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Tuberous sclerosis—what’s new?
Simultaneous detection of mitochondrial DNA depletion and single-exon deletion in the deoxyguanosine gene using array-based comparative genomic hybridisation
With new prenatal testing, will babies with Down syndrome slowly disappear?
Antioxidant enzymes in blood of patients with Friedreich's ataxia
Nova et Vetera
Medical News
Hiatus hernia.
NEWS AND NOTES
Regular Review: Interferon for treatment: the dust settles
ABC of clinical genetics. Treatment of genetic disorders.
Hereditary (primary) haemochromatosis.
Trusses.
Searching for gastrinomas.
London scientists blame NHS reforms for brain drain
Screening for cystic fibrosis Should begin with cascade screening
Serum C4 concentration and risk of atherosclerosis
Human genome moves closer to reality
Gene transfer produces angiogenesis
Parkinson's disease genetics comes of age
Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study
New interventions in hearing impairment
The promise of human genetic databases
US approves new anti-leukaemia drug
New life form to be created
The changing face of familial colorectal cancer
Tetraparesis associated with colchicine is probably due to inhibition by verapamil of the P-glycoprotein efflux pump in the blood-brain barrier
Meeting the challenge of antibiotic resistance
Unravelling the secrets of ageing
Colleagues of dismissed Karolinska professor issue letter of support
Designing prevention programmes to reduce incidence of dementia: prospective cohort study of modifiable risk factors
Notes on Books
Galactose Diabetes
Genetic Effects of Radiation
Geographical Variation in Leukaemia Mortality in Relation to Background Radiation and Other Factors
Clinical Aspects of Genetics
Genetics and Rheumatic Diseases
Medicine and the Media
The Manchester regional screening programme: a 10-year exercise in patient and family care.
Mutational analysis of the high affinity immunoglobulin E receptor β subunit gene in asthma
Glutathione S-transferase P1 (GSTP1) polymorphism in patients with chronic obstructive pulmonary disease
Recent advances in molecular biological techniques and their relevance to pulmonary research
Early aberrant gene expression in primary non-small cell carcinomas: a future diagnostic tool?
Neutrophilic inflammation and IL-8 levels in induced sputum of alpha-1-antitrypsin PiMZ subjects
Association of inducible nitric oxide synthase with asthma severity, total serum immunoglobulin E and blood eosinophil levels
The alveolar epithelium can initiate the extrinsic coagulation cascade through expression of tissue factor
Unravelling the complex genetics of inflammatory bowel disease
Multiple Epiphysial Dysplasia
Gross impairment of hepatic drug metabolism in a patient with chronic liver disease.
Policies on drugs in the new Europe.
Minerva
Building bodies
Minerva
How should another Camelford be managed?
Preventing insulin dependent diabetes mellitus.
Scientists grow sperm from germ cells
Vascular disease: the next target for local molecular therapeutics
Atherosclerotic disease and cognitive decline
The clinical promise of molecular pathology
Biological influences on criminal behaviour: how good is the evidence?
Report identifies research priorities in Britain
Britain to boost competitiveness and science
Influence of vitamin D receptor genotype on bone mineral density in postmenopausal women: a twin study in Britain
Recent Advances: Psychiatry
Vitamin D receptor genotype and bone mineral density
Second opinions for patients with cancer
Recurrence of malignant tumours in the head and neck
Science, medicine, and the future: Molecular genetic approaches to understanding disease
Do neuroleptic drugs hasten cognitive decline in dementia?
Gene variation linked to cervical cancer
The origins and molecular basis of antibiotic resistance
Unifactorial models are not appropriate for multifactorial disease
Polymorphism in high density lipoprotein paraoxonase gene and risk of acute myocardial infarction in men: prospective nested case-control study
Severe osteogenesis imperfecta: new therapeutic options?
Mutation increases cancer risk in carriers of BRCA2
Rules on gene therapy are tightened after leukaemia alert
Adjuvant trastuzumab for breast cancer: An increasingly common ethical and economic conundrum
Drug for leukaemia can lead to heart failure
Reduced risk of ulcerative colitis after appendicectomy
Type 2 Gaucher disease: the collodion baby phenotype revisited
Interleukin-6 G(−174)C polymorphism is associated with mental retardation in cystic periventricular leucomalacia in preterm infants
Phenotypic diversity in siblings with partial androgen insensitivity syndrome
Molecular biology and genetics of allergy and asthma
Clinical and molecular findings in IPEX syndrome
Medical News
The Staphylococcal Menace
Systemic lupus erythematosus.
Oncogenes and the origins of human cancer.
Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16.
ABC of clinical genetics. Special issues.
ABC of clinical genetics. Gene structure and function.
Presymptomatic testing for Huntington's disease in the United Kingdom. The United Kingdom Huntington's Disease Prediction Consortium.
NOTES
Minerva
Fortnightly Review: Familial breast cancer
Cutaneous T cell lymphomas
Researchers in US dispute first case of AIDS
Correction
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