daniel_reichart
@danielreichart3
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Cardiology LMU Munich | Postdoc@Seidman Lab | Harvard Medical School | scRNAseq
Joined December 2019
Excited to see our new story.@ScienceMagazine! 881,081 nuclei from.healthy and diseased hearts were deeply.characterized with insights into shared and.distinct signatures across genotypes!.Amazing team work, @ericl_lindberg.@HenrikeMaatz @HMSGenetics
science.org
A single-cell atlas of the heart identifies cellular interactions and pathways involved in two types of cardiomyopathy.
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RT @zhh_ch: Day 2 #PCHFLondon2024 @zhh_ch @TomLuscher @eleanorwicks @RuthAmstein @johncleland Treatment (old & the new). @WilfredMullens #d….
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Fünf für München: Provinz, Pumpenforschung, Poetry-Slam.via @sz
sueddeutsche.de
Brandon Miller hat beim Bundeswettbewerb für Musical gewonnen, Anna Aichers Fotoband wurde ausgezeichnet.
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RT @NatureBiotech: From AI to the Y chromosome (and everything in between) .Our editors pick their favorite research articles from 2023 htt….
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RT @GeneCenter_LMU: 🎇🥳Happy to share that Daniel Reichart has been awarded with a funding of two million euros by the German Research Foun….
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RT @LMU_Muenchen: Congrats! The German Research Foundation @dfg_public is awarding four LMU researchers through the Emmy Noether and Heisen….
lmu.de
The funded projects deal with new biomarkers of ageing, quantum simulations, the journey of immune cells through the body and media usage strategies.
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RT @davidrliu: Today we report in @NatureBiotech the development of dual-AAV in vivo delivery systems for prime editors that can support ef….
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RT @davidrliu: Today we report in @NatureMedicine a study led by Christine & Jonathan Seidman’s lab in which we used adenine base editing i….
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RT @EricTopol: Exciting to see genome editing of hypertrophic cardiomyopathy to correct the pathogenic variant in the humanized mouse model….
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RT @EricTopol: A 2nd @NatureMedicine report today showing prevention of hypertrophic cardiomyopathy in mice via genome editing, reinforcing….
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RT @Transactivator: Happy to share our latest paper on a broad new application of CRISPR for treatment of heart disease. Ablation of CaMKI….
science.org
Removing oxidative activation sites in CaMKIIδ by base editing sustains heart function after ischemia-reperfusion injury.
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RT @GOuditResearch: Harvard’s Dr. Christine E. Seidman to Receive the 2022 Research Achievement Award, the Association’s Highest Honor http….
newsroom.heart.org
Embargoed until 7 a.m. CT / 8 a.m. ET Wednesday, Oct. 26, 2022 DALLAS, Oct. 26, 2022 – The American Heart Association is presenting its 2022 Research Achievement Award to Christine E. Seidman, M.D.,...
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RT @dquiat: Excited to share results from a collaboration with @md_timberlake and many others to study genetic basis of craniofacial micros….
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RT @Ele_Adami: Just sharing this again, because I heart it and because today it's #WorldHeartDay 💗🫀. #SciArt
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RT @grunewaju: Boston RT party!🧬So excited about our #CRISPR prime editing work, out @NatureBiotech today – great @JoungLab team work w/ Br….
nature.com
Nature Biotechnology - A split prime editor architecture facilitates screening and engineering of improved variants.
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RT @grunewaju: Extremely excited to kickstart my lab @TU_Muenchen with Emmy Noether support from @dfg_public. I’m very grateful to @JKeithJ….
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RT @stemcellpodcast: On this week's episode: an atlas for #HeartFailure 🗺️ 🫀. @DanielReichart3, @EricL_Lindberg, Henrike Maatz, & their col….
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RT @LaskerFDN: #snRNAseq of ventricles from heart failure patients reveals distinct transcriptional states in #cardiomyopathy. Eg, #fibrobl….
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RT @ericl_lindberg: The data of our recent heart failure snRNAseq study (@danielreichart3, @HubnerLab, @MDC_Berlin) are now online. You can….
cellxgene.cziscience.com
Find, download, and visually explore curated and standardized single cell datasets.
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RT @EricTopol: Laying the groundwork for individualized, molecular basis interventions for some people w/cardiomyopathy and heart failure,….
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RT @GOuditResearch: Researchers pinpoint genetic defects that cause heart failure, pointing the way to more targeted treatments Folio http….
ualberta.ca
An international research team has identified individual genetic defects that cause heart failure, opening the door to more targeted diagnoses, preventive measures and treatments.
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