Bär M et al. |
Wavelength-dependent induction of CYP24A1-mRNA after UVB-triggered calcitriol synthesis in cultured human keratinocytes. |
2007 |
J. Invest. Dermatol. |
pmid:16902422
|
Jong Hee Chae CS et al. |
Identification of a novel DHCR7 mutation in a Korean patient with Smith-Lemli-Opitz syndrome. |
2007 |
J. Child Neurol. |
pmid:18006960
|
Gupta R et al. |
Photoprotection by 1,25 dihydroxyvitamin D3 is associated with an increase in p53 and a decrease in nitric oxide products. |
2007 |
J. Invest. Dermatol. |
pmid:17170736
|
Solcà C et al. |
Loss of apolipoprotein E exacerbates the neonatal lethality of the Smith-Lemli-Opitz syndrome mouse. |
2007 |
Mol. Genet. Metab. |
pmid:17197219
|
Yu H et al. |
Selective reconstitution of liver cholesterol biosynthesis promotes lung maturation but does not prevent neonatal lethality in Dhcr7 null mice. |
2007 |
BMC Dev. Biol. |
pmid:17408495
|
Chen TC et al. |
Factors that influence the cutaneous synthesis and dietary sources of vitamin D. |
2007 |
Arch. Biochem. Biophys. |
pmid:17254541
|
Holick MF et al. |
Vitamin D and skin physiology: a D-lightful story. |
2007 |
J. Bone Miner. Res. |
pmid:18290718
|
Sánchez-MartÃn CC et al. |
Cholesterol starvation induces differentiation of human leukemia HL-60 cells. |
2007 |
Cancer Res. |
pmid:17409448
|
Korade Z et al. |
Expression and p75 neurotrophin receptor dependence of cholesterol synthetic enzymes in adult mouse brain. |
2007 |
Neurobiol. Aging |
pmid:16887237
|
Blahakova I et al. |
Molecular screening of Smith-Lemli-Opitz syndrome in pregnant women from the Czech Republic. |
2007 |
J. Inherit. Metab. Dis. |
pmid:17994283
|
Weinhofer I et al. |
Peroxisomal cholesterol biosynthesis and Smith-Lemli-Opitz syndrome. |
2006 |
Biochem. Biophys. Res. Commun. |
pmid:16678134
|
Fernø J et al. |
Drug-induced activation of SREBP-controlled lipogenic gene expression in CNS-related cell lines: marked differences between various antipsychotic drugs. |
2006 |
BMC Neurosci |
pmid:17052361
|
Bijlsma MF et al. |
Repression of smoothened by patched-dependent (pro-)vitamin D3 secretion. |
2006 |
PLoS Biol. |
pmid:16895439
|
Patel S and Mishra BK |
Oxidation of cholesterol by a biomimetic oxidant, cetyltrimethylammonium dichromate. |
2006 |
J. Org. Chem. |
pmid:16626135
|
Koide T et al. |
Negative regulation of Hedgehog signaling by the cholesterogenic enzyme 7-dehydrocholesterol reductase. |
2006 |
Development |
pmid:16687448
|
Weintrob N et al. |
Low estriol levels in the maternal triple-marker screen as a predictor of isolated adrenocorticotropic hormone deficiency caused by a new mutation in the TPIT gene. |
2006 |
Pediatrics |
pmid:16390921
|
Cohen MM |
Holoprosencephaly: clinical, anatomic, and molecular dimensions. |
2006 |
Birth Defects Res. Part A Clin. Mol. Teratol. |
pmid:17001700
|
Nowaczyk MJ et al. |
DHCR7 mutation carrier rates and prevalence of the RSH/Smith-Lemli-Opitz syndrome: where are the patients? |
2006 |
Am. J. Med. Genet. A |
pmid:16906538
|
Chignell CF et al. |
Ultraviolet A sensitivity in Smith-Lemli-Opitz syndrome: Possible involvement of cholesta-5,7,9(11)-trien-3 beta-ol. |
2006 |
Free Radic. Biol. Med. |
pmid:16814115
|
Webb AR |
Who, what, where and when-influences on cutaneous vitamin D synthesis. |
2006 |
Prog. Biophys. Mol. Biol. |
pmid:16766240
|
De Fabo EC |
Initial studies on an in vivo action spectrum for melanoma induction. |
2006 |
Prog. Biophys. Mol. Biol. |
pmid:16624384
|
Megha O et al. |
Cholesterol precursors stabilize ordinary and ceramide-rich ordered lipid domains (lipid rafts) to different degrees. Implications for the Bloch hypothesis and sterol biosynthesis disorders. |
2006 |
J. Biol. Chem. |
pmid:16735517
|
Valencia A et al. |
7-Dehydrocholesterol enhances ultraviolet A-induced oxidative stress in keratinocytes: roles of NADPH oxidase, mitochondria, and lipid rafts. |
2006 |
Free Radic. Biol. Med. |
pmid:17145559
|
Vaughan DK et al. |
Light-induced exacerbation of retinal degeneration in a rat model of Smith-Lemli-Opitz syndrome. |
2006 |
Exp. Eye Res. |
pmid:16360150
|
Rebolj K et al. |
Steroid structural requirements for interaction of ostreolysin, a lipid-raft binding cytolysin, with lipid monolayers and bilayers. |
2006 |
Biochim. Biophys. Acta |
