How To Use Gene mutation In A Sentence
-
We analyzed gene mutations in patients who died of thrombotic events, using multiplex allele-specific polymerase chain reaction amplification.
-
Gene mutations are alterations in the DNA code.
-
Methods: Polymerase chain reaction-single strand conformation polymorphism(PCR-SSCP) was used to exclude known gene mutation of HGF from 2 familial gingival fibromatosis .
-
In Pompe disease, a gene mutation prevents the body from making or making enough of an enzyme called acid alpha-glucosidase, which is necessary for proper muscle functioning.
FDA Approves New Version of Genzyme Drug for Rare Disease
-
Enough premalignant cells are present in the bulk of stool to permit the analysis of tumour suppressor gene mutations by this technique.
-
For biliary duct cancers, p53 gene mutation is an important contributor to carcinogenesis.
-
Objective: To investigate the association between gene mutations of ion channel gene KCNQ1 and KCNH2 and familial paroxysmal atrioventricular junctional reentrant tachycardia (FPAVJRT).
-
Gene mutations are alterations in the DNA code.
-
Cadmium compounds are inactive or weakly active in gene mutation and other genotoxicity assays.
-
Objective: To exclude known gene mutation, 21 exon of SOS1 which had been certified by foreign country form 2 families with hereditary gingival fibromatosis .
-
EO is a direct-acting mutagen that reacts with nucleophilic molecules, including DNA, causing gene mutation and chromosome deletions in somatic cells.
-
Other workers have found ras gene mutations in between 39% and 47% of colorectal cancers.
-
When a subset of cells contains the same gene mutation or deletion like this, it's called to as gonadal mosaicism.
Frequently Asked Questions About Alagille Syndrome
-
Renn SC, Park JH, Rosbash M, Hall JC, Taghert PH (1999) A pdf neuropeptide gene mutation and ablation of PDF neurons each cause severe abnormalities of behavioral circadian rhythms in
PLoS ONE Alerts: New Articles
-
Brenner provided the basis in a publication from 1974, in which he broke new ground by demonstrating that specific gene mutations could be induced in the genome of C. elegans by the chemical compound EMS (ethyl methane sulphonate).
Press Release: The 2002 Nobel Prize in Physiology or Medicine
-
In 1974, Brenner demonstrated that specific gene mutations could be induced in the genome of C. elegans by the chemical compound EMS (ethyl methane sulphonate).
The Nobel Prize in Physiology or Medicine 2002
-
Gene mutation can occur at many levels - from single nucleotide polymorphisms, to the introduction of stop codons and longer stretches of DNA (whole genes, even) via intron/exon shuffling.
On Thursday, the Legg report will be published along with...
-
Objective: To investigate the association between gene mutations of ion channel gene KCNQ1 and KCNH2 and familial paroxysmal atrioventricular junctional reentrant tachycardia (FPAVJRT).
-
They studied a strain of mice with a gene mutation that causes them to have attacks of dyskinesia, or abnormal movements several times a day.
-
Alagille syndrome is an autosomal dominant disorder, which means someone who carries the Jagged1 gene mutation has a 50 percent chance of passing on that mutation to their child.
What Causes Alagille Syndrome?
-
The couples were put into three groups depending on the DNA of the men: men without the gene mutation, men with one copy of the mutant gene and men with both copies of the mutation.
-
With our range of tests we can detect 28 of the most common gene mutations present in 85 per cent of colon cancer patients.
Times, Sunday Times
-
The gene mutation appears to work by restricting calorie absorption at the cellular level.
-
Gene mutations occur spontaneously and can be induced by mutagenic agents such has high temperature, mustard gas, and radiation.
-
Objective: To investigate the association between gene mutations of ion channel gene KCNQ1 and KCNH2 and familial paroxysmal atrioventricular junctional reentrant tachycardia (FPAVJRT).
-
Objective : To analyze G 6 PD gene mutation in 168 Cantonese G 6 PD deficient male infants.
-
A woman who tests positive for the gene mutations may choose to undergo preventive procedures, such as mastectomy or oophorectomy, which might be unnecessary if a given mutation would not lead to cancer.
-
They were also tested for the common gene mutations that predispose to venous thromboembolism.
-
Conclusion Maybe there is no association with E237G gene mutation between asthma and atopy.
-
Conclusion Maybe there is no association with E237G gene mutation between asthma and atopy.
-
It's called exon skipping and basically patches over gene mutations that cause the disease.
Aspen Times - Top Stories
-
Every discovered Drosophila gene mutation is given a name, and Gill had called his mutation "fruity.
Homosexuality and Biology
-
Gene mutations occur spontaneously and can be induced by mutagenic agents such has high temperature, mustard gas, and radiation.
-
Objective To establish a method with high efficiency in detecting phenylalanine hydroxylase(PAH) gene mutations and hence to rapidly diagnose prenatal fetals with phenylketonuria .
-
Gene mutations are alterations in the DNA code.
-
Greece also doesn't have so-called Gram-negative bacteria with gene mutations known as NDM, IMP and OXA-48, which are common elsewhere, Pournaras said.
BusinessWeek.com -- Top News
-
Single strand conformation polymorphism (SSCP) essay and sequence analysis of the PCR product were used to ascertain the gene mutation.
-
Objective : To analyze G 6 PD gene mutation in 168 Cantonese G 6 PD deficient male infants.
-
Background and objective:The hypothesis of "two hit" model suggests that at least two classes of gene mutations are responsible for the leukemogenesis.
-
Gene mutational damage in the liver can be assessed in the transgenic animal mutation assay.
-
When a subset of gonadal cells (egg or sperm cells) contains the same gene mutation, but the mutation is not found in any other cells of the body.
Alagille Syndrome Glossary
-
The gene mutation causes a condition known as attenuated familial adenomatous polyposis (AFAP).
PhysOrg.com - latest science and technology news stories
-
Analyzer for barcode and fluorescence detection, results in an extremely flexible platform suited for those focused on a wide variety of applications using multiplexed assays, such as clinical diagnostics, gene mutation analysis, drug resistance genotyping, pharmaceutical drug discovery, and biodetection.
Business Wire Travel News
-
One finding: Anne inherited two gene mutations from her father that put her at risk for embolisms, as well as a third mutation from her mother associated with inherited thrombophilia, a disorder that increases the risk of clots.
Family Pioneers in Exploration of the Genome
