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Effects of freeze-thawing and intravenous infusion on mesenchymal stromal cell gene expression.

Mesenchymal stromal cells (MSC) are increasingly used as an investigative therapeutic product for immune disorders and degenerative disease. Typically, MSC are isolated from human tissue, expanded in culture and cryopreserved until usage. The safety and efficacy of MSC therapy will depend on the phenotypical and functional characteristics of MSC. The freeze-thawing procedure may change these chara

A review of the role of nurses and technicians in ST-elevation myocardial infarction (STEMI).

The role of nurses and technicians in the treatment of ST-elevation myocardial infarction (STEMI) by primary percutaneous coronary intervention (PPCI) is vital for the success of the multidisciplinary Heart Team. Several editorials have emphasised the importance of a holistic treatment which links each step of care to the next, a chain that is essential for quality and efficacy in the management o

Acute and sustained actions of hyperglycaemia on endothelial and glomerular barrier permeability

Microalbuminuria is an established marker of systemic endothelial dysfunction, which for patients with diabetes signals an increased risk of both diabetic nephropathy and cardiovascular complications. A better understanding of the pathogenesis of microalbuminuria is important in the quest of finding new approaches to treat patients with diabetes. Direct acute effects of episodes of hyperglycaemia

Loss of HIF-1α accelerates murine FLT-3ITD-induced myeloproliferative neoplasia.

Hypoxia-induced signaling is important for normal and malignant hematopoiesis. The transcription factor hypoxia-inducible factor-1α (HIF-1α) plays a crucial role in quiescence and self-renewal of hematopoietic stem cells (HSCs) as well as leukemia-initiating cells (LICs) of acute myeloid leukemia (AML) and chronic myeloid leukemia (CML). We have investigated the effect of HIF-1α loss on the phenot

Variation of the electron population by four units in the cluster series [(eta(5)-Cp ')(3)Mo3S4Co(L)](n+) (L = I, CO, PPh3, NO; n=0, 1)

The versatility of cuboidal Mo3S4Co clusters for the preparation of complexes with different numbers of valence shell electrons (VSE) in the cluster is described. The reaction of the geometrically incomplete cuboidal cluster salt [(eta(5)-Cp')(3)Mo3S4][pts] (pts = p-toluenesulfonate) with one molar equivalent of [Co-2(CO)(8)] afforded almost quantitatively the electroneutral 60 VSE cluster [(eta(5

ATPase activity of magnesium chelatase subunit I is required to maintain subunit D in vivo

During biosynthesis of chlorophyll, Mg2+ is inserted into protoporphyrin IX by magnesium chelatase. This enzyme consists of three different subunits of approximate to 40, 70 and 140 kDa. Seven barley mutants deficient in the 40 kDa magnesium chelatase subunit were analysed and it was found that this subunit is essential for the maintenance of the 70 kDa subunit, but not the 140 kDa subunit. The 40

Polymorphism and transcription of Mhc class I genes in a passerine bird, the great reed warbler

The class I genes of the major histocompatibility complex (Mhc) are here investigated for the first time in a passerine bird. The great reed warbler is a rare species in Sweden with a few semi-isolated populations. Yet, we found extensive Mhc class I variation in the study population. The variable exon 3, corresponding to the alpha(2) domain, was amplified from genomic DNA with degenerated primers

Warum können wir Fahrrad fahren

Beim Fahrradfahren arbeitet der Mensch als Regler. Das wird beim Balancieren des Fahrrades besonders offensichtlich, denn das Fahrrad ist instabil. In diesem Beitrag wird untersucht, unter welchen Bedingungen es möglich ist, das Fahrrad mit einem so einfachen Reglergesetz zu balancieren, dass Menschen dieses Reglergesetz ohne Mühe realisieren können. Dabei wird nicht nur die jedem Radfahrer bekann

Detection of alterations in all three exons of the peripherin/RDS gene in Swedish patients with retinitis pigmentosa using an efficient DGGE system

AIMS: To develop a sensitive mutation screening procedure suitable for routine analysis of the peripherin/RDS gene, and to estimate the nature and prevalence of peripherin/RDS gene mutations in Swedish patients with autosomal dominant retinitis pigmentosa. METHODS: To make the method as sensitive as possible, as many as eight segments, covering the three exons and the flanking intron sequences of