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Anticoagulation with or without Clopidogrel after Transcatheter Aortic-Valve Implantation.The roles of anticoagulation alone or with an antiplatelet agent after transcatheter aortic-valve implantation (TAVI) have not been well studied.
1844 related Products with: Anticoagulation with or without Clopidogrel after Transcatheter Aortic-Valve Implantation.Mouse(KM strain) normal t Acridine orange *10 mg mL Phosphatase Inhibitor (So Rabbit Anti-CD200R Orexin Rabbit Anti-HHV8 ORF50 Po Multiple organ normal tis Normal male rabbit multip Multiple organs tumor and BI-D1870; Appearance Pale Rabbit Anti-CD200R Orexin Rabbit Anti-HHV8 ORF50 Po Multiple organ normal fro
#32223104 // Save this To Up
[Sacral nerve magnetic stimulation combined with extracorporeal shockwave for the treatment of type-ⅢB chronic prostatitis].To investigate the clinical therapeutic effects of sacral nerve magnetic stimulation (SNMS) combined with extracorporeal shockwave (ECSW) in the treatment of type-ⅢB chronic prostatitis.
1579 related Products with: [Sacral nerve magnetic stimulation combined with extracorporeal shockwave for the treatment of type-ⅢB chronic prostatitis].Rat PAI-1 (wild type acti MOUSE ANTI CANINE DISTEMP NATIVE HUMAN PROLACTIN, P RABBIT ANTI GSK3 BETA (pS Mouse PAI-1 (wild type la Rabbit PAI-1 (wild type l Mouse PAI-1 (wild type ac Rat PAI-1 (wild type late 10x ELISA WASH BUFFER, Pr MOUSE ANTI HUMAN CD15, Pr Rat Forkhead Box P3(FOXP3 Porcine PAI-1 (wild type
#32223072 // Save this To Up
COVID-19 : Face Masks and Human-to-human Transmission.In December 2019, transmission of the novel coronavirus (SARS-CoV-2) that causes coronavirus disease 2019(COVID-19) occurred in Wuhan, China .And later the virus began to be transmitted from person to person .Face masks are a type of personal protective equipment used to prevent the spread of respiratory infections，it may be effective at helping prevent transmission of respiratory viruses and bacteria .Here, we share a case of face masks are be used to prevent the transmission of COVID-19 infection.
Rabbit Anti-PARP4 Polyclo Rabbit Anti-Human Androge Rabbit Anti-Human ATM (aa Recombinant Human Androge anti CD16 monoclonal anti Rabbit Anti-Human Androge Goat Anti-Human FACE1 ZMP Rabbit Anti-PARP4 Polyclo Rabbit Anti-Human Androge Anti RAGE (Receptor for A Goat Anti-Human Androgen CAR,CAR,Constitutive acti
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Frequency and management of non-obstetric fistula in the Democratic Republic of Congo: Experience from the Fistula Care Plus project.To describe the frequency, causes and post-repair outcomes of NOF in hospitals supported by the Fistula Care Plus (FC+) project in the Democratic Republic of Congo.
1679 related Products with: Frequency and management of non-obstetric fistula in the Democratic Republic of Congo: Experience from the Fistula Care Plus project.
#32223052 // Save this To Up
Potential association between oral mucosal nevus and melanoma: a preliminary clinicopathologic study.To assess potential association between oral nevi (ON) and nevus-associated melanoma (NAM), in which melanoma cells coexist with nevus cells.
1509 related Products with: Potential association between oral mucosal nevus and melanoma: a preliminary clinicopathologic study.Malignant melanoma, metas Malignant melanoma, metas Malignant melanoma, metas Malignant melanoma, metas Rabbit Anti-Human Androge Malignant melanoma test t Rabbit Anti-Melanoma HMB4 Androgen Receptor (Phosph Andrographolide CAS Numbe Rabbit Anti-Melanoma HMB4 Anti Androgen Receptor pr Androst-4-ene-3,6,17-trio
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Fulminant type 1 diabetes: A comprehensive review of an autoimmune condition.Fulminant type 1 diabetes (FT1D) is a subset of type 1 diabetes characterized by extremely rapid pancreatic β cell destruction with aggressive progression of hyperglycemia and ketoacidosis. It was initially classified as idiopathic type 1 diabetes due to the absence of autoimmune markers. However, subsequent studies provide evidences supporting the involvement of autoimmunity in rapid β cell loss in FT1D pathogenesis, which are crucial for FT1D being an autoimmune disease. This article highlights the role of immunological aspects in FT1D according to the autoimmune-associated genetic background, viral infection, innate immunity, adaptive immunity, and pancreas histology. This article is protected by copyright. All rights reserved.
