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ravening    
a. 猎食.狼吞虎咽的;贪婪的

猎食.狼吞虎咽的;贪婪的

ravening
adj 1: living by preying on other animals especially by catching
living prey; "a predatory bird"; "the rapacious wolf";
"raptorial birds"; "ravening wolves"; "a vulturine taste
for offal" [synonym: {predatory}, {rapacious}, {raptorial},
{ravening}, {vulturine}, {vulturous}]
2: excessively greedy and grasping; "a rapacious divorcee on the
prowl"; "ravening creditors"; "paying taxes to voracious
governments" [synonym: {rapacious}, {ravening}, {voracious}]
3: devouring or craving food in great quantities; "edacious
vultures"; "a rapacious appetite"; "ravenous as wolves";
"voracious sharks" [synonym: {edacious}, {esurient}, {rapacious},
{ravening}, {ravenous}, {voracious}, {wolfish}]


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  • 511345: Hereditary Hemochromatosis, DNA Analysis - Labcorp
    Three variants are analyzed: c 845G>A (p Cys282Tyr), commonly referred to as C282Y; c 187C>G (p His63Asp), commonly referred to as H63D; c 193A>T (p Ser65Cys), commonly referred to as S65C DNA Analysis of the HFE gene (NM_000410 4) is performed by PCR amplification followed by restriction enzyme digestion analyses
  • WHAT YOU SHOULD KNOW ABOUT GENETIC TESTING FOR HAEMOCHROMATOSIS
    The HFE gene is on chromosome 6 Two gene mutations If you inherit gene mutations from both your mother and your father, you are at risk of haemochromatosis, although many people never develop the disorder You will pass the altered gene on to your children and all your children will be carriers of at least one copy One gene mutation
  • About Hereditary Hemochromatosis - CDC
    Diagnosis A blood test can be used to screen people who may have hemochromatosis by measuring how much iron is in their blood Affected people with or without a known family history of hemochromatosis can be diagnosed through blood tests for excess iron in the body (called iron overload) followed by genetic testing
  • Hemochromatosis Gene (HFE) Test - Kaiser Permanente
    Hemochromatosis gene (HFE) testing is a blood test used to check for hereditary hemochromatosis, an inherited disorder that causes the body to absorb too much iron The iron then builds up in the blood, liver, heart, pancreas, joints, skin, and other organs In its early stages, hemochromatosis can cause joint and belly
  • Hereditary Hemochromatosis: Rapid Evidence Review | AAFP
    Genetic testing for the C282Y and H63D mutations of the HFE gene is recommended for first-degree relatives of people with hereditary hemochromatosis; screening does not need to begin until 18
  • Hereditary Hemochromatosis DNA Mutation Analysis | Test Detail | Quest . . .
    Hereditary Hemochromatosis DNA Mutation Analysis - Hereditary Hemochromatosis is an autosomal recessive disease that results in an abnormal build-up of iron in the body The C282Y and H63D are among the most common mutations in patients with hereditary hemochromatosis Penetrance of the mutations (phenotypic disease), including by individuals with compound heterozygous mutations, is variable
  • Genetic testing for haemochromatosis
    Our genetic testing service for haemochromatosis, at a glance Order a home-testing kit by post, get the results within 2 weeks How long does the service take? No This service will only test for the two most common mutations associated with genetic haemochromatosis, known as HFE mutations c282y, h63d and (optionally) S65C
  • General Practitioners’ Quick Guide to Genetic Haemochromatos
    Genetic Testing looks for the common genetic mutations which can predispose to GH This test can indicate the cause of iron loading and or the likelihood of a of a variant in the HFE (high iron) gene known as C282Y They have 2 copies because they inherit one copy from each parent This is known as C282Y homozygous C282Y H63D Heterozygous
  • HFE gene analysis - Gloucestershire Hospitals NHS Foundation Trust
    The most common form is caused by mutations in HFE gene and is known as type I HH The condition has an autosomal recessive mode of inheritance and depending on the population, 80-93% of individuals with type I HH are homozygous for the C282Y mutation, with almost all of the remainder being compound heterozygous for C282Y and H63D
  • Testing for HFE-related haemochromatosis - Australian Prescriber
    The diagnostic evaluation of people with suspected HFE-haemochromatosis changed following the discovery of the HFE gene in 1996 1 Blood tests for HFE genotyping should be considered in people with suspected iron overload, patients with a family history of HFE-haemochromatosis and cases of unexplained chronic liver disease with an increased transferrin saturation 12 ()





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