Dr Isabel Lopez Sanchez

Research Manager at Mito Foundation and mitochondrial scientist

[Dr Isabel Lopez Sanchez @DrIsabelLopez]

@MolMet_KI @jelenaamisic @mitopinionated @Carlos_T_Moraes @TheKailaLab Congratulations!!!

[Dr Isabel Lopez Sanchez @DrIsabelLopez]

@janellison @MitoPsychoBio @BaszuckiGroup Congratulations!

[Jelle van den Ameele @Jellevda]

📢We're hiring! Not one but FOUR roles in the @cam_mito team! All on one page now: https://t.co/4qEvMho8Wf Join us to do world-leading #singlecell🔬, #Bioinformatics📊or #clinicaltrials💊research on #MITO disease & #RareDisease, with @MRCMouseNetwork @wellcometrust @RosetreesT

[Dr Isabel Lopez Sanchez @DrIsabelLopez]

Join a dedicated team of genetic eye disease researchers in Melbourne!

[A/Prof Lauren Ayton @DrLaurenAyton]

We are hiring! Looking for a research nurse / study coordinator to join our team, to work with us on exciting genetic testing programs in inherited retinal disease. Read more here: https://t.co/1TKLaM9isc

[Centre for Eye Research Australia @EyeResearchAus]

Donated eye tissue plays a vital role in research to develop new treatments for glaucoma, inherited retinal disease and other sight disorders.

Thanks to your support, our researchers have better access to donated eye tissue through the purchase of a new tissue retrieval kit.

[ReMexER @ReMexER1]

Estamos a sólo 30 días de celebrar el Día Mundial de las Enfermedades Raras y el 4to Simposio Internacional del Día de las Enfermedades Raras #SIDERmx2024 para concientizar e informar sobre estas condiciones y los millones que viven con ellas en México, Latinoamérica y el Mundo👇

[Dr Isabel Lopez Sanchez @DrIsabelLopez]

@TheStrugglingS4 Surviving on an international student PhD scholarship - which was one third of the value of a local student scholarship

[CamRARE (Cambridge Rare Disease Network) @camraredisease]

For #RareDiseaseDay 29 Feb join this #research webinar. Our MD Jo & the @plrh_cambridge are talking about our @NIHRcommunity funded project to build a #RareDiseaseResearchNetwork platform to share patient led ideas, knowledge & to build partnerships

🎟️https://t.co/q9ee3EgVrw

[Dr. Amy Vincent (She/Her) [email protected] @AmyV91]

Interested in mitochondria, muscle and innovative imaging techniques? Want to do a PhD? We are looking for a motivated person to take up a PhD position with @UniofNewcastle with @mitomusclelab @bioImaging_NCL and @EMRSncl. Apply here https://t.co/AVrJjhbjVu @nuact_NCL DM for info

[CamRARE (Cambridge Rare Disease Network) @camraredisease]

Are you a #RareDisease researcher or an artist with an interest in science? Do you live within reach of #Cambridge or #London? Closing date 10 Jan to take part in a new ART-TRAnslations project with @lifearc1. Exhibit your work at their Translational Science Summit & RAREfest24

[Murdoch Children's Research Institute (MCRI) @MCRI_for_kids]

More great #grants news, with three #MCRI researchers awarded Strategic Grants for Outstanding Women (SGOW) by @UniMelb. Congrats to Dr Nicole Van Bergen, A/Prof Belinda McClaren & @JMVanslambrouck | @UniMelbMDHS #research #women #WomenInSTEM
More ➡️https://t.co/xtZya7ydR1

[Mito Foundation @AusMito]

Applications are now open for the Mito Foundation Booster Grant!

https://t.co/vNHecQFRAY

Due: 12 Jan '24

These Grants offer an exciting opportunity for researchers whose Ideas Grant application was deemed of high quality by the @NHMRC but was unsuccessful in securing funding.

[Centre for Eye Research Australia @EyeResearchAus]

We've joined @FightBlindness Consortium so rare genetic diseases get the same attention as more common conditions. A/Prof @DrLaurenAyton & the VENTURE team will pool research with other centres to improve results & bring in new clinical trials https://t.co/ofC2k5rzCJ @UniMelbMDHS

[Dr Isabel Lopez Sanchez @DrIsabelLopez]

Mito Foundation Awards celebrate outstanding contributions by people who've had a significant impact on the mito community.

See our award winners here: https://t.co/FPNwRMX3r4

@MitoAware #WorldMitoWeek #MitochondrialDisease #mito

[Mito Foundation @AusMito]

We are beyond excited to share our Mito Foundation Award winners!

Join us in celebrating these extraordinary people who've had a significant impact on the mito community.

See our award winners here: https://t.co/W42y8GpHbV

@MitoAware #WorldMitoWeek #MitochondrialDisease #mito

[Dr Isabel Lopez Sanchez @DrIsabelLopez]

@CPC_usyd @adiazvegas @SydneySOLES @Sydney_Science @davidjamesoz @eLife @eatlikeanimals @Sydney_Uni Congratulations Alexis!
@AusMito

[Mito Research @MitoResearch]

We're also pleased to share news from Dr Stroud (@thestroudlab).
He's developed a new diagnostic technique using quantitative proteomics. It has the potential to drastically improve mito diagnostic rates. Learn more: https://t.co/4rOPDRIscs
*MF #WMDW #MitoFoundation

[Mito Foundation @AusMito]

Celebrating our 100th grant for mito! 🎉We’ve committed over $8m towards funding research grants since 2010.

Find out more on our website https://t.co/RLbtehRgs0

#mito #mitochondrial #research #grants

[Mito Foundation @AusMito]

Research highlight 🔎 Identifying a genetic hotspot, the ATAD3 cluster, responsible for one of the most common causes of paediatric mito
@ae_frazier @MCRI_for_kids

[Mito Foundation @AusMito]

Research highlight 🔎 A confirmed genetic diagnosis for 160 people through clinical and research studies supported by Mito Foundation, including the Mito Flagship Project
@AusGenomics

[Mito Foundation @AusMito]

Research highlight 🔎Supporting the development of person-friendly clinical measures, including digital video assessments and computer-based cognitive assessments