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1 mice with a targeted disruption of the Batten disease gene (CLN3) display a progressive storage disorder
Макаров: у мышей с направленно разрушенным геном болезни Баттена (CLN3) обнаруживают прогрессирующую болезнь накопленияУниверсальный англо-русский словарь > mice with a targeted disruption of the Batten disease gene (CLN3) display a progressive storage disorder
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2 mice with a targeted disruption of the Batten disease gene display a progressive storage disorder
Макаров: (CLN3) у мышей с направленно разрушенным геном болезни Баттена (CLN3) обнаруживают прогрессирующую болезнь накопленияУниверсальный англо-русский словарь > mice with a targeted disruption of the Batten disease gene display a progressive storage disorder
См. также в других словарях:
CLN3 — Ceroid lipofuscinosis, neuronal 3 Identifiers Symbols CLN3; BTS; JNCL; MGC102840 External IDs … Wikipedia
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Synexpression — is a type of non random eukaryotic gene organization. Genes in a synexpression group may not be physically linked, but they are involved in the same process and they are coordinately expressed. It is expected that genes that function in the same… … Wikipedia
CLN5 — Ceroid lipofuscinosis, neuronal 5, also known as CLN5, is a human gene.cite web | title = Entrez Gene: CLN5 ceroid lipofuscinosis, neuronal 5| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=1203| accessdate … Wikipedia
Enfermedad de Batten — Herencia mendeliana autosómica recesiva: dos mutaciones de línea germinal (una de cada uno de los padres) para desarrollar la enfermedad; igualmente transmitida por hombres y mujeres … Wikipedia Español
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Cyclin — Cyclins are a family of proteins that control the progression of cells through the cell cycle by activating cyclin dependent kinase (Cdk) enzymes.[1] Contents 1 Function 2 Domain structure 3 … Wikipedia
Batten disease — Infobox Disease Name = Batten disease Caption = DiseasesDB = 31534 ICD10 = ICD10|E|75|4|e|70 ICD9 = ICD9|330.1 ICDO = OMIM = 204200 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D009472 Batten disease is a rare, fatal, autosomal… … Wikipedia
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