نتایج جستجو برای: lysosomal storage disease

تعداد نتایج: 1671181  

2017
Xiaolai Zhou Lirong Sun Oliver Bracko Ji Whae Choi Yan Jia Alissa L. Nana Owen Adam Brady Jean C. Cruz Hernandez Nozomi Nishimura William W. Seeley Fenghua Hu

Haploinsufficiency of progranulin (PGRN) due to mutations in the granulin (GRN) gene causes frontotemporal lobar degeneration (FTLD), and complete loss of PGRN leads to a lysosomal storage disorder, neuronal ceroid lipofuscinosis (NCL). Accumulating evidence suggests that PGRN is essential for proper lysosomal function, but the precise mechanisms involved are not known. Here, we show that PGRN ...

2015
Michelle Rothaug Stijn Stroobants Michaela Schweizer Judith Peters Friederike Zunke Mirka Allerding Rudi D’Hooge Paul Saftig Judith Blanz

The Lysosomal Associated Membrane Protein type-2 (LAMP-2) is an abundant lysosomal membrane protein with an important role in immunity, macroautophagy (MA) and chaperone-mediated autophagy (CMA). Mutations within the Lamp2 gene cause Danon disease, an X-linked lysosomal storage disorder characterized by (cardio)myopathy and intellectual dysfunction. The pathological hallmark of this disease is ...

Journal: :Journal of cell science 2012
Wanessa C Lima Florence Leuba Thierry Soldati Pierre Cosson

Mucolipidosis type IV is a poorly understood lysosomal storage disease caused by alterations in the mucolipin lysosomal Ca(2+) channel. In this study, we generated mucolipin-knockout Dictyostelium cells, and observed that lysosome exocytosis was markedly increased in these cells compared with wild-type cells. In addition, mucolipin-knockout cells were more resistant to Ca(2+) deprivation, and t...

Journal: :Journal of Cardiovascular Magnetic Resonance 2009
Dorota Piotrowska-Kownacka Lukasz Kownacki Marek Kuch Ewa Walczak Agnieszka Kosieradzka Anna Fidzianska Leszek Krolicki

Danon disease is a rare X-linked dominant lysosomal glycogen storage disease that can lead to severe ventricular hypertrophy and heart failure. We report a case of Danon disease with cardiac involvement evaluated with cardiovascular magnetic resonance, including late gadolinium enhancement and perfusion studies.

Journal: :BioImpacts : BI 2013
David A Wenger Paola Luzi Mohammad A Rafi

The name of lysosomal storage diseases stems from the fact that in this category of disorders specific undegraded materials are stored in the lysosomes. This is usually caused by a lysosomal enzyme deficiency and leads to a cascade of pathological outcomes. Apart from deficiency of lysosomal enzymes, lysosomal storage diseases also include deficiencies in proteins necessary for enzyme functioni...

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