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Kwaling Senapathy and doctors

Chalanachithram.com DB » New TF Industry Related » Archive through July 31, 2015 » Kwaling Senapathy and doctors « Previous Next »
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Linkmaster
Legend
Username: Linkmaster

Post Number: 48484
Registered: 02-2008
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Posted on Wednesday, July 29, 2015 - 04:15 pm:       


Starc:




neevu saamnyuduvi kaadu appaaa..
 

Starc
Junior Artist
Username: Starc

Post Number: 828
Registered: 03-2015
Posted From: 170.63.120.116

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Posted on Wednesday, July 29, 2015 - 04:09 pm:       

okay babai.. thanks for your inputs.

case details: tnbc mid 30s stg 4.. india lo chethulu ettesharu..

emi cheyyalo ardam kavadam ledu.. just reading through articles.
 

Senapathy
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Username: Senapathy

Post Number: 18067
Registered: 01-2009
Posted From: 137.131.20.144

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Posted on Wednesday, July 29, 2015 - 04:01 pm:       


Starc:




Annai, ilanti articles chala vasta untayi. Medical journals lo. They usually go positive with their findings. Not to discourage most of them do not result in a therapy.

But almost all rationally developed drugs have evolved from a sound scientific background such as this study. Mouse models nundi real life theraphy ki translate cheyyadam is a herculean task. If patients actuallt respond to this gene. My 2 cents. I will check back later at night. Busy today.
I am struck by the lightning of love and burnt beyond repair - Florentino Ariza

 

Starc
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Username: Starc

Post Number: 827
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Posted on Wednesday, July 29, 2015 - 03:53 pm:       

https://unclineberger.org/news/parise-cib1

Is this promising?

above link tho nikku details anni ardam avuthai.. so life mida home vadilesukovadamena?
 

Senapathy
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Username: Senapathy

Post Number: 18066
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Posted on Wednesday, July 29, 2015 - 03:47 pm:       


Starc:




Mouse genetics are not fully translatable to humans annai. But such data is usually promising and right direction. Monkey models are usually recommended for testing before human clinical trials, but again not a hard and fast rule

It might take any where between 10-15 years for a drug from inception to end of clinical trials. Usually each step is a hurdle and can be abandoned at that stage if results are negative

If there are already drugs for that pathway (and that protein), it is usually a head start. As pharamco kinetics are already in place.

General rule of thumb is most targets are not druggable. Anduke we are always searching for alternate ways. But we have to start somewhere. Hope it helps !
I am struck by the lightning of love and burnt beyond repair - Florentino Ariza

 

Starc
Junior Artist
Username: Starc

Post Number: 825
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Posted on Wednesday, July 29, 2015 - 03:42 pm:       

cancer
 

Vasu
Side Hero
Username: Vasu

Post Number: 8898
Registered: 10-2014
Posted From: 47.16.177.98

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Posted on Wednesday, July 29, 2015 - 03:40 pm:       


Starc:


amyloidosis?
Yes, we endorse you..... Edi Chee...anna Evadidi Chee...anna meeke saadhyam
Bala->Jr->Rajni->Mahesh->Prabhas/Rajamouli (Hence Proved)
 

Kantha_rao
Comedian
Username: Kantha_rao

Post Number: 1103
Registered: 11-2013
Posted From: 12.218.0.70

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Posted on Wednesday, July 29, 2015 - 03:38 pm:       

em disease ?
 

Starc
Junior Artist
Username: Starc

Post Number: 824
Registered: 03-2015
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Posted on Wednesday, July 29, 2015 - 03:37 pm:       

Senapathy,

USa lo oka mouse mida research chesi CIB1 protein is cause for the disease and it is proved in mouse ani icchadu..

next the drug trials should go in this direction in human ani cheppadu.. ee stage nunchi 3 phase human trials chesi FDA approval chesi market lo medicine ravadaniki enni samastaralu padutundi?

or instead of waiting can we use drugs which are in market already to block this protein?

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