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6S -"1-chloro-3-[(4-fluorobenzyl)oxy]-6-(pyrroline-1-ylcarbonyl)pyrrolo[1,2-a]prazosin-4(6H)-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 ...
- ... divided into 23 pairs. Two copies of chromosome 6, one copy inherited from each parent, form one of the pairs. Chromosome 6 spans about 171 million DNA building blocks (base ...
- ... linked glycosylation 12 homolog (S. cerevisiae, alpha-1,6-mannosyltransferase) asparagine-linked glycosylation 12 homolog (yeast, alpha- ...
- ... for making a protein called sodium/hydrogen exchanger 6 (Na+/H+ exchanger 6 or NHE6). Na+/H+ exchangers are found in ...
- ... instructions for producing an enzyme called N-acetylgalactosamine 6-sulfatase. This enzyme is located in lysosomes, which ... and recycle different types of molecules. N-acetylgalactosamine 6-sulfatase is involved in the breakdown of large ...
- ... provides instructions for making an enzyme called glucose 6-phosphatase. This enzyme is found on the membrane ... is involved in protein processing and transport. Glucose 6-phosphatase works together with the glucose 6-phosphate ...
- ... in children with bilateral striatal necrosis. ATP synthase 6 ATP synthase F0 subunit 6 ATP6 ATP6_HUMAN ATPase protein 6 ATPase-6 ATPASE6 mitochondrially encoded ATP synthase 6 ...
- ... Cluster of differentiation antigen 49f FLJ18737 integrin alpha 6 integrin alpha chain, alpha 6 Integrin alpha6 integrin, alpha 6 integrin, alpha-6 ITA6_HUMAN Lymphocyte antigen CD49F ...