Prokisch Lab

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Prokisch Lab

Prokisch Lab

@ProkischLab

OMICs, genetics, mitochondrial diseases and more | tweets by group members

Munich, Germany Bergabung Temmuz 2022
108 Mengikuti235 Pengikut
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Prokisch Lab
Prokisch Lab@ProkischLab·
Hello, #ScienceTwitter! We are scientists from Prokisch Lab in Munich, studying the diagnosis and treatments of genetic disorders, with a special focus on mitochondria. 💪 Tweets are from all lab members. Let's connect 👋
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Vamsi Mootha
Vamsi Mootha@VamsiMootha·
Hypoxia in a pill! Chronic, continuous 11% FIO2 suppresses brain pathology in models of mitochondrial disease and aging, but we need practical alternatives. We combine a Hb "left-shifter" with a HIF2a inhibitor to achieve therapeutic hypoxia in mice. jci.org/articles/view/…
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E-mit
E-mit@Emit38935125·
The GENOMIT Consortium is meeting this days in Barcellona (Spain). Different expertise, different skills, different countries: together to shed light on mitochondrial diseases. #MitoAwareness
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gagneurlab
gagneurlab@gagneurlab·
New concept for variant effect prediction. 'How bad' is the new 'how rare'. With DNA LMs we can ask how important a variant is for predicting other bases. This influence score correlates better with functional assays. This was not possible with alignment-based conservation.
Pedro Tomaz da Silva@pedrotomazsilva

We show that nucleotide dependencies indicate deleteriousness of human genetic variants more effectively than sequence alignment and DNA LM reconstruction. Example: promoter mutagenesis screen from Kircher et al.

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Anne O'Donnell-Luria
Anne O'Donnell-Luria@AnneOtation·
We explored why pathogenic variants are present in the gnomAD database for early-onset, severe, dominant conditions. Explanations identified for most but some likely due to incomplete penetrance though more study needed. 1/3
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Craig Porter
Craig Porter@bioblastgeek·
novel perspective suggesting high sustained energy expenditure may be net protective against cancer | Evolution, Medicine, and Public Health | Oxford Academic academic.oup.com/emph/article/1…
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The Journal of Inherited Metabolic Disease
Interesting new review article discussing how the rise in genomic investigations has placed an increased emphasis on the need for variant validation. Integrative -omics provide a complementary approach to better understand genomic findings. doi.org/10.1002/jimd.1…
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Rahul Gupta
Rahul Gupta@rahulg603·
Mitochondrial DNA mutations can lead to rare disease and accrue with age. But how does nuclear genome variation influence mtDNA variation? Here in >250k people, we find that nuclear variants can impact variation in the levels of mtDNA mutations. (1/5) medrxiv.org/content/10.110…
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Catalina Vasilescu, PhD
Catalina Vasilescu, PhD@_CVasilescu·
Prokisch Lab at beer garden, few weeks ago 🍻
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Prokisch Lab
Prokisch Lab@ProkischLab·
Hello, #ScienceTwitter! We are scientists from Prokisch Lab in Munich, studying the diagnosis and treatments of genetic disorders, with a special focus on mitochondria. 💪 Tweets are from all lab members. Let's connect 👋
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