Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jiuhong Pang"'
Autor:
Lianna J. Marks, Jennifer A. Oberg, Danielle Pendrick, Anthony N. Sireci, Chana Glasser, Carrie Coval, Rebecca J. Zylber, Wendy K. Chung, Jiuhong Pang, Andrew T. Turk, Susan J. Hsiao, Mahesh M. Mansukhani, Julia L. Glade Bender, Andrew L. Kung, Maria Luisa Sulis
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2017)
BackgroundThe advent of comprehensive genomic profiling has markedly advanced the understanding of the biology of pediatric hematological malignancies, however, its application to clinical care is still unclear. We present our experience integrating
Externí odkaz:
https://doaj.org/article/72d22ad9cdc54209a38fa6c39fc9b294
Autor:
Spiro P. Pantazatos, Stuart J. Andrews, Jane Dunning-Broadbent, Jiuhong Pang, Yung-yu Huang, Victoria Arango, Peter L. Nagy, J. John Mann
Publikováno v:
Neurobiology of Disease, Vol 79, Iss , Pp 123-134 (2015)
Low brain expression of the spermidine/spermine N-1 acetyltransferase (SAT1) gene, the rate-limiting enzyme involved in catabolism of polyamines that mediate the polyamine stress response (PSR), has been reported in depressed suicides. However, it is
Externí odkaz:
https://doaj.org/article/58c736dc47444775a30109872cdf9a5a
Autor:
Jiuhong Pang, Hongai Xia, Shijun Mi, Wen Zhang, Danielle Pendrick, Christopher Freeman, Helen Fernandes, Mahesh Mansukhani, Susan J Hsiao
Publikováno v:
Journal of Clinical Pathology. 76:276-280
Tumour mutational burden (TMB) is used to predict response to immunotherapies. Although several groups have proposed calculation methods for TMB, a clear consensus has not yet emerged. In this study, we explored TMB calculation approaches with a 586-
Autor:
Jiuhong Pang, Hongai Xia, Shijun Mi, Wen Zhang, Pendrick, Danielle, Freeman, Christopher, Fernandes, Helen, Mansukhani, Mahesh, Hsiao, Susan J.
Publikováno v:
Journal of Clinical Pathology; Apr2023, Vol. 76 Issue 4, p276-280, 6p
Publikováno v:
Methods Cell Biol
The maternally inherited mitochondrial DNA (mtDNA) is a circular 16,569-bp double stranded DNA that encodes 37 genes, twenty-four of which (2 rRNA and 22 tRNA) are necessary for transcription and translation of 13 polypeptides that are all subunits o
Publikováno v:
Journal of clinical pathology. 73(2)
AimMicrosatellite instability (MSI), a hallmark of DNA mismatch repair deficiency, is a key molecular biomarker with multiple clinical implications including the selection of patients for immunotherapy, identifying patients who may have Lynch syndrom
Autor:
Jane Dunning-Broadbent, Jiuhong Pang, Yung-yu Huang, J. John Mann, Peter L. Nagy, Victoria Arango, Spiro P. Pantazatos, Stuart J. Andrews
Publikováno v:
Neurobiology of Disease, Vol 79, Iss, Pp 123-134 (2015)
Low brain expression of the spermidine/spermine N-1 acetyltransferase (SAT1) gene, the rate-limiting enzyme involved in catabolism of polyamines that mediate the polyamine stress response (PSR), has been reported in depressed suicides. However, it is
Autor:
Helen Remotti, Andrew T. Turk, Andrew L. Kung, Danielle Pendrick, Hanina Hibshoosh, Stuart J. Andrews, Wendy K. Chung, Filemon S. Dela Cruz, Daniel Diolaiti, Peter L. Nagy, Jennifer A. Oberg, Rebecca J. Zylber, Julia L. Glade Bender, Anthony N. Sireci, Carrie Koval, Jiuhong Pang, Maria Luisa Sulis, Darrell J. Yamashiro, Mahesh M. Mansukhani, Susan J. Hsiao, James Garvin, Stephen G. Emerson
Publikováno v:
Genome Medicine
Background Molecular characterization has the potential to advance the management of pediatric cancer and high-risk hematologic disease. The clinical integration of genome sequencing into standard clinical practice has been limited and the potential
Publikováno v:
Journal of Clinical Pathology; Feb2020, Vol. 73 Issue 2, p83-89, 7p, 1 Diagram, 2 Charts, 2 Graphs
Autor:
Oberg, Jennifer A., Bender, Julia L. Glade, Sulis, Maria Luisa, Pendrick, Danielle, Sireci, Anthony N., Hsiao, Susan J., Turk, Andrew T., Cruz, Filemon S. Dela, Hibshoosh, Hanina, Remotti, Helen, Zylber, Rebecca J., Jiuhong Pang, Diolaiti, Daniel, Koval, Carrie, Andrews, Stuart J., Garvin, James H., Yamashiro, Darrell J., Chung, Wendy K., Emerson, Stephen G., Nagy, Peter L.
Publikováno v:
Genome Medicine; 12/23/2016, Vol. 8, p1-19, 19p