- eye mutations
- eye mutations.См. мутации окраски глаз.(Источник: «Англо-русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд-во ВНИРО, 1995 г.)
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eye mutations
Смотреть что такое "eye mutations" в других словарях:
Eye color — is a polygenic trait and is determined by the amount and type of pigments in the eye s iris.Wielgus AR, Sarna T. Melanin in human irides of different color and age of donors. Pigment Cell Res. 2005 Dec; 18(6):454 64. PMID 16280011.] Prota G, Hu… … Wikipedia
Evolution of the eye — The evolution of the eye has been a subject of significant study, as a distinctive example of a homologous organ present in a wide variety of taxa. The development of the eye is considered by some experts to be monophyletic; that is, all modern… … Wikipedia
Irish initial mutations — Irish, like all modern Celtic languages, is characterized by its initial consonant mutations. These mutations affect the initial consonant of a word under specific morphological and syntactic conditions. The mutations are an important tool in… … Wikipedia
мутации окраски глаз — eye mutations мутации окраски глаз. Oбширная серия мутаций у дрозофил, изменяющих уровень выработки глазных пигментов, что обусловливает широкий спектр изменчивости, М.о.г. широко используются в генетическом анализе к ним относятся рецессивные… … Молекулярная биология и генетика. Толковый словарь.
CRB1 — Crumbs homolog 1 (Drosophila), also known as CRB1, is a human gene.cite web | title = Entrez Gene: CRB1 crumbs homolog 1 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=23418| accessdate = ]… … Wikipedia
Collagen, type II, alpha 1 — (primary osteoarthritis, spondyloepiphyseal dysplasia, congenital) Identifiers Symbol COL2A1 Alt. symbols SEDC Entrez … Wikipedia
COL2A1 — protein Name=collagen, type II, alpha 1 (primary osteoarthritis, spondyloepiphyseal dysplasia, congenital) caption= width= HGNCid=2200 Symbol=COL2A1 AltSymbols=SEDC EntrezGene=1280 OMIM=120140 RefSeq=NM 001844 UniProt=P02458 PDB= ECnumber=… … Wikipedia
Disease, mitochondrial — Mutations (changes) in the mitochondrial chromosome are responsible for a number of disorders including, for example: An eye disease called Leber s hereditary optic atrophy; A type of epilepsy called MERRF which stands for Myoclonus Epilepsy with … Medical dictionary
Mitochondrial disease — Mutations (changes) in the mitochondrial chromosome are responsible for a number of disorders including, for example: An eye disease called Leber s hereditary optic atrophy; A type of epilepsy called MERRF which stands for Myoclonus Epilepsy with … Medical dictionary
evolution — evolutional, adj. evolutionally, adv. /ev euh looh sheuhn/ or, esp. Brit., /ee veuh /, n. 1. any process of formation or growth; development: the evolution of a language; the evolution of the airplane. 2. a product of such development; something… … Universalium
