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1.
Medicine (Baltimore) ; 103(29): e39047, 2024 Jul 19.
Artigo em Inglês | MEDLINE | ID: mdl-39029020

RESUMO

RATIONALE: Allan-Herndon-Dudley syndrome (AHDS) results from a pathogenic variant in the hemizygous subunit of the SLC16A2 gene, which encodes monocarboxylate transporter 8 and follows an X-linked recessive pattern. AHDS manifests as neuropsychomotor developmental delay, intellectual disability, movement disorders, and thyroid hormone abnormalities. It is frequently misdiagnosed as cerebral palsy or hypothyroidism. PATIENT CONCERNS: A 9-month-old male infant exhibited poor head control, hypodynamia, motor retardation, hypertonic limbs, and thyroid abnormalities. Despite levothyroxine supplementation and rehabilitation therapy, no improvements were observed. Whole-exome sequencing identified a novel nonsense mutation in SLC16A2 (c.124G > T, p.E42X), which unequivocally established the diagnosis. DIAGNOSES: AHDS was confirmed. INTERVENTIONS: Levothyroxine treatment commenced early in infancy, followed by 3 months of rehabilitation therapy, starting at 5 months of age. The combined administration of levothyroxine and methimazole was initiated at 1 year and 10 months of age, respectively. OUTCOMES: While improvements were noted in thyroid hormone levels, neurological developmental delays persisted. LESSONS: AHDS should be considered in patients presenting with atypical neurological features and thyroid hormone abnormalities such as elevated triiodothyronine and decreased thyroxine levels. The early utilization of exome sequencing aids in prompt diagnosis. The identified SLC16A2 nonsense mutation correlates with severe neurological phenotypes and adds to the spectrum of genetic variations associated with AHDS.


Assuntos
Códon sem Sentido , Transportadores de Ácidos Monocarboxílicos , Hipotonia Muscular , Atrofia Muscular , Simportadores , Humanos , Masculino , Transportadores de Ácidos Monocarboxílicos/genética , Lactente , Hipotonia Muscular/genética , Hipotonia Muscular/diagnóstico , Simportadores/genética , Atrofia Muscular/genética , Atrofia Muscular/diagnóstico , Fenótipo , Deficiência Intelectual Ligada ao Cromossomo X/genética , Deficiência Intelectual Ligada ao Cromossomo X/diagnóstico , Tiroxina/uso terapêutico , Hipertonia Muscular/genética , Hipertonia Muscular/diagnóstico , Sequenciamento do Exoma/métodos
2.
Ann Palliat Med ; 10(7): 7832-7840, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-34353070

RESUMO

BACKGROUND: Peritoneal dialysis (PD) uses the peritoneum as the dialysis membrane. PD is a simple operation for self-treatment at home, and has become the preferred option for most patients with chronic renal failure (CRF). This study aimed to explore the effect of a closed-loop health management (CLHM) system based on an Internet platform in patients with PD. METHODS: A total of 102 patients with PD who were admitted to Xuzhou Central Hospital from May 2019 to May 2020 were selected and randomly divided into two groups (n=51). The control group received routine care, and in the observation group a CLHM based on an Internet platform was introduced. The incidence of complications and changes in disease knowledge, nutritional status, quality of life (QOL) before and after the intervention were compared between groups. RESULTS: The incidences of peritonitis, tunnel entrance infection, poor drainage, and hypokalemia in the observation group were lower than in the control group (P<0.05). The disease-related knowledge mastery scores of the observation group were higher than those in the control group after 3 months of intervention (P<0.05). Malnutrition-inflammation score (MIS) and serum creatinine (SCr) in the observation group were lower than in the control group after 3 months of intervention (P<0.05), and the body mass index (BMI), albumin (ALB), and hemoglobin (Hb) of the observation group were higher than those of the control group (P<0.05). The QOL scores of the observation group were higher than those of the control group after 3 months of intervention (P<0.05). CONCLUSIONS: The application of a CLHM system based on an Internet platform to patients with PD could effectively reduce complications, and improve patients' knowledge of disease, nutritional status and QOL. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: ChiCTR2100046122.


