The Oncogenic Role of VWA8-AS1 , a Long Non-Coding RNA, in Epstein–Barr Virus-Associated Oral Squamous Cell Carcinoma: An Integrative Transcriptome and Functional Analysis.

Autor: Srisathaporn, Sawarot^1,2 (AUTHOR) sawarot.s@kkumail.com, Pientong, Chamsai^1,2 (AUTHOR) chapie@kku.ac.th, Heawchaiyaphum, Chukkris^1,2 (AUTHOR) thawaree.n@kkumail.com, Nukpook, Thawaree^1,2 (AUTHOR) sirinar@kku.ac.th, Aromseree, Sirinart^1,2 (AUTHOR), Ekalaksananan, Tipaya^1,2 (AUTHOR) chapie@kku.ac.th

Publikováno v: International Journal of Molecular Sciences. Dec2024, Vol. 25 Issue 23, p12565. 23p.

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome.

Autor: Evrony GD; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Cordero DR; Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA., Shen J; Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.; Laboratory of Molecular Medicine, Partners Personalized Medicine, Cambridge, Massachusetts 02139, USA., Partlow JN; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Yu TW; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Rodin RE; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Hill RS; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Coulter ME; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Lam AN; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Jayaraman D; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Gerrelli D; Institute of Child Health, University College London, London WC1N 1EH, United Kingdom., Diaz DG; Institute of Child Health, University College London, London WC1N 1EH, United Kingdom., Santos C; Institute of Child Health, University College London, London WC1N 1EH, United Kingdom., Morrison V; Institute of Child Health, University College London, London WC1N 1EH, United Kingdom., Galli A; Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom., Tschulena U; Division of Molecular Genome Analysis, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany., Wiemann S; Division of Molecular Genome Analysis, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany., Martel MJ; Department of Obstetrics and Gynecology, University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan S7N 5E5, Canada., Spooner B; Northern Medical Services, University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan S7K 0L4, Canada., Ryu SC; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Elhosary PC; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Richardson JM; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Tierney D; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA., Robinson CA; Department of Pathology, Royal University Hospital, University of Saskatchewan, Saskatoon, Saskatchewan S7N 0W8, Canada., Chibbar R; Department of Pathology, Royal University Hospital, University of Saskatchewan, Saskatoon, Saskatchewan S7N 0W8, Canada., Diudea D; Department of Pathology, Royal University Hospital, University of Saskatchewan, Saskatoon, Saskatchewan S7N 0W8, Canada., Folkerth R; Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA., Wiebe S; Department of Medical Imaging, Royal University Hospital, University of Saskatchewan, Saskatoon, Saskatchewan S7N 0W8, Canada., Barkovich AJ; Department of Radiology, University of California San Francisco, San Francisco, California 94143, USA., Mochida GH; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.; Pediatric Neurology Unit, Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA., Irvine J; Northern Medical Services, University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan S7K 0L4, Canada.; Population Health Unit, Mamawetan Churchill River and Keewatin-Yatthé Health Regions, and Athabasca Health Authority, La Ronge, Saskatchewan S0J 1L0, Canada., Lemire EG; Department of Pediatrics, Royal University Hospital, University of Saskatchewan, Saskatoon, Saskatchewan S7N 0W8, Canada., Blakley P; Department of Pediatrics, Royal University Hospital, University of Saskatchewan, Saskatoon, Saskatchewan S7N 0W8, Canada., Walsh CA; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA.; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.

Publikováno v: Genome research [Genome Res] 2017 Aug; Vol. 27 (8), pp. 1323-1335. Date of Electronic Publication: 2017 Jun 19.

Pulmonary lymphangitic carcinomatosis from squamous cell carcinoma of the cervix.

Autor: Kanthan R; Department of Pathology and Laboratory Medicine, University of Saskatchewan, Saskatoon, SK, Canada. rani.kanthan@saskatoonhealthregion.ca, Senger JL, Diudea D

Publikováno v: World journal of surgical oncology [World J Surg Oncol] 2010 Dec 03; Vol. 8, pp. 107. Date of Electronic Publication: 2010 Dec 03.

Circular RNA PVT1 Regulates Cell Proliferation, Migration, and Apoptosis by Stabilizing c-Myc and Downstream Target CXCR4 Expression in Acute Myeloid Leukemia.

Autor: Xian-Fu Sheng¹, Li-Li Hong¹, Lei Fan², Yu Zhang¹, Kai-Li Chen¹, Jie Mu¹, Si-yu Shen¹, Hai-Feng Zhuang¹ zhuanghaifeng5@163.com

Publikováno v: Turkish Journal of Hematology. 2023, Vol. 40 Issue 2, p82-91. 10p.

Timosaponin AIII Inhibits Migration and Invasion Abilities in Human Cervical Cancer Cells through Inactivation of p38 MAPK-Mediated uPA Expression In Vitro and In Vivo.

Autor: Chien, Hung-Ju^1,2 (AUTHOR), Liu, Chung-Jung^3,4 (AUTHOR), Ying, Tsung-Ho^5,6 (AUTHOR), Wu, Pei-Ju^1,5 (AUTHOR), Wang, Jiunn-Wei^3,4,7 (AUTHOR), Ting, Yi-Hsuan¹ (AUTHOR), Hsieh, Yi-Hsien^1,8 (AUTHOR) hyhsien@csmu.edu.tw, Wang, Shih-Chiang⁹ (AUTHOR) hyhsien@csmu.edu.tw

Publikováno v: Cancers. Jan2023, Vol. 15 Issue 1, p37. 14p.