Закреплённый твит
Gabriel Loeb
35 posts

Gabriel Loeb
@LoebLab
Seeking molecular mediators of kidney disease through human genetics, genomics, and novel experimental models. @UCSF, @UCSFNephrology
Присоединился Ağustos 2022
64 Подписки56 Подписчики

We are constantly thinking about how to integrate human genetics and better experimental models to identify the mechanisms of human disease @UCSFNephrology, @IHG_at_UCSF, @UCSFDOM . Funding for the next generation of medicine from @NIH.
Critiques and feedback welcome!
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Gabriel Loeb ретвитнул

What an awesome session on common variant CKD genetics @ASNKidney #KidneyWk @kidneyomicsamps @LoebLab @LimdiNita

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Gabriel Loeb ретвитнул
Gabriel Loeb ретвитнул

Incredible session on Genetics in Kidney Disease #KidneyWeek @ASNKidney
Outstanding organization & insightful talks by @Vishal_D_Patel #DanielGale #AliGharavi #GabrielLoeb
Grateful for the opportunity to present on Genetics of TMA🙏
Thx #ArleneChapman & #EmilieCornecLeGall
Sol Carriazo, Neph.@Nefrontera
🧬Very nice talk about genetics of TMA by @anuja_java at #KidneyWk 👉🏽 Interplay between genetics and triggers 👉🏽Who should we test?
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Thank you @ASNKidney! Our lab is very grateful to receive the 2025 Carl W. Gottschalk Research Scholar Grant. Read more about the work here: kidneycure.org/pages/qa.aspx?….
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@KSusztak @UCSFNephrology Grateful for the chance to learn from @ksusztak, @parkercwilson, and others @Penn and @PennKidney. So much science to be excited about.
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Gabriel Loeb ретвитнул

#Whyscience Day51🧠✨A strong finish to our Renal Grand rounds series by a rising star physician scientists @LoebLab @UCSFNephrology Pushing the frontiers of kidney genomics and single cell omics. The future of nephrology is bright🔆

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Exciting paper by @CanaudLab in @jclinicalinvest--doi.org/10.1172/JCI176…. 1) Somatic mutation as a (presumably) very rare cause of FSGS, 2) Targeting the mutated gene PIK3CA is helpful in multiple mouse FSGS models, 3) Activity of podocyte targeted therapy in mouse FSGS.
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@MazeInBiotech Very excited to see genetics loci translated into potential kidney therapeutics. SLC6A19 was one of the 138 kidney function genes we nominate in this @NatureGenet paper: rdcu.be/dTwye. How many others would make good targets?
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We are pleased to announce that the first participant has been dosed in our Phase 1 clinical trial evaluating MZE782. MZE782 is a potentially first-in-class, oral, small molecule targeting the solute transporter, SLC6A19, and has the potential to address chronic #kidneydisease (CKD) patients. Learn more about the MZE782 program here: businesswire.com/news/home/2024…

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