Results 1 - 10
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814
Tyrosine phosphorylation of paxillin and pp125FAK accompanies cell adhesion to extracellulax matrix: a role in cytoskeletal assembly
- J. Cell
, 1992
"... Abstract. Cells in culture reveal high levels of protein tyrosine phosphorylation in their focal adhesions, the regions where cells adhere to the underlying substratum. We have examined the tyrosine phosphorylation of proteins in response to plating cells on extracellular matrix substrata. Rat embry ..."
Abstract
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Cited by 152 (11 self)
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embryo fibroblasts, mouse Balb/c 3T3, and NIH 3T3 cells plated on fibronectin-coated surfaces revealed elevated phosphotyrosine levels in a cluster of proteins between 115 and 130 kD. This increase in tyrosine phosphorylation was also seen when rat embryo fibroblasts were plated on laminin or vitronectin
Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella
- J. Cell
, 2000
"... Abstract. Intraflagellar transport (IFT) is a rapid movement of multi-subunit protein particles along flagellar microtubules and is required for assembly and maintenance of eukaryotic flagella. We cloned and sequenced a Chlamydomonas cDNA encoding the IFT88 subunit of the IFT particle and identified ..."
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Cited by 97 (11 self)
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Abstract. Intraflagellar transport (IFT) is a rapid movement of multi-subunit protein particles along flagellar microtubules and is required for assembly and maintenance of eukaryotic flagella. We cloned and sequenced a Chlamydomonas cDNA encoding the IFT88 subunit of the IFT particle
Whole-Genome Sequence Assembly for Mammalian Genomes: Arachne 2
"... We previously described the whole-genome assembly program Arachne, presenting assemblies of simulated data for small to mid-sized genomes. Here we describe algorithmic adaptations to the program, allowing for assembly of mammalian-size genomes, and also improving the assembly of smaller genomes. Thr ..."
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Cited by 68 (2 self)
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. Three principal changes were simultaneously made and applied to the assembly of the mouse genome, during a six-month period of development: (1) Supercontigs (scaffolds) were iteratively broken and rejoined using several criteria, yielding a 64-fold increase in length (N50), and apparent elimination
Sequential Assembly of Centromeric Proteins in Male Mouse Meiosis
, 2008
"... The assembly of the mitotic centromere has been extensively studied in recent years, revealing the sequence and regulation of protein loading to this chromosome domain. However, few studies have analyzed centromere assembly during mammalian meiosis. This study specifically targets this approach on m ..."
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Cited by 1 (1 self)
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on mouse spermatocytes. We have found that during prophase I, the proteins of the chromosomal passenger complex Borealin, INCENP, and Aurora-B load sequentially to the inner centromere before Shugoshin 2 and MCAK. The last proteins to be assembled are the outer kinetochore proteins BubR1 and CENP-E. All
Impairs Mouse Primordial Follicle Assembly InVitro
"... Bisphenol-A (BPA) and diethylhexyl phthalate (DEHP) are estrogenic compounds widely used in commercial plastic products. Previous studies have shown that exposure to such compounds have adverse effects on various aspects of mammalian reproduction including folliculogene-sis. The objective of this st ..."
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of this study was to examine the effects of BPA and DEHP exposure on pri-mordial follicle formation. We found that germ cell nest breakdown and primordial follicle assembly were significantly reduced when new-born mouse ovaries were exposed to 10 or 100 lM BPA and DEHP in vitro. Moreover, BPA and DEHP exposure
Envelope Glycoprotein Interactions in Coronavirus Assembly
"... Abstract. Coronaviruses are assembled by budding into smooth membranes of the intermediate ERto-Golgi compartment. We have studied the association of the viral membrane glycoproteins M and S in the formation of the virion envelope. Using coimmunoprecipitation analysis we demonstrated that the M and ..."
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Cited by 35 (6 self)
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Abstract. Coronaviruses are assembled by budding into smooth membranes of the intermediate ERto-Golgi compartment. We have studied the association of the viral membrane glycoproteins M and S in the formation of the virion envelope. Using coimmunoprecipitation analysis we demonstrated that the M
Characterization of dominant and recessive assembly-defective mutations in mouse neurofilament NF-M
- J
, 1990
"... Abstract. We have generated a set of amino- and carboxy-terminal deletions of the neurofilament NF-M gene and determined the molecular consequences of forced expression of these mutant constructs in mouse fibroblasts. To follow the expression of mutant NF-M subunits in transfected cells, a 12 amino ..."
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Cited by 17 (1 self)
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Abstract. We have generated a set of amino- and carboxy-terminal deletions of the neurofilament NF-M gene and determined the molecular consequences of forced expression of these mutant constructs in mouse fibroblasts. To follow the expression of mutant NF-M subunits in transfected cells, a 12 amino
Intermediate filaments and initiation of desmosome assembly
- J. Cell
, 1985
"... ABSTRACT The desmosome junction is an important component in the cohesion of epithelial cells, especially epidermal keratinocytes. To gain insight into the structure and function of desmosomes, their morphogenesis has been studied in a primary mouse epidermal (PME) cell culture system. When these ce ..."
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Cited by 35 (5 self)
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ABSTRACT The desmosome junction is an important component in the cohesion of epithelial cells, especially epidermal keratinocytes. To gain insight into the structure and function of desmosomes, their morphogenesis has been studied in a primary mouse epidermal (PME) cell culture system. When
The p21(Cip1) and p27(Kip1) CDK ’inhibitors’ are essential activators of cyclin D-dependent kinases in murine fibroblasts.
- EMBO J
, 1999
"... The widely prevailing view that the cyclin-dependent kinase inhibitors (CKIs) are solely negative regulators of cyclin-dependent kinases (CDKs) is challenged here by observations that normal up-regulation of cyclin D-CDK4 in mitogen-stimulated fibroblasts depends redundantly upon p21 Cip1 and p27 K ..."
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Cited by 113 (2 self)
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Kip1 . Primary mouse embryonic fibroblasts that lack genes encoding both p21 and p27 fail to assemble detectable amounts of cyclin D-CDK complexes, express cyclin D proteins at much reduced levels, and are unable to efficiently direct cyclin D proteins to the cell nucleus. Restoration of CKI function
Results 1 - 10
of
814