Listing 1 - 3 of 3 |
Sort by
|
Choose an application
Dual specificity phosphatases (DUSPs) constitute a heterogeneous group of protein tyrosine phosphatases with the ability to dephosphorylate Ser/Thr and Tyr residues from proteins, as well as from other non-proteinaceous substrates including signaling lipids. DUSPs include, among others, MAP kinase (MAPK) phosphatases (MKPs) and small-size atypical DUSPs. MKPs are enzymes specialized in regulating the activity and subcellular location of MAPKs, whereas the function of small-size atypical DUSPs seems to be more diverse. DUSPs have emerged as key players in the regulation of cell growth, differentiation, stress response, and apoptosis. DUSPs regulate essential physiological processes, including immunity, neurobiology and metabolic homeostasis, and have been implicated in tumorigenesis, pathological inflammation and metabolic disorders. Accordingly, alterations in the expression or function of MKPs and small-size atypical DUSPs have consequences essential to human disease, making these enzymes potential biological markers and therapeutic targets. This Special Issue covers recent advances in the molecular mechanisms and biological functions of MKPs and small-size atypical DUSPs, and their relevance in human disease.
hematopoietic cells --- DEPArray --- n/a --- neuroblastoma --- liver steatosis --- MAPK phosphatase --- DUSP-4 --- granule neurons --- neuronal differentiation --- DUSP10 --- cytokines --- MAPKs --- single cell analysis --- macrophage --- asthma --- E. coli infection --- MAPK --- Cpp1 --- nucleotide receptors --- atypical DUSP --- RSV --- Pmp1 --- cannabinoids --- astrocytes --- sepsis --- influenza --- signaling --- triple-negative breast cancer (TNBC) --- differentiation --- HDAC6 (histone deacetylase isoform 6) --- atypical dual-specificity phosphatases --- microtubules --- respiratory viruses --- MK-STYX (MAPK (mitogen-activated protein kinase) phosphoserine/threonine/tyrosine-binding protein) --- dual-specificity phosphatase --- Msg5 --- TLR signaling --- mitogen-activated protein kinase --- fungal MKPs --- macrophages --- MAP Kinase Phosphatase-2 --- inflammation --- Sdp1 --- circulating tumor cells (CTCs) --- MAP kinases --- MAP kinase phosphatases --- P2X7 --- proliferation --- BDNF --- P2Y13 --- T cell --- hypertriglyceridemia --- integrated omics analysis --- post-translational modification --- rhinovirus --- protein stability --- ubiquitination --- dual-specificity phosphatases --- Mkp-1 --- cancer --- brain metastasis --- HER2 --- COPD --- pseudophosphatase
Choose an application
The book has 25 articles about the status and new directions in forensic genetics. Approximately half of the articles are invited reviews, and the remaining articles deal with new forensic genetic methods. The articles cover aspects such as sampling DNA evidence at the scene of a crime; DNA transfer when handling evidence material and how to avoid DNA contamination of items, laboratory, etc.; identification of body fluids and tissues with RNA; forensic microbiome analysis with molecular biology methods as a supplement to the examination of human DNA; forensic DNA phenotyping for predicting visible traits such as eye, hair, and skin colour; new ancestry informative DNA markers for estimating ethnic origin; new genetic genealogy methods for identifying distant relatives that cannot be identified with conventional forensic DNA typing; sensitive DNA methods, including single-cell DNA analysis and other highly specialised and sensitive methods to examine ancient DNA from unidentified victims of war; forensic animal genetics; genetics of visible traits in dogs; statistical tools for interpreting forensic DNA analyses, including the most used IT tools for forensic STR-typing and DNA sequencing; haploid markers (Y-chromosome and mitochondria DNA); inference of ethnic origin; a comprehensive logical framework for the interpretation of forensic genetic DNA data; and an overview of the ethical aspects of modern forensic genetics.
