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Platt Lab, Publications   All Platt Lab publications can be found at: Platt Lab, PubMed (full list) For individual publications, visit the Personnel page and click on an individual's PubMed link. Recent Publications Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium. 18953351 [PubMed - indexed for MEDLINE] Nat Med. 2008 Nov;14(11):1247-55. Epub 2008 Oct 26. Male germ cells require polyenoic sphingolipids with complex glycosylation for completion of meiosis: A link to ceramide synthase-3. PMID: 18308723 [PubMed - as supplied by publisher] J Biol Chem. 2008 Feb 27; [Epub ahead of print] N-butyldeoxygalactonojirimycin reduces brain ganglioside and GM2 content in neonatal Sandhoff disease mice. Neurochem Int. 2007 Dec 8; [Epub ahead of print] PMID: 18207611 [PubMed - as supplied by publisher N-butyldeoxynojirimycin causes weight loss as a result of appetite suppression in lean and obese mice. Diabetes Obes Metab. 2008 Feb;10(2):159-66. PMID: 18190430 [PubMed - in process] Modulation of human natural killer T cell ligands on TLR-mediated antigen-presenting cell activation. Proc Natl Acad Sci U S A. 2007 Dec 18;104(51):20490-5. Epub 2007 Dec 11. PMID: 18077358 [PubMed - indexed for MEDLINE] Accumulation of glucosylceramide in murine testis, caused by inhibition of beta-glucosidase 2: implications for spermatogenesis. J Biol Chem. 2007 Nov 9;282(45):32655-64. Epub 2007 Sep 11. PMID: 17848577 [PubMed - indexed for MEDLINE] Featured Publications Implications for invariant natural killer T cell ligands due to the restricted presence of isoglobotrihexosylceramide in mammals. Proc Natl Acad Sci U S A. 2007 Apr 3;104(14):5971-6. Epub 2007 Mar 19. PMID: 17372214 [PubMed - indexed for MEDLINE] Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease. Nat Med. 2007 Apr;13(4):439-47. Epub 2007 Mar 11. PMID: 17351625 [PubMed - indexed for MEDLINE] The sensitivity of murine spermiogenesis to miglustat is a quantitative trait: a pharmacogenetic study. Reprod Biol Endocrinol. 2007 Jan 22;5:1. PMID: 17241468 [PubMed - indexed for MEDLINE] Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase. Nat Genet. 2004 Nov;36(11):1225-9. Epub 2004 Oct 24. PMID: 15502825 [PubMed - indexed for MEDLINE] Storage solutions: treating lysosomal disorders of the brain. Nat Rev Neurosci. 2005 Sep;6(9):713-25. Review. PMID: 16049428 [PubMed - indexed for MEDLINE] < to top