Assuntos
Falência Renal Crônica , Diálise Peritoneal , Humanos , Internet , Falência Renal Crônica/terapia , Estado Nutricional , Qualidade de Vida
3.
Int J Mol Med ; 44(1): 67-78, 2019 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-31115486

RESUMO

Lysophosphatidic acid (LPA), a simple water­soluble glycerophospholipid with growth factor­like activity, regulates certain behaviors of multiple cancer types by binding to its receptor, LPA receptor 2 (LPA2). Notch1 is a key mediator in multiple human cancer cell types. The association between LPA2 and Notch1 in gastric cancer cells is not well known. The present study aimed to investigate the function of LPA2 and Notch1 in controlling the migration and invasion activities of SGC­7901 gastric cancer cells following stimulation with LPA. It was revealed that LPA may stimulate the expression of Notch1 and Hes family bHLH transcription factor 1, and the phosphorylation of protein kinase B which belongs to the Notch pathway. Furthermore, by performing transwell migration and invasion assays, immunofluorescent staining, analyzing the expression of markers for the epithelial­mesenchymal transition (EMT) and downregulating LPA2 and Notch1 expression, it was verified that LPA2 and Notch1 mediated the metastasis, invasion, EMT and rebuilding of the cytoskeleton of SGC­7901 cells upon LPA treatment. An immunoprecipitation assay revealed that LPA2 interacted with Notch1 in SGC­7901 cells. The present study may provide novel ideas and an experimental basis for identifying the factors that affect the functions of SGC­7901 cells.


Assuntos
Movimento Celular/efeitos dos fármacos , Lisofosfolipídeos/farmacologia , Proteínas de Neoplasias/metabolismo , Receptor Notch1/metabolismo , Receptores de Ácidos Lisofosfatídicos/metabolismo , Transdução de Sinais/efeitos dos fármacos , Neoplasias Gástricas/metabolismo , Linhagem Celular Tumoral , Humanos , Invasividade Neoplásica , Neoplasias Gástricas/patologia
4.
Fish Physiol Biochem ; 42(6): 1609-1619, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27277446

RESUMO

Synaptonemal complex protein 3 (Scp3), which is encoded by scp3, is a meiotic marker commonly used to trace the timing of gonadal differentiation in vertebrates. In the present study, the ricefield eel scp3 cDNA was cloned, and a fragment encoding amino acids 49 to 244 was overexpressed. The recombinant Scp3 polypeptide was purified and used to generate a rabbit anti-Scp3 polyclonal antiserum. In adult ricefield eels, scp3 mRNA was predominantly detected in the gonads and faintly detected in discrete brain areas. In the gonads, Scp3 immunoreactivities were shown to be localized to the germ cells, including meiotic primary growth oocytes, spermatocytes, and pre-meiotic spermatogonia. During early ovarian differentiation, immunoreactive Scp3 was not detected in the gonads of ricefield eels at 6 days post-hatching (dph) but was found to be abundantly localized in the cytoplasm of some oogonia at 7 dph, coinciding with the appearance of the ovarian cavity and ovarian differentiation. At 14 dph, strong Scp3 immunostaining was detected on one side of the nucleus with a distinct polarity in some germ cells, presumably at the leptotene stage. Consistent with these results, the expression of scp3 mRNA was faintly detected in the gonads of ricefield eels at 6 dph, increased at 8 dph, and then remained relatively high thereafter. Taken together, these results suggest that the appearance of immunoreactive Scp3 in oogonia could be a marker for early ovarian differentiation in ricefield eels. The translocation of the Scp3 protein from the cytoplasm to the nucleus in the oogonium of ricefield eels appears to be a controlled process that warrants further study.


Assuntos
Enguias , Proteínas de Peixes/genética , Proteínas de Peixes/metabolismo , Proteínas Nucleares/genética , Proteínas Nucleares/metabolismo , Ovário/metabolismo , Sequência de Aminoácidos , Animais , Sequência de Bases , Diferenciação Celular/genética , DNA Complementar/genética , Transtornos do Desenvolvimento Sexual/genética , Enguias/genética , Enguias/metabolismo , Feminino , Fígado/metabolismo , Masculino , Oócitos/metabolismo , Oogônios/metabolismo , Ovário/citologia , RNA Mensageiro/metabolismo , Processos de Determinação Sexual/genética , Espermatócitos/metabolismo , Espermatogônias/metabolismo , Testículo/citologia , Testículo/metabolismo
5.
Fish Physiol Biochem ; 41(6): 1515-25, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26202937

