390 results match your criteria: "UCLA School of Medicine 90095[Affiliation]"

The glucose transporter 1 (GLUT1) protein is underexpressed in human glioblastoma multiforme and is overexpressed in human cerebral hemangioblastoma. To gain in-sight into possible posttranscriptional mechanisms regulating the expression of the GLUT1 protein in human brain tumors, cytosolic proteins were prepared from these two tumors and used in RNase T1 protection assays that employed [32P]human GLUT1 synthetic RNA prepared from transcription plasmids. Gel shift mobility assays and ultra-violet light cross-linking studies demonstrated the formation of specific RNA/protein complexes that migrated with a mol mass of 120, 44, and 41 kD.

View Article and Find Full Text PDF

Immunophenotype analysis was used to characterize circulating lymphocyte subset levels in both rhesus monkeys that were chronically infected with SIVmac239 and in those that had resisted SIVmac239 infection as a result of prior vaccination with an attenuated SIV strain. Alterations in T, NK, and B cell subsets were compared with those previously identified in humans chronically infected with HIV [8-11, 14, 22]. The well-known decrease in CD4+ cell levels was observed in the SIVmac239-infected animals.

View Article and Find Full Text PDF

We studied the calcium compartmentation of the Ca overload induced by 50 min of metabolic inhibition (MI) in cultured neonatal rat cardiomyocytes. MI was achieved by application of 1 mM iodoacetic acid (IAA) and 10 mM 2-deoxyglucose (2-DOG) with omission of glucose in the perfusate. MI per se abolished spontaneous beating, but 10 mM caffeine pulses at 15, 30 and 45 min were able to induce contractile responses.

View Article and Find Full Text PDF

Background: [13N]Ammonia has been validated in dog studies as a myocardial blood flow tracer. Estimates of myocardial blood flow by [13N]ammonia were highly linearly correlated to those by the microsphere and blood sample techniques. However, estimates of myocardial blood flow with [13N]ammonia in humans have not yet been compared with those by an independent technique.

View Article and Find Full Text PDF

Clinical applications of stem cell factor.

Curr Opin Hematol

May 1996

Department of Medicine, UCLA School of Medicine 90095-6956, USA.

Stem cell factor is an early-acting hematopoietic cytokine that probably functions constitutively to support the proliferation and survival of pluripotent progenitor cells and to increase their receptivity to lineage commitment and differentiation in response to lineage-specific cytokines. Stem cell factor also can induce proliferation and activation of mast cells. In vitro and in vivo, stem cell factor has demonstrated synergy with other hematopoietic cytokines.

View Article and Find Full Text PDF

Glucose-galactose malabsorption (GGM) is an autosomal recessive disorder which presents with severe osmotic diarrhoea shortly after birth. Two proband siblings with GGM were previously demonstrated to contain a missense mutation (D28N) in the Na(+)-dependent glucose/galactose cotransporter (SGLT1) that accounts for the defect in sugar absorption. Prenatal screening for GGM was performed in two subsequent pregnancies in this large consanguineous family.

View Article and Find Full Text PDF

The influence of perinatal infective factors on ophthalmia neonatorum.

J Pediatr Ophthalmol Strabismus

November 1996

Department of Ophthalmology, Harbor-UCLA Medical Center, UCLA School of Medicine 90095-7001, USA.

Background: Ophthalmia neonatorum still blinds approximately 10,000 babies annually worldwide. Identification of contributory maternal perinatal factors could possibly predict which babies are at greater risk for this disease.

Methods: In a randomized prospective study of ophthalmia neonatorum in Kenya, we studied the effect of prophylaxis with povidone-iodine, silver nitrate, and erythromycin in 3117 neonates.

View Article and Find Full Text PDF

Black blood dual phase turbo FLASH MR imaging of the heart.

J Magn Reson Imaging

November 1996

Department of Radiological Sciences, UCLA School of Medicine 90095-1721, USA.

An MR imaging scheme for dark blood cardiac images acquired simultaneously in end diastolic and end systolic phases, in breath-hold times, is presented. The sequence consists of a magnetization preparation period followed by two segmented k-space acquisitions. Image quality was investigated with respect to different sequence parameters (optimal values are indicated in brackets): (a) echo time (TE)/repetition time (TR)/ flip angle (FA) (3/6.

View Article and Find Full Text PDF

The effects of immediate versus delayed cell separation, storage temperature, presence of serum, and type of anticoagulation on the natural killer (NK) cytotoxicity of human mononuclear cells were assessed. The NK cytotoxicity of Ficoll-Hypaque-separated peripheral blood mononuclear cells (PBMC) was tested in a 3-h chromium-51 release assay with K562 cells at various effector/target cell ratios. The NK activities of PBMC from blood anticoagulated with either heparin or EDTA and then immediately separated and assayed were not different (42.

View Article and Find Full Text PDF

The atherosclerosis-calcification link?

Curr Opin Lipidol

April 1996

Department of Medicine, UCLA School of Medicine 90095, USA.

Although previously believed to be a passive, degenerative process, there is increasing evidence that arterial calcification is actually an active, regulated process. In this review we address potential mechanisms of arterial calcification and, in particular, ways in which it is similar to bone formation. We also advance the hypothesis that particular factors present in atherosclerosis, such as lipids, may explain the co-localization of calcification and atherosclerosis in vivo.

