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Showing 1-7 of 7 results for "352-13-6" within Papers
Barry J Maurer et al.
Pediatric blood & cancer, 60(11), 1801-1808 (2013-07-03)
A phase I study was conducted to determine the maximum-tolerated dose, dose-limiting toxicities (DLTs), and pharmacokinetics of fenretinide (4-HPR) delivered in an oral powderized lipid complex (LXS) in patients with relapsed/refractory neuroblastoma. 4-HPR/LXS powder (352-2,210 mg/m(2) /day) was administered on Days
Raquel Rabionet et al.
Scientific reports, 9(1), 4579-4579 (2019-03-16)
Juvenile idiopathic arthritis (JIA) is a complex rheumatic disease with both autoimmune and autoinflammatory components. Recently, familial cases of systemic-onset JIA have been attributed to mutations in LACC1/FAMIN. We describe three affected siblings from a Moroccan consanguineous family with an
Yoshiaki Yano et al.
Biochemistry, 41(9), 3073-3080 (2002-02-28)
Investigation of interactions between hydrophobic model peptides and lipid bilayers is perhaps the only way to elucidate the principles of the folding and stability of membrane proteins (White, S. H., and Wimley, W. C. (1998) Biochim. Biophys. Acta 1367, 339-352).
Borys Kierdaszuk
Journal of fluorescence, 23(2), 339-347 (2012-12-13)
We examined the emission spectra and steady-state anisotropy of tyrosinate anion fluorescence with one-photon (250-310 nm), two-photon (570-620 nm) and three-photon (750-930 nm) excitation. Similar emission spectra of the neutral (pH 7.2) and anionic (pH 13) forms of N-acetyl-L-tyrosinamide (NATyrA) (pKa 10.6) were
Yuhjung J Tsai et al.
The Journal of allergy and clinical immunology, 118(6), 1242-1248 (2006-12-13)
The prostanoid DP receptor (PTGDR) gene on chromosome 14q22.1 has been identified as an asthma susceptibility gene. A haplotype with decreased transcription factor binding and transcription efficiency was associated with decreased asthma susceptibility in African American and white subjects. The
Takeshi Sakurai et al.
Psychiatric genetics, 16(6), 251-257 (2006-11-16)
An autism susceptibility locus (AUTS1, MIM#608636) has been identified in chromosome 7q31. NrCAM is a candidate gene for AUTS1 because it is expressed in the brain and encodes a receptor involved in nervous system development. Polymorphisms in NrCAM have been
Angélica María Sabogal-Guáqueta et al.
Biochimica et biophysica acta. Molecular basis of disease, 1866(8), 165797-165797 (2020-04-18)
Sporadic Alzheimer's disease (SAD) is the most common form of dementia, and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most frequent hereditary ischemic small vessel disease of the brain. Relevant biomarkers or specific metabolic signatures
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