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1.
AIP Adv ; 12(9): 095307, 2022 Sep.
Article in English | MEDLINE | ID: mdl-36110253

ABSTRACT

Faraday rotation is considered a gold standard measurement of the electronic spin polarization of an alkali metal vapor produced under optical pumping. However, during the production of large volumes of hyperpolarized xenon gas, transmission monitoring measurements, otherwise known as field cycling measurements, are generally employed to measure the spin polarization of alkali metal atoms in situ as this method is easier to implement than Faraday rotation on standard polarizer setups. Here, we present a simple, low-cost experimental setup to perform Faraday rotation measurements of the electronic spin polarization of alkali metal atoms that can be easily implemented on standard polarizer setups. We then compare Rb polarization measurements obtained with the Faraday rotation method to those obtained with the transmission monitoring method. To our knowledge, a direct comparison of these methods has never been made. Overall, we found good agreement between the two methods, but at low Rb density and high laser power, we found evidence of nonlinear magneto-optical effects that may prevent Faraday rotation from being used under these conditions.

2.
Oncogene ; 36(6): 731-745, 2017 02 09.
Article in English | MEDLINE | ID: mdl-27477696

ABSTRACT

microRNA (miRNA) dysregulation is a common feature of cancer cells, but the complex roles of miRNAs in cancer are not fully elucidated. Here, we used functional genomics to identify oncogenic miRNAs in non-small cell lung cancer and evaluate their impact on response to epidermal growth factor (EGFR)-targeting therapy. Our data demonstrate that miRNAs with an AAGUGC motif in their seed sequence increase both cancer cell proliferation and sensitivity to EGFR inhibitors. Global transcriptomics, proteomics and target prediction resulted in the identification of several tumor suppressors involved in the G1/S transition as AAGUGC-miRNA targets. The clinical implications of our findings were evaluated by analysis of AAGUGC-miRNA expression in multiple cancer types, supporting the link between this miRNA seed family, their tumor suppressor targets and cancer cell proliferation. In conclusion, we propose the AAGUGC seed motif as an oncomotif and that oncomotif-miRNAs promote cancer cell proliferation. These findings have potential therapeutic implications, especially in selecting patients for EGFR-targeting therapy.


Subject(s)
Carcinoma, Non-Small-Cell Lung/genetics , Lung Neoplasms/genetics , MicroRNAs/genetics , Base Sequence , Carcinogenesis/genetics , Carcinoma, Non-Small-Cell Lung/metabolism , Carcinoma, Non-Small-Cell Lung/pathology , Cell Proliferation/genetics , Humans , Lung Neoplasms/metabolism , Lung Neoplasms/pathology , MicroRNAs/biosynthesis , Nucleotide Motifs , Signal Transduction
4.
Acta Reumatol Port ; 39(3): 262-4, 2014.
Article in English | MEDLINE | ID: mdl-25326407

ABSTRACT

UNLABELLED: Systemic Sclerosis (SSc) is a chronic disease of the connective tissue, whose pathogenesis involves abnormalities of the immunological system. It has a variable course and there is a subgroup of patients with rapidly progressive disease or unresponsive to conventional treatment. These patients can benefit from intensive immunosuppression and autologous hematopoietic stem cell transplant. CLINICAL CASE: 19-year-old (y.o.) woman diagnosed with SSc at the age of 13 y.o. with cutaneous, vascular and articular involvement with initial response to methotrexate. Three years later the disease progressed with severe digestive involvement (dysphagia, delayed gastric emptying and weight loss) needing gastrostomy for nutritional support. She was treated with cyclophosphamide without improvement In May 2012 she had an autologous transplant with myeloablative regimen (BEAM): carmustine 300 mg/m2x1 day; etoposido 120 mg/kgx4 days; cytarabine 120 mg/kg 12/12:hx4 days; melphalan 140 mg/m2x1 day. A year and a half after transplantation she is asymptomatic, without any signs or symptoms of the disease, feeds by mouth and the gastric emptying study is normal. Currently she is free of medication.


