gene mutation

A partial tandem duplication is a type of gene mutation that occurs when a section of a gene is repeated, like a stutter in the gene's DNA.

But one naturally occurring AHR-2 variant, the result of a gene mutation, proves a very poor mate, Wirgin's team has found.

Conclusion: E2 of NF2 gene mutation might be one of the critical factor in the tumorogenesis of acoustic neuromas .

They say they may be able to use drugs to trigger a similar gene mutation in people to encourage hair to grow on bald patches.

Pedigree analysis showed that the porcine HCM may be inherited, and was not caused by a single gene mutation.

The genesis may be related to its viral infection, gene mutation, environmental agent, and other hematological systemic disease.

To investigate further, the researchers studied 1051 HCV patients and found that 35% carried at least one HFE gene mutation.

The gene mutation theory of cancer's origins, however, predicts that the disease should be quite common in newborns .

The frequency of two CETP gene mutation had no significant difference in patients and controls.

DNA sequencing plasmids encoding sequence into the correct position, no gene mutation, consistent with the design.

Change the time, the gene mutation that future generations of Apple's become very tall, please Apple.

BRAF gene mutation has been confirmed to be closely related to the dedifferentiation of papillary thyroid carcinoma.

Genetic analysis demonstrates that the phenotypes of the mutant were caused by a recessive single gene mutation.

Studies have shown that prolactin gene and prolactin receptor gene mutation would give rise to animal breeding dysfunction.

Oxidation DNA adducts can interrupt the growth of normal cells, induce gene mutation and alter the normal gene transcription.

But the impact on the risk of breast cancer in post-menopausal women with a BRCA1 gene mutation was unclear, Narod's team said.

Scientists have discovered a group of people in Ecuador with a rare gene mutation that could reveal ways to extend the human life span.

It has been widely applied in gene analysis, detection of gene mutation and genetic disease.

DHPLC can be applied for high-throughput screening of gene mutation.

Previous research has shown that gene mutation in SHANK3 is associated with delayed language abilities, learning disability, and ASDs.

People with this gene mutation, Dr. Karsenty said, had jawbones so dense it was difficult to extract their teeth.

The team thought this protection might come from the same gene mutation that made these people so small.

Objective To discuss the cloning method for detecting the HPRT gene mutation of rats.

About 40% of these patients have a KRAS gene mutation, and respond poorly to such antibodies.

Objective To explore SCA3 gene mutation in the patients with inherited spinocerebellar ataxia.

Gene mutation analysis was performed for patients with BH4 deficiency and their parents.

For instance, many primates cannot make vitamin C, because of a gene mutation.

The researchers are not yet certain how the gene mutation works to shift people's sleep time.

Therefore, the detection of BRCA1 and BRCA2 gene mutation will be valuable for the prognosis of breast cancer.

Phenylketonuria (PKU) is one kinds of autosomal recessive disease caused by phenylalanine hydroxylase(PAH) gene mutation.

It could just be a single gene mutation.

His research is mainly concerned with gene mutation .

This review is about the gene mutation and phenotype of CYP3A4.

Variations of flower color are related to gene mutation and pollination pattern and so on.

The disease is caused by gene mutation.

Objective To study and compare the HPRT gene mutation in rat soma cells induced by internal exposure to radionuclides using cloning method.

To study the relationships between the expression level of PTEN gene, gene mutation and occurrence and development of glioma.

BACKGROUND & AIM: To study the antagonistic effect of propolis on gene_mutation induced by thiotepa and other strong mutagens .

Crossing experiments revealed that a single recessive gene mutation (yellow) gives rise to the yellow phenotype of Rana rugosa in Japan.

