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European Journal of Haematology|July 18, 2013
DNA interstrand cross-link repair: understanding role of Fanconi anemia pathway and therapeutic implicationsPallavi Shukla, Avani Solanki, Kanjaksha Ghosh, et al.Plos One|January 16, 2020
Mitochondrial DNA variations and mitochondrial dysfunction in Fanconi anemiaAvani Solanki, Aruna Rajendran, Sheila Mohan, et al.Plos One|January 23, 2016
FANCA Gene Mutations with 8 Novel Molecular Changes in Indian Fanconi Anemia PatientsAvani Solanki, Purvi Mohanty, Pallavi Shukla, et al.Leukemia Research|December 27, 2016
Characterization of two novel FANCG mutations in Indian Fanconi anemia patientsAvani Solanki, C Kumar Selvaa, Frenny Sheth, et al.Molecular Biology Reports|March 29, 2021
Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemiaMerin George, Avani Solanki, Purvi Mohanty, et al.Human Mutation|September 29, 2021
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjectsMerin George, Avani Solanki, Niranjan Chavan, et al.Human Mutation|September 13, 2019
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in IndiaFrank X Donovan, Avani Solanki, Minako Mori, et al.Pageof 1