RESUMO

Growth hormone (GH) is a single-chain polypeptide hormone mainly secreted by somatotropes of the anterior pituitary gland and is an important regulator of somatic growth in vertebrates including teleosts. In this study, a polyclonal antiserum against ricefield eel Gh was generated and the expression of Gh at the mRNA and protein levels was analyzed. Both RT-PCR and western blot analysis showed that Gh was predominantly expressed in the pituitary glands of ricefield eels. The immunoreactive Gh signals were localized to the multicellular layers of the adenohypophysis adjacent to the neurohypophysis in ricefield eels. Ontogenetic analysis showed that immunoreactive Gh signals could be detected in the pituitary glands of ricefield eel embryos as early as 3 days post-fertilization. During the sex change from female to male, the levels of the immunoreactive Gh signals in the pituitary glands of the ricefield eels peaked at the intersexual stage. These results suggest that Gh in the pituitary glands may be associated with embryonic development before hatching, as well as with the sex change in the adult ricefield eels, possibly via the classical endocrine manner.


Assuntos
Enguias/crescimento & desenvolvimento , Hormônio do Crescimento/fisiologia , Processos de Determinação Sexual , Animais , Transtornos do Desenvolvimento Sexual/embriologia , Enguias/embriologia , Feminino , Larva/fisiologia , Masculino , Hipófise/embriologia , RNA Mensageiro/metabolismo
7.
Zhonghua Yan Ke Za Zhi ; 41(7): 652-5, 2005 Jul.
Artigo em Chinês | MEDLINE | ID: mdl-16080903

RESUMO

OBJECTIVE: To study characteristics of the publication of Chinese Journal of Ophthalmology during years of 2001 to 2004. METHODS: Statistic method was used to retrieve the following parameters of Chinese Journal of Ophthalmology: numbers of articles, columns, citation frequencies, grants support, time lag from accepted to publication. RESULTS: The journal published 926 pieces of papers and 16 reports during years of 2001 to 2004. There were 24 columns; citation rates were 89.98%; papers published in the journal 19.53% got grant support. The times lag for publication was relatively longer. CONCLUSIONS: Chinese Journal of Ophthalmology is a high quality, specialized and core periodical in china.


Assuntos
Bibliometria , Oftalmologia , Publicações Periódicas como Assunto/estatística & dados numéricos , China , História do Século XXI , Publicações Periódicas como Assunto/história , Publicações Periódicas como Assunto/tendências
9.
Zhonghua Nei Ke Za Zhi ; 44(12): 918-21, 2005 Dec.
Artigo em Chinês | MEDLINE | ID: mdl-16409730

RESUMO

OBJECTIVE: To identify and analyze the scientific level and quality of the articles published in Chinese Journal of Internal Medicine. METHOD: Using the database of the Chinese Medical Citation Index (CMCI), the numbers and distribution of the cited original articles in Chinese Journal of Internal Medicine from 2000 to 2004 were analyzed according to the method of citation analysis. RESULT: The percentage of cited papers in all the published articles was 47.10% during the period, the average times of citation of an original article by other researchers is 4.30 and the top cited frequency was 133. There were 250 articles being cited 5 or more (25.43% of the total papers), and the times of citation from them were 2834 (67.01% of the total). 983 cited articles were written by 845 authors from different countries. The author of the most frequently cited articles wrote 6 papers and the authors with one cited paper were 751 (88.88% of all the authors). The cited authors were from 31 municipalities and provinces as well as from other countries. Beijing, Guangdong and Shanghai were in the front of the list of places with authors being frequently cited. Beijing was the top of the rank (44.74% of total authors). There were 266 institutes cited and the most frequently cited institute was Peking Union Medical College Hospital of Peking Union Medical College and Chinese Academy of Medical Sciences. There were 685 citing journals and the self-citing rate is 3.52%. CONCLUSIONS: The Chinese Journal of Internal Medicine has published high quality articles. As a core medical journal, it is the one of the most important information resources for the medical researchers.


Assuntos
Bibliometria , Medicina Interna , Publicações Periódicas como Assunto/estatística & dados numéricos , China
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