Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Edna D'Souza"'
Autor:
Merin Thomas, Vandana Jain, Bhushan Sonawane, Edna D’Souza, M. Vijay Kumar, Raman Mohan Singh
Publikováno v:
JPC – Journal of Planar Chromatography – Modern TLC. 35:627-633
Autor:
Najmuddin Mulani, Abhay B. Fulke, Edna D'Souza, Aashna Monga, M. Nageswar Rao, Aayushi Maloo, Anirudh Ram
Publikováno v:
Marine Pollution Bulletin. 192:114955
Publikováno v:
Indian Journal of Human Genetics
Aim: The presence of circulatory cell-free fetal DNA in maternal plasma has found new applications in non-invasive risk-free prenatal diagnosis. Materials and Methods: We made use of a size separation approach along with real time polymerase chain re
Autor:
Ramesh Z. Patel, Pratibha Sawant, Anita Nadkarni, Kanjaksha Ghosh, Roshan B. Colah, Reema Surve, Edna D'Souza, Dilip C. Master, Dipika Mohanty, Ajit Gorakshakar, Supriya Phanasgaonkar
Publikováno v:
British Journal of Haematology. 149:739-747
Although the average frequency of beta-thalassaemia carriers in India is 3-4% and the prevalent mutations have been studied, no micromapping has been done. This is the first attempt to provide an accurate estimate of the frequencies of beta-thalassae
Publikováno v:
Cytometry Part B: Clinical Cytometry. :175-180
Background Isolation of adequate numbers of fetal cells circulating in the maternal circulation is the major hurdle in developing noninvasive prenatal diagnostic procedures. We used flow cytometry and a combination of different monoclonal antibodies
Autor:
Pratibha Sawant, Kanjaksha Ghosh, Ajit Gorakshakar, Roshan B. Colah, Anita Nadkarni, Edna D'Souza, Dipika Mohanty
Publikováno v:
American Journal of Clinical Pathology. 130:202-209
Our purpose was to develop and evaluate isolation and enrichment of fetal erythroblasts and a nested polymerase chain reaction (PCR) approach using fetal erythroblasts for detecting the β-globin gene mutations for a noninvasive prenatal diagnosis of
Autor:
Roshan, Colah, Ajit, Gorakshakar, Supriya, Phanasgaonkar, Edna, D'Souza, Anita, Nadkarni, Reema, Surve, Pratibha, Sawant, Dilip, Master, Ramesh, Patel, Kanjaksha, Ghosh, Dipika, Mohanty
Publikováno v:
British journal of haematology. 149(5)
Although the average frequency of beta-thalassaemia carriers in India is 3-4% and the prevalent mutations have been studied, no micromapping has been done. This is the first attempt to provide an accurate estimate of the frequencies of beta-thalassae
Publikováno v:
International journal of laboratory hematology. 32(1 Pt 1)
Accurate estimation of hemoglobin (Hbs) A, Hb A(2), Hb F and abnormal Hb is required for diagnosis of hemoglobinopathies and genetic counseling. High pressure liquid chromatography (HPLC) is the most suitable approach available. But for 70% of the ru
Autor:
Reema Surve, Ajit Gorakshakar, Supriya Phanasgaonkar, Khushnooma Italia, Anita Nadkarni, Roshan B. Colah, Edna D'Souza, Pratibha Sawant
Publikováno v:
Indian journal of pediatrics. 74(7)
An accurate diagnosis of beta -thalassemia carriers, homozygous patients and identification of different structural hemoglobin variants is important for epidemiological studies as well as for management and prevention of the major hemoglobin disorder
Publikováno v:
Hemoglobin. 31(1)
Prenatal diagnosis is an option for couples at risk of having a child affected with hemoglobinopathies. Chorionic villus sampling (CVS) and cordocentesis are accurate but a finite risk of fetal loss exists. A non invasive, risk free strategy that has