-
1دورية أكاديمية
المؤلفون: V J Arun, Anuradha Deorukhkar, Aboobacker Mohamed Rafi, Deepak Charles, Rati Devendra, Susheela J Innah, Prabhakar Kedar
المصدر: Asian Journal of Transfusion Science, Vol 16, Iss 1, Pp 128-131 (2022)
مصطلحات موضوعية: glucose-6-phosphate dehydrogenase, methemoglobinemia, novel mutation, Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
-
2دورية أكاديمية
المصدر: BMC Medical Genomics, Vol 14, Iss 1, Pp 1-7 (2021)
مصطلحات موضوعية: Adenylate kinase deficiency, Enzymopathies, Prenatal diagnosis, Congenital hemolytic anemia, Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1755-8794
-
3دورية أكاديمية
المؤلفون: Rati Devendra, Vinod Gupta, Somashekhar S. Biradar, Pradeep Bhat, Shantharam Hegde, S. L. Hoti, Malay B. Mukherjee, Harsha V. Hegde
المصدر: Annals of Human Biology, Vol 47, Iss 1, Pp 55-58 (2020)
مصطلحات موضوعية: g6pd, mutation, microsatellite repeat sequences, g6pd a- mutation, siddis, Biology (General), QH301-705.5, Human anatomy, QM1-695, Physiology, QP1-981
وصف الملف: electronic resource
-
4
المؤلفون: Rashmi Dongerdiye, Meghana Bokde, Tejashree Anil More, Arati Saptarshi, Rati Devendra, Ashish Chiddarwar, Prashant Warang, Prabhakar Kedar
المصدر: Annals of Hematology. 102:1029-1036
مصطلحات موضوعية: Hematology, General Medicine
-
5
المصدر: BMC Medical Genomics, Vol 14, Iss 1, Pp 1-7 (2021)
BMC Medical Genomicsمصطلحات موضوعية: Prenatal diagnosis, Adenylate kinase deficiency, Biology, QH426-470, medicine.disease_cause, Enzymopathies, Loss of heterozygosity, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, medicine, Genetics, Gene, Internal medicine, Genetics (clinical), Sanger sequencing, Mutation, Psychomotor retardation, Congenital hemolytic anemia, Anemia, Hemolytic, Congenital Nonspherocytic, medicine.disease, RC31-1245, genomic DNA, 030220 oncology & carcinogenesis, symbols, medicine.symptom, Research Article, 030215 immunology
-
6
المصدر: Molecular genetics and genomics : MGG.
مصطلحات موضوعية: Genetics, General Medicine, Molecular Biology
-
7
المؤلفون: B. Suresh, Rashmi Dongerdiye, Prabhakar Kedar, Sujatha Jagadeesh, Rati Devendra, Aruna Rajendran, Prashant Warang
المصدر: Journal of Clinical Pathology. 74:620-624
مصطلحات موضوعية: 0301 basic medicine, Genetics, Proband, Hexokinase, Mutation, Anemia, General Medicine, 030105 genetics & heredity, Biology, medicine.disease, medicine.disease_cause, Pathology and Forensic Medicine, 03 medical and health sciences, chemistry.chemical_compound, Hexokinase deficiency, 030104 developmental biology, chemistry, medicine, Glycolysis, Gene, Exome sequencing
-
8
المصدر: Annals of Hematology. 99:715-727
مصطلحات موضوعية: Male, Models, Molecular, Hemolytic anemia, Congenital Anemia, Iron Overload, Adolescent, Protein Conformation, Hydrops Fetalis, Pyruvate Kinase, Mutation, Missense, India, Biology, Anemia, Hemolytic, Congenital, medicine.disease_cause, Ion Channels, Mice, Structure-Activity Relationship, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, medicine, Animals, Humans, Missense mutation, Computer Simulation, Amino Acid Sequence, Child, Genetic Association Studies, Genes, Dominant, Sanger sequencing, Genetics, Mutation, Anemia, Iron-Deficiency, Sequence Homology, Amino Acid, Genetic disorder, High-Throughput Nucleotide Sequencing, Hematology, General Medicine, medicine.disease, Child, Preschool, 030220 oncology & carcinogenesis, Mutation testing, symbols, Female, Sequence Alignment, Congenital hemolytic anemia, 030215 immunology
-
9
المؤلفون: Prashant Warang, Prabhakar Kedar, Anuja Kulkarni, Rati Devendra, Ashish Chiddarwar, Vinod Gupta
المصدر: Human Mutation. 41:737-748
مصطلحات موضوعية: Models, Molecular, Genotype, Protein Conformation, CYB5R3, Genes, Recessive, Prenatal diagnosis, Disease, Biology, medicine.disease_cause, Methemoglobinemia, Structure-Activity Relationship, 03 medical and health sciences, Genetics, medicine, Humans, Genetic Predisposition to Disease, Gene, Alleles, Genetic Association Studies, Genetics (clinical), 030304 developmental biology, 0303 health sciences, Mutation, Molecular pathology, 030305 genetics & heredity, medicine.disease, Phenotype, Amino Acid Substitution, Congenital Methemoglobinemia, Cytochrome-B(5) Reductase
-
10
المؤلفون: S.L. Hoti, Pradeep Bhat, Shantharam Hegde, Malay B. Mukherjee, Harsha V. Hegde, Rati Devendra, Somashekhar S. Biradar, Vinod Gupta
المصدر: Annals of Human Biology. 47:55-58
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Aging, Adolescent, Physiology, Epidemiology, India, Glucosephosphate Dehydrogenase, Biology, Young Adult, 03 medical and health sciences, 0302 clinical medicine, hemic and lymphatic diseases, parasitic diseases, Prevalence, Genetics, Humans, 030216 legal & forensic medicine, Child, Aged, Public Health, Environmental and Occupational Health, nutritional and metabolic diseases, Middle Aged, Glucosephosphate Dehydrogenase Deficiency, 030104 developmental biology, Mutation, Mutation (genetic algorithm), Female