Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Milind Chanekar"'
Autor:
Shital Munde, Shaikhali Barodawala, Kunjal Lila, Raj Jatale, Shibani Ramchandran, Milind Chanekar, Gauri Pradhan, Kirti Chadha
Publikováno v:
Cancer Research, Statistics, and Treatment, Vol 7, Iss 1, Pp 11-18 (2024)
Background: Accurate molecular testing in non-small-cell lung cancer (NSCLC) is of paramount importance for treatment, prediction, and prognostication. Objectives: We aimed to comprehensively describe the clinicopathological and molecular profile of
Externí odkaz:
https://doaj.org/article/788ba6e3d7644a39b7c2913e1a412d2d
Autor:
Pratiksha Chheda, Shailesh Pande, Tavisha Dama, Sushant Vinarkar, Milind Chanekar, Shweta Limaye, Nilesh Shah, Kirti Chadha
Publikováno v:
Cancer Research, Statistics, and Treatment, Vol 3, Iss 1, Pp 32-41 (2020)
Introduction: There is a growing need for BRCA1/BRCA2 mutation frequencies among hereditary breast and ovarian carcinoma (HBOC) cases, specifically determined on the grounds of personal and family history profiles in the Indian population. The curren
Externí odkaz:
https://doaj.org/article/c3d2281013cc474b8d8d3b8a24af8fd3
Autor:
Sandeep Warghade, Jyothi Britto, Reshma Haryan, Tejaswi Dalvi, Rajesh Bendre, Pratiksha Chheda, Sunmeet Matkar, Yogita Salunkhe, Milind Chanekar, Nilesh Shah
Publikováno v:
Journal of Laboratory Physicians, Vol 10, Iss 01, Pp 073-079 (2018)
CONTEXT: Hemoglobinopathies constitute the world's most common genetically inherited red blood cell disorder. Screening and accurate identification of hemoglobin (Hb) variants have become increasingly important in antenatal diagnosis and prevention o
Externí odkaz:
https://doaj.org/article/ae7f33f43a934fe9aed25c811dd49911
Autor:
Milind Chanekar, Kirti Chadha, Shailesh Pande, Pratiksha Chheda, Tavisha Dama, Nilesh Shah, Shweta Limaye, Sushant Vinarkar
Publikováno v:
Cancer Research, Statistics, and Treatment, Vol 3, Iss 1, Pp 32-41 (2020)
Introduction: There is a growing need for BRCA1/BRCA2 mutation frequencies among hereditary breast and ovarian carcinoma (HBOC) cases, specifically determined on the grounds of personal and family history profiles in the Indian population. The curren
Autor:
Milind Chanekar, Anurita Pais, Pratiksha Chheda, Rajesh Bendre, Yogita Salunkhe, Nilesh Shah, Tavisha Dama, Shailesh Pande
Publikováno v:
Molecular Diagnosis & Therapy. 22:353-359
Huntington’s disease (HD) is an autosomal-dominant neurodegenerative disorder with an average age at onset of 40 years. It is a polyglutamine (polyQ) disorder that is caused by an increase in the number of CAG repeats in the huntingtin (HTT) gene.
Autor:
Jyothi Britto, Nilesh Shah, Yogita Salunkhe, Tejaswi Dalvi, Milind Chanekar, Reshma Haryan, Pratiksha Chheda, Rajesh Bendre, Sandeep Warghade, Sunmeet Matkar
Publikováno v:
Journal of Laboratory Physicians
Journal of Laboratory Physicians, Vol 10, Iss 01, Pp 073-079 (2018)
Journal of Laboratory Physicians, Vol 10, Iss 01, Pp 073-079 (2018)
CONTEXT: Hemoglobinopathies constitute the world's most common genetically inherited red blood cell disorder. Screening and accurate identification of hemoglobin (Hb) variants have become increasingly important in antenatal diagnosis and prevention o