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History (55)
Transport of hydroxyzine and triprolidine across bovine olfactory mucosa: role of passive diffusion in the direct nose-to-brain uptake of small molecules.
Cultured M?ller cells from mammals can synthesize and accumulate retinyl esters.
Solid lipid nanoparticles (SLN) of tretinoin: potential in topical delivery.
Segregation and disparities in health services use.
Publishing nutrition research: a review of sampling, sample size, statistical analysis, and other key elements of manuscript preparation, Part 2.
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Characterization of kinesin switch I mutations that cause hereditary spastic paraplegia.
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Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands.
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Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia.
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Motor protein mutations cause a new form of hereditary spastic paraplegia.
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MitCHAP-60 and Hereditary Spastic Paraplegia SPG-13 Arise from an Inactive hsp60 Chaperonin that Fails to Fold the ATP Synthase ?-Subunit.
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Pathogenic mutation of spastin has gain-of-function effects on microtubule dynamics.
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