IRIS
TRAVERSA, ALICE
 Distribuzione geografica
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Continente #
AS - Asia 7
NA - Nord America 4
EU - Europa 3
Totale 14
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Nazione #
SG - Singapore 7
US - Stati Uniti d'America 4
IT - Italia 3
Totale 14
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Città #
Singapore 6
Rome 3
Ashburn 1
Council Bluffs 1
Seattle 1
Totale 12
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Nome #
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration 3
Unusual Segregation of APP Mutations in Monogenic Alzheimer Disease 3
Sialylated human milk oligosaccharides program cognitive development through a non-genomic transmission mode 3
Polyethylene Micro/Nanoplastics Exposure Induces Epithelial-Mesenchymal Transition in Human Bronchial and Alveolar Epithelial Cells 3
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritance 2
Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis 2
GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlations 2
Additional lesions identified by genomic microarrays are associated with an inferior outcome in low-risk chronic lymphocytic leukaemia patients 2
Exposure to 3′sialyllactose‐poor milk during lactation impairs cognitive capabilities in adulthood 2
Exploring non-coding genetic variability in ACE2: Functional annotation and in vitro validation of regulatory variants 2
Genomic and physiological resilience in extreme environments are associated with a secure attachment style 2
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation 1
Small 7p22.3 microdeletion: case report of Snx8 haploinsufficiency and neurological findings 1
Small RNAs and tooth development: The role of microRNAs in tooth agenesis and impaction 1
Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies 1
Novel SMAD4 mutation causing Myhre syndrome 1
Potassium Channel {KCNH}1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis 1
Mutations impairing GSK3-mediated MAF phosphorylation cause cataract, deafness, intellectual disability, seizures, and a down syndrome-like facies 1
Long-term consequences of reduced availability and compensatory supplementation of sialylated HMOs on cognitive capabilities 1
SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline 1
MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variants 1
Totale 36
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Categoria #
all - tutte 352
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 352
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/20241 0 0 0 0 0 0 0 0 1 0 0 0
2024/202535 0 0 0 0 0 35 0 0 0 0 0 0
Totale 36