36 related articles for article (PubMed ID: 8661037)
1. Identification of a testis-expressed creatine transporter gene at 16p11.2 and confirmation of the X-linked locus to Xq28.
Iyer GS; Krahe R; Goodwin LA; Doggett NA; Siciliano MJ; Funanage VL; Proujansky R
Genomics; 1996 May; 34(1):143-6. PubMed ID: 8661037
[TBL] [Abstract][Full Text] [Related]
2. Chromosomal localization of the human renal sodium phosphate transporter to chromosome 5: implications for X-linked hypophosphatemia.
Ghishan FK; Knobel S; Dasuki M; Butler M; Phillips J
Pediatr Res; 1994 Apr; 35(4 Pt 1):510-3. PubMed ID: 8047391
[TBL] [Abstract][Full Text] [Related]
3. The Role of Preclinical Models in Creatine Transporter Deficiency: Neurobiological Mechanisms, Biomarkers and Therapeutic Development.
Ghirardini E; Calugi F; Sagona G; Di Vetta F; Palma M; Battini R; Cioni G; Pizzorusso T; Baroncelli L
Genes (Basel); 2021 Jul; 12(8):. PubMed ID: 34440297
[TBL] [Abstract][Full Text] [Related]
4. Metabolic Basis of Creatine in Health and Disease: A Bioinformatics-Assisted Review.
Bonilla DA; Kreider RB; Stout JR; Forero DA; Kerksick CM; Roberts MD; Rawson ES
Nutrients; 2021 Apr; 13(4):. PubMed ID: 33918657
[TBL] [Abstract][Full Text] [Related]
5. Amino Acid Transporter SLC6A14 (ATB
Nałęcz KA
Front Cell Dev Biol; 2020; 8():594464. PubMed ID: 33195271
[TBL] [Abstract][Full Text] [Related]
6. High expression of SLC6A10P contributes to poor prognosis in lung adenocarcinoma.
Yuan K; Gao ZJ; Yuan WD; Yuan JQ; Wang Y
Int J Clin Exp Pathol; 2018; 11(2):720-726. PubMed ID: 31938158
[TBL] [Abstract][Full Text] [Related]
7. 16p11.2 transcription factor
Haller M; Au J; O'Neill M; Lamb DJ
Proc Natl Acad Sci U S A; 2018 Feb; 115(8):E1849-E1858. PubMed ID: 29432158
[TBL] [Abstract][Full Text] [Related]
8. SNF-10 connects male-derived signals to the onset of sperm motility in C. elegans.
Fenker KE; Stanfield GM
Worm; 2015; 4(1):e1003002. PubMed ID: 26430556
[TBL] [Abstract][Full Text] [Related]
9. X-linked creatine transporter deficiency: clinical aspects and pathophysiology.
van de Kamp JM; Mancini GM; Salomons GS
J Inherit Metab Dis; 2014 Sep; 37(5):715-33. PubMed ID: 24789340
[TBL] [Abstract][Full Text] [Related]
10. SLC6 transporters: structure, function, regulation, disease association and therapeutics.
Pramod AB; Foster J; Carvelli L; Henry LK
Mol Aspects Med; 2013; 34(2-3):197-219. PubMed ID: 23506866
[TBL] [Abstract][Full Text] [Related]
11. The creatine transporter gene paralogous at 16p11.2 is expressed in human brain.
Bayou N; M'rad R; Belhaj A; Daoud H; Zemni R; Briault S; Helayem MB; Ben Jemaa L; Chaabouni H
Comp Funct Genomics; 2008; 2008():609684. PubMed ID: 18509488
[TBL] [Abstract][Full Text] [Related]
12. Creatine synthesis and transport during rat embryogenesis: spatiotemporal expression of AGAT, GAMT and CT1.
Braissant O; Henry H; Villard AM; Speer O; Wallimann T; Bachmann C
BMC Dev Biol; 2005 May; 5():9. PubMed ID: 15918910
[TBL] [Abstract][Full Text] [Related]
13. A creatine transporter is operative at the brush border level of the rat jejunal enterocyte.
Tosco M; Faelli A; Sironi C; Gastaldi G; Orsenigo MN
J Membr Biol; 2004 Nov; 202(2):85-95. PubMed ID: 15702372
[TBL] [Abstract][Full Text] [Related]
14. Pharmacokinetics of the dietary supplement creatine.
Persky AM; Brazeau GA; Hochhaus G
Clin Pharmacokinet; 2003; 42(6):557-74. PubMed ID: 12793840
[TBL] [Abstract][Full Text] [Related]
15. Synaptic uptake and beyond: the sodium- and chloride-dependent neurotransmitter transporter family SLC6.
Chen NH; Reith ME; Quick MW
Pflugers Arch; 2004 Feb; 447(5):519-31. PubMed ID: 12719981
[TBL] [Abstract][Full Text] [Related]
16. Acute and moderate-term creatine monohydrate supplementation does not affect creatine transporter mRNA or protein content in either young or elderly humans.
Tarnopolsky M; Parise G; Fu MH; Brose A; Parshad A; Speer O; Wallimann T
Mol Cell Biochem; 2003 Feb; 244(1-2):159-66. PubMed ID: 12701826
[TBL] [Abstract][Full Text] [Related]
17. Human skeletal muscle creatine transporter mRNA and protein expression in healthy, young males and females.
Murphy RM; Tunstall RJ; Mehan KA; Cameron-Smith D; McKenna MJ; Spriet LL; Hargreaves M; Snow RJ
Mol Cell Biochem; 2003 Feb; 244(1-2):151-7. PubMed ID: 12701825
[TBL] [Abstract][Full Text] [Related]
18. Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.
Corzo D; Gibson W; Johnson K; Mitchell G; LePage G; Cox GF; Casey R; Zeiss C; Tyson H; Cutting GR; Raymond GV; Smith KD; Watkins PA; Moser AB; Moser HW; Steinberg SJ
Am J Hum Genet; 2002 Jun; 70(6):1520-31. PubMed ID: 11992258
[TBL] [Abstract][Full Text] [Related]
19. Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms.
Crosier M; Viggiano L; Guy J; Misceo D; Stones R; Wei W; Hearn T; Ventura M; Archidiacono N; Rocchi M; Jackson MS
Genome Res; 2002 Jan; 12(1):67-80. PubMed ID: 11779832
[TBL] [Abstract][Full Text] [Related]
20. Creatine and the creatine transporter: a review.
Snow RJ; Murphy RM
Mol Cell Biochem; 2001 Aug; 224(1-2):169-81. PubMed ID: 11693194
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]