Isolation and structural organization of the human preproenkephalin B gene.Horikawa S., Takai T., Toyosato M., Takahashi H., Noda M., Kakidani H., Kubo T., Hirose T., Inayama S.[...], Numa S.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 306:611-614 (1983)Cited in1
Complete sequencing and characterization of 21,243 full-length human cDNAs.Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H.[...], Sugano S.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]TissueAmygdalaCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Genet. 36:40-45 (2004)Cited in99+99+
The DNA sequence and comparative analysis of human chromosome 20.Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K.[...], Rogers J.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 414:865-871 (2001)Cited in99+99+
No title available.Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H.[...], Venter J.C.Cited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)Submission Submitted to EMBL/GenBank/DDBJ databases (SEP-2005)Cited in99+
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).The MGC Project TeamView abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]TissueBrainCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenome Res. 14:2121-2127 (2004)Cited in99+99+
NMR and structural model of dynorphin A (1-17) bound to dodecylphosphocholine micelles.Tessmer M.R., Kallick D.A.View abstractCited forSTRUCTURE BY NMR OF DYNORPHIN A(1-17)CategoriesStructureSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBiochemistry 36:1971-1981 (1997)Cited in1
Dynorphin peptides differentially regulate the human kappa opioid receptor.Chen Y., Chen C., Liu-Chen L.-Y.View abstractCited forFUNCTIONCategoriesFunctionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCLife Sci. 80:1439-1448 (2007)Cited in1
Big dynorphin as a putative endogenous ligand for the kappa-opioid receptor.Merg F., Filliol D., Usynin I., Bazov I., Bark N., Hurd Y.L., Yakovleva T., Kieffer B.L., Bakalkin G.View abstractCited forFUNCTIONCategoriesFunctionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Neurochem. 97:292-301 (2006)Cited in1Mapped to5
Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23.Bakalkin G., Watanabe H., Jezierska J., Depoorter C., Verschuuren-Bemelmans C., Bazov I., Artemenko K.A., Yakovleva T., Dooijes D.[...], Verbeek D.S.View abstractCited forVARIANTS SCA23 SER-138; SER-211; TRP-212 AND CYS-215, CHARACTERIZATION OF VARIANTS SCA23 SER-138; SER-211; TRP-212 AND CYS-215CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCAm. J. Hum. Genet. 87:593-603 (2010)Cited in1Mapped to3
No title available.Bakalkin G., Watanabe H., Jezierska J., Depoorter C., Verschuuren-Bemelmans C., Bazov I., Artemenko K.A., Yakovleva T., Dooijes D.[...], Verbeek D.S.Cited forERRATUM OF PUBMED:21035104SourceUniProtKB reviewed (Swiss-Prot)Am. J. Hum. Genet. 87:736-736 (2010)Cited in1
Perturbations of model membranes induced by pathogenic dynorphin A mutants causing neurodegeneration in human brain.Madani F., Taqi M.M., Warmlander S.K., Verbeek D.S., Bakalkin G., Graslund A.View abstractCited forVARIANTS SCA23 SER-211; TRP-212 AND CYS-215, CHARACTERIZATION OF VARIANTS SCA23 SER-211; TRP-212 AND CYS-215CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBiochem. Biophys. Res. Commun. 411:111-114 (2011)Cited in1Mapped to3
The frequency of spinocerebellar ataxia type 23 in a UK population.Fawcett K., Mehrabian M., Liu Y.T., Hamed S., Elahi E., Revesz T., Koutsis G., Herscheson J., Schottlaender L.[...], Houlden H.View abstractCited forVARIANT SCA23 TYR-22, VARIANT GLN-25CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Neurol. 260:856-859 (2013)Cited in1Mapped to3
Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases.Jezierska J., Stevanin G., Watanabe H., Fokkens M.R., Zagnoli F., Kok J., Goas J.Y., Bertrand P., Robin C.[...], Verbeek D.S.View abstractCited forVARIANTS SCA23 CYS-206; HIS-206 AND ASP-227CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Neurol. 260:1807-1812 (2013)Cited in1Mapped to3