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pro vyhledávání: '"Christine Briggs"'
Autor:
Christine Briggs
HCA does not provide the Case Selection Protocol. We will provide a link to the project publication for the purposes of providing the required protocol DOI to huBMAP.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de0887af507509ee4f8c98599369d5a9
https://doi.org/10.17504/protocols.io.bwxwpfpe
https://doi.org/10.17504/protocols.io.bwxwpfpe
Autor:
Edward A. Rietman, Christine Briggs, Afshin Beheshti, Kathleen P. Wilkie, Lili Ma, Lynn Hlatky, Nava Almog
Publikováno v:
Transcription
Tumor dormancy is a highly prevalent stage in cancer progression. We have previously generated and characterized in vivo experimental models of human tumor dormancy in which micro-tumors remain occult until they spontaneously shift into rapid tumor g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef644331beed9772a7641009336eda8c
https://doi.org/10.4161/trns.25558
https://doi.org/10.4161/trns.25558
Autor:
Lakshmanan K. Iyer, Christine Briggs, Caroline S. Vallaster, Richard H. Karas, Qing Lu, Gavin R. Schnitzler, Iris Z. Jaffe, Stephanie Erdkamp, Kazutaka Ueda
Publikováno v:
Molecular and cellular endocrinology. 442
The unliganded form of the estrogen receptor is generally thought to be inactive. Our prior studies, however, suggested that unliganded estrogen receptor alpha (ERα) exacerbates adverse vascular injury responses in mice. Here, we show that the prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b012b36dac5ac79e0db44c97500af6b7
https://pubmed.ncbi.nlm.nih.gov/27888004
https://pubmed.ncbi.nlm.nih.gov/27888004
Autor:
Ani Manichaikul, Vidu Garg, Qing Ma, Satish Rajagopal, Dita Obler, Leslie B. Smoot, Kari Boardman, Christine Briggs, D. Woodrow Benson, Karl W. Broman, Aoy Tomita-Mitchell, Deepak Srivastava, William T. Pu, Jie Shen, Elizabeth Goldmuntz
Publikováno v:
Journal of Molecular and Cellular Cardiology. 43:677-685
The transcription factor GATA4 is essential for heart morphogenesis. Heterozygous mutation of GATA4 causes familial septal defects. However, the phenotypic spectrum of heterozygous GATA4 mutation is not known. In this study, we defined the cardiac ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8ba82621647798177d4694a516addf1
https://doi.org/10.1016/j.yjmcc.2007.06.004
https://doi.org/10.1016/j.yjmcc.2007.06.004
Autor:
Christine Briggs, Jin Li, Matthew H. Kulke, Harvey J. Mamon, Sandra M. Gaston, Ewa Sicinska, Massimo Loda, Raffaella Zamponi, Shuji Ogino, Charles S. Fuchs, Lilin Wang, Fengfei Wang, Carlos Hader, Elizabeth A. Maher, G. Mike Makrigiorgos
Publikováno v:
The Journal of Molecular Diagnostics. 9:441-451
The need to apply modern technologies to analyze DNA from diverse clinical samples often stumbles on suboptimal sample quality. We developed a simple approach to assess DNA fragmentation in minute clinical samples of widely different origin and the l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18d54b9609e3637397be42d651571910
https://doi.org/10.2353/jmoldx.2007.070004
https://doi.org/10.2353/jmoldx.2007.070004
Autor:
Yulei Wang, Kai C. Sonntag, Tsung-Ung W. Woo, Christine Briggs, Lakshmanan K. Iyer, Benjamin Kong
The degeneration of substantia nigra (SN) dopamine (DA) neurons in sporadic Parkinson׳s disease (PD) is characterized by disturbed gene expression networks. Micro(mi)RNAs are post-transcriptional regulators of gene expression and we recently provide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e1da6fd4341d7ba8fbc9d74568ff194
https://europepmc.org/articles/PMC4522231/
https://europepmc.org/articles/PMC4522231/
Autor:
Francisco A. Bonilla, Christine Briggs, Marjorie A. Oettinger, Trudy N. Small, Jana L. Mooster, Keiichi Yamanaka, Manish J. Butte, Adam G. W. Matthews
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 4, p e0121489 (2015)
PloS one, vol 10, iss 4
PLoS ONE, Vol 10, Iss 4, p e0121489 (2015)
PloS one, vol 10, iss 4
Omenn syndrome is a primary immunodeficiency disorder, featuring susceptibility to infections and autoreactive T cells and resulting from defective genomic rearrangement of genes for the T cell and B cell receptors. The most frequent etiologies are h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f559ed97f47f2b2a8e59c99ff5d8d838
http://europepmc.org/articles/PMC4388548
http://europepmc.org/articles/PMC4388548
Autor:
Michael P. Whyte, Sarju G. Mehta, Christine Briggs, Sheena Ramdeen, Barbara McGillivray, Deborah V. Novack, Giles D. J. Watts, Sara Jane Hamilton, Virginia Kimonis, Steven Mumm
Publikováno v:
American Journal of Medical Genetics Part A. :322-330
We report on an unusual family with an autosomal dominant limb-girdle type of myopathy and bone fragility. This family was previously reported by Henry et al. [1958] as autosomal dominant progressive limb girdle “muscular dystrophy” with propensi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83b4fd314c7fe79e932e3d2cb510a122
https://doi.org/10.1002/ajmg.a.31008
https://doi.org/10.1002/ajmg.a.31008
Autor:
Giannoula Klement, J. Tyson McDonald, Ingolf A. Tuerk, Douglas Schneider, Aleksandr Perepletchikov, Christine Briggs, Michael J. Peluso, Lynn Hlatky, Heather Szelag
Publikováno v:
International journal of radiation biology. 90(3)
Despite concerns over risks from exposure to low-dose ionizing radiations encountered in the environment and workplace, the molecular consequences of these exposures, particularly at representative doses and dose-rates, remains poorly understood.Usin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d369856be877db9e2cc842288502351
https://pubmed.ncbi.nlm.nih.gov/24397407
https://pubmed.ncbi.nlm.nih.gov/24397407
Autor:
Hartmut Wohlrab, Amanda Haefele, Erzebet Ligeti, Christine Briggs, Leesa Mincone, Anne Phelps
Publikováno v:
Biochemistry. 40:2080-2086
The mitochondrial phosphate transport protein (PTP) has six (A--F) transmembrane (TM) helices per subunit of functional homodimer with all mutations referring to the subunit of the homodimer. In earlier studies, conservative replacements of several r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18b72311f38bf21768aa294bb247d5cc
https://doi.org/10.1021/bi002206i
https://doi.org/10.1021/bi002206i