#geneticmodifier - Twitter Hashtag

about 2 years ago

@TarunMamidi7 We are also making use of @TarunMamidi7's #DITTO approach for other #RareDisease, #UndiagnosedDisease, or #GeneticModifier projects e.g. #MECFS #CysticFibrosis #PraderWilliSyndrome #PediatricThyroidCancer #Ciliopathies and in our @uabmedicine #CPAM for #PrecisionAnimalModeling :D

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Genetics in Medicine @GIMJournal

almost 4 years ago

A rare example of a #geneticmodifier! Read Parodi et al’s recent work on overexpression of mitochondrial SARS2 as a #geneticmodifier of spastic paraplegia type 4 to learn more #HSP #SPG4 https://t.co/pNVsQ3BHMD

GIMJournal's tweet photo. A rare example of a #geneticmodifier! Read Parodi et al’s recent work on overexpression of mitochondrial SARS2 as a #geneticmodifier of spastic paraplegia type 4 to learn more #HSP #SPG4 https://t.co/pNVsQ3BHMD https://t.co/80bfouameA

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Kevin T Booth @KevinTBooth

over 4 years ago

Data presented by Monique Weaver from @MORL_UIowa suggests that there is a #geneticmodifier for TECTA-related #deafness and that the modifier might be COL6A5. #ARO2022 @AROMWM @UIowaGenetics @RJHS1953 @IowaOto

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Markus Riessland @RiesslandLab

over 7 years ago

Thanks again to the whole lab for making it possible. Great story! #sma #genetics #geneticmodifier https://t.co/anH0xHe33x https://t.co/7fbiOYYvUd

Brunhilde Wirth @BrunhildeWirth

over 7 years ago

The Cologne Medical Faculty Award for the best publication 2017 goes to Markus, Anna and Svenja from @BrunhildeWirth at Institute of Human Genetics @UKKoeln for the identification of a novel SMA protective gene, NCALD @CureSMA @SMAEurope @SMANewsToday

BrunhildeWirth's tweet photo. The Cologne Medical Faculty Award for the best publication 2017 goes to Markus, Anna and Svenja from @BrunhildeWirth at Institute of Human Genetics @UKKoeln for the identification of a novel SMA protective gene, NCALD @CureSMA @SMAEurope @SMANewsToday https://t.co/K5EbRm47FN

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Yalda Jamshidi @YaldaJamshidi

about 8 years ago

Nice talk from @tuuliel showing combination of #raredisease #genetics and regulatory variants as #geneticmodifier #eshg2018 https://t.co/e6VpNlUhul

Edoardo Giacopuzzi @Supergecko

about 8 years ago

TL: Regulatory variants contribute to incomplete penetrance of human traits by tuning expression of WT and mutant disease gene alleles https://t.co/6DphJjIRoe #eshg2018

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UCL Huntington’s Disease Centre @UCLHD

about 9 years ago

Researchers can now try to target this #geneticmodifier of #Huntingtonsdisease to develop new therapies to slow HD progression @UCLHD (8)

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Richard Wang @RichardTWang

about 10 years ago

@DuchenneConnect Seeking DNA from duchenne boys and men. https://t.co/hDJ3V0TXvZ or PM me at @RichardTWang #geneticmodifier #ppmdconnect

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