Results 31 -
40
of
253
for
Blood group B
- ... ALDOB gene provides instructions for making the aldolase B enzyme. This enzyme is one of a group of three aldolase enzymes that are responsible for breaking down certain molecules in cells throughout the body. Four identical aldolase B enzymes need to be attached (bound) to each ...
- ... Dotsch J, Muller-Wiefel DE, Hoyer P; Study Group Members of the Gesellschaft fur Padiatrische Nephrologie; Knebelmann B, Pirson Y, Grunfeld JP, Niaudet P, Cochat P, ...
- ... disorder called myelodysplastic syndrome (MDS). MDS comprises a group of conditions in which immature blood cells fail to develop normally, resulting in too ...
- ... chain or the binding of the A and B chains to form insulin, leading to impaired blood glucose control. More About This Health Condition MedlinePlus ... SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, ... Group; Hattersley AT, Ellard S. Insulin mutation screening in ...
- ... of glutamate formiminotransferase deficiency, a buildup of certain B vitamins called folates in the blood. It is unclear how the mutations result in ...
- ... of blood clots. More About This Health Condition Blood Coagulation Factor II coagulation factor II coagulation factor II (thrombin) prothrombin B-chain PT Q7Z7P3_HUMAN serine protease Tests of ...
- ... risk of developing metabolic syndrome, which is a group of conditions that include high blood glucose levels during prolonged periods without food (fasting), ...
- ... chain or the binding of the A and B chains to form insulin, leading to impaired blood glucose control.Permanent neonatal diabetes mellitus can also ... SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, ... Group; Hattersley AT, Ellard S. Insulin mutation screening in ...
- ... M, Novelli V, Giorgio G, Barra A, Franco B; Oral-Facial-Digital Type I (OFDI) Collaborative Group. Mutational spectrum of the oral-facial-digital type ...
- ... JA, MacDonald J, Saisawat P, Ashraf S, Ovunc B, Zenker M, Hildebrandt F; Gesselschaft fur Paediatrische Nephrologie (GPN) Study Group. Nineteen novel NPHS1 mutations in a worldwide cohort ...