Assignmenta of the human creatine transporter type 2 (SLC6A10) to chromosome band 16p11.2 by in situ hybridization

Cytogenetics and Cell Genetics

Volumn 76, Issue 1-2, 1997, Pages 19-

  Xu, W ^a   Liu, L ^a   Gorman, P A ^b   Sheer, D ^b   Emson, P C ^c  

^a Rayne Institute   (United Kingdom)

^b IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

^c BABRAHAM INSTITUTE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; COMPLEMENTARY DNA; CREATINE; CREATINE TRANSPORTER;

ARTICLE; CHROMOSOME 16; CHROMOSOME MAP; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE;

BASE SEQUENCE; CARRIER PROTEINS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 16; CREATINE; DNA, COMPLEMENTARY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MEMBRANE TRANSPORT PROTEINS; MOLECULAR SEQUENCE DATA;

EID: 0030631982     PISSN: 03010171     EISSN: 1424859X     Source Type: Journal    
DOI: 10.1159/000134503     Document Type: Article

References (3)

1. Iyer GS, Krahe R, Goodwin LA, Doggelt N, Siciliano MJ, Funanage VL, Proujansky: Identification of a test-expressed creatine transporter gene at 16p 11.2 and confirmation of the X-linked locus to Xq28. Genomics 34:143-146 (1996).
2. Nash SR, Giro B, Kingsmore S, et al.: Cloning, pharmacological characterization and genomic localization of the human creatine transporter. Receptors Channels 2:165-174 (1994).
3. Xu W, Gorman P, Sheer D, Bates G, Kishimolo J, Liu L, Emson P: Regional localization of the gene coding for human brain nitric oxide synthase (NOS1) to 12q24.2-» 12q24.3 bv fluorescent in situ hybridization. Cytogenet Cell Genetic 64:62-63 (1993).