[cite web | title = Entrez Gene: SLC16A2 solute carrier family 16, member 2 (monocarboxylic acid transporter 8)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6567| accessdate = ] ] PBB_Summary
section_title =
summary_text =
ee also
* Solute carrier family
References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Halestrap AP, Meredith D |title=The SLC16 gene family-from monocarboxylate transporters (MCTs) to aromatic amino acid transporters and beyond. |journal=Pflugers Arch. |volume=447 |issue= 5 |pages= 619–28 |year= 2004 |pmid= 12739169 |doi= 10.1007/s00424-003-1067-2
*cite journal | author=Friesema EC, Jansen J, Heuer H, "et al." |title=Mechanisms of disease: psychomotor retardation and high T3 levels caused by mutations in monocarboxylate transporter 8. |journal=Nature clinical practice. Endocrinology & metabolism |volume=2 |issue= 9 |pages= 512–23 |year= 2006 |pmid= 16957765 |doi= 10.1038/ncpendmet0262
*cite journal | author=Grüters A |title=Thyroid hormone transporter defects. |journal=Endocrine development |volume=10 |issue= |pages= 118–26 |year= 2007 |pmid= 17684393 |doi= 10.1159/0000106823
*cite journal | author=Lafrenière RG, Carrel L, Willard HF |title=A novel transmembrane transporter encoded by the XPCT gene in Xq13.2. |journal=Hum. Mol. Genet. |volume=3 |issue= 7 |pages= 1133–9 |year= 1995 |pmid= 7981683 |doi=
*cite journal | author=Andersson B, Wentland MA, Ricafrente JY, "et al." |title=A "double adaptor" method for improved shotgun library construction. |journal=Anal. Biochem. |volume=236 |issue= 1 |pages= 107–13 |year= 1996 |pmid= 8619474 |doi= 10.1006/abio.1996.0138
*cite journal | author=Yu W, Andersson B, Worley KC, "et al." |title=Large-scale concatenation cDNA sequencing. |journal=Genome Res. |volume=7 |issue= 4 |pages= 353–8 |year= 1997 |pmid= 9110174 |doi=
*cite journal | author=Price NT, Jackson VN, Halestrap AP |title=Cloning and sequencing of four new mammalian monocarboxylate transporter (MCT) homologues confirms the existence of a transporter family with an ancient past. |journal=Biochem. J. |volume=329 ( Pt 2) |issue= |pages= 321–8 |year= 1998 |pmid= 9425115 |doi=
*cite journal | author=Debrand E, Heard E, Avner P |title=Cloning and localization of the murine Xpct gene: evidence for complex rearrangements during the evolution of the region around the Xist gene. |journal=Genomics |volume=48 |issue= 3 |pages= 296–303 |year= 1998 |pmid= 9545634 |doi= 10.1006/geno.1997.5173
*cite journal | author=Friesema EC, Ganguly S, Abdalla A, "et al." |title=Identification of monocarboxylate transporter 8 as a specific thyroid hormone transporter. |journal=J. Biol. Chem. |volume=278 |issue= 41 |pages= 40128–35 |year= 2003 |pmid= 12871948 |doi= 10.1074/jbc.M300909200
*cite journal | author=Dumitrescu AM, Liao XH, Best TB, "et al." |title=A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene. |journal=Am. J. Hum. Genet. |volume=74 |issue= 1 |pages= 168–75 |year= 2004 |pmid= 14661163 |doi=
*cite journal | author=Friesema EC, Grueters A, Biebermann H, "et al." |title=Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation. |journal=Lancet |volume=364 |issue= 9443 |pages= 1435–7 |year= 2004 |pmid= 15488219 |doi= 10.1016/S0140-6736(04)17226-7
*cite journal | author=Heuer H, Maier MK, Iden S, "et al." |title=The monocarboxylate transporter 8 linked to human psychomotor retardation is highly expressed in thyroid hormone-sensitive neuron populations. |journal=Endocrinology |volume=146 |issue= 4 |pages= 1701–6 |year= 2005 |pmid= 15661862 |doi= 10.1210/en.2004-1179
*cite journal | author=Brockmann K, Dumitrescu AM, Best TT, "et al." |title=X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene. |journal=J. Neurol. |volume=252 |issue= 6 |pages= 663–6 |year= 2005 |pmid= 15834651 |doi= 10.1007/s00415-005-0713-3
*cite journal | author=Schwartz CE, May MM, Carpenter NJ, "et al." |title=Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene. |journal=Am. J. Hum. Genet. |volume=77 |issue= 1 |pages= 41–53 |year= 2005 |pmid= 15889350 |doi= 10.1086/431313
*cite journal | author=Friesema EC, Kuiper GG, Jansen J, "et al." |title=Thyroid hormone transport by the human monocarboxylate transporter 8 and its rate-limiting role in intracellular metabolism. |journal=Mol. Endocrinol. |volume=20 |issue= 11 |pages= 2761–72 |year= 2007 |pmid= 16887882 |doi= 10.1210/me.2005-0256
*cite journal | author=Olsen JV, Blagoev B, Gnad F, "et al." |title=Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. |journal=Cell |volume=127 |issue= 3 |pages= 635–48 |year= 2006 |pmid= 17081983 |doi= 10.1016/j.cell.2006.09.026
*cite journal | author=Jansen J, Friesema EC, Kester MH, "et al." |title=Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine. |journal=J. Clin. Endocrinol. Metab. |volume=92 |issue= 6 |pages= 2378–81 |year= 2007 |pmid= 17356046 |doi= 10.1210/jc.2006-2570
PBB_Controls
update_page = yes
require_manual_inspection = no
update_protein_box = yes
update_summary = yes
update_citations = yes
