snRPN

snRPN
small nuclear ribonucleoprotein polypeptide N

Medical dictionary. 2011.

Поможем сделать НИР

Look at other dictionaries:

  • SNRPN upstream reading frame protein — SNRPN upstream reading frame, also known as SNURF, is a human gene.cite web | title = Entrez Gene: SNURF SNRPN upstream reading frame| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=8926| accessdate = ] PBB …   Wikipedia

  • snRPN — • small nuclear ribonucleoprotein polypeptide N …   Dictionary of medical acronyms & abbreviations

  • Small nuclear ribonucleoprotein polypeptide N — Small nuclear ribonucleoprotein polypeptide N, also known as SNRPN, is a human gene.cite web | title = Entrez Gene: SNRPN small nuclear ribonucleoprotein polypeptide N| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

  • PAR1 (gene) — Prader Willi/Angelman region 1 Identifiers Symbols PAR1; D15S227E External IDs OMIM …   Wikipedia

  • Angelman syndrome — Infobox Disease Name = Angelman Syndrome Caption = DiseasesDB = 712 ICD10 = ICD10|Q|93|5|q|90 ICD9 = ICD9|759.89 ICDO = OMIM = 105830 MeshID = D017204 Angelman syndrome (AS) is a neuro genetic disorder characterized by intellectual and… …   Wikipedia

  • Prader-Willi syndrome — Infobox Disease Name = Prader Willi syndrome Caption = DiseasesDB = 10481 ICD10 = ICD10|Q|87|1|q|80 ICD9 = ICD9|759.81 ICDO = OMIM = 176270 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 1880 MeshID = D011218 Prader Willi syndrome… …   Wikipedia

  • Small Nucleolar RNA SNORD64 — SNORD64 (also known as HBII 13) is a non coding RNA (ncRNA) molecule which functions in the biogenesis (modification) of other small nuclear RNAs (snRNAs). This type of modifiying RNA is located in the nucleolus of the eukaryotic cell which is a… …   Wikipedia

  • SNRPB — Small nuclear ribonucleoprotein polypeptides B and B1, also known as SNRPB, is a human gene.cite web | title = Entrez Gene: SNRPB small nuclear ribonucleoprotein polypeptides B and B1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… …   Wikipedia

  • Prader-Willi-Syndrom — Klassifikation nach ICD 10 Q87.1 Angeborene Fehlbildungssyndrome, die vorwiegend mit Kleinwuchs einhergehen (inkl.: Prader Willi Syndrom) …   Deutsch Wikipedia

  • Síndrome de Prader-Willi — Este artículo o sección tiene un estilo difícil de entender para los lectores interesados en el tema. Si puedes, por favor edítalo y contribuye a hacerlo más accesible para el público general, sin eliminar los detalles técnicos que interesan a… …   Wikipedia Español

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”