Expression Analysis and Protein Localization of the Human HPC-1/Syntaxin 1A, a Gene Deleted in Williams Syndrome

Author： Botta A.   Sangiuolo F.   Calza L.   Giardino L.   Potenza S.   Novelli G.   Dallapiccola B.  

Publisher： Elsevier

ISSN： 0888-7543

Source： Genomics, Vol.62, Iss.3, 1999-12, pp. : 525-528

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Mapping of the Human HPC-1/Syntaxin 1A Gene (STX1A) to Chromosome 7 Band q11.2

By Nakayama T.   Fujiwara T.   Miyazawa A.   Asakawa S.   Shimizu N.   Shimizu Y.   Mikoshiba K.   Akagawa K.  

Genomics, Vol. 42, Iss. 1, 1997-05 ,pp. : 173-176

Academic Press

Access to resources Recommend Favorite

A Novel Human Gene,WSTF,Is Deleted in Williams Syndrome

By Lu X.   Meng X.   Morris C.A.   Keating M.T.  

Genomics, Vol. 54, Iss. 2, 1998-12 ,pp. : 241-249

Elsevier

Access to resources Recommend Favorite

Integration of a c-myc Transgene Results in Disruption of the Mouse Gtf2ird1 Gene, the Homologue of the Human GTF2IRD1 Gene Hemizygously Deleted in Williams-Beuren Syndrome

By Durkin M.E.   Keck-Waggoner C.L.   Popescu N.C.   Thorgeirsson S.S.  

Genomics, Vol. 73, Iss. 1, 2001-04 ,pp. : 20-27

Elsevier

Access to resources Recommend Favorite

A Novel Human GeneFKBP6Is Deleted in Williams Syndrome

By Meng X.   Lu X.   Morris C.A.   Keating M.T.  

Genomics, Vol. 52, Iss. 2, 1998-09 ,pp. : 130-137

Elsevier

Access to resources Recommend Favorite

KCNE1-like Gene Is Deleted in AMME Contiguous Gene Syndrome: Identification and Characterization of the Human and Mouse Homologs

By Piccini M.   Vitelli F.   Seri M.   Galietta L.J.V.   Moran O.   Bulfone A.   Banfi S.   Pober B.   Renieri A.  

Genomics, Vol. 60, Iss. 3, 1999-09 ,pp. : 251-257

Elsevier

Access to resources Recommend Favorite