Subject(s)
Hematopoietic Stem Cell Transplantation , Scleroderma, Systemic/surgery , Female , Humans , Severity of Illness Index , Transplantation, Autologous , Young Adult
5.
J Chem Phys ; 136(20): 204509, 2012 May 28.
Article in English | MEDLINE | ID: mdl-22667573

ABSTRACT

For more than three decades, the classical or mean-field picture describing the distant dipolar field has been almost always simplified to an effective field proportional to the local longitudinal magnetization, differing only by a scale factor of 1.5 for homomolecular (identical resonance frequency) and heteromolecular interactions. We re-examine the underlying assumptions, and show both theoretically and experimentally that the mathematical framework needs to be modified for modern applications such as imaging. We demonstrate new pulse sequences which produce unexpected effects; for example, modulating an arbitrarily small fraction of the magnetization can substantially alter the frequency evolution. Thus, matched gradient pulse pairs (a seemingly innocuous module in thousands of existing pulse sequences) can alter the time evolution in highly unexpected ways, particularly with small flip angle pulses such as those used in hyperpolarized experiments. We also show that specific gradient pulse combinations can retain only dipolar interactions between unlike spins, and the dipolar field can generate a secular Hamiltonian proportional to I(x).


Subject(s)
Algorithms , Magnetic Resonance Spectroscopy/methods , Acetone/chemistry , Magnetic Phenomena
6.
Bone Marrow Transplant ; 47(8): 1095-8, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22080970

ABSTRACT

Late-onset hemorrhagic cystitis (HC) after allogeneic hematopoietic stem cell transplantation (HSCT) has been associated with BK virus (BKV). Antiviral drugs are of limited efficacy and the optimal treatment for HC has not yet been established. Hyperbaric oxygen (HBO) may benefit these patients. We, therefore, retrospectively evaluated the effectiveness of HBO therapy in 16 patients with HC after allogeneic HSCT. All 16 patients had macroscopic hematuria and BKV infection. Patients received 100% oxygen in a hyperbaric chamber at 2.1 atmospheres for 90 min, 5 days per week, with a median 13 treatments (range, 4-84). Fifteen patients (94%) showed complete resolution of hematuria. Median urinary DNA BKV titers declined after HBO (P<0.05). Patients started on HBO earlier after diagnosis of HC responded sooner (P<0.05). HBO was generally well tolerated and proved to be a reliable option for this difficult to manage condition.


Subject(s)
BK Virus , Bone Marrow Transplantation , Cystitis/therapy , Hemorrhage/therapy , Hyperbaric Oxygenation/methods , Polyomavirus Infections/therapy , Adolescent , Adult , Cystitis/diagnosis , Cystitis/etiology , Female , Hematologic Diseases/diagnosis , Hematologic Diseases/therapy , Hemorrhage/diagnosis , Hemorrhage/etiology , Humans , Infant , Male , Middle Aged , Polyomavirus Infections/diagnosis , Polyomavirus Infections/etiology , Retrospective Studies , Time Factors , Transplantation, Homologous
7.
J Chem Phys ; 129(5): 054502, 2008 Aug 07.
Article in English | MEDLINE | ID: mdl-18698909

ABSTRACT

This report introduces a new approach that enhances nonlinear solution magnetic resonance signals from intermolecular dipolar interactions. The resulting signals can theoretically be as large as the full equilibrium magnetization. Simple, readily implemented pulse sequences using square-wave magnetization modulation simultaneously refocus all even order intermolecular multiple quantum coherences, leading to a substantial net signal enhancement, complex nonlinear dynamics, and improved structural sensitivity under realistic conditions.


Subject(s)
Magnetics , Linear Models , Magnetic Resonance Spectroscopy
8.
Rev Neurol ; 40(8): 479-81, 2005.
Article in Spanish | MEDLINE | ID: mdl-15861329

ABSTRACT

INTRODUCTION: Neonatal stroke (NNS) incidence appears to be increasing over the last years. This is believed to be a consequence of diagnostic accuracy rather than a real amplification of this entity. Nowadays, NNS incidence is estimated to be 1:4000 full newborns. CASE REPORT: Child with left middle cerebral artery territory infarction in which several thromboembolic risk factors were documented both in the child (neonatal sepsis and factor V Leiden) and his mother (lupus anticoagulant, pre-eclampsy and factor V Leiden). CONCLUSIONS: This case supports the increasing evidence in recent reports that association of multiple prothrombotic risk factors (maternal and foetal) is present in NNS genesis. This way the authors agree that wide prothrombotic study may be of crucial interest in identifying subjacent thrombophilic disease, even when an exogenous risk factor is present.


