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sandeep
Last Update: 2023-09-22
Usage Frequency: 1
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kon sandeep
sandeep kon h
Last Update: 2020-12-29
Usage Frequency: 1
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sandeep thakur
sandeep thakur
Last Update: 2016-07-21
Usage Frequency: 4
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sandeep name ringtone
sandeep name ringtones
Last Update: 2017-03-17
Usage Frequency: 3
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i love to me sandeep
i love to me sandeep.
Last Update: 2021-06-09
Usage Frequency: 1
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sandeep ka rashifal kya hai
sandeep's horoscope
Last Update: 2024-01-26
Usage Frequency: 31
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whatsapp status by name sandeep
whatsapp status name
Last Update: 2018-06-09
Usage Frequency: 2
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aap gajab haste hai sandeep jee
you have got a lot of sandeep jee
Last Update: 2018-07-15
Usage Frequency: 1
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mr sandeep se baat karni hai english translation
mr sandeep se baat karni hai english translation
Last Update: 2020-12-19
Usage Frequency: 1
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Reference:
sandeep tomar aapko koi bahut miss kar raha hai
sandeep tomar aapko koi bahut miss kar raha hai
Last Update: 2020-10-23
Usage Frequency: 1
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byee dear may be your trust stay as long as you believe in sandeep
i don't even like him
Last Update: 2020-11-15
Usage Frequency: 1
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my name is sandeep dandekar my name in your status mera naam hi meri phchan h
my name is sandeep dandekar my name, my name, my identity is in your status
Last Update: 2017-01-24
Usage Frequency: 1
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dear sandeep ji main apko last 20 days se bol raha hu ki aap walia ji se baat kar lo lekin aap unse koi baat nahi kar rahe h
dear sandeep ji main apko last 20 days se bol raha hu ki aap walia ji se baat kar lo lekin aap unse koi baat nahi kar rahe h
Last Update: 2021-05-31
Usage Frequency: 1
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sandeep kumar rawat ki tarah se dil se É आपको या आपके sb परिवार को इस पवन संसार पर दिल से मुबारक बात देते हुए कामना करते हैं भगवान आपकी मनोकामना पुरी करे हैप्पी दीपावली
sandeep kumar rawat ki tarah se dil se aapko or aapke sb pariwari ko is pawan awasr par dil se mubarak bat dete hue kamna krte hai bhagwan aapki manokamna puri kare happy dipawali
Last Update: 2023-11-11
Usage Frequency: 1
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duchenne muscular dystrophy, a severe type of muscle weakness that usually begins at an early age and worsens quickly, may soon have a new strategy of treatment through genetic regulation. there is no known cure for duchenne muscular dystrophy. treatments usually aim to control symptoms to improve quality of life. sandeep eswarappa, assistant professor indian institute of science (iisc), bengaluru one of the 21 recipients of this year’s swarnajayanti fellowship of the department of science and technology (dst), government of india proposes to supress the disease-causing premature stop codon or the genetic process that initiates these diseases. he is trying to bring about the suppression through translational readthrough, a gene regulatory principle found in humans, yeasts, bacteria and drosophila which takes place with the variation of the genetic code. prof. sandeep’s group has been developing strategies to induce translational readthrough across genetic diseases caused by non-sense mutations --a change in dna that causes a protein to terminate or end its translation earlier than expected. they were successful in achieving this in vitro in case of thalassemia and are working on other disease models. this research work has been published in the scientific journal ‘biochemistry’ recently. with the swarna jayanti fellowship, they will extend it to duchenne muscular dystrophy. if successful, this project may lead to novel therapeutics for the treatment of genetic diseases like thalassemia, duchenne muscular dystrophy, haemophilia. in case of any protein formation genetic information present in the genome is first transcribed into an mrna, which in turn is translated into a protein. protein synthesis or translation is executed by macromolecular machinery called ribosomes. ribosomes start this process at a specific location on an mrna called ‘start codon’ and terminate at a stop signal called ‘stop codon’. in case of diseases with nonsense mutations, such mutations result in premature stop signal in mrna often resulting in non-functional truncated protein. prof. sandeep eswarappa’s laboratory at iisc has shown that in certain mrnas, under certain conditions, translating ribosomes misread the stop signal and continue till they encounter another stop signal. in this translational readthrough process, a longer protein is synthesized with an extension. this extension might change the properties of the protein. the experiments carried out by his group have revealed that such long prote “the knowledge we have already gained from our experiment have opened an unexpected avenue to treat genetic diseases caused by non-sense mutations like duchenne muscular dystrophy, haemophilia and so on,” said prof. sandeep.
duchenne muscular dystrophy, a severe type of muscle weakness that usually begins at an early age and worsens quickly, may soon have a new strategy of treatment through genetic regulation. there is no known cure for duchenne muscular dystrophy. treatments usually aim to control symptoms to improve quality of life. sandeep eswarappa, assistant professor indian institute of science (iisc), bengaluru one of the 21 recipients of this year’s swarnajayanti fellowship of the department of science and technology (dst), government of india proposes to supress the disease-causing premature stop codon or the genetic process that initiates these diseases. he is trying to bring about the suppression through translational readthrough, a gene regulatory principle found in humans, yeasts, bacteria and drosophila which takes place with the variation of the genetic code. prof. sandeep’s group has been developing strategies to induce translational readthrough across genetic diseases caused by non-sense mutations --a change in dna that causes a protein to terminate or end its translation earlier than expected. they were successful in achieving this in vitro in case of thalassemia and are working on other disease models. this research work has been published in the scientific journal ‘biochemistry’ recently. with the swarna jayanti fellowship, they will extend it to duchenne muscular dystrophy. if successful, this project may lead to novel therapeutics for the treatment of genetic diseases like thalassemia, duchenne muscular dystrophy, haemophilia. in case of any protein formation genetic information present in the genome is first transcribed into an mrna, which in turn is translated into a protein. protein synthesis or translation is executed by macromolecular machinery called ribosomes. ribosomes start this process at a specific location on an mrna called ‘start codon’ and terminate at a stop signal called ‘stop codon’. in case of diseases with nonsense mutations, such mutations result in premature stop signal in mrna often resulting in non-functional truncated protein. prof. sandeep eswarappa’s laboratory at iisc has shown that in certain mrnas, under certain conditions, translating ribosomes misread the stop signal and continue till they encounter another stop signal. in this translational readthrough process, a longer protein is synthesized with an extension. this extension might change the properties of the protein. the experiments carried out by his group have revealed that such long proteins can have different localization, stability and function. “the knowledge we have already gained from our experiment have opened an unexpected avenue to treat genetic diseases caused by non-sense mutations like duchenne muscular dystrophy, haemophilia and so on,” said prof. sandeep.
Last Update: 2021-03-15
Usage Frequency: 1
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