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P Warang

Showing results (1-10 of 7) with videos related to

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International Journal of Laboratory Hematology|November 15, 2011
A new simple approach for the determination of pyrimidine 5'-nucleotidase activity in human erythrocytes using an ELISA readerP Warang, P Kedar, K Ghosh, et al.
European Journal of Clinical Investigation|January 27, 2010
Five alpha globin chain variants identified during screening for haemoglobinopathiesS Nair, A Nadkarni, P Warang, et al.
Annals of Hematology|March 1, 2020
Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in IndiaTejashree Anil More, Rashmi Dongerdiye, Rati Devendra, et al.
Clinical Genetics|November 26, 2013
Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in IndiaP P Warang, P S Kedar, C Shanmukaiah, et al.
Clinical Genetics|September 2, 2008
Spectrum of novel mutations in the human PKLR gene in pyruvate kinase-deficient Indian patients with heterogeneous clinical phenotypesP Kedar, T Hamada, P Warang, et al.
Hemoglobin|September 8, 2022
Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell DiseasePrashant P Warang, Nikhil S Shinde, Vinod D Umare, et al.
International Journal of Hematology|August 12, 2019
Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approachPrabhakar S Kedar, Hideo Harigae, Etsuro Ito, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
International Journal of Laboratory Hematology|November 15, 2011
A new simple approach for the determination of pyrimidine 5'-nucleotidase activity in human erythrocytes using an ELISA readerP Warang, P Kedar, K Ghosh, et al.
European Journal of Clinical Investigation|January 27, 2010
Five alpha globin chain variants identified during screening for haemoglobinopathiesS Nair, A Nadkarni, P Warang, et al.
Annals of Hematology|March 1, 2020
Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in IndiaTejashree Anil More, Rashmi Dongerdiye, Rati Devendra, et al.
Clinical Genetics|November 26, 2013
Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in IndiaP P Warang, P S Kedar, C Shanmukaiah, et al.
Clinical Genetics|September 2, 2008
Spectrum of novel mutations in the human PKLR gene in pyruvate kinase-deficient Indian patients with heterogeneous clinical phenotypesP Kedar, T Hamada, P Warang, et al.
Hemoglobin|September 8, 2022
Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell DiseasePrashant P Warang, Nikhil S Shinde, Vinod D Umare, et al.
International Journal of Hematology|August 12, 2019
Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approachPrabhakar S Kedar, Hideo Harigae, Etsuro Ito, et al.
Pageof 1