Results 1 -
10
of
967
for
6S -"2-amino-6-(3'-methoxybiphenyl-3-yl)-3,6-dimethyl-5,6-dihydropyrimidin-4(3H)-one"
Did you mean 6S -"2-amino-6-(3'-methoxybiphenyl-3-yl)-3,6-dimethyl-5,6-dihydropyrimidine-4(3H)-one"?
- Glucose-6-phosphate dehydrogenase deficiency is a genetic disorder that affects red blood cells, which carry oxygen from the lungs to tissues throughout the ...
- Dystonia 6 is one of many forms of dystonia, which is a group of conditions characterized by involuntary movements, twisting (torsion) and tensing of various muscles, ...
- Spinocerebellar ataxia type 6 (SCA6) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with coordination ...
- ... down a type of sugar molecule called glucose 6-phosphate. The breakdown of this molecule produces the ... SLC37A4 genes prevent the effective breakdown of glucose 6-phosphate. Glucose 6-phosphate that is not broken ...
- ... pathway; in this step, a molecule called glucose-6-phosphate is converted to another molecule called fructose-6-phosphate.When GPI remains a single molecule (a ...
- ... Fructose aldolase B deficiency Fructose intolerance Fructose-1,6-biphosphate aldolase deficiency Fructose-1-phosphate aldolase deficiency ... to hereditary fructose intolerance. FEBS Lett. 2002 Nov 6;531(2):152-6. doi: 10.1016/s0014- ...
- ... of diabetes that first appears within the first 6 months of life and persists throughout the lifespan. ... common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by ...
- ... related hypomyelinating leukodystrophy Genetic Testing Registry: Hypomyelinating leukodystrophy 6 Hypomyelination with atrophy of basal ganglia and cerebellum ...
- ... symptoms of the condition. Mitochondrial DNA depletion syndrome 6 MPV17-associated hepatocerebral MDS MTDPS6 Navajo familial neurogenic ... NNH Genetic Testing Registry: Mitochondrial DNA depletion syndrome 6 (hepatocerebral type) Navajo neurohepatopathy National Organization for Rare ...
- ... usually appear during childhood, most commonly around age 6. The first signs of the condition are typically ... 77. doi: 10.1086/321970. Epub 2001 Jul 6. Citation on PubMed or Free article on PubMed ...