View Article and Find Full Text PDF

A very stable cell line has been generated that produces monoclonal antibody to VIP designated as CURE.V55. This hybridoma was produced by fusion of spleen cells from an immunized Robertsonian mouse containing the translocated 8.

View Article and Find Full Text PDF

The pp52 gene encodes an intracellular, F-actin-binding phosphoprotein (also designated LSP1 and WP34) postulated to function in cytoskeleton dynamics and cell motility. We previously reported that different mRNA isoforms are expressed from this gene in cells of the leukocyte lineage versus mesodermally derived cells. These tissue-specific mRNA isoforms are identical except for 5'-untranslated regions and sequences coding for unique N-termini of 23 and 21 amino acids, respectively.

View Article and Find Full Text PDF

We model the space between the junctional sarcoplasmic reticulum (JSR) membrane and the inner leaflet of the transverse tubular ("T") sarcolemmal (SL) membrane, the diadic cleft, with respect to calcium (Ca) concentration and movement. The model predicts the following: 1) Ca influx via the "L" channel increases [Ca] to 1 microM within a distance of 50 nm from the channel mouth in < 500 microseconds. This is sufficient to trigger Ca release from a domain of 9 "feet.

View Article and Find Full Text PDF

Quantification of serial tumor glucose metabolism.

J Nucl Med

March 1996

Department of Molecular and Medical Pharmacology, UCLA School of Medicine 90095-6948, USA.

Unlabelled: We developed a method to improve the quantitative precision of FDG-PET scans in cancer patients. The total-lesion evaluation method generates a correlation coefficient (r) constrained Patlak parametric image of the lesion together with three calculated glucose metabolic indices: (a) the total-lesion metabolic index ("KT-tle", ml/min/lesion); (b) the total-lesion voxel index ("VT-tle", voxels/lesion); and (c) the global average metabolic index ("KV-tle", ml/min/voxel).

Methods: The glucose metabolic indices obtained from conventional region of interest (ROI) and multiplane evaluation were used as standards to evaluate the accuracy of the total-lesion evaluation method.

View Article and Find Full Text PDF

Despite their uniform histologic appearance, pediatric low-grade astrocytomas (LGA) often exhibit a rather unpredictable clinical course. It is presently unclear whether certain specific genetic, immunologic and/or metabolic features underlie these observed variations. In order to address this question we examined the tumor distribution of choline compounds (Cho), creatine (Cr) and N-acetyl aspartate (NAA) in seven children with midline LGA by means of proton magnetic resonance spectroscopy imaging (H-MRSI).

View Article and Find Full Text PDF

Striking variations exist, across individuals, in the internal and external geometry of the brain. Such normal variations in the size, orientation, topology, and geometric complexity of cortical and subcortical structures have complicated the problem of quantifying deviations from normal anatomy and of developing standardized neuroanatomical atlases. This paper describes the design, implementation, and results of a technique for creating a three-dimensional (3D) probabilistic surface atlas of the human brain.

View Article and Find Full Text PDF

There is a dearth of knowledge on the radiobiology of palliative radiotherapy, but some of the principles relevant to radical radiation treatments can be applied to the palliative situation. Nevertheless with minimal animal or human data available, it would appear that this area can be a fertile one for future study, although many of the difficulties and problems inherent in this type of research must be acknowledged and addressed.

View Article and Find Full Text PDF

Vestibular and auditory disorders.

Curr Opin Neurol

February 1996

Department of Neurology, UCLA School of Medicine 90095-1769, USA.

Benign positional vertigo, the most common cause of vertigo, can now be cured with a simple bedside maneuver. A series of recent publications have clarified the pathophysiology of benign positional vertigo and documented the efficacy of particle repositioning maneuvers for treating the condition. The number of genetic loci and abnormal genes associated with inherited auditory and vestibular disorders is rapidly expanding.

View Article and Find Full Text PDF

Background: Hin is a member of an extended family of site-specific recombinases--the DNA invertase/resolvase family--that catalyze inversion or deletion of DNA. DNA inversion by Hin occurs between two recombination sites and requires the regulatory protein Fis, which associates with a cis-acting recombinational enhancer sequence. Hin recombinase dimers bind to the two recombination sites and assemble onto the Fis-bound enhancer to generate an invertasome structure, at which time they become competent to catalyze DNA cleavage and strand exchange.

View Article and Find Full Text PDF

Many children with end-stage renal disease have significant urinary tract problems other than irreversible loss of native kidney function. These significant other urinary tract problems, if not corrected prior to transplantation, may significantly increase recipient mortality, graft loss, and patient morbidity. These other urinary tract problems may cause hydroureteronephrosis in the transplanted kidney, lead to an increased incidence of graft rejection, be the source of sepsis after subsequent immunosuppression, and cause hypertension.

View Article and Find Full Text PDF

Intestinal intraepithelial lymphocytes (IEL) are a population of cells consisting mostly of CD8+ T lymphocytes. Although their function is unknown, because of their location within the epithelium it has been postulated that IEL may be involved in defense against infection of the gut mucosa by pathogens including viruses. To address this issue, we have examined IEL populations from BALB/c mice systemically infected with lymphocytic choriomeningitis virus (LCMV).

View Article and Find Full Text PDF