نتایج جستجو برای: growth defects

تعداد نتایج: 939617  

     Background and purpose: Tissue engineering and cell therapy, as promising therapies, provide the opportunity to repair bone lesions and defects. Combined scaffolds, synthetic and natural polymers can provide a suitable structure for differentiation of Wharton Jelly mesenchymal stem cells (WJ-MSCs) into bone. In current study, the effect of lyophilized blood growth factors in promoting the ...

Journal: :Nano letters 2013
Karla Hillerich Kimberly A Dick Cheng-Yen Wen Mark C Reuter Suneel Kodambaka Frances M Ross

By combining in situ and ex situ transmission electron microscopy measurements, we examine the factors that control the morphology of "hybrid" nanowires that include group III-V and group IV materials. We focus on one materials pair, GaP/Si, for which we use a wide range of growth parameters. We show through video imaging that nanowire morphology depends on growth conditions, but that a general...

Journal: :Genetics 2000
J M Singer G J Hermann J M Shaw

The actin cytoskeleton is required for many aspects of cell division in yeast, including mitochondrial partitioning into growing buds (mitochondrial inheritance). Yeast cells lacking MDM20 function display defects in both mitochondrial inheritance and actin organization, specifically, a lack of visible actin cables and enhanced sensitivity to Latrunculin A. mdm20 mutants also exhibit a temperat...

2010
W. Qian M. Skowronski K. Doverspike L. B. Rowland D. K. Gaskill

Structural investigations of organometallic vapor phase epitaxy grown #-GaN films using high-resolution transmission electron microscopy and scanning force microscopy have revealed the presence of tunnel-like defects with 35–500 Å radii that are aligned along the growth direction of the crystal and penetrate the entire epilayer. These defects, which are termed ‘‘nanopipes,’’ terminate on the fr...

Journal: :Cell 2013
Nisha Padmanabhan Dongxin Jia Colleen Geary-Joo Xuchu Wu Anne C. Ferguson-Smith Ernest Fung Mark C. Bieda Floyd F. Snyder Roy A. Gravel James C. Cross Erica D. Watson

The importance of maternal folate consumption for normal development is well established, yet the molecular mechanism linking folate metabolism to development remains poorly understood. The enzyme methionine synthase reductase (Mtrr) is necessary for utilization of methyl groups from the folate cycle. We found that a hypomorphic mutation of the mouse Mtrr gene results in intrauterine growth res...

Journal: :Human molecular genetics 2001
E A Lindsay A Baldini

Chromosome 22q11.2 heterozygous deletions cause the most common deletion syndrome, including the DiGeorge syndrome phenotype. Using a mouse model of this deletion (named Df1) we show that the aortic arch patterning defects that occur in heterozygously deleted mice (Df1/+) are associated with a differentiation impairment of vascular smooth muscle in the 4th pharyngeal arch arteries (PAAs) during...

Journal: :The Journal of Cell Biology 1995
F Verde J Mata P Nurse

To identify new genes involved in the control of cell morphogenesis in the fission yeast Schizosaccharomyces pombe we have visually screened for temperature-sensitive mutants that show defects in cell morphology. We have isolated and characterized 64 mutants defining 19 independent genes, 10 of which have not been previously described. One class of mutants, defining 12 orb genes, become round a...

Journal: :Genetics 2008
Jason Z Morris Leah Bergman Anna Kruyer Mikhail Gertsberg Adriana Guigova Ronald Arias Monika Pogorzelska

Rapid larval growth is essential in the development of most metazoans. In this article, we show that bene, a gene previously identified on the basis of its oogenesis defects, is also required for larval growth and viability. We show that all bene alleles disrupt gatA, which encodes the Drosophila homolog of glutamyl-tRNA(Gln) amidotransferase subunit A (GatA). bene alleles are now referred to a...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Duanwu Zhang Wataru Tomisato Lijing Su Lei Sun Jin Huk Choi Zhao Zhang Kuan-Wen Wang Xiaoming Zhan Mihwa Choi Xiaohong Li Miao Tang Jose M Castro-Perez Sara Hildebrand Anne R Murray Eva Marie Y Moresco Bruce Beutler

The recessive N-ethyl-N-nitrosourea-induced phenotype toku is characterized by delayed hair growth, progressive hair loss, and excessive accumulation of dermal cholesterol, triglycerides, and ceramides. The toku phenotype was attributed to a null allele of Gk5, encoding glycerol kinase 5 (GK5), a skin-specific kinase expressed predominantly in sebaceous glands. GK5 formed a complex with the ste...

Journal: :Physical review letters 2010
M J Kramer M I Mendelev R E Napolitano

In situ x-ray diffraction (XRD) coupled with molecular dynamics (MD) simulations have been used to quantify antisite defect trapping during crystallization. Rietveld refinement of the XRD data revealed a marked lattice distortion which involves an a axis expansion and a c axis contraction of the stable C11b phase. The observed lattice response is proportional in magnitude to the growth rate, su...

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