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UnknownDiscovery and structural characterisation of new fold type IV-transaminases exemplify the diversity of this enzyme fold.
Not available
S-EPMC5131300 | biostudies-literature
TranscriptomicsPatterns of histone H3 Lysine 27 monomethylation and erythroid cell-type specific gene expression [expression]
ERYTHROID CELL-TYPE SPECIFIC GENE EXPRESSION Post-translational histone modifications, acting alone or in a context-dependent manner, influence numerous cellular processes via their regulation of gene expression. Monomethylation of histone H3 lysine 27 (K27me1) is a poorly understood histone modific...
ORGANISM(S): Homo sapiens 
2011-12-06 | E-GEOD-32135 | biostudies-arrayexpress
UnknownPlasma plant sterol levels do not reflect cholesterol absorption in children with Smith-Lemli-Opitz syndrome.
Not available
S-EPMC3092779 | biostudies-literature
UnknownA blood test for cerebrotendinous xanthomatosis with potential for disease detection in newborns.
Not available
S-EPMC3927472 | biostudies-literature
UnknownRapid healing of cutaneous leishmaniasis by high-frequency electrocauterization and hydrogel wound care with or without DAC N-055: a randomized controlled phase IIa trial in Kabul.
Not available
S-EPMC3923720 | biostudies-literature
UnknownThyroid Hormone Status in Sitosterolemia Is Modified by Ezetimibe.
Not available
S-EPMC5572543 | biostudies-literature
ProteomicsProteome analysis of the MO3.13 cell line from human oligodendrocytes
MO3.13 is an immortal human-human hybrid cell line that express phenotypic characteristics of primary oligodendrocytes. It was created by fusing a 6-thioguanine-resistant mutant of the human rhabdomyosarcoma RD (cancer of skeletal muscle) with adult human oligodendrocytes by a lectin-enhanced polyet...
ORGANISM(S): Homo Sapiens (ncbitaxon:9606) 
2019-06-12 | MSV000083971 | MassIVE
UnknownEvaluation of miglustat as maintenance therapy after enzyme therapy in adults with stable type 1 Gaucher disease: a prospective, open-label non-inferiority study.
Not available
S-EPMC3552937 | biostudies-literature
UnknownNeurovascular injury with complement activation and inflammation in COVID-19.
Not available
S-EPMC9278212 | biostudies-literature
UnknownLoss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.
Not available
S-EPMC12910011 | biostudies-literature
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