Soma Meran
1.4K posts

Soma Meran
@SomaMeran
Nephrologist scientist and mother. All views are my own
Beigetreten Ağustos 2011
379 Folgt220 Follower

@RoshanaMN If Kurds fight, we will be fighting for our own rights and freedom, and certainly not for installing Reza Pahlavi, whose father massacred and oppressed us just as much as the current regime.
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Iranians are understandably worried about arming the Kurds to resist given the spectre of the separatist movement, especially with how IRGC framed them
But many are hoping the Kurds fight for Iran, perhaps they will turn out to be Irans saviours, time will tell, and we all really hope Trump has done his homework here
Kurds for Iran 🙏🏻 We hope
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It’s #GivingTuesday! Donate to the Academy to help fund life-saving research 🔬✨
Support researchers like Dr Soma Meran, whose time in our SUSTAIN programme helped drive forward her work to uncover new treatments for kidney failure.
👉 Donate today: bit.ly/44Dc1Cv

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ISHAS Seminar Series is back! 7th Oct - 11 AM ET - 10 AM CT - 4 PM GMT. Teams eur03.safelinks.protection.outlook.com/?url=https%3A%…
Speakers:
Dr Rebecca Mellema - Layilin as a Modulator of Platelets & Thromboinflammation
Prof Jochen Zimmer - Molecular insights into HA synthesis & length control
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Check out the new KDIGO IgAN/IgAV Guideline Key Takeaways!
IgAN: kdigo.co/KDIGO-IgAN-Gui…
IgAV: kdigo.co/KDIGO-Guidelin…
These resources are designed to provide clinicians with quick and practical access to the most important points from the new KDIGO guideline on managing #IgAN and #IgAV.


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Our new report, looking into rare kidney diseases in the UK, has uncovered shocking statistics in diagnosis delays, inconsistent care, and long waits for new treatments, with the impact being more severe for children.
Rare kidney diseases include over 150 distinct diseases that, while individually uncommon, are estimated to collectively affect around 160,000 people in the UK.
Following our findings, we are calling on government to deliver faster diagnosis, ensure children can be included in clinical trials, and commit investment into research and services so families are no longer left behind.
Sandra Currie OBE, chief executive of Kidney Research UK, said: “This report provides the first real insight into the significant impact of rare kidney diseases and, importantly, lays out a clear path for action. We need faster and more accurate diagnoses, smoother transitions between child and adult services, and better inclusion of children in clinical trials so they are no longer last in line for innovation.”
Head to our report to see our 10 key findings and 14 recommendations: bit.ly/47Wdp5Z
Do you live with or know someone living with a rare disease? We’d love to hear your experiences in the comments.

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The kidney stroma in development and disease nature.com/articles/s4158…
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HA2025 kicks off with ISHAS president Melanie Simpson opening with HA is bigger than the kidney 😂 @ISHAS_org

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Calling all hyaluronan researchers- its time to register for HA 2025! Don't miss this meeting with ishas.org/ha-2025/regist…
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Bone quality relies on hyaluronan synthesis - Insights from mice with complete knockout of hyaluronan synthase expr… pubmed.ncbi.nlm.nih.gov/39736893/
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Hyaluronan provokes inflammation but suppresses phagocytotic function in macrophages pubmed.ncbi.nlm.nih.gov/39615286/
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Super chickens..Interesting concept ..
#B6" target="_blank" rel="nofollow noopener">jci.org/articles/view/…
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Reminder to join the ISHAS webinar on Nov 19th
International Society for Hyaluronan Sciences@ISHAS_org
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@TheWKRU @CUSystemsImmu well done to Irina Grigorieva
International Society for Hyaluronan Sciences@ISHAS_org
ISHAS are pleased to announce the Sept 2025 Grant Awards results: Congratulations to Irina Grigorieva from Cardiff University for a Research Grants Award and Sudhir Varma (University of Houston) & Karen Mifsud (Bristol University) for Travel Grants 🎉
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