pmid:16857161
|
Correa-Cerro LS et al. |
Development and characterization of a hypomorphic Smith-Lemli-Opitz syndrome mouse model and efficacy of simvastatin therapy. |
2006 |
Hum. Mol. Genet. |
pmid:16446309
|
Mukherjee S et al. |
Retinoids in the treatment of skin aging: an overview of clinical efficacy and safety. |
2006 |
Clin Interv Aging |
pmid:18046911
|
Everitt AV et al. |
Dietary approaches that delay age-related diseases. |
2006 |
Clin Interv Aging |
pmid:18047254
|
Bandeira F et al. |
Vitamin D deficiency: A global perspective. |
2006 |
Arq Bras Endocrinol Metabol |
pmid:17117289
|
Bijlsma MF et al. |
A dual role for 7-dehydrocholesterol reductase in regulating Hedgehog signalling? |
2006 |
Development |
pmid:17008445
|
Klein GL |
Burn-induced bone loss: importance, mechanisms, and management. |
2006 |
J Burns Wounds |
pmid:16921418
|
Richards MJ et al. |
Lipid hydroperoxide formation in the retina: correlation with retinal degeneration and light damage in a rat model of Smith-Lemli-Opitz syndrome. |
2006 |
Exp. Eye Res. |
pmid:16199034
|
Silva L et al. |
Nystatin-induced lipid vesicles permeabilization is strongly dependent on sterol structure. |
2006 |
Biochim. Biophys. Acta |
pmid:16626629
|
Vantieghem K et al. |
UVB-induced production of 1,25-dihydroxyvitamin D3 and vitamin D activity in human keratinocytes pretreated with a sterol delta7-reductase inhibitor. |
2006 |
J. Cell. Biochem. |
pmid:16365879
|
Lin X et al. |
A targeted apoB38.9 mutation in mice is associated with reduced hepatic cholesterol synthesis and enhanced lipid peroxidation. |
2006 |
Am. J. Physiol. Gastrointest. Liver Physiol. |
pmid:16455790
|
Tadjuidje E and Hollemann T |
Cholesterol homeostasis in development: the role of Xenopus 7-dehydrocholesterol reductase (Xdhcr7) in neural development. |
2006 |
Dev. Dyn. |
pmid:16752377
|
Tulenko TN et al. |
A membrane defect in the pathogenesis of the Smith-Lemli-Opitz syndrome. |
2006 |
J. Lipid Res. |
pmid:16258167
|
Rottiers V et al. |
Hormonal control of C. elegans dauer formation and life span by a Rieske-like oxygenase. |
2006 |
Dev. Cell |
pmid:16563875
|
Valencia A and Kochevar IE |
Ultraviolet A induces apoptosis via reactive oxygen species in a model for Smith-Lemli-Opitz syndrome. |
2006 |
Free Radic. Biol. Med. |
pmid:16458195
|
Jezela-Stanek A et al. |
Maternal urinary steroid profiles in prenatal diagnosis of Smith-Lemli-Opitz syndrome: first patient series comparing biochemical and molecular studies. |
2006 |
Clin. Genet. |
pmid:16451140
|
Matsumoto H et al. |
[Smith-Lemli-Opitz syndrome]. |
2006 |
Nippon Rinsho |
pmid:17022594
|
Kovarova M et al. |
Cholesterol deficiency in a mouse model of Smith-Lemli-Opitz syndrome reveals increased mast cell responsiveness. |
2006 |
J. Exp. Med. |
pmid:16618793
|
Vantieghem K et al. |
Dermal fibroblasts pretreated with a sterol Delta7-reductase inhibitor produce 25-hydroxyvitamin D3 upon UVB irradiation. |
2006 |
J. Photochem. Photobiol. B, Biol. |
pmid:16824767
|
Vantieghem K et al. |
UVB-induced 1,25(OH)2D3 production and vitamin D activity in intestinal CaCo-2 cells and in THP-1 macrophages pretreated with a sterol Delta7-reductase inhibitor. |
2006 |
J. Cell. Biochem. |
pmid:16598763
|
Tint GS et al. |
The use of the Dhcr7 knockout mouse to accurately determine the origin of fetal sterols. |
2006 |
J. Lipid Res. |
pmid:16651660
|
Gondré-Lewis MC et al. |
Abnormal sterols in cholesterol-deficiency diseases cause secretory granule malformation and decreased membrane curvature. |
2006 |
J. Cell. Sci. |
pmid:16636072
|
Yoshiyama T et al. |
Neverland is an evolutionally conserved Rieske-domain protein that is essential for ecdysone synthesis and insect growth. |
2006 |
Development |
pmid:16763204
|
Lehmann B |
The vitamin D3 pathway in human skin and its role for regulation of biological processes. |
2005 Nov-Dec |
Photochem. Photobiol. |
pmid:16162035
|
Matsumoto Y et al. |
R352Q mutation of the DHCR7 gene is common among Japanese Smith-Lemli-Opitz syndrome patients. |
2005 |
J. Hum. Genet. |
pmid:16044199
|
Cardoso ML et al. |
Molecular studies in Portuguese patients with Smith-Lemli-Opitz syndrome and report of three new mutations in DHCR7. |
2005 |
Mol. Genet. Metab. |
pmid:15979035
|