Runa Hamid (@RunaHamid) profile picture

Senior Scientist @TIGS_India. Former DST PI at CCMB #Neurobiology#Drosophila#RGDs Retweets are not endorsements. Views are personal.

Bengaluru
Joined April 2020
Photo by Runa Hamid (@RunaHamid)Photo by Runa Hamid (@RunaHamid)Photo by Runa Hamid (@RunaHamid)Photo by Runa Hamid (@RunaHamid)Photo by Runa Hamid (@RunaHamid)Photo by Runa Hamid (@RunaHamid)Photo by Runa Hamid (@RunaHamid)Photo by Runa Hamid (@RunaHamid)Photo by Runa Hamid (@RunaHamid)Photo by Runa Hamid (@RunaHamid)
Zepto supplied expired product yesterday loaded with fungus. This is extremely serious, irresponsible and pathetic. Violation of food safety act ! On raising the issue it simply returned the money. @ZeptoNow @fssaiindia @jagograhakjago
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Resolution update- received an apology call from @ZeptoNow with an assurance that Zepto will initiate appropriate enquiry into the matter.
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Say hello to our speakers for GeneticsDeCoded - 4! Join us for a day of talks, ideas, and conversations that decode the world of #genetics for everyone 📍 @GardenCityUni, Bengaluru 🗓️ Monday, 17 August 2026 | 10 - 4 Register now🔗forms.cloud.microsoft/r/3BhJ…
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Runa Hamid retweeted
Wasps inject their eggs into Drosophila larvae. The eggs mature in the larva, consuming the latter. But some larvae are able to escape such a fate by killing the wasp eggs + they can pass the abilities too! 1/2 @ShaguftaK_2711 @Ravina2_Saini @RunaHamid @3RakeshMishra
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Teaming to make ‘Rare Visible‘
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@BLiSC_India campus students presented a skit on neuromuscular disorder challenges! Through shared commitment, we reaffirm our dedication to advancing #RareDisease research & care. Thank you to everyone who joined us—let's make #Rare visible! ✨ 3/3
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@RunaHamid and @deeptrivedivyas gave brief talks as researchers and shared nuances about rare diseases A special thanks to Keya Hatkar, an young author and a disability advocate for a thought provoking session on the need for #inclusivity and awareness on rare diseases 2/3
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On #RareDiseaseDay2025, we came together to raise awareness & foster discussions on #rarediseases with @NCBS_Bangalore The event started off with an insightful live art competition, where the participants expressed their creativity on the canvas on the theme What is rare? 1/3
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Day 3 Join us in raising awareness for #RareDiseases! Today we want you to know: How many people are affected by rare diseases worldwide & in #India? Help us spread the word by reposting & sharing with @NCBS_Bangalore @BLiSC_India Let's make rare visible! #RareDiseaseDay2025
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Did you know, Why is #February considered as the #RareDisease Month? We've launched a campaign on Rare Genetic Disorders and we'll be sharing one #RareDisease fact every day until 28th of this month! Stay tuned! Let’s make #rare visible! @NCBS_Bangalore @BLiSC_India
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Day 5 Join us in raising awareness for #RareDiseases! Today we want you to know: Which age group is the most affected with #RareDiseases? with @NCBS_Bangalore @BLiSC_India Spread the word by reposting & sharing Let's make rare visible! #RareDiseaseDay2025
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Day 4 Join us in raising awareness for #RareDiseases! Today we want you to know: The diversity of #rarediseases Visit 𝙂𝙚𝙣𝙏𝙄𝙂𝙎: db.tigs.res.in/gentigs/index… with @NCBS_Bangalore @BLiSC_India Spread the word by reposting & sharing Let's make rare visible! #RareDiseaseDay2025
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Unleash your creativity, spread the word, share your talent, and amplify the voices of the rare disease community. Submit your entries in different categories with the theme: 'What is Rare?' lnkd.in/dBKRKjmK
This year the #RareDiseaseDay is observed on 28 Feb. We along with @NCBS_Bangalore are pleased to announce a few contests with the theme 'What is #Rare?' for all to participate! More details: forms.gle/oGUtXFgQonYjaR916 Celebrate creativity & raise awareness for #rarediseases!
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This year the #RareDiseaseDay is observed on 28 Feb. We along with @NCBS_Bangalore are pleased to announce a few contests with the theme 'What is #Rare?' for all to participate! More details: forms.gle/oGUtXFgQonYjaR916 Celebrate creativity & raise awareness for #rarediseases!
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Frustrated with axis bank customer care. Called 8 times since 21st Nov. Every time a new reference no is given for the same problem with assurance but no solution provided. Worst ever experience!!! @AxisBank @AxisBankSupport
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Nothing has happened yet and tomorrow is the date of payment!!! My CBIL is getting spoiled due the careless attitude of Axis bank officials… such a pathetic state of affairs!!! @AxisBank @AxisBankSupport
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Update - Just now I received another service request number but without any solution yet again. @AxisBank @AxisBankSupport your work flow is highly inefficient and it is going on and on… I have lost all hopes that my issue be resolved..
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If you are working on any aspect of RGD, don't miss your chance to present at the #REDRESS2024 Summit on Rare Genetic Disorders! Submit your poster abstracts by 22nd Oct and be part of impactful discussions with leading experts/stakeholders under one roof. @TIGS_India
📢#REDRESS 2024 We are back with the 3rd edition of Rare #Genetic Diseases Research Summit (REDRESS-2024)! Abstract submission to REDRESS-2024 poster presentations is now open! Extended deadline to apply: 22 Oct For details visit: bit.ly/3MNsbjC With @ORDIndia
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Sir Ratan Tata was an epitome of entrepreneurship, integrity & philanthropic vision which transformed the social & economic fabric of our nation. Your legacy will live on! Privileged & proud to be part of TIGS !
Today, we stand in solemn tribute of Mr. Ratan N Tata, whose visionary leadership played a pivotal role in founding TIGS. His passion for advancing science for the betterment of humanity will forever be a part of our mission. 1/2
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Every step counts towards raising awareness about these unique medical challenges. Let’s keep pushing for research on early diagnosis and therapeutics…and inclusivity in healthcare. @TIGS_India #runforacause #RareDiseaseAwareness
Lace up your shoes and join us as we run to raise awareness and support for those fighting rare diseases. Together, we can make a difference! Organised by @ORDIndia #RareDiseaseAwareness #RunForACause 🏃‍♂️💪#Racefor7 @TIGS_India
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