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A molecular approach to the classification of von Willebrand disease
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
Prognostic factors in acute myeloid leukaemia
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
A 'two-hit' model of cystogenesis in autosomal dominant polycystic kidney disease?
TRENDS IN MOLECULAR MEDICINE
Control of developmental timing in animals
NATURE REVIEWS GENETICS
Plant evolution and development in a post-genomic context
NATURE REVIEWS GENETICS
A genetic profile of contemporary Jewish populations
NATURE REVIEWS GENETICS
Development of genetic hypotheses in essential hypertension
JOURNAL OF HUMAN GENETICS
Gene targeting in Physcomitrella patens
CURRENT OPINION IN PLANT BIOLOGY
The other, forgotten genome: mitochondrial DNA and mental disorders
MOLECULAR PSYCHIATRY
Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A
HAEMOPHILIA
Gene polymorphism in IgA nephropathy
NEPHROLOGY
Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with centralconduction slowing
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
Screening for mutations in a genetically heterogeneous disorder: DHPLC versus DNA sequence for mutation detection in multiple genes causing Charcot-Marie-Tooth neuropathy
GENETICS IN MEDICINE
Role of major histocompatibility complex class III genes in recurrent spontaneous abortions
FRONTIERS IN BIOSCIENCE
Molecular genetic analysis of virulence in Mannheimia (Pasteurella) haemolytica
FRONTIERS IN BIOSCIENCE
The secretion pathway in filamentous fungi: A biotechnological view
FUNGAL GENETICS AND BIOLOGY
Lysosomal ceroid depletion by drugs: Therapeutic implications for a hereditary neurodegenerative disease of childhood
NATURE MEDICINE
Biomarkers for early detection of colon cancer
CLINICAL CANCER RESEARCH
Marginal-zone B-cell lymphoma of extranodal mucosa-associated lymphoid tissue type: Molecular genetics provides new insights into pathogenesis
ADVANCES IN ANATOMIC PATHOLOGY
Richer color experience in observers with multiple photopigment opsin genes
PSYCHONOMIC BULLETIN & REVIEW
Hamartomatous polyposis syndromes: Molecular genetics, neoplastic risk, and surveillance recommendations
ANNALS OF SURGICAL ONCOLOGY
Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients
HUMAN MUTATION
Mutations of the human polycystic kidney disease 2 (PKD2) gene
HUMAN MUTATION
Rapid detection by fluorescent multiplex PCR of exon deletions and duplications in the C1 inhibitor gene of hereditary angioedema patients
HUMAN MUTATION
Candida albicans Int1p interacts with the septin ring in yeast and hyphal cells
MOLECULAR BIOLOGY OF THE CELL
Primary congenital glaucoma: Three case reports on novel mutations and combinations of mutations in the GLC3A (CYP1B1) gene
JOURNAL OF GLAUCOMA
Gene-environment interplay in oppositional defiant and conduct disorder
CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA
Polymorphic markers in the SRD5A2 gene and prostate cancer risk: A population-based case-control study
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
Analyses of MYC, ERBB2, and CCND1 genes in benign and malignant thyroid follicular cell tumors by real-time polymerase chain reaction
THYROID
Defensive resin biosynthesis in conifers
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY
Sarcoidosis
INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE
Genetic models of hypertension in experimental animals
EXPERIMENTAL NEPHROLOGY
Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families
EUROPEAN JOURNAL OF HUMAN GENETICS
DNA variation at the rp49 gene region in Drosophila madeirensis and D-subobscura from Madeira: inferences about the origin of an insular endemic species
JOURNAL OF EVOLUTIONARY BIOLOGY
Multiple paternity and mating patterns in the American alligator, Alligator mississippiensis
MOLECULAR ECOLOGY
Phylogeography, population history and conservation genetics of jaguars (Panthera onca, Mammalia, Felidae)
MOLECULAR ECOLOGY
Functional characterization of human N-acetyltransferase 2 (NAT2) single nucleotide polymorphisms
PHARMACOGENETICS
Regulation of steroidogenic enzymes and a novel testicular RNA helicase
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
Genome-wide variation in the human and fruitfly: a comparison
CURRENT OPINION IN GENETICS & DEVELOPMENT
Breeding systems and genome evolution
CURRENT OPINION IN GENETICS & DEVELOPMENT
A common mutation of low-density lipoprotein receptor gene is associated with essential hypertension among Japanese
JOURNAL OF HUMAN HYPERTENSION
Recent advances in molecular genetics of breast cancer
JOURNAL OF MOLECULAR MEDICINE-JMM
New developments in the pathology of skull base tumors
VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
Insurance and genetics - Options to prevent undesirable consequences
GESUNDHEITSWESEN
Expression of the orpk disease gene during kidney development and maturation
PEDIATRIC NEPHROLOGY
Neuroblastoma, one century after Pepper: Which genes?
ARCHIVES DE PEDIATRIE
Purification and characterization of an oligo-isomaltosaccharide synthase from a Streptococcus sobrinus glucosyltransferase-I deficient mutant.
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
Novel genomic imbalances and chromosome translocations involving c-myc gene in Burkitt's lymphoma
LEUKEMIA
Preliminary interspecific genetic maps of the Populus genome constructed from RAPD markers
GENOME
Construction of a framework map in Pinus contorta subsp latifolia using random amplified polymorphic DNA markers
GENOME
Two genes involved in human familial hypertension
M S-MEDECINE SCIENCES
Color vision anomalies and the genetics of aging.
