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JAG1

  • JAG1
  • Protein found in humans

    Jagged1 (JAG1) is one of five cell surface proteins (ligands) that interact with four receptors in the mammalian Notch signaling pathway. The Notch signaling

    JAG1

    JAG1

    JAG1

  • Alagille syndrome
  • Medical condition

    caused by a loss of function mutations in JAG1 (Jagged1), and less commonly in NOTCH2 (Notch homolog 2). The JAG1 mutation is either intragenic and found

    Alagille syndrome

    Alagille syndrome

    Alagille_syndrome

  • K. Christopher Garcia
  • American scientist

    Delta-like 4 (DLL4) and Jagged1 (Jag1) as a means of stabilizing the complexes for co-crystallization. Notch1-DLL4 and Notch1-Jag1 structures were determined

    K. Christopher Garcia

    K. Christopher Garcia

    K._Christopher_Garcia

  • Ovarian cancer
  • Cancer originating in or on the ovary

    with CSF-1 50% FOXL2 point mutation (402 C to G) adult granulosa cell ~100% JAG1 amplification 2% JAG2 amplification 3% KRAS amplification mucinous and low-grade

    Ovarian cancer

    Ovarian cancer

    Ovarian_cancer

  • MIRN21
  • Non-coding RNA in the species Homo sapiens

    Notable targets include: ANP32A, BTG2, Bcl2, P12/CDK2AP1, HNRPK, IL-12p35, JAG1, MEF2C, hMSH2, PDCD4, PTEN, RECK, RhoB, SMARCA4, TGFBRII, SPRY1, SPRY2, TP63

    MIRN21

    MIRN21

    MIRN21

  • Aidonia
  • Jamaican Deejay

    clash for classmates and friends, writing his own lyrics and formed the JAG1 (Jah A Guide)(JOP) crew with friends. After being expelled, he relocated

    Aidonia

    Aidonia

    Aidonia

  • Tetralogy of Fallot
  • Type of congenital heart defect

    include: JAG1 codes for ligands within the Notch family of proteins and is highly expressed in the developing heart. Mutations of the JAG1 gene can lead

    Tetralogy of Fallot

    Tetralogy of Fallot

    Tetralogy_of_Fallot

  • Basal cell
  • General cell type

    studied precursor to gastric cancer. Furthermore, if the genes coding for Jag1 or Jag2 are mutated or deleted, this can cause a disruption of the critical

    Basal cell

    Basal cell

    Basal_cell

  • List of genetic disorders
  • recessive Adrenoleukodystrophy ABCD1 (X) recessive 1:17,000 Alagille syndrome JAG1, NOTCH2 dominant 1:30,000-50,000 ADULT syndrome TP63 dominant Aicardi–Goutières

    List of genetic disorders

    List_of_genetic_disorders

  • Notch proteins
  • Protein family

    Takahashi T, Kosaki K (2007). "Screening for Alagille syndrome mutations in the JAG1 and NOTCH2 genes using denaturing high-performance liquid chromatography"

    Notch proteins

    Notch proteins

    Notch_proteins

  • Sertoli cell
  • Cells found in human testes which help produce sperm

    immune cells) B7/H1 – decreasing proliferation of effector T-cells Jagged1 (JAG1) – induction of Foxp3 transcription factor expression in naive T lymphocytes

    Sertoli cell

    Sertoli cell

    Sertoli_cell

  • Cholestasis
  • Impaired flow of bile from the liver to the small intestine

    genes involved in the Notch signaling pathway. Most have a mutation of the JAG1 gene, while a small minority have a mutation of the NOTCH2 gene. A variety

    Cholestasis

    Cholestasis

    Cholestasis

  • Chromosome 20
  • Human chromosome

    (hsp70) member 12b ITPA: encoding enzyme Inosine triphosphate pyrophosphatase JAG1: jagged 1 (Alagille syndrome) JPH2: encoding protein Junctophilin 2 KIAA1755:

    Chromosome 20

    Chromosome 20

    Chromosome_20

  • Syndromes affecting the heart
  • genetic (Autosomal dominant inheritance: loss of function mutations in either JAG1 or NOTCH2) Congenital heart problems e.g. pulmonary artery stenosis (common)

    Syndromes affecting the heart

    Syndromes affecting the heart

    Syndromes_affecting_the_heart

  • Notch 2
  • Protein found in humans

    Hajdu–Cheney syndrome. NOTCH2 has been shown to interact with: Delta-like 1 GSK3B, JAG1, and JAG2. GRCh38: Ensembl release 89: ENSG00000134250 – Ensembl, May 2017

    Notch 2

    Notch 2

    Notch_2

  • List of OMIM disorder codes
  • 608688; ATIC Alagille syndrome 2; 610205; NOTCH2 Alagille syndrome; 118450; JAG1 Aland Island eye disease; 300600; CACNA1F Albinism, brown oculocutaneous;

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

  • HES1
  • Protein found in humans

    expression. HES1 has been shown to target at least Notch ligands: Dll1, Jagged1 (Jag1), and Neurogenin-2., Dll1, as with other Notch ligands, has been shown to

    HES1

    HES1

    HES1

  • List of human clusters of differentiation
  • CD339 JAG1 (Jagged 1). One of five cell surface proteins (ligands) that interact with 4 receptors in the mammalian Notch signaling pathway. The JAG1 gene

    List of human clusters of differentiation

    List_of_human_clusters_of_differentiation

  • List of human protein-coding genes 4
  • Q6IE81 7886 JADE2 HGNC:22984; Q9NQC1 7887 JADE3 HGNC:22982; Q92613 7888 JAG1 HGNC:6188; P78504 7889 JAG2 HGNC:6189; Q9Y219 7890 JAGN1 HGNC:26926; Q8N5M9

    List of human protein-coding genes 4

    List_of_human_protein-coding_genes_4

  • EGF-like domain
  • Protein domain

    FBN1; FBN2; FBN3; GAS6; HABP2; HBEGF; HEG1; HGFAC; HMCN1; HSPG2; ITGB5; JAG1; JAG2; LDLR; LRP1; LRP10; LRP1B; LRP2; LRP4; LRP5; LRP6; LRP8; LTBP1; LTBP2;

    EGF-like domain

    EGF-like domain

    EGF-like_domain

  • HPG80
  • state. This is due to the fact that when the Wnt pathway is inactivated, the JAG1 gene is repressed, inducing inactivation of the Notch pathway which plays

    HPG80

    HPG80

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