Neutral Sphingomyelinase (SMPD3) Deficiency Causes a Novel Form of Chondrodysplasia and Dwarfism That Is Rescued by Col2A1-Driven smpd3 Transgene Expression-Reference-Cited by-同舟云学术

Neutral Sphingomyelinase (SMPD3) Deficiency Causes a Novel Form of Chondrodysplasia and Dwarfism That Is Rescued by Col2A1-Driven smpd3 Transgene Expression

Published:2007-07 Issue:1 Volume:171 Page:153-161
ISSN:0002-9440
Container-title:The American Journal of Pathology
language:en
Short-container-title:The American Journal of Pathology

Author:

Stoffel Wilhelm,Knifka Jutta,Koebke Jürgen,Niehoff Anja,Jenke Britta,Holz Barbara,Binczek Erika,Günter Robert Heinz

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

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3. Characterization and subcellular localization of murine and human magnesium-dependent neutral sphingomyelinase;Tomiuk;J Biol Chem,2000

4. Acid sphingomyelinase-deficient mice mimic the neurovisceral form of human lysosomal storage disease (Niemann-Pick disease);Otterbach;Cell,1995

5. Neutral sphingomyelinase 1 deficiency in the mouse causes no lipid storage disease;Zumbansen;Mol Cell Biol,2002

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