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TBX3

  • TBX3
  • Protein-coding gene in the species Homo sapiens

    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

    TBX3

    TBX3

    TBX3

  • Dun gene
  • Dilution gene

    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

    Dun gene

    Dun gene

    Dun_gene

  • Virginia Papaioannou
  • Developmental biologist

    human syndromes such as DiGeorge syndrome (TBX1) and ulnar mammary syndrome (TBX3). Her work has been important for understanding how these genes control cell

    Virginia Papaioannou

    Virginia_Papaioannou

  • T-box
  • Genes that affect limb and heart development

    (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

    T-box

    T-box

    T-box

  • Micromastia
  • Abnormally underdeveloped breasts

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

    Micromastia

    Micromastia

    Micromastia

  • Atrial fibrillation
  • Irregular beating of the atria of the heart

    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

    Atrial fibrillation

    Atrial fibrillation

    Atrial_fibrillation

  • Ulnar–mammary syndrome
  • Human disease

    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). Another

    Ulnar–mammary syndrome

    Ulnar–mammary syndrome

    Ulnar–mammary_syndrome

  • Bay (horse)
  • Hair coat color of horses

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

    Bay (horse)

    Bay (horse)

    Bay_(horse)

  • Agouti (coloration)
  • Animal fur with multiple color bands on each hair

    Maria Cecilia T; Barsh, S.; Andersson, Leif (2016). "Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color

    Agouti (coloration)

    Agouti (coloration)

    Agouti_(coloration)

  • Sorraia
  • Breed of horse

    deposited asymmetrically around each growing hair, under the control of the TBX3 transcription factor, which determines how melanocytes are distributed in

    Sorraia

    Sorraia

    Sorraia

  • TBX2
  • Protein-coding gene in the species Homo sapiens

    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

    TBX2

    TBX2

    TBX2

  • Terbium
  • Chemical element with atomic number 65 (Tb)

    and water. 2 Tb(s) + 3 H2SO4 → 2 Tb3+ + 3 SO42− + 3 H2(g) 2 Tb + 3 X2 → 2 TbX3 (X = F, Cl, Br, I) 2 Tb(s) + 6 H2O → 2 Tb(OH)3 + 3 H2(g) Terbium oxidizes

    Terbium

    Terbium

    Terbium

  • Equine coat color genetics
  • Genetics behind the equine coat color

    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

    Equine coat color genetics

    Equine coat color genetics

    Equine_coat_color_genetics

  • List of human transcription factors
  • ENSG00000122145 T-box Known motif – In vivo/Misc source [907] AGGTGWSAAWTTCACACCT TBX3 ENSG00000135111 T-box Known motif – High-throughput in vitro [908] YVACACSH

    List of human transcription factors

    List_of_human_transcription_factors

  • Primitive markings
  • Hair coloration in some equine

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

    Primitive markings

    Primitive markings

    Primitive_markings

  • Amastia
  • Absence of the breast and nipple

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

    Amastia

    Amastia

  • Trichoplax
  • Genus of Placozoa

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

    Trichoplax

    Trichoplax

    Trichoplax

  • Ectopic pacemaker
  • Cardiac condition

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

    Ectopic pacemaker

    Ectopic pacemaker

    Ectopic_pacemaker

  • Genome-wide association study
  • Study of genetic variants in different individuals

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

    Genome-wide association study

    Genome-wide association study

    Genome-wide_association_study

  • Sooty horse
  • Trait characterized by black or darker hairs mixed into a horse's coat

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

    Sooty horse

    Sooty horse

    Sooty_horse

  • Black butterflyfish
  • Species of fish

    ADW: Chaetodon_flavirostris AFD: Chaetodon_flavirostris BOLD: 160000 CoL: TBX3 FishBase: 6527 GBIF (old): 2385545 iNaturalist: 97160 IRMNG: 10826748 ITIS:

    Black butterflyfish

    Black butterflyfish

    Black_butterflyfish

  • Chromosome 12
  • Human chromosome

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

    Chromosome 12

    Chromosome 12

    Chromosome_12

  • Taosheng Huang
  • American geneticist and physician scientist

    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

    Taosheng Huang

    Taosheng_Huang

  • Terbium compounds
  • Chemical compounds with at least one terbium atom

    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

    Terbium compounds

    Terbium compounds

    Terbium_compounds

  • List of OMIM disorder codes
  • with severe limb deficiency; 276820; WNT7A Ulnar–mammary syndrome; 181450; TBX3 Urocanase deficiency; 276880; UROC1 Urofacial syndrome; 236730; HPSE2 Usher

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

  • BCL9
  • Protein-coding gene in humans

    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

    BCL9

    BCL9

    BCL9

  • Jun dimerization protein 2
  • Protein-coding gene in the species Homo sapiens

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

    Jun dimerization protein 2

    Jun dimerization protein 2

    Jun_dimerization_protein_2

  • TBX22
  • Protein-coding gene in the species Homo sapiens

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

    TBX22

    TBX22

    TBX22

  • TCF/LEF family
  • Group of genes

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

    TCF/LEF family

    TCF/LEF family

    TCF/LEF_family

  • List of human protein-coding genes 8
  • Q969Z0 16410 TBX1 HGNC:11592; O43435 16411 TBX2 HGNC:11597; Q13207 16412 TBX3 HGNC:11602; O15119 16413 TBX4 HGNC:11603; P57082 16414 TBX5 HGNC:11604; Q99593

    List of human protein-coding genes 8

    List_of_human_protein-coding_genes_8

  • Tbx18 transduction
  • Medical intervention

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

    Tbx18 transduction

    Tbx18_transduction

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