Research & information: general --- Biology, life sciences --- Genetics (non-medical) --- TaqMan SNP genotyping --- OpenArray™ system --- forensic DNA phenotyping --- forensic DNA typing --- animal forensics --- wildlife forensics --- cat STRs --- dog STRs --- cyt b --- COI --- biogeographic ancestry --- pigmentation --- skin color --- externally visible characteristics --- forensic genetics --- eye colour --- rs12913832 --- DNA phenotyping --- domestic dog (Canis familiaris) --- canine DNA phenotyping --- forensic --- proof of concept study --- evidence --- Y-STR --- mtDNA --- mitochondria --- bio-geographical ancestry --- massively parallel sequencing --- ancestry informative markers --- SNPs --- 1000 Genomes --- Human Origins SNP array --- FDP --- HIrisPlex-S --- DEPArray --- ancestry prediction --- phenotype prediction --- next-generation sequencing --- single-cell genomics --- single-cell sequencing --- mixture deconvolution --- low template DNA --- ltDNA --- probabilistic genotyping --- EuroForMix --- DNAStatistX --- STRmixTM --- DNA forensics --- DNA mixture --- mixture interpretation --- single-cell --- clustering algorithm --- number of contributors --- consensus profile --- cross-amplification --- microsatellites --- Strigiformes --- illegal trade --- kinship --- nocturnal raptors --- review --- body fluid --- organ --- tissue --- identification --- mRNA --- DNA methylation --- activity level --- massively parallel sequencing (MPS) --- next-generation sequencing (NGS) --- short tandem repeat (STR) --- sequence analysis --- software --- DNA transfer --- DNA persistence --- DNA prevalence --- DNA recovery --- activity level evaluation --- forensic science --- ethics --- ethics as lived practice --- decision-making --- genetic databasing --- forensic genealogy --- forensic epigenetics --- communication --- database --- SNP --- next generation sequencing --- hybridization capture --- bone --- transfer --- persistence --- activity --- Bayesian networks --- burglary --- CODIS --- touch DNA --- crime scene --- authorized --- sampling --- short tandem repeat --- forensic microbiology --- microbiome --- physical appearance --- human genome variation --- DNA-based prediction --- investigative leads --- forensic DNA intelligence --- forensic genomics --- degraded DNA --- mitochondrial DNA --- forensic DNA profiling --- ancient DNA --- human identification --- ancestry --- biostatistics --- clustering --- classification --- distance based --- likehood --- hypothesis tests --- DNA molecules --- decontamination --- cleaning strategies --- Romanov family --- next generation sequencing (NGS) --- heteroplasmy --- single nucleotide polymorphism (SNP) --- kinship analyses --- biological sexing --- DNA --- principles of interpretation --- investigative --- evaluative --- reporting --- LR --- propositions --- activity issues --- TaqMan SNP genotyping --- OpenArray™ system --- forensic DNA phenotyping --- forensic DNA typing --- animal forensics --- wildlife forensics --- cat STRs --- dog STRs --- cyt b --- COI --- biogeographic ancestry --- pigmentation --- skin color --- externally visible characteristics --- forensic genetics --- eye colour --- rs12913832 --- DNA phenotyping --- domestic dog (Canis familiaris) --- canine DNA phenotyping --- forensic --- proof of concept study --- evidence --- Y-STR --- mtDNA --- mitochondria --- bio-geographical ancestry --- massively parallel sequencing --- ancestry informative markers --- SNPs --- 1000 Genomes --- Human Origins SNP array --- FDP --- HIrisPlex-S --- DEPArray --- ancestry prediction --- phenotype prediction --- next-generation sequencing --- single-cell genomics --- single-cell sequencing --- mixture deconvolution --- low template DNA --- ltDNA --- probabilistic genotyping --- EuroForMix --- DNAStatistX --- STRmixTM --- DNA forensics --- DNA mixture --- mixture interpretation --- single-cell --- clustering algorithm --- number of contributors --- consensus profile --- cross-amplification --- microsatellites --- Strigiformes --- illegal trade --- kinship --- nocturnal raptors --- review --- body fluid --- organ --- tissue --- identification --- mRNA --- DNA methylation --- activity level --- massively parallel sequencing (MPS) --- next-generation sequencing (NGS) --- short tandem repeat (STR) --- sequence analysis --- software --- DNA transfer --- DNA persistence --- DNA prevalence --- DNA recovery --- activity level evaluation --- forensic science --- ethics --- ethics as lived practice --- decision-making --- genetic databasing --- forensic genealogy --- forensic epigenetics --- communication --- database --- SNP --- next generation sequencing --- hybridization capture --- bone --- transfer --- persistence --- activity --- Bayesian networks --- burglary --- CODIS --- touch DNA --- crime scene --- authorized --- sampling --- short tandem repeat --- forensic microbiology --- microbiome --- physical appearance --- human genome variation --- DNA-based prediction --- investigative leads --- forensic DNA intelligence --- forensic genomics --- degraded DNA --- mitochondrial DNA --- forensic DNA profiling --- ancient DNA --- human identification --- ancestry --- biostatistics --- clustering --- classification --- distance based --- likehood --- hypothesis tests --- DNA molecules --- decontamination --- cleaning strategies --- Romanov family --- next generation sequencing (NGS) --- heteroplasmy --- single nucleotide polymorphism (SNP) --- kinship analyses --- biological sexing --- DNA --- principles of interpretation --- investigative --- evaluative --- reporting --- LR --- propositions --- activity issues
