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br Materials and methods br
2018-10-24
Materials and methods Results Discussion It is known that mutation types of SOD1 affect not only enzymatic activity and protein half-life of SOD1, but also age at onset and the survival time of SOD1-ALS patients (Hayward et al., 2002) (Borchelt et al., 1994) (Regal et al., 2006). However, t
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Using the combination of a mitogen
2018-10-24
Using the combination of a mitogen-activated protein kinase kinase (MEK) inhibitor, PD0325901 (PD03), and a glycogen synthase kinase 3 (GSK3) inhibitor, CHIR99021 (CHIR), which will hereafter be referred to as 2i, mouse ESCs (mESCs) are maintained in a ground state (Ying et al., 2008). CHIR activate
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The molecular mechanisms controlling the establishment of im
2018-10-24
The molecular mechanisms controlling the establishment of imprinting at the GNAS cluster and leading to the methylation defects in PHP1B are mostly unknown, in part because of a paucity of suitable animal models and lack of accessible Gsα-imprinted human tissues. During the murine embryonic developm
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Taken together our results demonstrate
2018-10-24
Taken together, our results demonstrate an essential role for STAT5 in the regulation of adult IESC homeostasis and response to intestinal injury and regeneration. Functionally, genetic activation of Stat5 increases IESC regeneration to replenish injured intestinal epithelia, conferring resistance t
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However before application in a clinical
2018-10-24
However before application in a clinical context, a number of issues still need to be considered. Indeed, SSC transplantation in cancer patients requires techniques to exclude cancer cell contamination, because implantation of as few as 20 leukemic norepinephrine bitartrate can result in cancer rela
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Introduction Due to their potential
2018-10-24
Introduction Due to their potential to differentiate into all cell types of the three primary germ layers, embryonic stem diltiazem hcl (ESCs) are perfectly suited to investigate early developmental processes such as heart development (Wobus, 2001). The investigation of cardiac cell subtype specif
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Genome wide association studies GWASs represent
2018-10-24
Genome-wide association studies (GWASs) represent another unbiased approach that has proven particularly successful in humans for gene discovery of numerous disease phenotypes (Hindorff et al., 2015). Encouraged by this success, GWASs also have been proposed in mice using a recently developed panel
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br Discussion br Experimental Procedures br Author
2018-10-24
Discussion Experimental Procedures Author Contributions Acknowledgments We thank members of the Azrieli Center for Stem Cells and Genetic Research at the Hebrew University for their contribution, and especially Mordecai Peretz for assistance with the figures, and Ido Sagi for critical re
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Transplantation of RPE cells may be a treatment
2018-10-24
Transplantation of RPE cells may be a treatment for retinal diseases, such as age-related macular degeneration (AMD). Many experimental clinical applications of allogeneic RPE cells for the treatment of AMD have been attempted (Algvere, 1997; Algvere et al., 1999; Kaplan et al., 1999; Peyman et al.,
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br Experimental Procedures br Author Contributions br Acknow
2018-10-24
Experimental Procedures Author Contributions Acknowledgments The authors thank Matthew Deater and the Grompe laboratory for supplying C57BL/6 Fancd2+/− mice and antibodies, and Michael Garbati for the advice on LY2228820. We are indebted to members of the Flow Cytometry Core Laboratory at O
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Here we provide the first definitive evidence that
2018-10-24
Here we provide the first definitive evidence that an alternative airway progenitor cell, marked by expression of SOX2, is the predominant cell of origin for nascent KRT5+ trpv1 antagonist after influenza infection. This was true for nascent KRT5+ cells that emerge in the airways and those that app
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The correct deposition of m C into RNAs is essential
2018-10-24
The correct deposition of m5C into RNAs is essential for normal development. Loss-of-function mutations in the NSUN2 gene in both mouse and human cause growth retardation and neurodevelopmental deficits including microcephaly, as well as defects in cognition and motor function (Blanco and Frye, 2014
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There is widespread recognition of the complementary value o
2018-10-24
There is widespread recognition of the complementary value of hiPSCs in disease modeling. Indeed, a number of studies have revealed mutant HTT-related molecular and cellular abnormalities using human pluripotent stem cells and differentiated cells, e.g., alterations in transcriptomes, proteomes, ATM
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Yet at the same time the extent of human variability
2018-10-24
Yet at the same time the extent of human variability, of which we are only beginning to take the full measure, poses an important practical problem for the field of iPSC-based modeling. Given background genetic differences between individuals, the key question is which experimental designs and degre
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In this contribution we consider the geometric modeling
2018-10-24
In this contribution we consider the geometric modeling of middle-size fullerenes growth beginning with C32; namely C34, C36, C38, C40, C42, C44, C46, C48, C50, C52, C54, C56, C58, and C60. We have studied their growth at first obtaining their graphs, what is simpler, and then designing their struct
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