Comparative study of gene mutation between Chinese patients with familial and sporadic hypertrophic cardiomyopathy

Study of the relation between prothrombin gene mutation and cerebral thrombosis

Pathological features and gene mutation analysis in two pedigrees of diffuse palmoplantar keratoderma

Study of the Relation between Prothrombin Gene Mutation and Thrombosis

Analysis of gene mutation in patients with tuberous sclerosis complex with polymerase chain reaction-single strand conformation polymorphism

Detection of telomerase activity and K-ras gene mutation in pancreatic juice and its diagnostic value in pancreatic cancer

Progress on Study of Somatic - cell Gene Mutation as Radiation Biological Dosimeter

Clinical and gene mutation studies on a Chinese pedigree with glucocorticoid-remediable aldosteronism

Detection of mitochondrial gene mutation in aminoglycoside antibiotic induced deafness families

Detection of vector gene mutation by single strand conformation polymorphism with capillary electrophoresis

Analysis of ethambutol drug-resistance gene mutation in Mycobacterium tuberculosis by specific endonuclease

Hematological changes and related gene mutation of post-severe acute respiratory syndrome patients with osteonecrosis

Gene mutation in the oncogenic transformation process of immortalized human bronchial epithelial cells induced by cyclophosphamide

Investigation of relationship between mannose binding protein gene mutation and infectious diseases

Relationship Between PTEN Gene Mutation and Microsatellite Alteration in Sporadic Colorectal Cancer

Analysis of the gene mutation of vitelline macular dystrophy in a family with Best disease

Application of Half- denaturing High Performance Liquid Chromatography in Drug- resistance Gene Mutation

Relationships between E-cadherin gene mutation, its abnormal protein expression and metastasis of laryngeal cancer

Several Physiological Factors Influencing Chloroplast Gene Mutation of Sunflower by Mutagen N-methyl-N-nitrosourea

HPRT Gene Mutation Frequency in Peripheral Blood Lymphocytes in Nasopharyngeal Carcinoma Patients

Study on HPRT gene mutation of rat peripheral blood lymphocytes induced by internal exposure to radionuclides using cloning method

Study on the Gene Mutation of Quinolone-resistant Mycobacterium tuberculosis Isolated from Sichuan Province

Gene mutation analysis of a Chinese family of congenital long QT syndromes

Gene mutation in the tumorigenic transformation process of immortalized human bronchial epithelial cells induced by thiotepa

Detection of S-gene mutation strain in vertical transmission of HBV and its significance

Study on the optic neuropathy induced response protein gene mutation in Chinese patients with primary open-angle glaucoma

Association Between Phospholamban Gene Mutation and Dilated Cardiomyopathy in the Chengdu Area

Analysis of Gene Mutation in the Low Density Lipoprotein Receptor Genes of one Familial Hypercholesterolemia Genealogy

Influence of individual radiation sensitivity on GPA gene mutation frequency in medical diagnostic X-ray workers

Experiment Study on the Diagnostic Value of Bile K-ras Gene Mutation Responsible to the Hepatic Metastasis of Pancreatic Cancer

Chronic family benign pemphigus gene mutation and molecular biologic pathogenesis

Study on tetrahydrobiopterin metabolism and gene mutation for dopa-responsive dystonia-a family report

Overview of relationship between EGFR gene mutation and efficacy and acquired drug resistance of gefitinib

Study on HPRT Gene Mutation of Rat Spleen Lymphocytes Induced by Internal Exposure to Radio-nuclides Using Cloning Method

Gene mutation detection in a cleidocranial dysplasia family

Fibrillin-1 gene mutation in Chinese patients with Marfan syndrome and its gene diagnosis by haplotype analysis

Polymorphism of Parkin gene mutation in familial or sporadic patients with primary Parkinson disease

Genotoxicity Comparison between Gasoline- and Methanol-fueled Exhaust by TK Gene Mutation Assay

Germline APC gene mutation in patients with familial adenomatous polyposis: a preliminary study

Effect of cystic fibrosis transmembrane conductance regulator gene mutation on male fertility

Research of Cucumber Gene Mutation (Sexual Changes) Induced By High-Voltage Static Electricity

Detection of gene mutation and genetic analysis of a patient with type 3 von Willebrand disease

Study on the relationship between K-ras gene mutation and respiratory syncytial virus infection in lung cancer

Clinical study on effect of common methylenetetrahydrofolate reductase gene mutation on coronary artery disease in hypertension

