Sökning: WFRF:(Jauhiainen Suvi) > (2020) > Mapping endothelial...
Fältnamn | Indikatorer | Metadata |
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000 | 03950naa a2200457 4500 | |
001 | oai:DiVA.org:uu-426315 | |
003 | SwePub | |
008 | 201130s2020 | |||||||||||000 ||eng| | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4263152 URI |
024 | 7 | a https://doi.org/10.7554/eLife.614132 DOI |
040 | a (SwePub)uu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Orsenigo, Fabriziou FIRC Inst Mol Oncol Fdn IFOM, Vasc Biol Unit, Milan, Italy.4 aut |
245 | 1 0 | a Mapping endothelial-cell diversity in cerebral cavernous malformations at single-cell resolution |
264 | 1 | b eLife Sciences Publications, Ltd,c 2020 |
338 | a electronic2 rdacarrier | |
520 | a Cerebral cavernous malformation (CCM) is a rare neurovascular disease that is characterized by enlarged and irregular blood vessels that often lead to cerebral hemorrhage. Loss-of-function mutations to any of three genes results in CCM lesion formation; namely, KRIT1, CCM2, and PDCD10 (CCM3). Here, we report for the first time in-depth single-cell RNA sequencing, combined with spatial transcriptomics and immunohistochemistry, to comprehensively characterize subclasses of brain endothelial cells (ECs) under both normal conditions and after deletion of Pdcd10 (Ccm3) in a mouse model of CCM. Integrated single-cell analysis identifies arterial ECs as refractory to CCM transformation. Conversely, a subset of angiogenic venous capillary ECs and respective resident endothelial progenitors appear to be at the origin of CCM lesions. These data are relevant for the understanding of the plasticity of the brain vascular system and provide novel insights into the molecular basis of CCM disease at the single cell level. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Cell- och molekylärbiologi0 (SwePub)301082 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Cell and Molecular Biology0 (SwePub)301082 hsv//eng |
700 | 1 | a Conze, Lei Liuu Uppsala universitet,Vaskulärbiologi4 aut0 (Swepub:uu)leliu102 |
700 | 1 | a Jauhiainen, Suviu Uppsala universitet,Vaskulärbiologi4 aut0 (Swepub:uu)suvja782 |
700 | 1 | a Corada, Monicau FIRC Inst Mol Oncol Fdn IFOM, Vasc Biol Unit, Milan, Italy.4 aut |
700 | 1 | a Lazzaroni, Francescau FIRC Inst Mol Oncol Fdn IFOM, Vasc Biol Unit, Milan, Italy.4 aut |
700 | 1 | a Malinverno, Matteou FIRC Inst Mol Oncol Fdn IFOM, Vasc Biol Unit, Milan, Italy.4 aut |
700 | 1 | a Sundell, Veronicau Uppsala universitet,Institutionen för immunologi, genetik och patologi4 aut |
700 | 1 | a Cunha, Sara Isabelu Uppsala universitet,Institutionen för immunologi, genetik och patologi4 aut |
700 | 1 | a Brännstrom, Johanu Uppsala universitet,Institutionen för immunologi, genetik och patologi4 aut |
700 | 1 | a Globisch, Maria A.u Uppsala universitet,Vaskulärbiologi4 aut0 (Swepub:uu)margl506 |
700 | 1 | a Maderna, Claudiou FIRC Inst Mol Oncol Fdn IFOM, Vasc Biol Unit, Milan, Italy.4 aut |
700 | 1 | a Lampugnani, Maria Graziau FIRC Inst Mol Oncol Fdn IFOM, Vasc Biol Unit, Milan, Italy.;Mario Negri Inst Pharmacol Res, Milan, Italy.4 aut |
700 | 1 | a Magnusson, Peetrau Uppsala universitet,Vaskulärbiologi4 aut0 (Swepub:uu)petrmagn |
700 | 1 | a Dejana, Elisabettau Uppsala universitet,Vaskulärbiologi,FIRC Inst Mol Oncol Fdn IFOM, Vasc Biol Unit, Milan, Italy.4 aut0 (Swepub:uu)elide443 |
710 | 2 | a FIRC Inst Mol Oncol Fdn IFOM, Vasc Biol Unit, Milan, Italy.b Vaskulärbiologi4 org |
773 | 0 | t eLIFEd : eLife Sciences Publications, Ltdg 9q 9x 2050-084X |
856 | 4 | u https://doi.org/10.7554/eLife.61413y Fulltext |
856 | 4 | u https://uu.diva-portal.org/smash/get/diva2:1504639/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-426315 |
856 | 4 8 | u https://doi.org/10.7554/eLife.61413 |
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