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Anatomical and physiological variation of the hyoid musculature during swallowing in infant pigs.
Iterative design of emetine-based prodrug targeting fibroblast activation protein (FAP) and dipeptidyl peptidase IV DPPIV using a tandem enzymatic activation strategy.
Homology cloning of protein kinase and phosphoprotein phosphatase sequences of Dictyostelium discoideum.
Comparison of Atmospheric Fungal Spore Concentrations between Two Main Cities in the Caribbean Basin.
A confirmatory model for substance use among Japanese American and part-Japanese American adolescents.
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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.
Academic Article
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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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Spastic Paraplegia, Hereditary
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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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Huckaba, Thomas
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Pathogenic mutation of spastin has gain-of-function effects on microtubule dynamics.
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Bernal, Ricardo
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Gonzalez, Michael J
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Mottamal, Madhusoodanan
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Davidson, Michael
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