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Roshan B Colah

Showing results (11-20 of 86) with videos related to

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Blood Cells, Molecules & Diseases|December 6, 2012
Effect of a group of genetic markers around the 5' regulatory regions of the β globin gene cluster linked to high HbF on the clinical severity of β thalassemiaPooja Dabke, Roshan B Colah, K Ghosh, et al.
Hemoglobin|March 17, 2007
An improved flow cytometric approach for isolation of fetal cells from maternal blood for non invasive prenatal diagnosis of hemoglobinopathiesEdna D'Souza, Swati Kulkarni, Roshan B Colah, et al.
Clinical Chemistry and Laboratory Medicine|September 24, 2014
Spectrum of red cell abnormalities in undiagnosed hemolytic anemias and methemoglobinemias: a single center experiencePrashant Warang, Prabhakar Kedar, Kanjaksha Ghosh, et al.
American Journal of Hematology|February 18, 2011
Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: compound heterozygous for NADH-cytochrome b5 reductase gene mutationsPrabhakar S Kedar, Prashant Warang, Kanjaksha Ghosh, et al.
Indian Journal of Pediatrics|November 28, 2006
Red cell pyruvate kinase deficiency in neonatal jaundice cases in IndiaPrabhakar S Kedar, Prashant Warang, Roshan B Colah, et al.
Haematologia|June 14, 2003
Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian familiesPrabhakar S Kedar, Roshan B Colah, Kanjaksha Ghosh, et al.
Gene|November 14, 2012
UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adultsSelma D'Silva, Roshan B Colah, Kanjaksha Ghosh, et al.
Gene|May 29, 2014
Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonatesSelma D'Silva, Roshan B Colah, Kanjaksha Ghosh, et al.
Blood Cells, Molecules & Diseases|August 19, 2004
Molecular basis of G6PD deficiency in IndiaSridevi Sukumar, Malay B Mukherjee, Roshan B Colah, et al.
Journal of Community Genetics|February 14, 2019
Haemoglobinopathies in India: estimates of blood requirements and treatment costs for the decade 2017-2026Sujata Sinha, Tulika Seth, Roshan B Colah, et al.
Pageof 9

Showing results (11-20 of 86) with videos related to

Sort By:
Pageof 9
Blood Cells, Molecules & Diseases|December 6, 2012
Effect of a group of genetic markers around the 5' regulatory regions of the β globin gene cluster linked to high HbF on the clinical severity of β thalassemiaPooja Dabke, Roshan B Colah, K Ghosh, et al.
Hemoglobin|March 17, 2007
An improved flow cytometric approach for isolation of fetal cells from maternal blood for non invasive prenatal diagnosis of hemoglobinopathiesEdna D'Souza, Swati Kulkarni, Roshan B Colah, et al.
Clinical Chemistry and Laboratory Medicine|September 24, 2014
Spectrum of red cell abnormalities in undiagnosed hemolytic anemias and methemoglobinemias: a single center experiencePrashant Warang, Prabhakar Kedar, Kanjaksha Ghosh, et al.
American Journal of Hematology|February 18, 2011
Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: compound heterozygous for NADH-cytochrome b5 reductase gene mutationsPrabhakar S Kedar, Prashant Warang, Kanjaksha Ghosh, et al.
Indian Journal of Pediatrics|November 28, 2006
Red cell pyruvate kinase deficiency in neonatal jaundice cases in IndiaPrabhakar S Kedar, Prashant Warang, Roshan B Colah, et al.
Haematologia|June 14, 2003
Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian familiesPrabhakar S Kedar, Roshan B Colah, Kanjaksha Ghosh, et al.
Gene|November 14, 2012
UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adultsSelma D'Silva, Roshan B Colah, Kanjaksha Ghosh, et al.
Gene|May 29, 2014
Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonatesSelma D'Silva, Roshan B Colah, Kanjaksha Ghosh, et al.
Blood Cells, Molecules & Diseases|August 19, 2004
Molecular basis of G6PD deficiency in IndiaSridevi Sukumar, Malay B Mukherjee, Roshan B Colah, et al.
Journal of Community Genetics|February 14, 2019
Haemoglobinopathies in India: estimates of blood requirements and treatment costs for the decade 2017-2026Sujata Sinha, Tulika Seth, Roshan B Colah, et al.
Pageof 9