Info
- Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.
Advances in Forensic Genetics
| Advances in Forensic Genetics |
| Autore | Morling Niels |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 electronic resource (516 p.) |
| Soggetto topico |
Research & information: general
Biology, life sciences Genetics (non-medical) |
| Soggetto non controllato |
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 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910585942303321 |
Morling Niels
|
||
| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Boreal Bird Ecology, Management and Conservation
| Boreal Bird Ecology, Management and Conservation |
| Autore | McNulty Stacy A |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 electronic resource (158 p.) |
| Soggetto topico |
Research & information: general
Biology, life sciences Genetics (non-medical) |
| Soggetto non controllato |
boreal
buffering climate change forest bird macroclimate population decline protected areas topographic heterogeneity bird distribution and abundance boreal birds Canada Warbler Cardellina canadensis Zonation reserve design Euphagus carolinus nest success post-fledging rusty blackbird survivorship streams wetlands range periphery spruce-fir forests range shift community dynamics red squirrel wetland point count remotely sensed landscape data unmarked boreal forest clear-cutting conservation forest management old-growth forest Picoides dorsalis Black Belt Prairie citizen science machine learning niche modeling group size habitat use species distribution models Rusty Blackbird boreal wetlands aquatic macroinvertebrates foraging ecology occupancy modeling genetic diversity glacial refugia phylogeography |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910580215103321 |
|
McNulty Stacy A
|
||
| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Genes : fatos e fantasias
| Genes : fatos e fantasias |
| Autore | Garcia Eloi S |
| Pubbl/distr/stampa | SciELO Books - Editora FIOCRUZ, 2006 |
| Descrizione fisica | 1 electronic resource (124 p.) |
| Soggetto topico | Genetics (non-medical) |
| Soggetto non controllato | Genetics (non-medical) |
| ISBN | 9786557081020 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | por |
| Altri titoli varianti | Genes |
| Record Nr. | UNINA-9910557279203321 |
|
Garcia Eloi S
|
||
| SciELO Books - Editora FIOCRUZ, 2006 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Genetic Conditions Affecting the Skeleton : Congenital, Idiopathic Scoliosis and Arthrogryposis
| Genetic Conditions Affecting the Skeleton : Congenital, Idiopathic Scoliosis and Arthrogryposis |
| Autore | Giampietro Philip |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 electronic resource (172 p.) |
| Soggetto topico |
Research & information: general
Biology, life sciences Genetics (non-medical) |
| Soggetto non controllato |
spinal curvatures
scoliosis idiopathic DNA methylation pyrosequencing estrogen receptor 1 ESR1 scoliosis progression adolescent idiopathic scoliosis idiopathic scoliosis exome sequencing spine polygenic variants musculoskeletal disease cytoskeleton extracellular matrix contracture arthrogryposis congenital POC5 cilia genetics spine deformity genetic predisposition complex trait model animal genome wide association study genetic linkage study Amyoplasia DECIPHER (DatabasE of genomiC variation and Phenotype in Humans using Ensemble Resources) CNV (copy number variant) DA (distal arthrogryposis) IPA (ingenuity pathway analysis) HPO (human phenotype ontology) akinesia MYOD IGF2 FGFR1 (Fibroblast growth factor receptor 1) genetic variations congenital scoliosis monozygotic twin epigenome-wide association study bone discordant curve severity differentially methylated region congenital vertebral malformation copy number variant CNV CHRNG distal arthrogryposis type 8 Escobar multiple pterygium syndrome MYH3 protein tyrosine kinase 7 (PTK7) whole exome sequencing |
| ISBN | 3-0365-5976-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Genetic Conditions Affecting the Skeleton |
| Record Nr. | UNINA-9910639995403321 |
|
Giampietro Philip
|
||
| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Genetics and Genomics of Pulmonary Arterial Hypertension
| Genetics and Genomics of Pulmonary Arterial Hypertension |
| Autore | Southgate Laura |
| Pubbl/distr/stampa | Basel, : MDPI Books, 2022 |
| Descrizione fisica | 1 electronic resource (188 p.) |
| Soggetto topico |
Research & information: general
Biology, life sciences Genetics (non-medical) |
| Soggetto non controllato |
pulmonary arterial hypertension
massive parallel sequencing NGS digenic inheritance and genetics BMPR2 promoter pathogenic variant heritable pulmonary arterial hypertension genetic analysis NGS gene panel BMPR2 TBX4 GDF2 EIF2AK4 genomics pediatrics lung disease endothelial cells smooth muscle cells DNA damage DNA repair expression quantitative trait locus eQTL blood genetics exome sequencing molecular genetics paediatrics bone morphogenetic protein receptor type 2 heritable familial estrogen estradiol penetrance gender PAH forward phenotyping forward genetics reverse genetics reverse phenotyping intermediate phenotypes whole-genome sequencing epigenetic inheritance genetic heterogeneity phenotypic heterogeneity pulmonary hypertension bone morphogenetic protein receptor 2 signaling repurposed drugs pharmaceuticals miRNA clinical trials |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910595078603321 |
|
Southgate Laura
|
||
| Basel, : MDPI Books, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Genetics of Hearing Impairment
| Genetics of Hearing Impairment |
| Autore | del Castillo Ignacio |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 electronic resource (314 p.) |
| Soggetto topico |
Research & information: general
Biology, life sciences Genetics (non-medical) |
| Soggetto non controllato |
inner ear
