T-box transcription factor TBX3 is a protein that in humans is encoded by the TBX3 gene. T-box 3 (TBX3) is a member of the T-box gene family of transcription...

pattern of TBX3 expression mirrored the pattern of pigment deposition in the hair, that is, TBX3 was found wherever the pigment was not. TBX3 was not found...

Congenital causes include ulnar–mammary syndrome (caused by mutations in the TBX3 gene), Poland syndrome, Turner syndrome, and congenital adrenal hyperplasia...

(TBXT) the first found (in mice) TBR1 (TBR1) TBX1 (TBX1) TBX2 (TBX2) TBX3 (TBX3) TBX4 (TBX4) TBX5 (TBX5) TBX6 (TBX6) TBX10 (TBX10) TBX15 (TBX15) TBX18...

tapering to a prominent chin, and a broad nose. It has been associated with TBX3. This gene is located on the long arm of chromosome 12 (12q24.21).[citation...

Sundström E, Berglund J, et al. (February 2016). "Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color...

Sundström E, Berglund J, et al. (February 2016). "Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color...

ENSG00000122145 T-box Known motif – In vivo/Misc source [907] AGGTGWSAAWTTCACACCT TBX3 ENSG00000135111 T-box Known motif – High-throughput in vitro [908] YVACACSH...

diluted. Zygosity for Dun can be determined with a DNA test. The Dun locus is TBX3 on equine chromosome 8. The molecular cause behind the dun coat colors is...

ADW: Chaetodon_flavirostris AFD: Chaetodon_flavirostris BOLD: 160000 CoL: TBX3 FishBase: 6527 GBIF: 2385545 iNaturalist: 97160 IRMNG: 10826748 ITIS: 169598...

different variants associated with transcription factor coding-genes, such as TBX3 and TBX5, NKX2-5 o PITX2, which are involved in cardiac conduction regulation...

and water. 2 Tb (s) + 3 H2SO4 → 2 Tb3+ + 3 SO2−4 + 3 H2↑ 2 Tb + 3 X2 → 2 TbX3 (X = F, Cl, Br, I) 2 Tb (s) + 6 H2O → 2 Tb(OH)3 + 3 H2↑ Terbium oxidizes...

They are associated with genes that encode transcription factors, such as TBX3 and TBX5, NKX2-5 or PITX2, involved in the regulation of cardiac conduction...

family of genes that share a common DNA-binding domain, the T-box. Tbx2 and Tbx3 are the only T-box transcription factors that act as transcriptional repressors...

HGNC:17443 Q969Z0 16392 TBX1 HGNC:11592 O43435 16393 TBX2 HGNC:11597 Q13207 16394 TBX3 HGNC:11602 O15119 16395 TBX4 HGNC:11603 P57082 16396 TBX5 HGNC:11604 Q99593...

from these discoveries, he was the very first to establish the link between TBX3 and cancer. Huang has contributed towards basic science and clinical research...

already been possible to identify several genes, such as Brachyury and TBX2/TBX3, which are homologous to corresponding base-pair sequences in eumetazoans...

family 8 member B1 TBC1D15: encoding protein TBC1 domain family member 15 TBX3: encoding protein T-box transcription factor 3 TCHP: encoding protein Trichoplein...

Wong, L.Y. Elaine; Bakker, Martijn L.; Clout, Danielle E.; et al. (2007). "Tbx3 controls the sinoatrial node gene program and imposes pacemaker function...

diagnosed as amastia simultaneously, all of them are carriers of mutations in TBX3 gene. This mutation could cause various abnormalities, not only amastia,...

Sundström E, Berglund J, et al. (February 2016). "Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color...

domain HD1 of BCL9 (and BCL9L) has recently been shown to be interacting with TBX3 in the context of intestinal carcinogenesis; this interaction mediates some...

MIchel; Basler, Konrad; Moor, Andreas E; Cantù, Claudio (18 August 2020). "TBX3 acts as tissue-specific component of the Wnt/β-catenin transcriptional complex"...

delocalized in a conduction band. Terbium can form four trihalides in the form TbX3 (X=F, Cl, Br, I), which, except the fluoride, are easily soluble in water...

with severe limb deficiency; 276820; WNT7A Ulnar–mammary syndrome; 181450; TBX3 Urocanase deficiency; 276880; UROC1 Urofacial syndrome; 236730; HPSE2 Usher...

disorders: mutations in TBX5 cause Holt–Oram syndrome, whereas mutations in TBX3 cause ulnar–mammary syndrome. Mutations in TBX22 cause X-linked cleft palate...

Differentiation of Sinus Node Myocardium Are Independently Regulated by Tbx18 and Tbx3. Circulation Research. 104: 388-397. Kapoor, N., Liang, W., Marbán, E., and...

JDP2 is involved in neutrophil differentiation and transcription factor Tbx3-mediated osteoclastogenesis for host defense and bone homeostasis. Methylome...