Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Jisha Elias"'
Autor:
Snigdha Majumder, Rakshit Shah, Jisha Elias, Yogesh Mistry, Karunakaran Coral, Priyanka Shah, Anand Kumar Maurya, Bharti Mittal, Jason K D'Silva, Sakthivel Murugan, Lakshmi Mahadevan, Rekha Sathian, V L Ramprasad, Papia Chakraborty, Ravi Gupta, Amitabha Chaudhuri, Arati Khanna-Gupta
Publikováno v:
PLoS ONE, Vol 13, Iss 9, p e0203845 (2018)
Familial adenomatous polyposis (FAP) is an inherited condition arising from genetic defects in the Adenomatous polyposis coli (APC) gene. Carriers with mutations in the APC gene develop polyps in the colon and rectum which if not managed, transition
Externí odkaz:
https://doaj.org/article/2ae8ce8f8fa7419cbd38a330a9843017
Autor:
Snigdha Majumder, Rakshit Shah, Jisha Elias, Yogesh Mistry, Coral Karunakaran, Priyanka Shah, Anand Kumar Maurya, Bharti Mittal, Jason K. D'Silva, Lakshmi Mahadevan, Rekha Sathian, Ravi Gupta, Amitabha Chaudhuri, Arati Khanna- Gupta
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue-Supplement, Pp 252-252 (2017)
Familial Adenomatous Polyposis (FAP) is characterized by the manifestation of adenomatous polyps in the colon and rectum at an early age (mean age of 16), which if left untreated, leads to aggressive and fatal tumors by the age of 40 years. FAP is ca
Externí odkaz:
https://doaj.org/article/9f87281882344ebc81e4aba4b1109b33
Autor:
Jisha Elias, Coral Karunakaran, Snigdha Majumder, Malini Manoharan, Rakshit Shah, Yogesh Mistry, Rajesh Ramanuj, Niraj Bhatt, Arati Khanna- Gupta
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue-Supplement, Pp 254-254 (2017)
Lynch syndrome (Hereditary Non Polyposis Colorectal Cancer, HNPCC) is one of the most common hereditary familial colorectal cancers (CRC) with an autosomal dominant pattern of inheritance. It accounts for 2-5% of the total CRCs reported worldwide. Al
Externí odkaz:
https://doaj.org/article/f2f73c4b56fa45c08cf47d5dc86c6d11
Autor:
Coral Karunakaran, Jisha Elias, Nitin Mandoli, Anand K. Maurya, Rajesh Kantharia, Yogesh Mistry, Kartikeyen Jain, Ravi Gupta, Amit Chaudhuri, Arati Khanna- Gupta
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue-Supplement, Pp 245-245 (2017)
Head and neck squamous cell carcinoma (HNSCC) is the sixth most common malignancy globally, but ranks first in India because of the extensive use of tobacco, betel-quid and alcohol. Despite, the availability of aggressive treatments, the survival for
Externí odkaz:
https://doaj.org/article/9c79ad8e8e24477fb3fe375193aab2ab
Autor:
Vasumathi Kode, Yogesh Mistry, Lakshmi Mahadevan, Snigdha Majumder, Karunakaran Coral, Papia Chakraborty, Bharti Mittal, Arati Khanna-Gupta, Malini Manoharan, Priyanka Shah, Sakthivel Murugan Sm, Rakshit Shah, Jisha Elias, Ravi Gupta, Anjali Kumari, Amitabha Chaudhuri
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-14 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-14 (2018)
Lynch syndrome (LS) is a cancer predisposition disorder wherein patients have a 70–80% lifetime risk of developing colorectal cancers (CRC). Finding germline mutations in predisposing genes allows for risk assessment of CRC development. Here we rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec7da21f96bc9c0302e7f49a733ed1c0
https://doi.org/10.1038/s41598-018-30466-x
https://doi.org/10.1038/s41598-018-30466-x
Autor:
Sakthivel Murugan, Arati Khanna-Gupta, Vedam L. Ramprasad, Yogesh Mistry, Papia Chakraborty, Priyanka Shah, Ravi Gupta, Snigdha Majumder, Bharti Mittal, Lakshmi Mahadevan, Jisha Elias, Rakshit Shah, Jason K. D’Silva, Karunakaran Coral, Anand Kumar Maurya, Rekha Sathian, Amitabha Chaudhuri
Publikováno v:
PLoS ONE
PLoS ONE, Vol 13, Iss 9, p e0203845 (2018)
PLoS ONE, Vol 13, Iss 9, p e0203845 (2018)
Familial adenomatous polyposis (FAP) is an inherited condition arising from genetic defects in the Adenomatous polyposis coli (APC) gene. Carriers with mutations in the APC gene develop polyps in the colon and rectum which if not managed, transition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::846692412666e69dedee7264957c3c91
https://doi.org/10.1371/journal.pone.0203845
https://doi.org/10.1371/journal.pone.0203845
Autor:
Ravi Gupta, Arati Khanna Gupta, Nitin Mandoli, Jisha Elias, Rajesh A Kantharia, Yogesh Mistry, Coral Karunakaran, Anand Kumar Maurya, Amit Chaudhuri, Kartikeyen Jain
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue-Supplement, Pp 245-245 (2017)
Head and neck squamous cell carcinoma (HNSCC) is the sixth most common malignancy globally, but ranks first in India because of the extensive use of tobacco, betel-quid and alcohol. Despite, the availability of aggressive treatments, the survival for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92bea4a3f76a229696735fda95f499fa
https://doi.org/10.24870/cjb.2017-a230
https://doi.org/10.24870/cjb.2017-a230
Autor:
Arati Khanna Gupta, Rakshit Shah, Coral Karunakaran, Anand Kumar Maurya, Snigdha Majumder, Yogesh Mistry, Jason K. D’Silva, Jisha Elias, Priyanka Shah, Lakshmi Mahadevan, Rekha Sathian, Amitabha Chaudhuri, Bharti Mittal, Ravi Gupta
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue-Supplement, Pp 252-252 (2017)
Familial Adenomatous Polyposis (FAP) is characterized by the manifestation of adenomatous polyps in the colon and rectum at an early age (mean age of 16), which if left untreated, leads to aggressive and fatal tumors by the age of 40 years. FAP is ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f1c9db577294f9c227b7f39f039af92
Autor:
Coral Karunakaran, Snigdha Majumder, Rakshit Shah, Malini Manoharan, Niraj Bhatt, Arati Khanna Gupta, Rajesh Ramanuj, Yogesh Mistry, Jisha Elias
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue-Supplement, Pp 254-254 (2017)
Lynch syndrome (Hereditary Non Polyposis Colorectal Cancer, HNPCC) is one of the most common hereditary familial colorectal cancers (CRC) with an autosomal dominant pattern of inheritance. It accounts for 2-5% of the total CRCs reported worldwide. Al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::096e6d1bb519e2c59573a9824f85d8a4
Autor:
Majumder, Snigdha1, Shah, Rakshit2, Elias, Jisha1,2, Mistry, Yogesh2, Coral, Karunakaran1, Shah, Priyanka1, Maurya, Anand Kumar1 amitc@medgenome.com, Mittal, Bharti1, D’Silva, Jason K.1, Murugan, Sakthivel1, Mahadevan, Lakshmi1, Sathian, Rekha1, Ramprasad, V. L.1, Chakraborty, Papia3, Gupta, Ravi1, Chaudhuri, Amitabha1,3, Khanna-Gupta, Arati1 arati.g@medgenome.com
Publikováno v:
PLoS ONE. 9/26/2018, Vol. 13 Issue 9, p1-18. 18p.