Subject(s)
Infant, Newborn , Stroke/diagnosis , Stroke/etiology , Thrombophilia/complications , Child, Preschool , Factor V , Humans , Infant , Infarction, Middle Cerebral Artery/diagnosis , Infarction, Middle Cerebral Artery/etiology , Infarction, Middle Cerebral Artery/pathology , Male , Risk Factors , Stroke/pathology , Thrombophilia/diagnosis , Thrombophilia/pathology
9.
Rev. neurol. (Ed. impr.) ; 40(8): 479-481, 16 abr., 2005. ilus, tab
Article in Es | IBECS | ID: ibc-037068

ABSTRACT

Introducción. La frecuencia del accidente vascular cerebral (AVC) neonatal ha aumentado de manera significativa en los últimos años. Ello puede deberse no tanto a un aumento real del número de casos, como a una mayor certeza en su diagnóstico. Actualmente, su incidencia se ha calculado en un caso por cada 4.000 nacimientos. Caso clínico. Lactante con AVC en el área de la arteria cerebral media izquierda, del cual se disponía de información documentada sobre factores de riesgo (FR) tromboembólicos hereditarios y adquiridos, tanto en el niño (factor V de Leiden y sepsis neonatal) como en la madre (factor V de Leiden, lupus anticoagulante y preeclampsia). Conclusiones. Este caso apoya la evidencia, progresivamente observada en la literatura, de que el AVC neonatal es el resultado de una asociación de diversos FR trombótico (maternos y fetales). En este sentido, los autores consideran importante la investigación sistemática del niño y de su madre, teniendo en cuenta la identificación de una posible enfermedad trombofílica, incluso cuando se haya identificado un factor de riesgo exógeno


Introduction. Neonatal stroke (NNS) incidence appears to be increasing over the last years. This is believed to be a consequence of diagnostic accuracy rather than a real amplification of this entity. Nowadays, NNS incidence is estimated to be 1:4000 full newborns. Case report. Child with left middle cerebral artery territory infarction in which several thrombo-embolic risk factors were documented both in the child (neonatal sepsis and factor V Leiden) and his mother (lupus anticoagulant, pre-eclampsy and factor V Leiden). Conclusions. This case supports the increasing evidence in recent reports that association of multiple prothrombotic risk factors (maternal and foetal) is present in NNS genesis. This way the authors agree that wide prothrombotic study may be of crucial interest in identifying subjacent thrombophilic disease, even when an exogenous risk factor is present


Subject(s)
Male , Infant , Humans , Stroke/complications , Infant, Newborn, Diseases , Thrombophilia/diagnosis , Risk Factors , Factor V/analysis , Antibodies, Antiphospholipid/analysis , Pregnancy Complications
10.
Clin Lab Haematol ; 26(5): 319-21, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15485460

ABSTRACT

We evaluate a technique for genotyping HNA-1a, -1b and -1c antigens, resorting to fluorescence-primed allele-specific polymerase chain reaction (FPAS-PCR), and determine the frequency of the different genotypes in a normal Portuguese population. Our results indicate that the FPAS-PCR system is a reliable and simple tool for genotyping the neutrophil Fcgamma receptor IIIB antigens. The HNA-1a, -1b and -1c gene frequencies of 42.98, 84.21 and 6.14%, respectively, found in this study are similar to those reported for other white populations.


Subject(s)
Antigens, CD/immunology , Antigens/analysis , Neutrophils/immunology , Polymerase Chain Reaction/methods , Receptors, IgG/immunology , Alleles , Fluorescence , GPI-Linked Proteins , Gene Frequency , Genotype , Humans , Portugal/epidemiology
11.
Clin Lab Haematol ; 26(4): 297-300, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15279669

ABSTRACT

The authors report the case of a 9-year-old Caucasian girl, born in northern Portugal, with chronic nonspherocytic haemolytic anaemia and without family history of anaemia. The aethiological study of this anaemia revealed pyruvate kinase deficiency (PKD), because of two previously described mutations (426Arg-->Trp and 510Arg-->Gln). Since the blood smear revealed features not fully compatible with PKD diagnosis, additional tests were performed for the propositus and her parents, namely red blood cell membrane protein analysis. A decrease in proteins band 3 (15%) and 4.2 (18%) was found in the propositus. Her father presented only a decrease in band 3 (11%). Coexistence of PKD and erythrocyte membrane proteins deficiency in the same patient is very uncommon. Our findings suggest that a careful blood smear observation may lead to the identification of a combined deficiency in erythrocyte membrane proteins and enzymopathies.