Measuring the HPRT Gene Mutation in Rat after Exposure to Radon and Its Daughters

Study on the chondriosome gene mutation of the deaf children induced by antibiotics

Study on correlation factor of chronic benzene poisoning risk with glycophorin A gene mutation assay

GNE gene mutation analysis in a family of distal myopathy with rimmed vacuoles

TH gene mutation in Chinese patients with autosomal recessive dopa-responsive dystonia

Causes of Congenital Heart Disease -Gene Mutation and Chromosome Aberration

Screening and sequence analysis of TIGR gene mutation in patients with primary open angle glaucoma

Screening and sequence analysis of TIGR gene mutation in patients with primary open angle glaucoma

Germline E-cadherin gene mutation screening in familial gastric cancer kindreds

Up-Date Development of Molecular Detecting Technology on Gene Mutation and Single Nucleotide Polymorphism

Study on Fas gene mutation and amino acid variation in thymus tissue of patients with myasthenia gravis

An update on correlation between PTEN gene mutation and human inherited cancer syndrome

The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7

Relationship between HBV core gene promoter gene mutation and serum HBeAg and HBV DNA contents

Study on relationship between melanocortin-4 receptor gene mutation and obesity in Chinese population of Shanghai area

Gene mutation and hereditary endocrine and metabolic diseases

Research into Gene Mutation in Development of Congenital Atrial Septal Defect and Ventricular Septal Defect

Rapid detection of gene mutation in isoniazid-resistant M. Tuberculosis

The Relationship between AT Gene Mutation and Esophagus Cancer and Colon Cancer

Gene Mutation of Tau Protein and Neurodegenerative Diseases

Relation of gene mutation of hypertension related gene 1 with the occurrence of essential hypertension

A novel RPGR gene mutation in a Chinese family with X-linked dominant retinitis pigmentosa

Molecular Detecting Technology on Gene Mutation

Report of Gene Mutation Hot Spots Analysis in One Congenital Cataract Pedigree

Detection of Gene Mutation in Cardiovascular Disease

Gene Mutation Mechanism of Resistance to Fluoroquinolone in E. Coli

Study on gene mutation in a dystrophic epidermolysis bullosa family

Study on the Pedigree with Thyrotropin Receptor Gene Mutation

Gene mutation and apoptosis of pancreatic carcinoma

Cigarette smoking index and K-ras gene mutation in bronchoalveolar lavage fluid in patients with lung cancer

A novel KIT gene mutation from a family with piebaldism in the southern part of China

Detection of fibroblast growth factor receptor 3 gene mutation at nucleotide 1138 site in congenital achondroplasia patients

Study on Gene Mutation and Trace Element Content in Esophageal Mucosa

Discussion on Cloning Method for Detecting the HPRT Gene Mutation of Rats

Study on Gene Mutation of 21-hydroxylase Deficiency in Congenital Adrenal Hyperplasia

Spindle poisons induce tk gene mutation in mouse lymphoma cells

Acrylamide Induce tk Gene Mutation in Mouse Lymphoma Cells

Correlation between K-ras gene mutation and non-small cell lung cancer

Effects of depleted uranium on cell survival and gene mutation

Gene Mapping in Chinese Pedigree with Hereditary Leukonychia Totalis and Identification of Keratin 7 Gene Mutation

Analysis of Rb gene mutation in squamous cell carcinoma of larynx

Novel HERG gene mutation and congenital long QT syndrome

The Possible Consequence of LPL Gene Mutation

Application of DNA Chips in the Analysis of Gene Mutation in HBV

The chemical mutagenesis and the gene mutation of inner ear

Gene mutation in pituitary adenomas of human

A novel KIT gene mutation results in piebaldism

Mode of Regional Development Strategy Based on Gene Mutation Principle

Studies of tk Gene Mutation by Hydroxylammonium Nitrate

Bcl 10 gene mutation in hepatocellular carcinoma

An Improved Genetic Algorithm Based on Gene Mutation

Association of insulin promoter factor-1 gene mutation with the pathogenesis of diabetes in Shanghai