search for: receptors

...-rich flanking regions N-terminal,Cysteine-rich flanking regions C-terminal LEUCINE-RICH TRANSMEMBRANE PROTEINS Biological process unclassified - A_51_P100174 NM_008613.2 - MEIOSIS-SPECIFIC NUCLEAR STRUCTURAL PROTEIN 1 Developmental processes Meiosis A_51_P100218 NM_134198.1 Vomeronasal receptors type 1,GPCRs rhodopsin-like superfamily VOMERONASAL PHEROMONE RECEPTOR Signal transduction,Sensory perception Cell surface receptor mediated signal transduction,Pheromone response A_51_P100227 NM_023579.4 HEAT,Importin-betas N-terminal,Armadillo-like helical IMPORTIN BETA-3,IMPORTIN BETA In...

Hi, I have the following data frame: > print(mydatframe) __DATAFRAME__ V1 V2 V3 1 1007_s_at DDR1 discoidin domain receptor tyrosine kinase 1 2 1053_at RFC2 replication factor C (activator 1) 2, 40kDa 3 117_at HSPA6 heat shock 70kDa protein 6 (HSP70B') __END__ Is there a way to create a hash with V2 as Key and V3 as its value? - Gundala Viswanath Jakarta - Indonesia

Hi, I have the following data file to be parsed and captured as a data frame: __DATA__ #GDS_ID GENE_NAME GENE_DESCRIPTION GENE_FUNCTION 1007_s_at | DDR1 | discoidin domain receptor tyrosine kinase 1 | protein-coding 1053_at | RFC2 | replication factor C (activator 1) 2, 40kDa | protein-coding 117_at | HSPA6 | heat shock 70kDa protein 6 (HSP70B') | protein-coding __END__ In particular it is

Dear all, Here is my code which am using to combine 5th column from different data sets. Here is the function to do my job genesymbol.append.file <-NULL gene.column <- NULL readGeneSymbol <- function(files,genesymbol.column=5){ for(i in fnames){ temp <- read.table(fnames,header=T,sep="\t",stringsAsFactors=F,quote="\"")

Dear R-helpers: I am trying to fit a multivariate Cox proportional hazards model, modelling survival outcome as a function of treatment and receptor status. The data look like below: # structure of the data str(sample.data) List of 4 $ survobj : Surv [1:129, 1:2] 0.8925+ 1.8836+ 2.1191+ 5.3744+ 1.6099+ 5.2567 0.2081+ 0.2108+ 0.2683+ 0.4873+ ... ..- attr(*, "dimnames")=List of 2

Hello. I'm running some asterisks in a small voip provider in Brazil and we're having some problems with a analogic channel bank. When I make calls using analogic extensions, I have a crystal clear quality, but the receptor have a lot of noise and echo. We tested the situation using SIP, E1 links, GSM links, analogic trunks (FXO ports) and we always have the same symptons My

Hello all, I'm trying to create a heatmap using 2 matrices I have: z and v. Both matrices represent different correlations for the same independent variables. The problem I have is that I wish to have the values from matrix z to be represented by color intensity while having the values from matrix v to be represented by circle size. I currently have the following in front of me and an unsure

Dear list, Has anyone created a version of SSmicmen that allows testing for group differences? The basic Michaelis-Menten equation is: (Bmax * X) / (Kd + X). The nlme package allows modeling of random effects for Bmax and Kd as needed, but I curious how I can build in group differences? I have receptor binding data for strains of mice, and following Pinheiro and Bates' lead in their

Actualizaci?n De La Norma Sobre Descargas De Aguas Residuales CONFERENCIA VIRTUAL EN VIVO | 25 de Julio 2023 informaci?n El 11 de marzo de 2022 fue publicada en el Diario Oficial de la Federaci?n la actualizaci?n de la NOM-001-SEMARNAT-2021 que sustituye a la NOM-001-SEMARNAT-1996, la cual entrar? el presente a?o y ser? obligatoria para las personas f?sicas o morales que realicen descargas de

