| NOUN | dyskeratosis | dyskeratoses |
NOUN article.ind sg | pl
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- Dyskeratosis congenita {f} <DKC / DC> = dyskeratosis congenita <DKC / DC>
- Dyskeratosis follicularis {f} = Darier's disease <DAR> [also: Darier disease] [Dyskeratosis follicularis, Keratosis follicularis]
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- They have been implicated in some hereditary disorders, such as dyskeratosis congenita.
- They have been implicated in some hereditary disorders, such as dyskeratosis congenita.
- Hereditary mutations in PARN lead to the bone marrow failure disease dyskeratosis congenita which is caused by defective telomerase RNA processing and degradation in patients.
- DKC (dyskeratosis congenita) patients are all characterized by the defective maintenance of telomeres leading to problems with stem cell regeneration.
- Hereditary benign intraepithelial dyskeratosis is a rare type of genodermatosis that may occur in infancy and early childhood, its symptoms often appear in the patients' eyes and mouths.
- The term "dyskaryosis" is not to be confused with "dyskeratosis".
- Dyskeratosis congenita – Mutations in the assembled snRNPs are also found to be a cause of dyskeratosis congenita, a rare syndrome that presents by abnormal changes in the skin, nails and mucous membrane.
- Main cause of mortality in these patients are related to bone marrow failure. Nearly 80% of the patients of dyskeratosis congenita develop bone marrow failure.
- Another example is the haploinsufficiency of telomerase reverse transcriptase which leads to anticipation in autosomal dominant dyskeratosis congenita.
- Both upper respiratory tract disease and cutaneous dyskeratosis have caused precipitous population declines and die-offs across the entire range of this charismatic species.
- All of the patients with such mutations exhibited dyskeratosis, arthritis, recurrent fever episodes, recurrent elevated CRP (from "C-reactive protein") levels and vitamin A deficiency.
- They have been implicated in some hereditary disorders, such as dyskeratosis congenita.
- Hereditary benign intraepithelial dyskeratosis is a rare In the eye it appears as gelatinous plaques on bulbar perilimbal conjunctiva.
- Hoyeraal–Hreidasson syndrome is a very rare multisystem X-linked recessive disorder characterized by excessively short telomeres and is considered a severe form of dyskeratosis congenita.
- In contrary, inactivating mutations in both alleles of WRAP53β causes dyskeratosis congenita, indicating that this protein acts as tumor suppressor, rather than an oncogene.
- They have been implicated in some hereditary disorders, such as dyskeratosis congenita.
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