Choose an application
The book has 25 articles about the status and new directions in forensic genetics. Approximately half of the articles are invited reviews, and the remaining articles deal with new forensic genetic methods. The articles cover aspects such as sampling DNA evidence at the scene of a crime; DNA transfer when handling evidence material and how to avoid DNA contamination of items, laboratory, etc.; identification of body fluids and tissues with RNA; forensic microbiome analysis with molecular biology methods as a supplement to the examination of human DNA; forensic DNA phenotyping for predicting visible traits such as eye, hair, and skin colour; new ancestry informative DNA markers for estimating ethnic origin; new genetic genealogy methods for identifying distant relatives that cannot be identified with conventional forensic DNA typing; sensitive DNA methods, including single-cell DNA analysis and other highly specialised and sensitive methods to examine ancient DNA from unidentified victims of war; forensic animal genetics; genetics of visible traits in dogs; statistical tools for interpreting forensic DNA analyses, including the most used IT tools for forensic STR-typing and DNA sequencing; haploid markers (Y-chromosome and mitochondria DNA); inference of ethnic origin; a comprehensive logical framework for the interpretation of forensic genetic DNA data; and an overview of the ethical aspects of modern forensic genetics.
TaqMan SNP genotyping --- OpenArray™ system --- forensic DNA phenotyping --- forensic DNA typing --- animal forensics --- wildlife forensics --- cat STRs --- dog STRs --- cyt b --- COI --- biogeographic ancestry --- pigmentation --- skin color --- externally visible characteristics --- forensic genetics --- eye colour --- rs12913832 --- DNA phenotyping --- domestic dog (Canis familiaris) --- canine DNA phenotyping --- forensic --- proof of concept study --- evidence --- Y-STR --- mtDNA --- mitochondria --- bio-geographical ancestry --- massively parallel sequencing --- ancestry informative markers --- SNPs --- 1000 Genomes --- Human Origins SNP array --- FDP --- HIrisPlex-S --- DEPArray --- ancestry prediction --- phenotype prediction --- next-generation sequencing --- single-cell genomics --- single-cell sequencing --- mixture deconvolution --- low template DNA --- ltDNA --- probabilistic genotyping --- EuroForMix --- DNAStatistX --- STRmixTM --- DNA forensics --- DNA mixture --- mixture interpretation --- single-cell --- clustering algorithm --- number of contributors --- consensus profile --- cross-amplification --- microsatellites --- Strigiformes --- illegal trade --- kinship --- nocturnal raptors --- review --- body fluid --- organ --- tissue --- identification --- mRNA --- DNA methylation --- activity level --- massively parallel sequencing (MPS) --- next-generation sequencing (NGS) --- short tandem repeat (STR) --- sequence analysis --- software --- DNA transfer --- DNA persistence --- DNA prevalence --- DNA recovery --- activity level evaluation --- forensic science --- ethics --- ethics as lived practice --- decision-making --- genetic databasing --- forensic genealogy --- forensic epigenetics --- communication --- database --- SNP --- next generation sequencing --- hybridization capture --- bone --- transfer --- persistence --- activity --- Bayesian networks --- burglary --- CODIS --- touch DNA --- crime scene --- authorized --- sampling --- short tandem repeat --- forensic microbiology --- microbiome --- physical appearance --- human genome variation --- DNA-based prediction --- investigative leads --- forensic DNA intelligence --- forensic genomics --- degraded DNA --- mitochondrial DNA --- forensic DNA profiling --- ancient DNA --- human identification --- ancestry --- biostatistics --- clustering --- classification --- distance based --- likehood --- hypothesis tests --- DNA molecules --- decontamination --- cleaning strategies --- Romanov family --- next generation sequencing (NGS) --- heteroplasmy --- single nucleotide polymorphism (SNP) --- kinship analyses --- biological sexing --- DNA --- principles of interpretation --- investigative --- evaluative --- reporting --- LR --- propositions --- activity issues
Listing 1 - 3 of 3 |
Sort by
|