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missense suppressor

См. также в других словарях:

  • missense — As used in genetics, a mutation that causes a sequence such that there is a substitution of one amino acid residue for another. m. suppression a mutation in tRNA that allows for incorporation of an amino acid …   Medical dictionary

  • Von Hippel-Lindau tumor suppressor — The Von Hippel Lindau tumor suppressor protein is encoded by the VHL gene and when inactivated is associated with Von Hippel Lindau disease. PBB Summary section title = summary text = Von Hippel Lindau syndrome (VHL) is a dominantly inherited… …   Wikipedia

  • Mutation — A permanent change, a structural alteration, in the DNA or RNA. In humans and many other organisms, mutations occur in DNA. However, in retroviruses like HIV, mutations occur in RNA which is the genetic material of retroviruses. In most cases,… …   Medical dictionary

  • CYLD (gene) — Cylindromatosis (turban tumor syndrome) PDB rendering based on 1ixd …   Wikipedia

  • Ataxia telangiectasia — Infobox Disease Name = Ataxia Telangiectasia Caption = DiseasesDB = 1025 ICD10 = ICD10|G|11|3|g|10 ICD9 = ICD9|334.8 ICDO = OMIM = 208900 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 691 eMedicine mult = eMedicine2|oph|319 MeshID = D001260 …   Wikipedia

  • Cylindromatosis — (turban tumor syndrome), also known as CYLD, is a human gene.cite web | title = Entrez Gene: CYLD cylindromatosis (turban tumor syndrome)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=1540| accessdate = ] …   Wikipedia

  • Neurofibromin 1 — PDB rendering based on 1nf1 …   Wikipedia

  • Neurofibromatosis — Classification and external resources Back of an elderly woman with neurofibromatosis ICD 10 Q …   Wikipedia

  • List of genetic engineering topics — NOTOC # 3 end 5 end A Acentric chromosome Achondroplasia Active site Adam s Curse Adaptation Adenine Adenosine Adenosine diphosphate Adenovirus ADP Ala Alagille syndrome Albino Alcoholism Alkylating agent Allele Allele frequency Alleles… …   Wikipedia

  • Lethal white syndrome — (LWS), also called overo lethal white syndrome (OLWS), lethal white overo (LWO), and overo lethal white foal syndrome (OLWFS), is an autosomal genetic disorder most prevalent in the American Paint Horse. Affected foals are born after the full 11… …   Wikipedia

  • RHAG — Rh associated glycoprotein, also known as RHAG, is a human gene.cite web | title = Entrez Gene: RHAG Rh associated glycoprotein| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=6005| accessdate = ] RHAG has… …   Wikipedia

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