
Gabriel Loeb
@LoebLab
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Seeking molecular mediators of kidney disease through human genetics, genomics, and novel experimental models. @UCSF, @UCSFNephrology
Joined August 2022
Thank you @ASNKidney! Our lab is very grateful to receive the 2025 Carl W. Gottschalk Research Scholar Grant. Read more about the work here:
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RT @KSusztak: #Whyscience Day51🧠✨A strong finish to our Renal Grand rounds series by a rising star physician scientists @LoebLab @UCSFNe….
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Exciting paper by @CanaudLab in @jclinicalinvest-- 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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RT @MazeInBiotech: We are pleased to announce that the first participant has been dosed in our Phase 1 clinical trial evaluating MZE782. MZ….
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RT @doctorveera: Great paper that dissects the genetics of kidney function by combining GWAS results with data from single cell ATAC sequen….
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RT @UCSFNephrology: Very important new study out today by Gabe Loeb, MD, PhD, Assistant Prof : 56% of kidney function heritability localize….
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RT @ReiterLab: Please read and critique our new paper on the genetic determinants of human kidney function @NatureGenet:..
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A missense variant in a high risk APOL1 allele ameliorates risk of kidney disease in humans and also blocks channel function, solid human genetic evidence that channel activity —>pathogenesis. Amazing from @ahungkidney and @MazeInBiotech at #KIDNEYWEEK2022.
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RT @ecorneclegall: Nephrogenetic session #KidneyWk Prof Jan Halbritter from @ChariteBerlin advocates for recognizing CKD unknown (or not ye….
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