Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Reena Das

Showing results (181-190 of 279) with videos related to

Pageof 28
Sort By:
The Journal of Molecular Diagnostics : JMD|February 24, 2018
Optimal Reference Gene Selection for Expression Studies in Human ReticulocytesAnu Aggarwal, Manu Jamwal, Ganesh K Viswanathan, et al.
European Journal of Haematology|January 30, 2014
Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian populationThiyagaraj Mayuranathan, Janakiram Rayabaram, Reena Das, et al.
Journal of Microscopy and Ultrastructure|May 12, 2025
Bone Marrow Erythroblastic Dysplasia on Morphology Correlates Significantly with Flow Cytometric Apoptosis and Peripheral Blood EryptosisChander Hans, Prashant Sharma, Rahul Saini, et al.
Pathology|November 6, 2017
First report of Mediterranean stomatocytosis/macrothrombocytopenia in an Indian family: a diagnostic dilemmaManu Jamwal, Anu Aggarwal, Arindam Maitra, et al.
European Journal of Haematology|January 4, 2023
Hematological and genetic profiles of persons with co-inherited heterozygous β-thalassemia and supernumerary α-globin genesDurga Devi Sundaresan, Jasbir Kaur Hira, Sanjeev Chhabra, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 31, 2026
Combining conventional and reticulocyte metrics enhances Iron deficiency detection in asymptomatic individualsMugdha Gautam, Prashant Sharma, Arnab Pal, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 5, 2015
Coagulation factor VIII, IX and XI levels in north Indian patients with venous thromboembolism: first study from IndiaAbhijit Chougule, Sweta Rajpal, Jasmina Ahluwalia, et al.
Hemoglobin|February 11, 2022
Hb Mizuho (<i>HBB</i>: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation SequencingDiksha D Yadav, Manu Jamwal, Namrata Singh, et al.
World Journal of Gastroenterology|June 26, 2007
Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north IndiaBarjinderjit Kaur Dhillon, Reena Das, Gurjeewan Garewal, et al.
Pediatric Blood & Cancer|September 17, 2013
Risk factors for thromboembolism and pulmonary artery hypertension following splenectomy in children with hereditary spherocytosisAnirban Das, Deepak Bansal, Jasmina Ahluwalia, et al.
Pageof 28

Showing results (181-190 of 279) with videos related to

Sort By:
Pageof 28
The Journal of Molecular Diagnostics : JMD|February 24, 2018
Optimal Reference Gene Selection for Expression Studies in Human ReticulocytesAnu Aggarwal, Manu Jamwal, Ganesh K Viswanathan, et al.
European Journal of Haematology|January 30, 2014
Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian populationThiyagaraj Mayuranathan, Janakiram Rayabaram, Reena Das, et al.
Journal of Microscopy and Ultrastructure|May 12, 2025
Bone Marrow Erythroblastic Dysplasia on Morphology Correlates Significantly with Flow Cytometric Apoptosis and Peripheral Blood EryptosisChander Hans, Prashant Sharma, Rahul Saini, et al.
Pathology|November 6, 2017
First report of Mediterranean stomatocytosis/macrothrombocytopenia in an Indian family: a diagnostic dilemmaManu Jamwal, Anu Aggarwal, Arindam Maitra, et al.
European Journal of Haematology|January 4, 2023
Hematological and genetic profiles of persons with co-inherited heterozygous β-thalassemia and supernumerary α-globin genesDurga Devi Sundaresan, Jasbir Kaur Hira, Sanjeev Chhabra, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 31, 2026
Combining conventional and reticulocyte metrics enhances Iron deficiency detection in asymptomatic individualsMugdha Gautam, Prashant Sharma, Arnab Pal, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 5, 2015
Coagulation factor VIII, IX and XI levels in north Indian patients with venous thromboembolism: first study from IndiaAbhijit Chougule, Sweta Rajpal, Jasmina Ahluwalia, et al.
Hemoglobin|February 11, 2022
Hb Mizuho (<i>HBB</i>: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation SequencingDiksha D Yadav, Manu Jamwal, Namrata Singh, et al.
World Journal of Gastroenterology|June 26, 2007
Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north IndiaBarjinderjit Kaur Dhillon, Reena Das, Gurjeewan Garewal, et al.
Pediatric Blood & Cancer|September 17, 2013
Risk factors for thromboembolism and pulmonary artery hypertension following splenectomy in children with hereditary spherocytosisAnirban Das, Deepak Bansal, Jasmina Ahluwalia, et al.
Pageof 28