2416 related Products with: Fulminant type 1 diabetes: A comprehensive review of an autoimmune condition.Dengue Type 1 Antibody Angiotensin II Type 1 (AT Anti adenovirus type 5 he Angiotensin II Type 1 (AT Anti PCOLE 1 (Procollagen Dengue Type 2 Antibody Anti adenovirus type 5 he Anti CACNA1b(Voltage depe Angiotensin II Type 1 (AT Anti-adenovirus type 5 he Dengue Type 3 Antibody fibronectin type III and
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Mixed phenotype acute leukemia (MPAL): biological profile, clinical characteristic and treatment outcomes: report of the population-based study.The aim of this population-based, retrospective study was to analyze biological and clinical features and treatment results in children diagnosed with MPAL in all Polish pediatric oncology centers between 2007 and 2018.
2527 related Products with: Mixed phenotype acute leukemia (MPAL): biological profile, clinical characteristic and treatment outcomes: report of the population-based study.Multiple organ tumor tiss pCAMBIA1380 Vector (No Re CSL Gradient Thermal Cycl Feline Leukemia virus ant Kidney cancer test tissue Lung carcinoma and normal MultiGene Gradient therm Human Mouse Phospho-Stat Androstadienone C19H26O C Tissue Pre Treatment Kit Multiple organs tumor and Pancreatic cancer and nor
#32223016 // Save this To Up
Yap1 is required for maintenance of adult RPE differentiation.Nuclear YAP1 plays a critical role in regulation of stem cell proliferation, tissue regeneration, and organ size in many types of epithelia. Due to rapid turnover of most epithelial cell types, the cytoplasmic function of YAP1 in epithelial cells has not been well studied. The retinal pigment epithelium (RPE) is a highly polarized epithelial cell type maintained at a senescence state, and offers an ideal cell model to study the active role of YAP1 in maintenance of the adult epithelial phenotype. Here, we show that the cytoplasmic function of YAP1 is essential to maintain adult RPE differentiation. Knockout of Yap1 in the adult mouse RPE caused cell depolarization and tight junction breakdown, and led to inhibition of RPE65 expression, diminishment of RPE pigments, and retraction of microvilli and basal infoldings. These changes in RPE further prompted the loss of adjacent photoreceptor outer segments and photoreceptor death, which eventually led to decline of visual function in older mice between 6 and 12 months of age. Furthermore, nuclear β-catenin and its activity were significantly increased in mutant RPE. These results suggest that YAP1 plays an important role in active inhibition of Wnt/β-catenin signaling, and is essential for downregulation of β-catenin nuclear activity and prevention of dedifferentiation of adult RPE.
Rabbit Anti-IEX1 Differen Rabbit Anti-IEX1 Differen NATIVE HUMAN PROLACTIN, P MOUSE ANTI HUMAN CD19 RPE Mouse Anti-Ca19.9 Sialyl Rabbit Anti-IEX1 Differen Rabbit Anti-IEX1 Differen MOUSE ANTI CANINE DISTEMP Rabbit Anti-IEX1 Differen Rabbit Anti-IEX1 Differen 10x ELISA WASH BUFFER, Pr MOUSE ANTI APAAP COMPLEX,
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Maternal administration of bisphenol A alters the microglial profile in the neocortex of mouse weanlings.Bisphenol A is known to cause abnormal neurogenesis in the developing neocortex. The mechanisms of bisphenol A toxicity concerning neuroinflammatory-related endpoints are incompletely characterized. To evaluate the microglial morphology and the gene expression of pro-inflammatory cytokines in the newborn neocortex, ICR mice were exposed to bisphenol A 200 μg/kg/day on gestational day 6 through postpartum day 21. Weanlings exposed during pre- and post-natal period to bisphenol A showed an increased number of amoeboid-type microglia, a microglial differentiation disruption (the M1/M2 microglial ratio), and an abnormal expression of genes encoding pro-inflammatory factors. These findings suggest that the well-known neurodevelopmental toxicity of bisphenol A may be related to an increased microglial activation and neuroinflammation in the neocortex. This article is protected by copyright. All rights reserved.
2973 related Products with: Maternal administration of bisphenol A alters the microglial profile in the neocortex of mouse weanlings.FDA Standard Frozen Tissu Mouse Anti-Bacteroides th FDA Standard Frozen Tissu FDA Standard Frozen Tissu Normal mouse multiple org FDA Standard Frozen Tissu FDA Standard Frozen Tissu Multiple organ tumor tiss FDA Standard Frozen Tissu Thermal Shaker with cooli Mouse Anti-Influenza B Vi Mouse Anti-Influenza-A HA
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