chromosomal rearrangement

chromosomal rearrangement
Медицина: хромосомная перестройка

Универсальный англо-русский словарь. . 2011.

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  • Chromosomal translocation — of the 4th and 20th chromosome. In genetics, a chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes. A gene fusion may be created when the translocation joins two otherwise… …   Wikipedia

  • Chromosomal inversion — A clay model showing why heterozygous inversion loops are visible in polytene chromosome preparations …   Wikipedia

  • Y-chromosomal Adam — Y chromosome in descendants of one human male In human genetics, Y chromosomal Adam ( Y MRCA) is the theoretical most recent common ancestor (MRCA) from whom all living people are descended patrilineally (tracing back along the paternal lines of… …   Wikipedia

  • genetic disease, human — Introduction       any of the diseases and disorders that are caused by mutations in one or more genes (gene).       With the increasing ability to control infectious and nutritional diseases in developed countries, there has come the realization …   Universalium

  • Chromosome 15 (human) — Human chromosome 15 Chromosome 15 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 15 spans about 106 million base pairs (the building material of DNA) and represents between 3% and 3 …   Wikipedia

  • Robertsonian translocation — is a common form of chromosomal rearrangement that occurs in the five acrocentric human chromosome pairs, namely 13, 14, 15, 21, and 22. They are named after the American insect geneticist W. R. B. Robertson, who first described a Robertsonian… …   Wikipedia

  • MYL3 — Myosin, light chain 3, alkali; ventricular, skeletal, slow, also known as MYL3, is a human gene.cite web | title = Entrez Gene: MYL3 myosin, light chain 3, alkali; ventricular, skeletal, slow| url =… …   Wikipedia

  • ABCD1 — is a protein that transfers fatty acids into peroxisomes. A deficiency is associated with adrenoleukodystrophy. PBB Summary section title = summary text = The protein encoded by this gene is a member of the superfamily of ATP binding cassette… …   Wikipedia

  • CBFB — Core binding factor, beta subunit, also known as CBFB, is a human gene. PBB Summary section title = summary text = The protein encoded by this gene is the beta subunit of a heterodimeric core binding transcription factor belonging to the… …   Wikipedia

  • MYH11 — Myosin, heavy chain 11, smooth muscle, also known as MYH11, is a human gene.cite web | title = Entrez Gene: MYH11 myosin, heavy chain 11, smooth muscle| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=4629|… …   Wikipedia

  • PATZ1 — POZ (BTB) and AT hook containing zinc finger 1 Rendering based on PDB 2EPP …   Wikipedia


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