To estimate saturation binding parameters Bmax and Kd in a receptor saturation binding experiment, I use the following nonlinear equation and the nls() function: bmax*X*dummy ------------ + ns*X + background = total binding kd+X where X is concentration, and dummy is an indicator to allow shared estimation of the nonspecific binding parameter ns. This equation describes two fitted

Hello all. I'm struggling to get Centos 4 to recognize my Dell Powervaul 132T tape changer. The system doesnt create a device node for it. [root at orion scotty]# cat /proc/scsi/scsi Attached devices: Host: scsi0 Channel: 00 Id: 06 Lun: 00 Vendor: SEAGATE Model: DAT DAT72-052 Rev: A060 Type: Sequential-Access ANSI SCSI revision: 03 Host: scsi1 Channel: 00 Id: 01 Lun:

Hi I' ve just installed TE410P and asterisk-0.7.2 from tar.gz on fedora core 1. When i start asterisk it shows me this: /usr/lib/asterisk/modules/chan_zap.so: undefined symbol: ast_pickup_call Apr 19 16:52:32 WARNING[-1085304704]: loader.c:358 load_modules: Loading module chan_zap.so failed! Where do i look, how can i debug? Thanks in advance Jorge Verastegui G RedCetus S.R.L

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Dear R-helpers: I am trying to fit a multivariate Cox proportional hazards model, modelling survival outcome as a function of treatment and receptor status. The data look like below: # structure of the data str(sample.data) List of 4 $ survobj : Surv [1:129, 1:2] 0.8925+ 1.8836+ 2.1191+ 5.3744+ 1.6099+ 5.2567 0.2081+ 0.2108+ 0.2683+ 0.4873+ ... ..- attr(*, "dimnames")=List of 2

Job Title : Postdoctoral Position in Biostatistics/Bioinformatics Background The joint research unit between bioM?rieux, international leader in in vitro diagnostic, and Hospices Civils de Lyon, second-largest University Hospital Network in France, develops a research program dedicated to the study of injury induced immunosuppression. This program aims at (i) describing and understanding the

Hello, in my company we want to implement a Two-Factor authentication in servers with Solaris(8 or 9) and HP-UX (11 or 11i). The authentication server will be a RSA. We want to use OpenSSH to ask for authorization twice, first with PAM, and then to the RSA server. I like to know if somebody already implemented. Thanks for your help Uriel Quintana La informaci?n contenida en este correo

Se não pode visualizar este e-mail corretamente, clique aqui <http://www.almasoma.pt/newsletter--terapia-para-bebes-aprenda-a-ajuda-los> . <http://www.almasoma.pt/> Formação em Terapia para Bebés Lisboa, Outono 2013 - Primavera 2016 Workshop: "Baby Clinic", 6 e 7 de Abril de 2013 Conferência de Apresentação, 5 de Abril de 2013 Karlton Terry Pioneiro da assistência aos

BioInformatics Scientist Job Code: 10-TR25 Location: Cambridge, MA Description We are seeking a highly motivated, independent bioinformatics scientist to join a group of scientists, analysts and programmers to develop tools and methodologies for large-scale gene expression data analysis. The group supports a variety of research projects in target and drug discovery as well as biomarker

Hello, I have a seemingly simple problem that a tab-delimited file can't be read in. > annoTranscripts <- read.table("matched.txt", sep = '\t', stringsAsFactors = FALSE) Error in scan(file, what, nmax, sep, dec, quote, skip, nlines, na.strings, : line 5933 did not have 12 elements However, all lines do have 12 columns. > lines <-

...//rcytoscape.systemsbiology.net/versions/current/gallery/TCGA/subnet.TCGA.02.0014.png This portrays 1) gene expression (green: under-expression; red: over-expression) 2) copy number (blue: high, black: low) 3) gene type (node shape: hexagons are kinases, arrows are ligands, diamonds are receptors, circles for everything else) 4) mutation status (not SNPs, but non-synonymous amino acid substitutions) 5) in the context of gene relationships, from KEGG A vignette for a larger version of this network is nearly complete. The Cytoscape network map is created from data and R code. -...