Rett Syndrome | Cellular and molecular basis of Rett syndrome

Rett Syndrome | Cellular and molecular basis of Rett syndrome | Treatment of Rett Syndrome.

Рет қаралды 3,238

5 ай бұрын

This video talks about Rett Syndrome | Cellular and molecular basis of Rett syndrome | Treatment of Rett Syndrome.
Refrences: www.nature.com/articles/s4158...
www.nature.com/articles/nrg3897
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Пікірлер: 15

@girogiro-vh5pz 2 ай бұрын

Thanks this is perhaps the best explanation of RED syndrome that I have seen.

@animatedbiologywitharpan 2 ай бұрын

Could you please help me by sharing my contents with your friends group/ college group. I put huge efforts in making these videos but unfortunately not a lot of people are watching this.

@earth2k66 Күн бұрын

CRE-LOXP and CRISPR CAS9 are the sharpest tools we have available in modern Molecular Biology. I firmly believe there is nothing impossible to achieve with these in the right hands.

@priyashankar510 4 ай бұрын

Excellent Narration about the Rett...so far never posted. CONGRATS. can u pl. Inform me, how to proceed about it for treatment,since my daughter is having same complaint. Please help us....Awaiting Sir.

@animatedbiologywitharpan 4 ай бұрын

This FDA approved drug is now available in USA market. Email the the company such that you can import it in India

@glinnes456 2 ай бұрын

Another great video! I have one question though: as PSD95 is present in glutamatergic/excitatory neurons, wouldn't that mean that excitatory transmission is disturbed because of the loss of post-synaptic spines? How is that linked to overall too much excitation (E/I (im)balance) in Rett syndrome though? Or did I misunderstand something there? I'd be curious to know if you have an answer :) Thank you!

@animatedbiologywitharpan 2 ай бұрын

PSD95 stabilizes and regulates excitatory synaptic receptors, crucial for synaptic plasticity and strength. It indirectly influences inhibitory synapses to maintain excitatory/inhibitory balance. Dysregulation of PSD95 is linked to disorders like autism and schizophrenia, underscoring its importance in neural circuit stability and overall brain function. For more details refer to this research article. www.ncbi.nlm.nih.gov/pmc/articles/PMC2526002/#:~:text=AMPA%20receptors%20directly%20associate%20with,decreased%20excitation%2C%20or%20increased%20inhibition.

@arvindrajput5328 5 ай бұрын

What is the function of chromosome13 in rett syndrome

@animatedbiologywitharpan 5 ай бұрын

Rett syndrome is a neurodevelopmental disorder primarily caused by mutations in the MECP2 gene located on chromosome X. Chromosome 13 is not directly implicated in Rett syndrome. The role of chromosome 13 in Rett syndrome is not significant, as the key gene involved, MECP2, is located on chromosome X. However, chromosome 13 and other chromosomes may still indirectly influence various aspects of neurodevelopment and gene regulation, potentially impacting the severity or presentation of Rett syndrome symptoms.