BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 27176626)

  • 1. The AP-2 Transcription Factor APTF-2 Is Required for Neuroblast and Epidermal Morphogenesis in Caenorhabditis elegans Embryogenesis.
    Budirahardja Y; Tan PY; Doan T; Weisdepp P; Zaidel-Bar R
    PLoS Genet; 2016 May; 12(5):e1006048. PubMed ID: 27176626
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Char Syndrome a novel mutation and new insights: A clinical report.
    Massaad E; Tfayli H; Awwad J; Nabulsi M; Farra C
    Eur J Med Genet; 2019 Dec; 62(12):103607. PubMed ID: 30579973
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Char syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd finger.
    Babaoğlu K; Oruç M; Günlemez A; Gelb BD
    Anadolu Kardiyol Derg; 2012 Sep; 12(6):523-4. PubMed ID: 22728731
    [No Abstract]   [Full Text] [Related]  

  • 4. Caenorhabditis elegans anillin (ani-1) regulates neuroblast cytokinesis and epidermal morphogenesis during embryonic development.
    Fotopoulos N; Wernike D; Chen Y; Makil N; Marte A; Piekny A
    Dev Biol; 2013 Nov; 383(1):61-74. PubMed ID: 24016757
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transcription factor AP-2beta in development, differentiation and tumorigenesis.
    Raap M; Gierendt L; Kreipe HH; Christgen M
    Int J Cancer; 2021 Sep; 149(6):1221-1227. PubMed ID: 33720400
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel missense mutation in TFAP2B associated with Char syndrome and central diabetes insipidus.
    Edward HL; D'Gama AM; Wojcik MH; Brownstein CA; Kenna MA; Grant PE; Majzoub JA; Agrawal PB
    Am J Med Genet A; 2019 Jul; 179(7):1299-1303. PubMed ID: 31012281
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus.
    Satoda M; Zhao F; Diaz GA; Burn J; Goodship J; Davidson HR; Pierpont ME; Gelb BD
    Nat Genet; 2000 May; 25(1):42-6. PubMed ID: 10802654
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Research progress of genetic research on Char syndrome].
    Zhao M; Fan L; Xiang R
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Jun; 41(6):758-760. PubMed ID: 38818565
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mechanical forces drive neuroblast morphogenesis and are required for epidermal closure.
    Wernike D; Chen Y; Mastronardi K; Makil N; Piekny A
    Dev Biol; 2016 Apr; 412(2):261-77. PubMed ID: 26923492
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The PAF1 complex is involved in embryonic epidermal morphogenesis in Caenorhabditis elegans.
    Kubota Y; Tsuyama K; Takabayashi Y; Haruta N; Maruyama R; Iida N; Sugimoto A
    Dev Biol; 2014 Jul; 391(1):43-53. PubMed ID: 24721716
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A study of familial Char syndrome involving the TFAP2B gene with a focus on facial shape characteristics.
    Nyboe D; Kreiborg S; Darvann T; Dunø M; Nissen KR; Hove HB
    Clin Dysmorphol; 2018 Jul; 27(3):71-77. PubMed ID: 29683802
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The conserved zinc finger protein VAB-23 is an essential regulator of epidermal morphogenesis in Caenorhabditis elegans.
    Pellegrino MW; Gasser RB; Sprenger F; Stetak A; Hajnal A
    Dev Biol; 2009 Dec; 336(1):84-93. PubMed ID: 19799893
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phospholipase C-epsilon regulates epidermal morphogenesis in Caenorhabditis elegans.
    Vázquez-Manrique RP; Nagy AI; Legg JC; Bales OA; Ly S; Baylis HA
    PLoS Genet; 2008 Mar; 4(3):e1000043. PubMed ID: 18369461
    [TBL] [Abstract][Full Text] [Related]  

  • 14. AP-2β is a transcriptional regulator for determination of digit length in tetrapods.
    Seki R; Kitajima K; Matsubara H; Suzuki T; Saito D; Yokoyama H; Tamura K
    Dev Biol; 2015 Nov; 407(1):75-89. PubMed ID: 26277217
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Developmental stage-dependent transcriptional regulatory pathways control neuroblast lineage progression.
    Feng G; Yi P; Yang Y; Chai Y; Tian D; Zhu Z; Liu J; Zhou F; Cheng Z; Wang X; Li W; Ou G
    Development; 2013 Sep; 140(18):3838-47. PubMed ID: 23946438
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder.
    Mani A; Radhakrishnan J; Farhi A; Carew KS; Warnes CA; Nelson-Williams C; Day RW; Pober B; State MW; Lifton RP
    Proc Natl Acad Sci U S A; 2005 Feb; 102(8):2975-9. PubMed ID: 15684060
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CDC-42 Orients Cell Migration during Epithelial Intercalation in the Caenorhabditis elegans Epidermis.
    Walck-Shannon E; Lucas B; Chin-Sang I; Reiner D; Kumfer K; Cochran H; Bothfeld W; Hardin J
    PLoS Genet; 2016 Nov; 12(11):e1006415. PubMed ID: 27861585
    [TBL] [Abstract][Full Text] [Related]  

  • 18. KCTD1 mutants in scalp‑ear‑nipple syndrome and AP‑2α P59A in Char syndrome reciprocally abrogate their interactions, but can regulate Wnt/β‑catenin signaling.
    Hu L; Chen L; Yang L; Ye Z; Huang W; Li X; Liu Q; Qiu J; Ding X
    Mol Med Rep; 2020 Nov; 22(5):3895-3903. PubMed ID: 33000225
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tissue-Specific Functions of
    Refai O; Smit RB; Votra S; Pruyne D; Mains PE
    G3 (Bethesda); 2018 Jul; 8(7):2277-2290. PubMed ID: 29720391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A genetic screen for temperature-sensitive morphogenesis-defective Caenorhabditis elegans mutants.
    Jud MC; Lowry J; Padilla T; Clifford E; Yang Y; Fennell F; Miller AK; Hamill D; Harvey AM; Avila-Zavala M; Shao H; Nguyen Tran N; Bao Z; Bowerman B
    G3 (Bethesda); 2021 Apr; 11(4):. PubMed ID: 33713117
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.