BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 17914448)

  • 1. RSPO4 is the major gene in autosomal-recessive anonychia and mutations cluster in the furin-like cysteine-rich domains of the Wnt signaling ligand R-spondin 4.
    Brüchle NO; Frank J; Frank V; Senderek J; Akar A; Koc E; Rigopoulos D; van Steensel M; Zerres K; Bergmann C
    J Invest Dermatol; 2008 Apr; 128(4):791-6. PubMed ID: 17914448
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.
    Bergmann C; Senderek J; Anhuf D; Thiel CT; Ekici AB; Poblete-Gutierrez P; van Steensel M; Seelow D; Nürnberg G; Schild HH; Nürnberg P; Reis A; Frank J; Zerres K
    Am J Hum Genet; 2006 Dec; 79(6):1105-9. PubMed ID: 17186469
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia.
    Blaydon DC; Ishii Y; O'Toole EA; Unsworth HC; Teh MT; Rüschendorf F; Sinclair C; Hopsu-Havu VK; Tidman N; Moss C; Watson R; de Berker D; Wajid M; Christiano AM; Kelsell DP
    Nat Genet; 2006 Nov; 38(11):1245-7. PubMed ID: 17041604
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in R-spondin 4 (RSPO4) underlie inherited anonychia.
    Ishii Y; Wajid M; Bazzi H; Fantauzzo KA; Barber AG; Blaydon DC; Nam JS; Yoon JK; Kelsell DP; Christiano AM
    J Invest Dermatol; 2008 Apr; 128(4):867-70. PubMed ID: 17805348
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel nonsense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a Pakistani family.
    Wasif N; Ahmad W
    Pediatr Dermatol; 2013; 30(1):139-41. PubMed ID: 22300369
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation in the RSPO4 gene in a patient with autosomal recessive anonychia.
    Khalil S; Hayashi R; Daou L; Staiteieh SA; Abbas O; Bergqvist C; Nemer G; Shimomura Y; Kurban M
    Clin Exp Dermatol; 2017 Apr; 42(3):313-315. PubMed ID: 28247548
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I).
    Khan TN; Klar J; Nawaz S; Jameel M; Tariq M; Malik NA; Baig SM; Dahl N
    BMC Med Genet; 2012 Dec; 13():120. PubMed ID: 23234511
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The R-spondin protein family.
    de Lau WB; Snel B; Clevers HC
    Genome Biol; 2012; 13(3):242. PubMed ID: 22439850
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mouse cristin/R-spondin family proteins are novel ligands for the Frizzled 8 and LRP6 receptors and activate beta-catenin-dependent gene expression.
    Nam JS; Turcotte TJ; Smith PF; Choi S; Yoon JK
    J Biol Chem; 2006 May; 281(19):13247-13257. PubMed ID: 16543246
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Wnt signalling ligand RSPO4, causing inherited anonychia, is not mutated in a patient with congenital nail hypoplasia/aplasia with underlying skeletal defects.
    Seitz CS; van Steensel M; Frank J; Senderek J; Zerres K; Hamm H; Bergmann C
    Br J Dermatol; 2007 Oct; 157(4):801-2. PubMed ID: 17596144
    [No Abstract]   [Full Text] [Related]  

  • 11. Loss-of-function point mutations and two-furin domain derivatives provide insights about R-spondin2 structure and function.
    Li SJ; Yen TY; Endo Y; Klauzinska M; Baljinnyam B; Macher B; Callahan R; Rubin JS
    Cell Signal; 2009 Jun; 21(6):916-25. PubMed ID: 19385064
    [TBL] [Abstract][Full Text] [Related]  

  • 12. R-Spondin family members regulate the Wnt pathway by a common mechanism.
    Kim KA; Wagle M; Tran K; Zhan X; Dixon MA; Liu S; Gros D; Korver W; Yonkovich S; Tomasevic N; Binnerts M; Abo A
    Mol Biol Cell; 2008 Jun; 19(6):2588-96. PubMed ID: 18400942
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel missense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a consanguineous Pakistani family.
    Chishti MS; Kausar N; Rafiq MA; Amin M; Ahmad W
    Br J Dermatol; 2008 Mar; 158(3):621-3. PubMed ID: 18070203
    [No Abstract]   [Full Text] [Related]  

  • 14. Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3.
    Hsu CK; Romano MT; Nanda A; Rashidghamat E; Lee JYW; Huang HY; Songsantiphap C; Lee JY; Al-Ajmi H; Betz RC; Simpson MA; McGrath JA; Tziotzios C
    J Invest Dermatol; 2017 May; 137(5):1176-1179. PubMed ID: 28087452
    [No Abstract]   [Full Text] [Related]  

  • 15. R-spondins in cutaneous biology: nails and cancer.
    Blaydon DC; Philpott MP; Kelsell DP
    Cell Cycle; 2007 Apr; 6(8):895-7. PubMed ID: 17426450
    [TBL] [Abstract][Full Text] [Related]  

  • 16.
    Niu J; Guan J; Li R; Li X; Zhai J; Qi J; He Y
    Int J Mol Sci; 2018 Jun; 19(7):. PubMed ID: 29966290
    [No Abstract]   [Full Text] [Related]  

  • 17. R-spondins: novel matricellular regulators of the skeleton.
    Knight MN; Hankenson KD
    Matrix Biol; 2014 Jul; 37():157-61. PubMed ID: 24980904
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Structural basis for R-spondin recognition by LGR4/5/6 receptors.
    Wang D; Huang B; Zhang S; Yu X; Wu W; Wang X
    Genes Dev; 2013 Jun; 27(12):1339-44. PubMed ID: 23756652
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structures of Wnt-antagonist ZNRF3 and its complex with R-spondin 1 and implications for signaling.
    Peng WC; de Lau W; Madoori PK; Forneris F; Granneman JC; Clevers H; Gros P
    PLoS One; 2013; 8(12):e83110. PubMed ID: 24349440
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Syndecan-4 inhibits Wnt/β-catenin signaling through regulation of low-density-lipoprotein receptor-related protein (LRP6) and R-spondin 3.
    Astudillo P; Carrasco H; Larraín J
    Int J Biochem Cell Biol; 2014 Jan; 46():103-12. PubMed ID: 24275095
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.