FCD 524 DRIVER

Please review our privacy policy. February 6, Last modified: Do not show this banner again. National Institutes of Health. ProtoNet; Automatic hierarchical classification of proteins More Integrated resource of protein families, domains and functional sites More

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However, in contrast to leukocytes the interactions were not restricted to venules, but were also observed in small arterioles. In summary, additional data is needed to determine the clinical significance of this variant.

The aim of our present study was, therefore, to establish a model to investigate the microcirculation in the mouse small intestine. Ensembl bacterial and archaeal genome annotation project More Besides 52 perfusion, leukocyte-endothelial cell interaction was analyzed in postcapillary venules of the intestinal submucosa using rhodamine-6G as an in vivo leukocyte stain.

K7RQ16 Primary citable accession number: Help criteria provided, multiple submitters, no conflicts 2 stars out fce maximum of 4 stars. National Institutes of Health. Uncertain significance Last evaluated: Database of comparative protein structure models More You are using a version of browser that may not display all the features of this website. Do not show this banner again. Please review our privacy policy.

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Sarotech FCD() Free Driver Download (Official) for Windows 98SE

Automatic assertion inferred from database entries i. Pfam protein domain database More Using this model in combination with gene-targeted mice or monoclonal antibodies it is possible to investigate the molecular mechanisms of intestinal inflammation reactions. Unreviewed – Annotation score: December 5, This is version 35 of the entry and version 1 of the sequence.

Conserved Domains Database More It is useful for tracking sequence updates. Systems used to automatically annotate proteins with high accuracy:.

Select item s and click on “Add to basket” to create your own collection here entries max. The algorithm is described in the ISO standard. This variant’s association with FCD has not been reported in other affected individuals, which, taken together with the presumed autosomal dominant inheritance pattern of FCD, does not support a strong correlation between this variant and FCD.

This is version 35 of the entry and version 1 of the sequence. ClinVar Relating variation to medicine. This variant has also been identified in the heterozygous state in one individual with late onset Fuchs corneal dystrophy FCDhowever hearing status was not reported Riazuddin EMBL nucleotide sequence database More In a separate group rhodamine-6G-labeled syngeneic platelets were infused to analyze platelet-endothelial cell interactions quantitatively in vivo.

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May 23, Number of submission s: Select the link destinations: Interpretation Help Clinical significance: Click here to see the new Variation Report design!

FCD domain-containing protein

Automatic assertion according to rules i. Clinical assertions Summary evidence Supporting observations Help.

Although this variant has been seen in the general population, its frequency is not high enough to rule out a pathogenic role. Help Review status:

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