hedges, R. W.
Publicado em 1975

Skp2 inhibits FOXO1 in tumor suppression through ubiquitin-mediated degradation

Por Huang, Haojie, Regan, Kevin M., Wang, Fang, Wang, Diping, Smith, David I, van Deursen, Jan M. A., Tindall, Donald J.
Publicado em 2005

The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8

Por Gemmill, Robert M., West, James D., Boldog, Ferenc, Tanaka, Naotake, Robinson, Linda J., Smith, David I., Li, Frederick, Drabkin, Harry A.
Publicado em 1998

Mechanisms of Genomic Instabilities Underlying Two Common Fragile-Site-Associated Loci, PARK2 and DMD, in Germ Cell and Cancer Cell Lines

Por Mitsui, Jun, Takahashi, Yuji, Goto, Jun, Tomiyama, Hiroyuki, Ishikawa, Shunpei, Yoshino, Hiroyo, Minami, Narihiro, Smith, David I., Lesage, Suzanne, Aburatani, Hiroyuki, Nishino, Ichizo, Brice, Alexis, Hattori, Nobutaka, Tsuji, Shoji
Publicado em 2010

Discovery of recurrent t(6;7)(p25.3;q32.3) translocations in ALK-negative anaplastic large cell lymphomas by massively parallel genomic sequencing

Por Feldman, Andrew L., Dogan, Ahmet, Smith, David I., Law, Mark E., Ansell, Stephen M., Johnson, Sarah H., Porcher, Julie C., Özsan, Nazan, Wieben, Eric D., Eckloff, Bruce W., Vasmatzis, George
Publicado em 2011

Genome-Wide Characterization of Transcriptional Patterns in High and Low Antibody Responders to Rubella Vaccination

Por Haralambieva, Iana H., Oberg, Ann L., Ovsyannikova, Inna G., Kennedy, Richard B., Grill, Diane E., Middha, Sumit, Bot, Brian M., Wang, Vivian W., Smith, David I., Jacobson, Robert M., Poland, Gregory A.
Publicado em 2013

3' tag digital gene expression profiling of human brain and universal reference RNA using Illumina Genome Analyzer

Por Asmann, Yan W, Klee, Eric W, Thompson, E Aubrey, Perez, Edith A, Middha, Sumit, Oberg, Ann L, Therneau, Terry M, Smith, David I, Poland, Gregory A, Wieben, Eric D, Kocher, Jean-Pierre A
Publicado em 2009

Transcriptional Profiling by Sequencing of Oropharyngeal Cancer

Por Laborde, Rebecca R., Wang, Vivian W., Smith, Todd M., Olson, N. Eric, Olsen, Steven M., García, Joaquín J., Olsen, Kerry D., Moore, Eric J., Kasperbauer, Jan L., Tombers, Nicole M., Smith, David I.
Publicado em 2012

Mutations in CHEK2 Associated with Prostate Cancer Risk

Por Dong, Xiangyang, Wang, Liang, Taniguchi, Ken, Wang, Xianshu, Cunningham, Julie M., McDonnell, Shannon K., Qian, Chiping, Marks, Angela F., Slager, Susan L., Peterson, Brett J., Smith, David I., Cheville, John C., Blute, Michael L., Jacobsen, Steve J., Schaid, Daniel J., Tindall, Donald J., Thibodeau, Stephen N., Liu, Wanguo
Publicado em 2003

Tumor Transcriptome Sequencing Reveals Allelic Expression Imbalances Associated with Copy Number Alterations

Por Tuch, Brian B., Laborde, Rebecca R., Xu, Xing, Gu, Jian, Chung, Christina B., Monighetti, Cinna K., Stanley, Sarah J., Olsen, Kerry D., Kasperbauer, Jan L., Moore, Eric J., Broomer, Adam J., Tan, Ruoying, Brzoska, Pius M., Muller, Matthew W., Siddiqui, Asim S., Asmann, Yan W., Sun, Yongming, Kuersten, Scott, Barker, Melissa A., De La Vega, Francisco M., Smith, David I.
Publicado em 2010

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

Por Klein, Christopher J., Botuyan, Maria-Victoria, Wu, Yanhong, Ward, Christopher J., Nicholson, Garth A., Hammans, Simon, Hojo, Kaori, Yamanishi, Hiromitch, Karpf, Adam R., Wallace, Douglas C., Simon, Mariella, Lander, Cecilie, Boardman, Lisa A., Cunningham, Julie M., Smith, Glenn E., Litchy, William J., Boes, Benjamin, Atkinson, Elizabeth J., Middha, Sumit, Dyck, P. James, Parisi, Joseph E., Mer, Georges, Smith, David I., Dyck, Peter J.
Publicado em 2011

Genome-wide analysis reveals recurrent structural abnormalities of TP63 and other p53-related genes in peripheral T-cell lymphomas

Por Vasmatzis, George, Johnson, Sarah H., Knudson, Ryan A., Ketterling, Rhett P., Braggio, Esteban, Fonseca, Rafael, Viswanatha, David S., Law, Mark E., Kip, N. Sertac, Özsan, Nazan, Grebe, Stefan K., Frederick, Lori A., Eckloff, Bruce W., Thompson, E. Aubrey, Kadin, Marshall E., Milosevic, Dragana, Porcher, Julie C., Asmann, Yan W., Smith, David I., Kovtun, Irina V., Ansell, Stephen M., Dogan, Ahmet, Feldman, Andrew L.
Publicado no Blood (2012)