hearing impairment gene identification disease-causing mutations genetic epidemiology genotype&ndash phenotype correlations pathophysiological mechanisms omics genome editing gene therapy |
| ISBN | 3-0365-5224-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910637793003321 |
|
del Castillo Ignacio
|
||
| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Une histoire génétique : notre diversité, notre évolution, notre adaptation : Leçon inaugurale prononcée au Collège de France le jeudi 6 février 2020 / / Lluis Quintana-Murci
| Une histoire génétique : notre diversité, notre évolution, notre adaptation : Leçon inaugurale prononcée au Collège de France le jeudi 6 février 2020 / / Lluis Quintana-Murci |
| Autore | Quintana-Murci Lluis |
| Pubbl/distr/stampa | Paris, : Collège de France, 2021 |
| Altri autori (Persone) |
FischerAlain
Quintana-MurciLluis |
| Collana | Leçons inaugurales |
| Soggetto topico |
Science: general issues
Life sciences: general issues Evolution Genetics (non-medical) |
| Soggetto non controllato |
génétique
génétique des populations génomique génomique humaine diversité biologique immunologie diversité épidémiologie évolution diversité phénotypique |
| ISBN | 2-7226-0573-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | fre |
| Altri titoli varianti |
Une histoire génétique
Une histoire génétique |
| Record Nr. | UNINA-9910495760603321 |
|
Quintana-Murci Lluis
|
||
| Paris, : Collège de France, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
| Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019 |
| Autore | Butler Merlin G |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 electronic resource (256 p.) |
| Soggetto topico |
Research & information: general
Biology, life sciences Genetics (non-medical) |
| Soggetto non controllato |
autism spectrum disorders (ASD)
cancer overlapping genes and gene profiling super-pathways phenotypes and diseases molecular functions and processes 15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome imprinting parent-of-origin effects phenotype-genotype correlation autism developmental delays motor delays microbiome gut ProSAP2 Phelan McDermid Syndrome gut–brain interaction leaky gut IL-6 SHANK collapsin response mediator protein 4 autism spectrum disorder neurodevelopmental disorder whole-exome sequencing animal model sex different phenotypes 15q11.2 BP1–BP2 microdeletion (Burnside–Butler syndrome) NIPA1 NIPA2 CYFIP1 TUBGCP5 genes Prader–Willi and Angelman syndromes magnesium transporters and supplementation potential treatment options intellectual disability AMPA receptors NMDA receptors guanine nucleotide exchange factor synaptic plasticity Autism spectrum disorder ASD Obesity Overweight Body mass index BMI autism candidate genes synaptotagmin-like protein 4 (SYTL4) transmembrane protein 187 (TMEM187) SYTL4-protein structure STRING-protein-protein interaction expression profile microRNA- interactions autism spectrum disorders biological networks genomics multi-omics network diffusion data integration genetics quantitative traits stratification by trait severity heterogeneity reduction case-control association analysis fragile X syndrome RNA toxicity DNA methylation mosaicism pediatrics MS-QMA AmplideX cytokine monocyte β-glucan T cell cytokine trained immunity maternal immune activation epigenetics mice postnatal VPA injection SAM gene expression nanostring |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910566483203321 |
|
Butler Merlin G
|
||
| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020
| Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020 |
| Autore | Butler Merlin G |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 electronic resource (204 p.) |
| Soggetto topico |
Research & information: general
Biology, life sciences Genetics (non-medical) |
| Soggetto non controllato |
autism
ASD genetics heterogeneity syndromes assessment medications treatment causes autism spectrum disorders (ASDs) proteomics metabolomics interactomics disease biomarkers clinical decision support systems (CDSSs) phenotypic subgroups stratified by ASD severity simplex families DNA methylation subgroup-associated genes and biological functions Broader Autism Phenotype genetic autism spectrum disorder multiplex family genetic factors epigenetic factors environmental factors pervasive developmental disorder post-synaptic density CNV SNP gene fusion CACNA1C CaV1.2 short QT syndrome dental enamel defect bioinformatics human genetics pharmacogenomics 15q11.2 BP1-BP2 deletion Burnside-Butler syndrome clinical findings cognition neuropsychiatric behavior development genomic characterization exome sequencing protein–protein interaction 22q13.3 duplication auditory steady-state response ASSR SHANK3 biomarker auditory event-related potential ERP autism spectrum disorders intellectual disabilities |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910566463603321 |
|
Butler Merlin G
|
||
| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Root, Tuber and Banana Food System Innovations [[electronic resource] ] : Value Creation for Inclusive Outcomes
| Root, Tuber and Banana Food System Innovations [[electronic resource] ] : Value Creation for Inclusive Outcomes |
| Autore | Thiele Graham |
| Pubbl/distr/stampa | Cham, : Springer International Publishing AG, 2022 |
| Descrizione fisica | 1 online resource (583 p.) |
| Altri autori (Persone) |
FriedmannMichael
CamposHugo PolarVivian BentleyJeffery W |
| Soggetto topico |
Agricultural science
Genetics (non-medical) Business & management |
| Soggetto non controllato |
Scalling innovation
tropical crops banana cassava sweet potato yams agriculture value creation crop waste management digital pest control citizen science |
| ISBN | 3-030-92022-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910558693603321 |
|
Thiele Graham
|
||
| Cham, : Springer International Publishing AG, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
