Search Results - "Mukherjee, M B"

A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant by Devendra, R., Warang, P., Gupta, V., Chiddarwar, A., Kedar, P., Agarwal, M. B., Mukherjee, M. B.

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Identification of high oxygen affinity hemoglobin (Hb Andrew‐Minneapolis) in an Indian family by Mehta, P., Upadhye, D., Hariharan, P., Italia, K., Sawant, P., Nadkarni, A., Subramanian, G., Mukherjee, M. B.

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Molecular characterization of G6PD Insuli—a novel 989 CGC → CAC (330 Arg → His) mutation in the Indian population by Sukumar, S, Mukherjee, M.B, Colah, R.B, Mohanty, D

“…Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common red cell enzymopathy among humans. G6PD deficiency was reported in India more than 30…”
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G6PD deficiency and malaria in India by Mohanty, D., Sukumar, S., Mukherjee, M.B., Colah, R.B.

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Iron deficiency anaemia in sickle cell disorders in India by Mohanty, D, Mukherjee, M B, Colah, R B, Wadia, M, Ghosh, K, Chottray, G P, Jain, D, Italia, Y, Ashokan, K, Kaul, R, Shukla, D K, Muthuswamy, V

“…Iron deficiency anaemia (IDA) is uncommon in individuals with sickle cell disease (SCD) because of availability of an adequate iron source potentially from…”
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Effect of α‐thalassemia on sickle‐cell anemia linked to the Arab‐Indian haplotype in India by Mukherjee, Malay B., Lu, Chang Yong, Ducrocq, Rolande, Gangakhedkar, Raman R., Colah, Roshan B., Kadam, Megha D., Mohanty, Dipika, Nagel, Ronald L., Krishnamoorthy, Rajagopal

“…Two population groups from Western India with a high prevalence of the βs gene, one tribal (Valsad) and the other nontribal (Nagpur), were studied. The βs gene…”
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G6PD Namoru (208 T→ C) is the major polymorphic variant in the tribal populations in southern India by Chalvam, R., Mukherjee, M. B., Colah, R. B., Mohanty, D., Ghosh, K.

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Clinical examination and hematological data in asymptomatic & apparently healthy school children in a boarding school in a tribal area by Ghosh, K, Mukherjee, M B, Shankar, U, Kote, S L, Nagtilak, S B, Kolah, R B, Surve, R R, Tamankar, A A, Sukumar, S, Mohanty

“…In a boarding school of Maharashtra State of India 314 students (Bhil & Pawar) were examined clinically and blood was examined. Anemia was present in 16.2%…”
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A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India by Chalvam, R, Kedar, P S, Colah, R B, Ghosh, K, Mukherjee, M B

“…Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common red cell enzymopathy among humans. In India, G6PD Mediterranean, G6PD Orissa, and G6PD…”
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Milder clinical course of sickle cell disease in patients with alpha thalassemia in the Indian subcontinent by Mukherjee, M B, Colah, R B, Ghosh, K, Mohanty, D, Krishnamoorthy, R

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Red Cell Genetic Abnormalities, β-Globin Gene Haplotypes, and APOB Polymorphism in the Great Andamanese, A Primitive Negrito Tribe of Andaman and Nicobar Islands, India by MURHEKAR, K.M., MURHEKAR, M.V., MUKHERJEE, M.B., GORAKSHAKAR, A.C., SURVE, R., WADIA, M., PHANASGAONKAR, S., SHRIDEVI, S., ROSHAN, B. COLAH, MOHANTY, D.

“…The Great Andamanese are a primitive Negrito tribe of the Andaman and Nicobar Islands, India, with a total population of 37. We studied 29 individuals from…”
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The influence of alpha-thalassaemia on the haematological & clinical expression of sickle cell disease in western India by Mukherjee, M B, Surve, R, Tamankar, A, Gangakhedkar, R R, Ghosh, K, Lu, C Y, Krishnamoorthy, R, Colah, R, Mohanty, D

“…We evaluated the clinical and haematological features of 29 sickle cell anaemia patients with associated alpha-thalassaemia and 22 sickle cell homozygotes with…”
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Beta-thalassaemia heterozygotes with alpha-globin gene triplication by Colah, R B, Nadkarni, A H, Mukherjee, M B, Gorakshakar, A C, Surve, R, Mohanty, D

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Characterization of G6PD Rohini--a new class III Indian variant by Sayyed, Z, Mukherjee, M B, Mudera, V C, Colah, R, Gupte, S

“…A new Indian G6PD variant was detected in a 15 yr old Maratha male during a population screening programme in high school children in Bombay (India). The…”
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Hemoglobin sickle D Punjab-a case report by Mukherjee, M, Surve, R, Gangakhedkar, R, Mohanty, D, Colah, R

“…Compound heterozygosity for bS/bD results in a severe hemolytic anemia and a clinical syndrome similar to that of sickle cell disease. Here, we report a case…”
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Time to form a consortium to study the genetic polymorphism by using standard DNA markers by Ghosh, K, Mukherjee, M, Mohanty, D

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Identification of a novel S184F mutation causing glucose-6-phosphate-dehydrogenase deficiency in a tribal family of Madhya Pradesh, Central India by Devendra, R, Shanmugam, R, Singh, MPSS, Vishwakarma, CP, Godbhole, S, Singh, N, Gupta, V, Kedar, P, Mukherjee, MB

“…Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human erythroenzymopathy. G6PD deficiency in India is mainly due to the presence of the…”
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Red Cell Genetic Abnormalities, [Beta]-Globin Gene Haplotypes, and APOB Polymorphisms in the Great Andamanese, A Primitive Negrito Tribe of Andaman and Nicobar Islands, India by Murhekar, K. M, Murhekar, M. V, Mukherjee, M. B, Gorakshakar, A. C, Surve, R, Wadia, M, Phanasgaonkar, S, Shridevi, S, Colah, Roshan B, Mohanty, D

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Prevalence of clinically relevant (TA)n UGT1A1 promoter alleles in Indian neonates by D'Silva, Selma, Colah, Roshan B., Ghosh, Kanjaksha, Mukherjee, Malay B.

“…UDP-glucuronosyltransferase 1A1 (UG-T1A1) is the key enzyme for bilirubin conjugation. It is encoded by the UGT1A1 gene, which consists of five exons and is a…”
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Symptomatic presentation of a sickle cell heterozygote: An evaluation of genetic factors by Mukherjee, Malay B., Surve, Reema R., Gorakshakar, Ajit C., Gangakhedkar, Raman R., Colah, Roshan B., Mohanty, Dipika

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