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Bruno REVERSADE @reversade
Joined January 2010
  • Tweets 21
  • Following 60
  • Followers 166
2 Photos and videos
Bruno REVERSADE retweeted
Nicolas Rivron@NRivron
15 Feb 2023
Replying to @Carinejoubran @reversade @jacob_hanna @vlad_bndk @Shadi_Tarazi @mycomar @AlejandroAgCa @SShiokhi
😂 Here is my version of it. Good times.
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Bruno REVERSADE retweeted
Nature Genetics@NatureGenet
22 Jul 2022
‼️ PUBLISHED ONLINE @NatureGenet 📰 Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis 🧑🏿‍🤝‍🧑🏻 @reversade and team 👇🏿 <go.nature.com/3z23c4G>

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Bruno REVERSADE retweeted
Reversade Lab@ReversadeLab
10 Mar 2022
Check out our latest preprint! We describe the first human condition from the loss-of-function of the proto-oncogene RAF, that results in a neonatal lethal progeroid syndrome (1/3) medrxiv.org/content/10.1101/…

A Progeroid Syndrome Caused by RAF1 deficiency Underscores the importance of RTK signaling for...

Somatic and germline gain-of-function point mutations in RAF, the first oncogene to be discovered in humans, delineate a group of tumor-prone syndromes known as RASopathies. In this study, we...

medrxiv.org
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Bruno REVERSADE retweeted
Reversade Lab@ReversadeLab
27 May 2021
Loss of C2orf69 defines a fatal #autoinflammatory syndrome in humans and #zebrafish that evokes a glycogen storage-associated mitochondriopathy @AJHGNews Incredible collaboration between @fred_bard @MathuruLab @Holab_DukeNUS @MaurerStroh #mitochondria authors.elsevier.com/c/1d7lb…

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Bruno REVERSADE retweeted
De Sandre-Giovannoli Annachiara@DeGiovannoli
16 Sep 2020
Heureuse d’annoncer la parution de notre dernier article décrivant l’identification du gène responsable d’une nouvelle maladie rare, le syndrome “MADaM” (Dysplasie Acromandibulaire associée à MTX2”) dans Nature Communications. nature.com/articles/s41467-0…
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Bruno REVERSADE retweeted
Reversade Lab@ReversadeLab
15 Sep 2020
Loss of MTX2, a #mitochondria protein, causes mandibuloacral dysplasia, a #laminopathy - like #progeroid disorder. Our work links mitochondrial dysfunction to altered #nuclear morphology. #RareDisease #aging @NatureComms nature.com/articles/s41467-0…

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Bruno REVERSADE retweeted
Reversade Lab@ReversadeLab
25 Aug 2020
We studied fetuses with neural tube closure defects and identified a role of NUAK2, an essential #kinase, in #Hippo signaling. Modeled in patient derived cells and #organoid. Congrats Carine! #RareDisease #anacephaly #neuroscience #cytoskeleton
Journal of Experimental Medicine@JExpMed
25 Aug 2020
Bonnard, Reversade @ReversadeLab @Astarhq et al. report that NUAK2, operating on the Hippo signaling axis, is an essential kinase that regulates cytoskeletal processes that govern cell shape during neural tube closure. bit.ly/3jcE81h
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Bruno REVERSADE retweeted
Samantha Morris@morris_lab
23 Jun 2020
I invest a lot of energy trying to recruit postdocs to my lab. I haven't received a SINGLE non-immigrant postdoc application in the past five years
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Sience (fiction): frogs with extra limbs x.com/ReversadeLab/status/99…

Reversade Lab@ReversadeLab
24 May 2018
Paper in print version of @nature today. Controlling #limb numbers. This #Xenopus has rnf43/znrf3 mutation on the right (#polymelia) and rspo2 mutation on the left (#amelia). #wnt #devbio @the_Node nature.com/articles/s41586-0…
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ELABELA deficiency promotes preeclampsia and cardiovascular malformations in mice science.sciencemag.org/conte…
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#TheNoseGene: the Team @ReversadeLab discovers mutations in #SMCHD1 causing absent nose at birth #Arhinia.
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Bruno REVERSADE retweeted
AAAS@aaas
15 Dec 2016
This polo star won a prestigious match with help from six cloned horses. @sciencecohen of @ScienceMagazine explains. bit.ly/2gLptgi
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ELABELA Is an Endogenous Growth Factor that Sustains hESC Self-Renewal via the PI3K/AKT Pathway: Cell Stem Cell cell.com/cell-stem-cell/abst…
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