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Properties and units in the clinical laboratory sciences part XXIV. Properties and units in clinical molecular genetics (IUPAC Technical Report) in: Pure and Applied Chemistry Volume 90 Issue 7 (2018)
Properties and units in the clinical laboratory sciences part XXIV. Properties and units in clinical molecular genetics (IUPAC Technical Report) in: Pure and Applied Chemistry Volume 90 Issue 7 (2018)

Animal models and therapeutic prospects for CharcotMarieTooth disease
Animal models and therapeutic prospects for CharcotMarieTooth disease

PS mutations. Schematic representation of PS1, the most frequently... | Download Scientific Diagram
PS mutations. Schematic representation of PS1, the most frequently... | Download Scientific Diagram

Localization of mitofusin 2 (MFN2) mutations. Previously reported... | Download Scientific Diagram
Localization of mitofusin 2 (MFN2) mutations. Previously reported... | Download Scientific Diagram

Binding Partners of Alzheimer's Disease Proteins: Are They Physiologically Relevant?
Binding Partners of Alzheimer's Disease Proteins: Are They Physiologically Relevant?

Disease‐related mutations among Caribbean Hispanics with familial dementia - Lee - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Disease‐related mutations among Caribbean Hispanics with familial dementia - Lee - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Frontiers | Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants
Frontiers | Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants

MFN2 mutation distribution and genotype/ phenotype correlation in Charcot–Marie– Tooth type 2
MFN2 mutation distribution and genotype/ phenotype correlation in Charcot–Marie– Tooth type 2

IJMS | Free Full-Text | Hereditary and Sporadic Forms of Aβ-Cerebrovascular Amyloidosis and Relevant Transgenic Mouse Models
IJMS | Free Full-Text | Hereditary and Sporadic Forms of Aβ-Cerebrovascular Amyloidosis and Relevant Transgenic Mouse Models

Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased
Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased

PDF) Locus-Specific Mutation Databases for Neurodegenerative Brain Diseases
PDF) Locus-Specific Mutation Databases for Neurodegenerative Brain Diseases

MolGen - Global solutions provider of innovative DNA / RNA extraction
MolGen - Global solutions provider of innovative DNA / RNA extraction

Review Article: Genetics of Alzheimer Disease
Review Article: Genetics of Alzheimer Disease

Molecular genetics of Dravet syndrome
Molecular genetics of Dravet syndrome

Genetic analyses of early-onset Alzheimer's disease using next generation sequencing | Scientific Reports
Genetic analyses of early-onset Alzheimer's disease using next generation sequencing | Scientific Reports

Disease-Modifying Therapies in Frontotemporal Lobar Degeneration
Disease-Modifying Therapies in Frontotemporal Lobar Degeneration

Deletion of lrrk2 causes early developmental abnormalities and age-dependent increase of monoamine catabolism in the zebrafish brain | PLOS Genetics
Deletion of lrrk2 causes early developmental abnormalities and age-dependent increase of monoamine catabolism in the zebrafish brain | PLOS Genetics

Methods in Molecular Genetics Human Molecular Genetics
Methods in Molecular Genetics Human Molecular Genetics

Neurodegeneration and Cancer: Where the Disorder Prevails | Scientific Reports
Neurodegeneration and Cancer: Where the Disorder Prevails | Scientific Reports

MolGen - Global solutions provider of innovative DNA / RNA extraction
MolGen - Global solutions provider of innovative DNA / RNA extraction

Genetics of Early-Onset Alzheimer Dementia
Genetics of Early-Onset Alzheimer Dementia

Frontiers | A network of RNA and protein interactions in Fronto Temporal Dementia
Frontiers | A network of RNA and protein interactions in Fronto Temporal Dementia

PDF) novoSNP, a novel computational tool for sequence variation discovery | Christine Van Broeckhoven - Academia.edu
PDF) novoSNP, a novel computational tool for sequence variation discovery | Christine Van Broeckhoven - Academia.edu

Impact of Autosomal Recessive Juvenile Parkinson's Disease Mutations on the Structure and Interactions of the Parkin Ubiquitin
Impact of Autosomal Recessive Juvenile Parkinson's Disease Mutations on the Structure and Interactions of the Parkin Ubiquitin

High frequency of SH3TC2 mutations in Czech HMSN I patients
High frequency of SH3TC2 mutations in Czech HMSN I patients