Walter-Csomós Lab
@walterlab1
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We are a passionate and diligent team working in the field of immunology. Come and see how we strive for excellence in research and dabble in fun! #goscience
University of South Florida SP
Joined April 2020
Congratulations to our MD PhD students on their latest publication, Can we identify WHIM in infancy? Walter Lab is very proud of our teams hard work and dedication! 💪🏼👏🏼 https://t.co/Pe1CiiEgN8
#NBS #SCID #PID #PrimaryImmunodeficiency #WHIMSyndrome #Immunology #JMF
onlinelibrary.wiley.com
Newborn screening (NBS) for severe combined immunodeficiency (SCID) utilizing T-cell receptor excision circles (TRECs) has been implemented in all 50 states as of December 2018 and has been transfo...
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🧬Inborn Error of Immunity⚠️ - ADA2 deficiency 13 y-o girl ➡️ early-onset stroke, + immunodeficiency: recurrent skin infections, chronic Molluscum contagiosum, B cell deficiency, low serum IgA https://t.co/tYJE3uIoIe
#bioinformatics #iot #openscience #immunology #snrtg #genomics
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For #WorldKindnessDay, show some kindness to your friends & family living with #PrimaryImmunodeficiency. Living with a #ChronicIllness is extremely difficult, and living with an #InvisibleIllness comes with its own set of challenges. On #KindnessDay & every day, be kind ❤️
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Very proud of our young trainees and team members at JHACH 11th Annual Research Day. Go Walter-Csomós Lab, go! 🧪🧬🧠 #Immunology #JHACH #Research
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The Walter lab joined #RunForAllChildren at JHACH on Saturday! We are grateful for our USF/JHACH AI team Building Bridges for coming out to share this moment 💚 #GoBulls
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I signed up for the Run For All Children on Sep 10, 2022! Please join us team BuildingBridges in person or virtually.
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September is #NewbornScreening Awareness Month! We're sharing information about NBS for #SCID, our global #advocacy efforts, and family stories. In 2018, NBS for SCID was finally implemented across the USA. Learn more about the history of NBS at https://t.co/2udMfsrsVl 🧪
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Excited to share our recent collaborative work regarding PIK3CD deficiency. Check us out!!😀 Cellular Mechanisms Underlying B Cell Abnormalities in Patients With Gain-of-Function Mutations in the PIK3CD Gene
pubmed.ncbi.nlm.nih.gov
The present study suggests additional mechanistic insight into B cell pathology of APDS: (1) decreased peripheral B cell numbers may be due to the increased death of naïve B cells; (2) larger B cell...
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🗣️🗣️ Please take a look at our recent publication on partial RAG deficiency Partial RAG deficiency in humans induces dysregulated peripheral lymphocyte development and humoral tolerance defec…
pubmed.ncbi.nlm.nih.gov
The recombination-activating genes (RAG) 1 and 2 are indispensable for diversifying the primary B cell receptor repertoire and pruning self-reactive clones via receptor editing in the bone marrow;...
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Check out the Walter Lab's recent publication on a rare primary immunodeficiency, WHIM. Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients
pubmed.ncbi.nlm.nih.gov
Warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome (WS) is a combined immunodeficiency caused by gain-of-function mutations in the C-X-C chemokine receptor type 4 (CXCR4)...
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A lot of us take our immune systems for granted. #COVID19 #pandemic precautions - quarantining, masking, etc - gave us an example of how people with #PrimaryImmunodeficiency live every day, pre-COVID included. Join us to end the lifelong battle against illness for PI patients 💪
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Very clever! 😊
JMF Co-Founder Fred Modell shared this #joke for #NationalTellAJokeDay - Patient: "I have a ringing in my ears." Doctor: "Don't answer it!" Spread some laughter today. Reply with your best joke! 😂
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We proudly support research that creates a better understanding of Primary Immune Deficiency Disorders (#PIDDs) like WHIM, leading to better care & improved outcomes for patients. Thank you to all co-funders & congratulations to the authors on publishing this important work! 🥳
Congratulations @ChristophBGeier @WalterJolan & coauthors for their publication of research evaluating disease progression in an international cohort of #WHIM patients, identifying new genetic variants. Happy to support this research! @Info4PI Learn more:
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https://t.co/WONp9r6lgi Excited to share our international cohort of 66 patients with #WHIMSyndrome (+11 novel CXCR4 variants). Our mission is early diagnosis and targeted therapy. We thank our global collaborators, patients, their families and supporters @Info4PI @X4Pharma
link.springer.com
Journal of Clinical Immunology - Warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome (WS) is a combined immunodeficiency caused by gain-of-function mutations in the C-X-C...
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@X4Pharma @ChristophBGeier @WalterJolan Congratulations on publishing this important work on WHIM Syndrome! We are proud supporters of this research, which will lead to better disease management and improved outcomes for patients ♥
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Thank you @X4Pharma we appreciate your kind wishes
Congratulations @ChristophBGeier @WalterJolan & coauthors for their publication of research evaluating disease progression in an international cohort of #WHIM patients, identifying new genetic variants. Happy to support this research! @Info4PI Learn more:
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Excited to share. We are grateful for all our mentors, collaborators, team members, patients and families. https://t.co/0IyAtzxWzC
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Hard work pays off! The proof is in the pudding😎 Baby Nolan is gonna love his new paintings 🖌🖌🎨🎨
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