Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Ashraf Mannan"'
Autor:
Intezar Mehdi, K. Ramya, T.L. Suma, Ashraf Mannan, M.L. Sheela, Shanmukh Kattragada, B.S. Ajaikumar, Mithua Ghosh
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 8, Iss 2, Pp 80-84 (2023)
Background: Familial platelet disorder (FPD) with predisposition to acute myeloid leukemia (AML) is an autosomal dominant disease of the hematopoietic system that is caused by heterozygous mutations in RUNX1 gene. RUNX1 is frequently involved in the
Externí odkaz:
https://doaj.org/article/93f660e979b34122be4a70fcdfcc6e5a
Autor:
Chaitanyanand Koppiker, Ashwini Bapat, Siddharth Gahlaut, Naveen Luke, Jisha John, Rupa Mishra, Aishwarya Konnur, Namrata Namewar, Ruhi Reddy, Shaheen Shaikh, Rituja Banale, Smeeta Nare, Laleh Busheri, Asha Reddy, Ashraf Mannan, Sabarinathan Radhakrishnan, Selvi Radhakrishna, Santosh Dixit
Publikováno v:
Cancer Research. 82:LB561-LB561
Breast cancer is the most common cancer in Indian women with a high incidence of triple negative breast cancer (TNBC), an aggressive subtype of breast cancer associated with poor prognosis. The high TNBC prevalence (>25%) in India as compared to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dc00d780325e0b04ddedc73ab8c4ba3
https://doi.org/10.1158/1538-7445.am2022-lb561
https://doi.org/10.1158/1538-7445.am2022-lb561
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94327 (2014)
The Acp2 gene encodes the beta subunit of lysosomal acid phosphatase, which is an isoenzyme that hydrolyzes orthophosphoric monoesters. In mice, a spontaneous mutation in Acp2 results in severe cerebellar defects. These include a reduced size, abnorm
Externí odkaz:
https://doaj.org/article/5022ec9f6b4d4a8a9f312e628bc5cdb8
Autor:
Veena, Vedartham, Soumya, Sundaram, Sruthi S, Nair, Aparna, Ganapathy, Ashraf, Mannan, Ramshekhar, Menon
Publikováno v:
Ophthalmic genetics. 40(4)
Mutations in sequestosome 1 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9428a44b7788abd057a9aedd6be342e7
https://pubmed.ncbi.nlm.nih.gov/31525130
https://pubmed.ncbi.nlm.nih.gov/31525130
Autor:
Nalini Rao, Upasana Mukherjee, Sheela Ml, Mithua Ghosh, Basavalinga S. Ajaikumar, B Mahesh, Vaijayanti Gupta, Radheshyam Naik, U. Ashraf Mannan, Manjima Chatterjee, C T Satheesh, S. Patil, K. Murugan, Satish Sankaran
Publikováno v:
International Journal of Human Genetics. 16:120-127
Male breast carcinoma (MBC) is a rare cancer type that accounts 1 percent of the total breast cancer cases. This substantially invites diagnosis challenges and social burdens where the individual n...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e597adc08d6130565dea1e0bfbffd503
https://doi.org/10.1080/09723757.2016.11886287
https://doi.org/10.1080/09723757.2016.11886287
Autor:
Sheth, Harsh1 (AUTHOR), Pancholi, Dhairya1 (AUTHOR), Bhavsar, Riddhi1 (AUTHOR), Mannan, Ashraf2 (AUTHOR), Ganapathy, Aparna2 (AUTHOR), Chowdhury, Mayank3 (AUTHOR), Shah, Sudhir4 (AUTHOR), Solanki, Dhawal5 (AUTHOR), Sheth, Frenny1 (AUTHOR), Sheth, Jayesh1 (AUTHOR), Mannan, Ashraf U6 (AUTHOR)
Publikováno v:
Neurology India. Nov/Dec2021, Vol. 69 Issue 6, p1729-1736. 8p.
Autor:
Dhar, Subhra1 (AUTHOR), Mannan, Ashraf2 (AUTHOR), Singh, J3 (AUTHOR), Dhar, Sandipan4 (AUTHOR), Pradhan, Swetalina5 (AUTHOR), Mannan, Ashraf U6 (AUTHOR), Singh, J Jaya7 (AUTHOR)
Publikováno v:
Indian Journal of Pathology & Microbiology. Apr-Jun2022, Vol. 65 Issue 2, p465-467. 3p.
Autor:
Aravind, Sankaramoorthy1 (AUTHOR), Ashley, Berty2 (AUTHOR), Mannan, Ashraf3 (AUTHOR), Ganapathy, Aparna3 (AUTHOR), Ramesh, Keerthi2 (AUTHOR), Ramachandran, Aparna2 (AUTHOR), Nongthomba, Upendra4 (AUTHOR), Shastry, Arun2 (AUTHOR)
Publikováno v:
Indian Journal of Medical Research. Sep2019, Vol. 150 Issue 3, p282-289. 8p.
Autor:
Vedartham, Veena1 (AUTHOR), Sundaram, Soumya1 (AUTHOR) ssdr.soumya@gmail.com, Nair, Sruthi S1 (AUTHOR), Ganapathy, Aparna2 (AUTHOR), Mannan, Ashraf2 (AUTHOR), Menon, Ramshekhar1 (AUTHOR)
Publikováno v:
Ophthalmic Genetics. Aug2019, Vol. 40 Issue 4, p376-379. 4p.
Publikováno v:
Annals of Indian Academy of Neurology. Jul/Aug2020, Vol. 23 Issue 4, p539-541. 3p.