about
Molecular cloning and characterization of rab27a and rab27b, novel human rab proteins shared by melanocytes and plateletsComparison of the hydrolysis of the three types of natriuretic peptides by human kidney neutral endopeptidase 24.11Expression of DAX-1, the gene responsible for X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism, in the hypothalamic-pituitary-adrenal/gonadal axisEffect of short-term treatment with pivalic acid containing antibiotics on serum carnitine concentration--a risk irrespective of ageDideoxyfingerprinting (ddF) analysis of the type X collagen gene (COL10A1) and identification of a novel mutation (S671P) in a kindred with Schmid metaphyseal chondrodysplasiaRapid changes in carbohydrate metabolism in muscle induced by triiodothyronine; the role of glucose 1,6-bisphosphateBiotinylation of histones by human serum biotinidase: assessment of biotinyl-transferase activity in sera from normal individuals and children with biotinidase deficiency.Bioaccumulated chlorinated hydrocarbons and red/white blood cell parameters.Serum immunoreactive leptin concentrations in patients with anorexia nervosa before and after partial weight recovery.Nonenzymatic degradation and salvage of dietary folate: physicochemical factors likely to influence bioavailability.Oral ingestion of mannose elevates blood mannose levels: a first step toward a potential therapy for carbohydrate-deficient glycoprotein syndrome type I.Antigenic and functional conservation of an integrin I-domain in Saccharomyces cerevisiae.The human early pregnancy factor/chaperonin 10 gene family.Cathepsin K: isolation and characterization of the murine cDNA and genomic sequence, the homologue of the human pycnodysostosis gene.Identification of a ferritin light chain pseudogene near the glycerol kinase locus in Xp21 by cDNA amplification for identification of genomic expressed sequences.Differential evolution and expression of murine peroxisomal membrane protein genes.Expression of myogenic regulatory factors in normal and dystrophic mice: effects of IGF-1 treatment.Expression of PAX3 in Ewing's sarcoma family of tumors.Gender differences in serum leptin levels in humans.Role of lipid aldehydes in cataractogenesis: 4-hydroxynonenal-induced cataract.Serum pilocarpine esterase activity and response to oral pilocarpine.Substrate accessibility to cytosolic aspartate aminotransferase improves posthypoxic recovery of isolated rat heart.Proposed role for a combination of citric acid and ascorbic acid in the production of dietary iron overload: a fundamental cause of disease.Therapeutic potential and mechanism of action of oligonucleotides and ribozymes.Science and medicine at the millennium.Developmental expression of morphoregulatory genes in the mouse embryo: an analytical approach using a novel technology.Further evidence for multitopological localization of mammalian porin (VDAC) in the plasmalemma forming part of a chloride channel complex affected in cystic fibrosis and encephalomyopathy.Sulfation of chondroitin/dermatan sulfate by cystic fibrosis pancreatic duct cells is not different from control cells.Abnormal metabolism of mannose in families with carbohydrate-deficient glycoprotein syndrome type 1.DAX1 gene expression upregulated by steroidogenic factor 1 in an adrenocortical carcinoma cell line.Viruses in the pathogenesis of Kaposi's sarcoma--a review.Preimplantation polar body diagnosis.PCR diagnosis of viral pneumonitis from fixed-lung tissue in children.Batten disease and mitochondrial pathways of proteolysis.Toxicity of cationic lipid-ribozyme complexes in human prostate tumor cells can mimic ribozyme activity.Diagnosis of complex I deficiency in patients with lactic acidemia using skin fibroblast cultures.IGF-I does not mediate T-lymphoblast colony formation in response to estradiol, testosterone, 1,25(OH)2 vitamin D3, and triiodothyronine: studies in control and pygmy T-cell lines.Normal mitochondrial DNA and respiratory chain activity in familial dysautonomia fibroblasts.Retroviral vector-mediated transfer of the galactocerebrosidase (GALC) cDNA leads to overexpression and transfer of GALC activity to neighboring cells.The entire genomic sequence and cDNA expression of mouse alpha-galactosidase A.
P1433
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P1433
description
journal
@en
revista científica
@es
rivista scientifica
@it
wetenschappelijk tijdschrift van Academic Press
@nl
wissenschaftliche Fachzeitschrift
@de
name
Biochemical and molecular medicine
@ast
Biochemical and molecular medicine
@en
Biochemical and molecular medicine
@es
Biochemical and molecular medicine
@it
Biochemical and molecular medicine
@nl
type
label
Biochemical and molecular medicine
@ast
Biochemical and molecular medicine
@en
Biochemical and molecular medicine
@es
Biochemical and molecular medicine
@it
Biochemical and molecular medicine
@nl
prefLabel
Biochemical and molecular medicine
@ast
Biochemical and molecular medicine
@en
Biochemical and molecular medicine
@es
Biochemical and molecular medicine
@it
Biochemical and molecular medicine
@nl