Lysosomal Storage Diseases A class of ~50 genetic diseases, known as L ysosomal S torage D iseases (LSDs) are characterized by lysosomal dysfunction resulting in the accumulation of undegraded...
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HOUSTON LYSOSOMAL STORAGE DISEASE CENTER - HOME | utlyso.org Reviews
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Lysosomal Storage Diseases A class of ~50 genetic diseases, known as L ysosomal S torage D iseases (LSDs) are characterized by lysosomal dysfunction resulting in the accumulation of undegraded...
utlyso.org
OUR TEAM - HOUSTON LYSOSOMAL STORAGE DISEASE CENTER
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HOUSTON LYSOSOMAL STORAGE DISEASE CENTER. Kartik Venkatachalam, Ph.D. Director, UT Lysosomal Storage Disease Center. Assistant Professor, Department of Integrative Biology and Pharmacology. University of Texas, School of Medicine, Houston. Dr Venkatachalam's research involves the use of. Current funding related to LSDs: NIH R01, NS081301, "Alterations in synaptic growth and lipid-raft organization in a fly MLIV model". Email Dr. Venkatachalam. Dr Venkatachalam's lab website. Mary Kay Koenig, M.D. Dr Koen...
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HOUSTON LYSOSOMAL STORAGE DISEASE CENTER.
PARTNERS - HOUSTON LYSOSOMAL STORAGE DISEASE CENTER
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HOUSTON LYSOSOMAL STORAGE DISEASE CENTER. The Mucolipidosis type IV (MLIV) Foundation.
MISSION - HOUSTON LYSOSOMAL STORAGE DISEASE CENTER
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HOUSTON LYSOSOMAL STORAGE DISEASE CENTER.
INFORMATION - HOUSTON LYSOSOMAL STORAGE DISEASE CENTER
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HOUSTON LYSOSOMAL STORAGE DISEASE CENTER.
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HOUSTON LYSOSOMAL STORAGE DISEASE CENTER - HOME
HOUSTON LYSOSOMAL STORAGE DISEASE CENTER. A class of 50 genetic diseases, known as L. Iseases (LSDs) are characterized by lysosomal dysfunction resulting in the accumulation of undegraded material in cells throughout the body. Although LSDs affect cells regardless of tissue type, the neurological consequences of lysosomal dysfunction, which include severe locomotor and intellectual disabilities, cognitive deficits, and seizures, are especially intractable. For more information on LSDs.
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