Subject(s)
Anemia, Hemolytic, Congenital/etiology , Anion Exchange Protein 1, Erythrocyte/deficiency , Erythrocytes/metabolism , Pyruvate Kinase/deficiency , Pyruvate Metabolism, Inborn Errors/complications , Anemia, Hemolytic, Congenital/genetics , Anemia, Hemolytic, Congenital/metabolism , Anion Exchange Protein 1, Erythrocyte/genetics , Anion Exchange Protein 1, Erythrocyte/metabolism , Child , DNA Mutational Analysis , Erythrocytes/enzymology , Exons , Family Health , Female , Hematologic Tests , Heterozygote , Humans , Point Mutation , Pyruvate Kinase/genetics , Pyruvate Kinase/metabolism , Pyruvate Metabolism, Inborn Errors/genetics , Pyruvate Metabolism, Inborn Errors/metabolism
12.
Solid State Nucl Magn Reson ; 25(1-3): 153-9, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14698403

ABSTRACT

It has been recently recognized that residual intermolecular double-quantum coherences (iDQcs) provide a novel contrast mechanism to study heterogeneity in liquid systems. This is of much interest in the field of the physics of matter and biomedicine. Nowadays, literature concerning the behaviour of the iDQc signal originated by highly heterogeneous systems such as fluids in porous media is scarce. In this paper, we report and discuss our principal results about iDQc signal behaviour in confined liquid systems (trabecular bone, travertine, porous standard systems) and also some new results obtained on doped water in glass capillary pipes.


Subject(s)
Femur/chemistry , Glass/chemistry , Magnetic Resonance Spectroscopy/methods , Materials Testing/methods , Models, Chemical , Porosity , Water/chemistry , Adsorption , Animals , Capillary Action , Cattle , Humans , Phantoms, Imaging , Solutions/chemistry
13.
Magn Reson Imaging ; 21(3-4): 413-4, 2003.
Article in English | MEDLINE | ID: mdl-12850749

ABSTRACT

In heterogeneous systems the amplitude of the intermolecular double-quantum (DQ) signal depends on sample heterogeneity over a correlation distance dc=pi/(gammaGct). In this paper two different CRAZED-type sequences were applied in a porous medium phantom. One of these sequences gives rise to a DQ-T2 weighted signal, while the other one gives rise to a DQ-T2* weighted signal. Experimental results indicate that tuning of the correlation distance dc in a porous medium can alter the DQ signal in a manner which depends on the microstructure. This is evident only using the CRAZED-type sequence which gives rise to a DQ-T2* weighted signal.


Subject(s)
Magnetic Resonance Spectroscopy/methods , Phantoms, Imaging , Porosity
14.
Pediatr Med Chir ; 8(1): 3-8, 1986.
Article in Italian | MEDLINE | ID: mdl-3523446

ABSTRACT

Aplastic anaemia is a haematological syndrome in which pancytopenia is due to a depletion, damage of inhibition of hemopoietic stem cells. The pathogenetic factors are still unclear: damage or inhibition of hemopoietic stem cells may be direct or indirect mediated through changes in the cellular humoral environment; evidence is accumulating that in some cases these processes are of autoimmune nature. The prognostic evaluation is based on hematological parameters at diagnosis: severe aplastic anemia (SAA) is defined by the following criteria: neutrophils less than 0.5 X 10(9)/l; reticulocytes less than 0.5 X 10(9)/l and platelets less than 20 X 10(9)/l. Survival rates in children with SAA are poor; the probability of survival at 1 year from diagnosis being 10%. In this form treatment is based on supportive therapy (transfusion and prevention of infections) and on a specific therapy: immunosuppression and/or BMT. BMT is reserved to patient with an HLA identical sibling donor and may be curative in 70-80% of cases. To date the use of antilymphocytoglobulin in SAA has also given satisfactory results with a favorable response in 50-60% of cases.


Subject(s)
Anemia, Aplastic , Anemia, Aplastic/diagnosis , Anemia, Aplastic/etiology , Anemia, Aplastic/therapy , Antilymphocyte Serum/therapeutic use , Biopsy , Bone Marrow/pathology , Bone Marrow Transplantation , Child , Child, Preschool , Female , Graft vs Host Disease/etiology , Humans , Infant , Male , Prognosis , T-Lymphocytes/immunology
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