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American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 04/2011, Volume 300, Issue 4, pp. 833 - 842
Journal Article
Computer Communications, ISSN 0140-3664, 05/2016, Volume 82, pp. 49 - 58
Journal Article
Molecular Genetics and Metabolism Reports, ISSN 2214-4269, 06/2017, Volume 11, Issue C, pp. 24 - 29
G -gangliosidosis, AB variant is an extremely rare autosomal recessive inherited disorder caused by mutations in the gene that encodes G ganglioside activator... 
Gangliosidosis | GM2 ganglioside activator protein | Lysosomal storage disease | GM2 ganglioside | ganglioside activator protein | ganglioside | G
Journal Article
Critical Care, ISSN 1364-8535, 10/2018, Volume 22, Issue 1, pp. 251 - 251
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 2018, Volume 293, Issue 3, pp. 808 - 818
The cbb3 oxidase has a high affinity for oxygen and is required for growth of bacteria, including pathogens, in oxygen-limited environments. However, the... 
Index Medicus | Bioenergetics | bacteria | cytochrome oxidase | subunit interactions | membrane sub-complexes assembly | cbb3 cytochrome c oxidase biogenesis | membrane protein | respiration | protein assembly
Journal Article
Journal of Inherited Metabolic Disease, ISSN 1573-2665, 12/2010, Volume 33, Issue S3, pp. 409 - 412
To report the successful pregnancy of a woman with methylmalonic acidemia and hyperhomocysteinemia, cblC type [cobalamin C (cblC) deficiency] (MIM... 
Human Genetics | Biochemistry, general | Pediatrics | Internal Medicine | Medicine & Public Health | Metabolic Diseases | MEDICINE, RESEARCH & EXPERIMENTAL | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | Folic Acid - therapeutic use | Homocystinuria - therapy | Humans | Male | Vitamin B 12 Deficiency - therapy | Homocystinuria - metabolism | Amino Acid Metabolism, Inborn Errors - diagnosis | Young Adult | Amino Acid Metabolism, Inborn Errors - metabolism | Amino Acid Metabolism, Inborn Errors - genetics | DNA Mutational Analysis | Female | Aspirin - therapeutic use | Pregnancy Complications - metabolism | Vitamin B 12 Deficiency - metabolism | Platelet Aggregation Inhibitors - therapeutic use | Hydroxocobalamin - therapeutic use | Genetic Predisposition to Disease | Vitamin B 12 Deficiency - diagnosis | Vitamin B Complex - therapeutic use | Live Birth | Cells, Cultured | Treatment Outcome | Combined Modality Therapy | Pregnancy Complications - diagnosis | Amino Acid Metabolism, Inborn Errors - therapy | Diet, Protein-Restricted | Pregnancy | Carrier Proteins - genetics | Phenotype | Carnitine - therapeutic use | Pregnancy Complications - genetics | Vitamin B 12 Deficiency - genetics | Mutation | Homocystinuria - diagnosis | Homocystinuria - genetics | Vitamin B 12 - metabolism | Pregnancy Complications - therapy | Care and treatment | Aspirin | Pregnant women | Index Medicus
Journal Article
Molecular genetics and metabolism reports, ISSN 2214-4269, 06/2017, Volume 11, pp. 24 - 29
G -gangliosidosis, AB variant is an extremely rare autosomal recessive inherited disorder caused by mutations in the gene that encodes G ganglioside activator... 
Journal Article
Journal Article
Journal Article
Journal of Hand Surgery, ISSN 0363-5023, 2016, Volume 41, Issue 10, pp. e337 - e341
Journal Article