Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Qining Qian"'
Autor:
Chandni Desai, Jon Thomason, Qining Qian, Sarah L. Hall, Benjamin W. Darbro, Colleen Fullenkamp, Munir R. Tanas, Adam J. Dupuy, Nicole Merritt, Allyn M. Lambertz
Publikováno v:
Oncotarget
TAZ and YAP are transcriptional coactivators negatively regulated by the Hippo pathway that have emerged as key oncoproteins in several cancers including sarcomas. We hypothesized that loss of expression of the Hippo kinases might be a mechanism of a
Autor:
Qining Qian, Terry A. Braun, Mark D. Iannettoni, Scott K. Sherman, James R. Howe, Jessica E. Maxwell, Benjamin W. Darbro, Andrew M. Bellizzi
Publikováno v:
Cancer Genetics. 208:41-46
Germline mutations in the PTEN tumor-suppressor gene cause autosomal-dominant conditions such as Cowden and Bannayan–Riley–Ruvalcaba syndromes with variable presentations, including hamartomatous gastrointestinal tumors, dermatologic abnormalitie
Autor:
Aaron D. Bossler, Nitin J. Karandikar, Benjamin W. Darbro, Carol J. Holman, Jacqueline Lekostaj, Nancy S. Rosenthal, Bryan Steussy, Sergei Syrbu, Qining Qian
Publikováno v:
Laboratory Medicine
We report an instructive case of acute myeloid leukemia with histiocytic differentiation (acute histiocytic leukemia) arising in a patient, a 52-year-old woman with a history of follicular lymphoma. The results of genetic studies proved a clonal rela
Autor:
Stacia L. Phillips, Aloysius J. Klingelhutz, Qining Qian, Francoise A. Gourronc, Shivanand R. Patil, Benjamin W. Darbro
Publikováno v:
Virology. 340(2):237-244
To study the role of human papillomavirus (HPV) infection in the development of genetic instability, we transduced normal human airway and anogenital epithelial cells with various combinations of HPV-16 E6, E7, and the reverse transcriptase component
Autor:
Megan J Riker, Benjamin W. Darbro, Frances Solivan-Timpe, Qining Qian, John H. Fingert, Alan L. Robin, Kathy Miller, Robert F. Mullins, Ben R. Roos, Richard Van Rheeden
Publikováno v:
Ophthalmic genetics. 35(1)
The gene that causes normal tension glaucoma (NTG) in a large pedigree was recently mapped to a region of chromosome 12q14 (GLC1P) that contains the genes TBK1, XPOT, RASSF3, and GNS. We sought to investigate the structure of the chromosome 12q14 dup
Autor:
Elena V. Semina, Dimitri G. Trembath, Qining Qian, Shivanand R. Patil, Douglas H. Jones, Andrew F. Russo, Brad A. Amendt, Jeffrey C. Murray
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology. 70(2)
BACKGROUND: Rieger’s syndrome is an autosomal dominant disorder characterized by eye, tooth, and umbilical anomalies. A gene responsible for Rieger’s syndrome, PITX2, has previously been cloned using two patients with balanced translocations, t(4
Autor:
Steussy, Bryan, Lekostaj, Jacqueline, Qining Qian, Rosenthal, Nancy, Holman, Carol J., Syrbu, Sergei, Darbro, Benjamin, Bossler, Aaron, Karandikar, Nitin J.
Publikováno v:
Laboratory Medicine; May2016, Vol. 47 Issue 2, p155-157, 3p