Search Results - "Qian, Qining"

Functional Copy-Number Alterations as Diagnostic and Prognostic Biomarkers in Neuroendocrine Tumors by Vaughn, Hayley, Major, Heather, Kadera, Evangeline, Keck, Kendall, Dunham, Timothy, Qian, Qining, Brown, Bartley, Scott, Aaron, Bellizzi, Andrew M, Braun, Terry, Breheny, Patrick, Quelle, Dawn E, Howe, James R, Darbro, Benjamin

“…Functional copy-number alterations (fCNAs) are DNA copy-number changes with concordant differential gene expression. These are less likely to be bystander…”
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Analysis of two translocation breakpoints and identification of a negative regulatory element in patients with Rieger's syndrome by Trembath, Dimitri G., Semina, Elena V., Jones, Douglas H., Patil, Shivanand R., Qian, Qining, Amendt, Brad A., Russo, Andrew F., Murray, Jeffrey C.

“…BACKGROUND Rieger's syndrome is an autosomal dominant disorder characterized by eye, tooth, and umbilical anomalies. A gene responsible for Rieger's syndrome,…”
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A comprehensive evaluation of Hippo pathway silencing in sarcomas by Merritt, Nicole M, Fullenkamp, Colleen A, Hall, Sarah L, Qian, Qining, Desai, Chandni, Thomason, Jon, Lambertz, Allyn M, Dupuy, Adam J, Darbro, Benjamin, Tanas, Munir R

“…TAZ and YAP are transcriptional coactivators negatively regulated by the Hippo pathway that have emerged as key oncoproteins in several cancers including…”
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Leukemic Transdifferentiation of Follicular Lymphoma Into an Acute Histiocytic Leukemia in a 52-Year-Old Caucasian Woman by Steussy, Bryan, Lekostaj, Jacqueline, Qian, Qining, Rosenthal, Nancy, Holman, Carol J., Syrbu, Sergei, Darbro, Benjamin, Bossler, Aaron, Karandikar, Nitin J.

“…We report an instructive case of acute myeloid leukemia with histiocytic differentiation (acute histiocytic leukemia) arising in a patient, a 52-year-old woman…”
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TBK1 and Flanking Genes in Human Retina by Fingert, John H., Darbro, Benjamin W., Qian, Qining, Van Rheeden, Richard, Miller, Kathy, Riker, Megan, Solivan-Timpe, Frances, Roos, Ben R., Robin, Alan L., Mullins, Robert F.

“…Abstract Purpose: The gene that causes normal tension glaucoma (NTG) in a large pedigree was recently mapped to a region of chromosome 12q14 (GLC1P) that…”
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Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations by Sherman, Scott K, Maxwell, Jessica E, Qian, Qining, Bellizzi, Andrew M, Braun, Terry A, Iannettoni, Mark D, Darbro, Benjamin W, Howe, James R

“…Germline mutations in the PTEN tumor-suppressor gene cause autosomal-dominant conditions such as Cowden and Bannayan–Riley–Ruvalcaba syndromes with variable…”
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G-protein coupled receptor expression patterns delineate medulloblastoma subgroups by Whittier, Kelsey L, Boese, Erin A, Gibson-Corley, Katherine N, Kirby, Patricia A, Darbro, Benjamin W, Qian, Qining, Ingram, Wendy J, Robertson, Thomas, Remke, Marc, Taylor, Michael D, O'Dorisio, M Sue

“…Medulloblastoma is the most common malignant brain tumor in children. Genetic profiling has identified four principle tumor subgroups; each subgroup is…”
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Amplification of the chromosome 20q region is associated with expression of HPV-16 E7 in human airway and anogenital epithelial cells by Klingelhutz, Aloysius J., Qian, Qining, Phillips, Stacia L., Gourronc, Francoise A., Darbro, Benjamin W., Patil, Shivanand R.

“…To study the role of human papillomavirus (HPV) infection in the development of genetic instability, we transduced normal human airway and anogenital…”
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