Adam10 - OmicsDI

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Researcher, Department of Internal Medicine and Clinical Nutrition, Sahlgrenska Academy, University of Gothenburg, Box 424, 405 30 Göteborg, Sweden (1)
Proteomics and Cancer Cell Signaling Unit, German Cancer Research Center, Heidelberg,Germany (1)
1. Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan. 2. Molecular Medicine Research Center, Chang Gung University, Taoyuan 33302, Taiwan. 3. Department of Otolaryngology-Head and Neck Surgery, Chang Gung Memorial Hospital, Linkou 33305, Taiwan. 4. Research Center for Food and Cosmetic Safety, College of Human Ecology, Chang Gung University of Science and Technology, Taoyuan 33302, Taiwan. (1)
Department of Biotechnology and Food Engineering, Technion-Israel Institute of Technology, Haifa 3200003, Israel (1)
Lehrstuhl für Neuroproteomik, Technische Universität München und Neuroproteomik, Deutsches Zentrum für Neurodegenerative Erkrankungen, München (1)
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8Clinical Protein Science & Imaging, Biomedical Centre, Department of Biomedical Engineering, Lund University, Lund, Sweden (1)
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Translational Biomedical Proteomics, Institute of Molecular and Cell Biology, Singapore (1)

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Expression data from Adam10 knock out mice and wild type

Adam10, a cell surface protease, cleaving many proteins including TNF-alpha and E-cadherin. Here we investigate the genome wide effects of Adam10 knock out on the transcriptome. Commercial microarrays (Affymetrix Mouse Gene ST 1.0) were used to generate genome wide mRNA profiles. Mouse tissue sample...

ORGANISM(S): Mus musculus

2011-01-06 | E-GEOD-25480 | biostudies-arrayexpress

Systematic substrate identification reveals a central role for the metalloprotease ADAM10 in axon targeting and synapse function

Metzincin metalloproteases have major roles in intercellular communication by modulating the function of membrane proteins. One of the proteases is the a-disintegrin-and-metalloprotease 10 (ADAM10) which acts as alpha-secretase of the Alzheimer’s disease amyloid precursor protein. ADAM10 is also req...

ORGANISM(S): Mus musculus (Mouse)

2018-10-18 | PXD003426 | Pride

In vitro sheding activity of ADAM10

Investigation of the shading activity of the recombinant catalytic domain of ADAM10

ORGANISM(S): Homo sapiens (Human)

2023-05-17 | PXD040511 | Pride

Adam10 app alzheimer’s disease

Tetraspanin Tspan15 is an essential subunit of an ADAM10 scissor complex

A disintegrin and metalloprotease 10 (ADAM10) is essential for embryonic development and impacts on diseases such as cancer, Alzheimer’s and inflammatory diseases. ADAM10 is a ‘molecular scissor’ that proteolytically cleaves the extracellular region from over 100 substrates, including Notch, amyloi...

ORGANISM(S): Homo sapiens (Human)

2021-08-24 | PXD016508 | Pride

Tspan15 Adam10

Vascular endothelial ADAM10 governs liver homeostasis

The Role of ADAM10 in Liver Endothelial Cells in Regulating Hepatic Homeostasis

PRJEB103973 | ENA

Murine cartilage tissues (tibia): Control vs ADAM10 flox/flox-Col2a1-Cre

PRJNA594619 | ENA

Identification of ADAM10 interactors and N-glycosylation sites in SK-BR-3 cells

Immunoprecipitation of ADAM10-WT and ADAM10-4NQ interacting proteins were identified by mass spectrometry(MS));purified ADAM10 protein was subjected to Coomassie Blue Staining and LC-MS/MS in order to identify the N-glycosylation sites

ORGANISM(S): Homo Sapiens

2022-07-16 | PXD035378 |

Combined proteomics and CRISPR-Cas9 screens in PDX identify ADAM10 as essential for leukemia in vivo

Acute leukemias represent deadly malignancies which require better treatment. As challenge, treatment is counteracted by a microenvironment protecting dormant leukemia stem cells. To identify responsible surface proteins, we performed deep proteome profiling on minute numbers of dormant patient-deri...

ORGANISM(S): Homo sapiens (Human)

2023-07-24 | PXD036223 | Pride

Leukemia stem cell Proteome Adam10 Crispr Leukemia Dia pasef

Effect of ADAM10 depletion in human retinal microvascular endothelial cells (HRMVECs)

PRJNA1029964 | ENA

Targeting cardiomyocyte ADAM10 ectodomain shedding promotes survival early after myocardial infarction

PRJNA898315 | ENA

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