Gladstone M M - OmicsDI

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Unknown (959)
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Lab affiliation

Quantitative Biosciences Institute (QBI), University of California, San Francisco, San Francisco, CA USA J. David Gladstone Institutes, San Francisco, San Francisco, CA, USA Department of Bionengineer and Therapeutic Sciences, University of California, San Francisco, San Francisco, CA, USA (2)
Cellular and Molecular Pharmacology, Quantitative Biosciences Institute, Gladstone Institutes, University of California San Francisco, CA, USA (1)
Department of Medicine (GI Oncology), UCSF, United States (1)
Dept. Cellular Molecular Pharmacology, University of California - San Francisco (UCSF), USA (1)
Gladstone Institure for Immunology; The J David Gladstone Institutes; San Francisco, CA, USA (1)
Gladstone Institute of Neurological Disease, San Francisco, CA, USA; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA; Bakar Aging Research Institute, University of California, San Francisco, San Francisco, CA, USA. (1)
Gladstone Institutes (1)
Gladstone Institutes, San Francisco, CA, USA Quantitative Biosciences Institute (QBI), University of California, San Francisco, San Francisco, CA, USA Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, CA, USA (1)
Medicine, University of California San Francisco (1)
QBI COVID-19 Research Group (QCRG), San Francisco, CA, USA Quantitative Biosciences Institute (QBI), University of California San Francisco, San Francisco, CA, USA J. David Gladstone Institutes, San Francisco, CA, USA Department of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, CA, USA Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA (1)
Quantitative Biosciences Institute (QBI), J. David Gladstone Institutes, Department of Cellular and Molecular Pharmacology, University of California, San Francisco (1)
Quantitative Biosciences Institute (QBI), San Francisco, CA, USA; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, CA, USA;Gladstone Institute of Data Science and Biotechnology, J. David Gladstone Institutes, San Francisco, CA, USA (1)
Quantitative Biosciences Institute (QBI), University of California San Francisco, San Francisco, CA, USA Department of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, CA, USA The J. David Gladstone Institutes, San Francisco, CA, USA. (1)
Quantitative Biosciences Institute (QBI), University of California, San Francisco, CA 94158, USA. Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, CA 94158, USA. Department of Cellular and Molecular Pharmacology, University of California, San Francisco, CA 94158, USA. Gladstone Institute of Data Science and Biotechnology, J. David Gladstone Institutes, San Francisco, CA 94158, USA. (1)

Tags

xref:PubMed:31641121 (1)
xref:PubMed:33723017 (1)
xref:PubMed:32935097 (1)
xref:PubMed:29502971 (1)
xref:PubMed:17785846 (1)
xref:EuropePMC:PMC13085270 (1)

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Torsional twist of the SARS-CoV and SARS-CoV-2 SUD-N and SUD-M domains.

Not available

S-EPMC11837046 | biostudies-literature

Transcriptional Activity in Lymph Nodes During the Initiation and Progression of Autoimmune Encephalomyelitis

NOD mice (8- to 13-wk-old) were bred and maintained at the La Trobe University Central Animal House (Bundoora, Melbourne, Australia). All experiments were conducted in accordance with the Australian code of practice for the care and use of animals for scientific purposes (National Health and Medical...

ORGANISM(S): Mus musculus

2008-04-03 | E-GEOD-7461 | biostudies-arrayexpress

Gene expression of colon from control or VilCre;Ihhflox/flox mice

Ihh expression is required for intestinal stem cell niche development. Loss of Ihh leads to disruption of intestinal stem cell niche, which leads to abnormal stem cell development and epithelial cell differentiation. 3 paired control (C) and mutant (M) mice here harvested. Their colon tissues were a...

ORGANISM(S): Mus musculus

2010-06-16 | E-GEOD-18393 | biostudies-arrayexpress

A mosaic tetracycline resistance gene tet(S/M) detected in an MDR pneumococcal CC230 lineage that underwent capsular switching in South Africa.

Not available

S-EPMC7021099 | biostudies-literature

Quantitative Yeast Genetic Interaction Profiling of Bacterial Effector Proteins Uncovers a Role for the Human Retromer in Salmonella Infection.

Not available

S-EPMC6160342 | biostudies-literature

Discovery of Coronavirus Main Protease Inhibitors with Enhanced Brain Exposure and Potent Oral Efficacy in SARS-CoV-2 and MERS Infection Models.

Not available

S-EPMC12834036 | biostudies-literature

Structure-based discovery of highly bioavailable, covalent, broad-spectrum coronavirus M<sup>Pro</sup> inhibitors with potent in vivo efficacy.

Not available

S-EPMC12017303 | biostudies-literature

Expression data from H358

Tumors that show evidence of epithelial to mesenchymal transition (EMT) have been associated with metastasis, drug resistance, and poor prognosis. EMT may alter the molecular requirements for growth and survival in different contexts, but the underlying mechanisms remain incomplete. Given the hete...

ORGANISM(S): Homo sapiens

2014-01-01 | E-GEOD-52308 | biostudies-arrayexpress

Expression data from from hTR and hTERT knockdown in human CD4 T cells

We have found that knockdown of the human telomerase RNA template, hTR, induces Bim-mediated apoptosis independent of telomere length in primary human CD4 T cells, whereas knockdown of the telomerase enzymatic protein, hTERT does not induce apoptosis in the timeframe of our studies. We used microarr...

ORGANISM(S): Homo sapiens

2014-08-28 | E-GEOD-60855 | biostudies-arrayexpress

Vitamin C induces Tet-dependent DNA demethylation in ES cells to promote a blastocyst-like methylome [Affymetrix]

DNA methylation is a heritable epigenetic modification involved in gene silencing, imprinting, and the suppression of retrotransposons. Global DNA demethylation occurs in the early embryo and the germline and may be mediated by Tet (ten-eleven-translocation) enzymes, which convert 5-methylcytosine (...

ORGANISM(S): Mus musculus

2013-06-30 | E-GEOD-46319 | biostudies-arrayexpress

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