@CherquiLab

Lab of Dr. Stephanie Cherqui @UCSDHealth. Developing stem cell and gene therapy strategies for degenerative multi-systemic disorders.

 La Jolla, California
medschool.ucsd.edu/som/pediatrics/research/labs/cherqui/Pages/default.aspx
Joined October 2022
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  • Followers46
5Media
@CIRMnews is a proud sponsor of the Gene Therapy Initiative Symposium at @UCSDHealth, which bring together researchers and industry experts to share scientific discoveries and boost collaboration to advance cell and gene therapy treatments for patients everywhere. #gtiUCSD
A large group of people in an auditorium watch two speakers at a podium

ALT A large group of people in an auditorium watch two speakers at a podium

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Check out this report from @CherquiLab et al. "Rescue of Alzheimer's disease phenotype in a mouse model by transplantation of wild-type hematopoietic stem and progenitor cells", published in @CellReports #ASGCT2024 hubs.li/Q02wFqBN0
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Come checkout our Postdoc Veenita’s poster on Renal Fanconi Sundrome in Cystinosis @WORLDSymposia
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Excited to kick off @WORLDSymposia lysosomal disease conference this year by attending an important @CureSanfilippoF meeting on leveraging data to advance Sanfilippo therapeutic development! #lysosomes #genetherapy #hspc #sanfilippo #mps @UCSDHealth @MPSSociety
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We are thrilled for our project scientist Anusha to be 1 of 10 researchers receiving a $20,000 grant from @UpliftingAth! This grant will aid her research and support the 1 in 10 Americans diagnosed with a #RareDisease. upliftingathletes.org/2024/0…

Uplifting Athletes Crosses 1 Million Dollar Threshold with 2024 Young Investigator Draft Grants

Uplifting Athletes' 2024 Young Investigator Draft class will each be presented with a $20,000 grant to support their vital work in rare disease research.

upliftingathletes.org
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Excited to be at the @MPSSociety 37th Annual Family Conference to present some of my work at @CherquiLab on gene modified HSPC for MPSIIIC! @UCSDHealth #GeneTherapy #StemCells
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Backed by a $5M gift from Nancy & Geoffrey Stack Foundation, @UCSanDiego officially launches the Gene Therapy Initiative 🧬. Led by Drs. Cherqui & Muotri, the initiative will fuel research🔬+ gene therapies💉to benefit patients with #Genetics disorders today.ucsd.edu/story/uc-san-…

UC San Diego Launches Gene Therapy Initiative, Targeting Treatments for Rare Diseases

A $5 million gift from the Nancy and Geoffrey Stack Foundation has established the UC San Diego Gene Therapy Initiative to find novel therapies for children and adults with genetic diseases.

today.ucsd.edu
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Out now in @CellReports, Dr. Stephanie Cherqui's (@Cherqui_S) lab shows hematopoietic #StemCell transplants can protect against memory loss, neuroinflammation and β-amyloid build-up in a mouse model of #AlzheimersDisease 🧠 today.ucsd.edu/story/stem-ce…

Stem Cell Therapy Rescues Symptoms of Alzheimer’s Disease

Promising preclinical results from UC San Diego show hematopoietic stem cell therapy was effective in rescuing memory loss, neuroinflammation and beta amyloid build-up in a mouse model of Alzheimer’s...

today.ucsd.edu
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EXCITING STUDY! In new proof-of-concept study, Priyanka Mishra, Stephanie Cherqui et al. show #StemCell transplants may also be promising therapeutic against #AlzheimersDisease. @CherquiLab @ucsdstemcell @ljiresearch @CellReports doi.org/10.1016/j.celrep.202… today.ucsd.edu/story/stem-ce…
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Honoured to have been awarded one of the @ASGCTherapy 2023 outstanding poster award for my abstract on my work in the @CherquiLab @UCSDHealth on Hematopoeitic #stemcell #genetherapy for MPSIIIC funded by @MPSSociety & @CureSanfilippoF
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Great week for the Cherqui lab ⁦@ASGCTherapy⁩ presenting our latest work! #stemcell #genetherapy ⁦@UCSDHealth⁩ linkedin.com/posts/stephanie…

It has been an exciting week for my lab at the 26th American Society of Gene & Cell Therapy...

It has been an exciting week for my lab at the 26th American Society of Gene & Cell Therapy conference, I was happy to share positive data from the phase 1/2 clinical trial for hematopoietic stem...

linkedin.com
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Happy to be back presenting a poster at the @ASGCTherapy annual meeting on my work at @CherquiLab on #stemcell #GeneTherapy for Sanfilippo C funded by @MPSSociety & @CureSanfilippoF. Poster No. 649
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Cherqui Lab retweeted
Synthego@Synthego22 Mar 2023
🎧 NEW PODCAST 🎧 Professor @Cherqui_S is a pioneer in the field of #CRISPR cell and gene therapies. She speaks about her work on curing genetic diseases such as Friedreich's ataxia, obstacles in clinical development, and the future of CRISPR therapies 👉 hubs.li/Q01HM8kb0
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Thank you @rafaelabadell for representing our lab at @WORLDSymposia 2023. Also, a special acknowledgement goes out to @MPSSociety and @CureSanfilippoF for your fellowship supports!
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I am very happy and grateful to have received the fellowship award from the @CureSanfilippoF to continue my work investigating the use of #stemcell #genetherapy to treat Sanfilippo type C in the @CherquiLab @UCSDHealth
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Excited to share the FAID reel of 2022! It's a delightful visual summary of our recent conference. Our team has worked hard to make this event happen, and we couldn't be more proud of what we have achieved so far. #ClinicalTrials #GeneTherapy france-science.com/en/france…
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Congratulations to all of the recipients, including @AquilanoKatia, @Cherqui_S, and @USFHealth Together, we will #SlowStopReverse and #CureFA
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Professor Stephanie Cherqui of @UCSDMedSchool speaks to us about a prestigious grant from the California Institute for Regenerative Medicine, which will allow her team to bring a new CRISPR therapy for Friedreich’s ataxia to the clinic. Read more here: bit.ly/3WxA2nV
Stephanie Cherqui Ph.D is an Associate Professor in the Department of Paediatrics, Division of Genetics at the University of California San Diego. Her team is developing therapeutic strategies based on gene-edited haematopoietic stem and progenitor cell transplantation to treat Friedreich’s ataxia and other multi-systemic degenerative disorders. Photo courtesy of Stephanie Cherqui

ALT Stephanie Cherqui Ph.D is an Associate Professor in the Department of Paediatrics, Division of Genetics at the University of California San Diego. Her team is developing therapeutic strategies based on gene-edited haematopoietic stem and progenitor cell transplantation to treat Friedreich’s ataxia and other multi-systemic degenerative disorders. Photo courtesy of Stephanie Cherqui

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Replying to @CIRMnews
@CIRMnews We are grateful for the funding opportunity granted by the California Institute for Regenerative Medicine (CIRM) to develop a treatment for Friedreich’s ataxia (FA) patients using CRISPR/Cas9-mediated gene editing technology, a novel ex vivo gene therapy approach.
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Your support helps greatly in our effort to transition this project from bench to bedside.
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today.ucsd.edu/story/scienti… #CIRM #UCSD #CureFA

Scientists Receive $4.8M to Pursue Gene Therapy for ‘Incurable’ Disease

The California Institute for Regenerative Medicine has awarded UC San Diego researchers $4.8 million to advance a gene therapy to treat Friedreich’s ataxia, a rare but devastating neuromuscular...

today.ucsd.edu
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