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES
Identifying main evolutionary mechanisms shaping genetic variation of Leuciscus cephalus L. 1758 (Cyprinidae) in Western Greece: discordance between methods
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES
Insect photoperiodism and circadian clocks: Models and mechanisms
JOURNAL OF BIOLOGICAL RHYTHMS
The genetics of lipomatous tumors
SEMINARS IN DIAGNOSTIC PATHOLOGY
Positive and negative selection in the DAZ gene family
MOLECULAR BIOLOGY AND EVOLUTION
Contrasting patterns of X-linked and autosomal nucleotide variation in Drosophila melanogaster and Drosophila simulans
MOLECULAR BIOLOGY AND EVOLUTION
Recombination and the frequency spectrum in Drosophila melanogaster and Drosophila simulans
MOLECULAR BIOLOGY AND EVOLUTION
Nucleotide sequence variation at two genes of the phenylpropanoid pathway,the FAH1 and F3H genes, in Arabidopsis thaliana
MOLECULAR BIOLOGY AND EVOLUTION
Genetic modification of short rotation popular wood: Properties for ethanol fuel and fiber productions
CRITICAL REVIEWS IN PLANT SCIENCES
Behavioural-genetic perspectives on personality function
CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE
Relationship between increased longevity and stress resistance as assessedthrough gerontogene mutations in Caenorhabditis elegans
EXPERIMENTAL GERONTOLOGY
Estrogen receptor alpha in giant cell arteritis: A molecular genetic study
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
Clinical and EEG findings in 18 cases of late infantile neuronal ceroid lipofuscinosis
BRAIN & DEVELOPMENT
Genomic and spectral analyses of long to middle Wavelength-sensitive visual pigments of common marmoset (Callithrix jacchus)
GENE
Late-onset metachromatic leukodystrophy clinically presenting as isolated peripheral neuropathy: Compound heterozygosity for the IVS2+1G -> A mutation and a newly identified missense mutation (Thr408Ile) in a Spanish family
ANNALS OF NEUROLOGY
Enhanced central response to dehydration in mice lacking angiotensin AT(1a) receptors
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
The importance of gene order in expression of the red and green visual pigment genes and in color vision
COLOR RESEARCH AND APPLICATION
Red-green pigment gene analysis as a clinical diagnostic tool
COLOR RESEARCH AND APPLICATION
The importance of deleterious mutations of M pigment genes as a cause of color vision defects
COLOR RESEARCH AND APPLICATION
Testing hypotheses about visual pigments underlying deutan color vision
COLOR RESEARCH AND APPLICATION
The prevalence of defective color vision in Old World monkeys and apes
COLOR RESEARCH AND APPLICATION
A new mass screening test for color-vision deficiencies in children
COLOR RESEARCH AND APPLICATION
Mutational analysis of 85 mucopolysaccharidosis type I families: frequencyof known mutations, identification of 17 novel mutations and in vitro expression of missense mutations
HUMAN GENETICS
A novel nonsense mutation in the antithrombin III gene (Ser365 to stop) causing deep and mesenteric venous thromboses
THROMBOSIS AND HAEMOSTASIS
A novel mutation in the anti-mullerian hormone gene as cause of persistentmullerian duct syndrome
EUROPEAN JOURNAL OF PEDIATRICS
G-protein ss 3 subunit gene splice variant in obesity and overweight
INTERNATIONAL JOURNAL OF OBESITY
Molecular genetics of schizophrenia
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY
The molecular genetics of Thiobacillus ferrooxidans and other mesophilic, acidophilic, chemolithotrophic, iron- or sulfur-oxidizing bacteria
HYDROMETALLURGY
Molecular analysis of CYP-21 mutations for congenital adrenal hyperplasia in Singapore
HORMONE RESEARCH
Genetic diagnosis in cardiovascular medicine
ZEITSCHRIFT FUR KARDIOLOGIE
A novel chromosomal translocation t(3;5)(q12;p15.3) and loss of heterozygosity on chromosome 22 in a multifocal follicular variant of papillary thyroid carcinoma presenting with skin metastases
CLINICAL ENDOCRINOLOGY
From the chromosome to DNA: Restriction fragment length polymorphism analysis and its clinical application
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY
Atypical motor neuron disease and related motor syndromes
SEMINARS IN NEUROLOGY
The iab-7 polycomb response element maps to a nucleosome-free region of chromatin and requires both GAGA and pleiohomeotic for silencing activity
MOLECULAR AND CELLULAR BIOLOGY
RasC is required for optimal activation of adenylyl cyclase and Akt/PKB during aggregation
EMBO JOURNAL
Spt16-Pob3 and the HMG protein Nhp6 combine to form the nucleosome-bindingfactor SPN
EMBO JOURNAL
The sedimentary record of dinoflagellate cysts: looking back into the future of phytoplankton blooms
SCIENTIA MARINA
The morphological, immunophenotypic, cytogenetic, molecular genetic (MIC-M) classification of acute leukaemia
EXPERIMENTAL ONCOLOGY
Genome scan for blood pressure in Dutch dyslipidemic families reveals linkage to a locus on chromosome 4p
HYPERTENSION
Hypertension in an anthropological and evolutionary paradigm
HYPERTENSION
Characterization of the lipA gene encoding the major lipase from Pseudomonas aeruginosa strain IGB83
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
Gastric adenocarcinoma: pathomorphology and molecular pathology
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
Genes 'for' phenotypes: A modern history view
BIOLOGY & PHILOSOPHY
Paramecium genome survey: a pilot project
TRENDS IN GENETICS
Angiotensin-converting enzyme gene polymorphism and microvascular complications in Turkish type 2 diabetic patients
DIABETES RESEARCH AND CLINICAL PRACTICE
Molecular genetics of bipolar disorder
NEUROSCIENCE RESEARCH
Molecular genetics and gene expression in atherosclerosis
INTERNATIONAL JOURNAL OF CARDIOLOGY
Molecular enzymology of carnitine transfer and transport
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY
Histopathology and molecular genetics of hearing loss in the human
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY