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Значения термина molecular disease на английском
русский
врождённое заболевание португальский
anomalias genéticas испанский
anomalia genetica каталонский
malaltia genètica Disease that has material basis in genetic variations in the human genome.
Синонимы
Examples for "inborn"
Examples for "inborn"
1
No; it was something in them, something inborn and subtle and everlasting.
2
It takes a man all his inborn strength to fight hunger properly.
3
Fatty-acid metabolism plays a key role in acquired and inborn metabolic diseases.
4
The sight sets him thinking of the inborn sense of the bird.
5
Tact was inborn in Cunningham, as it had been in his father.
1
Autism is a heterogeneous disorder that can reveal a specific genetic disease.
2
Cancer is a genetic disease resulting from germline or somatic genetic aberrations.
3
Sharon Bernardi lost all seven of her children to a rare genetic disease.
4
This finding may contribute to clinical treatment of genetic disease or tissue repair.
5
The best-fit genetic disease model for this marker is a recessive genetic model.
1
I have xeroderma pigmentosum-XPfor short- arareand frequently fatal genetic disorder.
2
This is a genetic disorder that most people have never heard of.
3
Beta-thalassemia is a genetic disorder caused by mutations in the beta-globin gene.
4
Are these advantages as important as removing a genetic disorder from my genome?
5
Let's pretend I carry the gene responsible for a genetic disorder.
1
Mutations responsible for inherited disease may act by disrupting normal transcriptional splicing.
2
Cystic fibrosis is the most common life-threatening inherited disease in Ireland.
3
Cystic fibrosis is Ireland's most common life-threatening genetically inherited disease.
4
So Tessie Wartliz was suffering from an inherited disease commonly called "Greed."
5
Fanconi anemia (FA) is a recessive inherited disease characterized by defective DNA repair.
1
This had been a vow taken by him and his siblings in an effort to end generations of familial disorder.
1
Cobalamin C is a rare inborn disorder of metabolism that results in multisystemic abnormalities, including progressive visual deficits.
1
Three-year-old Isabella Santorum suffers from a rare genetic condition called trisomy 18.
2
Ditto for Mason Gulley, who had a genetic condition that affected his appearance.
3
SCD is a genetic condition that is present at birth.
4
Spinal muscular atrophy is a genetic condition that affects the nerves that control muscle movement.
5
Paul was born with Treacher Collins syndrome - a genetic condition which causes facial deformities.
1
I want to know if it could have been a hereditary disease.
2
A low origin is like an hereditary disease-itwill bear no strain.
3
Some terrible hereditary disease, are we planning a trip to the moon?
4
I will refrain, for instance, from bringing up the subject of hereditary disease.
5
Medical Matters: Medicine, like politics, can be a hereditary disease.
1
These transcription units represent candidate genes for multiple hereditary diseases, including HPC1.
2
Works with family trees and illnesses, Icelandic families and hereditary diseases, genetic diseases.
3
They are peculiarly indicative of hereditary diseases, especially lungs, heart, nerves, and spine.
4
Prevalence: Alpha-1 antitrypsin deficiency is one of the most common hereditary diseases in Caucasians of European descent.
5
I don't know about any hereditary diseases.
Использование термина molecular disease на английском
1
Interestingly, the latest advances in AMD research also highlight common molecular disease pathways with other neurodegenerative disorders.
2
Thus, there is a high clinical need for molecular disease biomarkers to aid in differentiating these distinct phenotypes.
3
These cells remain after IM therapy, even when apparently complete responses are achieved, and they probably explain molecular disease persistence.
4
These patients are typically younger and suffer from conditions caused by a known molecular disease mechanism and a peculiar sarcopenic phenotype.
5
Fluorogenic probes that signal the presence of specific DNA or RNA sequences are key enabling tools for molecular disease diagnosis and imaging studies.
6
Here, we performed whole exome sequencing in 79 consanguineous or familial cases of suspected nephronophthisis in order to determine the underlying molecular disease cause.
7
Molecular disease mechanisms downstream of functional SMN loss are still largely unknown.
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Translations for molecular disease
русский
португальский
испанский