These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 24954533)

  • 1. A new mutation in the gene ROR2 causes brachydactyly type B1.
    Huang D; Jiang S; Zhang Y; Liu X; Zhang J; He R
    Gene; 2014 Aug; 547(1):106-10. PubMed ID: 24954533
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A nonsense mutation in the gene ROR2 underlying autosomal dominant brachydactyly type B.
    Habib R; Amin-Ud-Din M; Ahmad W
    Clin Dysmorphol; 2013 Apr; 22(2):47-50. PubMed ID: 23238279
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel variant in the ROR2 gene underlying brachydactyly type B: a case report.
    Shao J; Liu Y; Zhao S; Sun W; Zhan J; Cao L
    BMC Pediatr; 2022 Sep; 22(1):528. PubMed ID: 36064339
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation screening in candidate genes in four Chinese brachydactyly families.
    Dong S; Wang Y; Tao S; Zheng F
    Ann Clin Lab Sci; 2015; 45(1):94-9. PubMed ID: 25696018
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family.
    Lv D; Luo Y; Yang W; Cao L; Wen Y; Zhao X; Sun M; Lo WH; Zhang X
    J Hum Genet; 2009 Jul; 54(7):422-5. PubMed ID: 19461659
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Genetic analysis of a Chinese pedigree affected with Brachydactyly type B1 due to a novel variant of ROR2 gene].
    Ren H; Zhao W; Jiang N; Li S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):561-564. PubMed ID: 38684301
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Mutation analysis of the pathogenic gene in a Chinese family with Brachydactyly type B1].
    Li CM; Wang FY; Sun WW; Han SL; Chang MX; Feng HG
    Yi Chuan; 2011 Feb; 33(2):147-52. PubMed ID: 21377971
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.
    Oldridge M; Fortuna AM; Maringa M; Propping P; Mansour S; Pollitt C; DeChiara TM; Kimble RB; Valenzuela DM; Yancopoulos GD; Wilkie AO
    Nat Genet; 2000 Mar; 24(3):275-8. PubMed ID: 10700182
    [TBL] [Abstract][Full Text] [Related]  

  • 9. One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.
    Afzal AR; Jeffery S
    Hum Mutat; 2003 Jul; 22(1):1-11. PubMed ID: 12815588
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes.
    Schwarzer W; Witte F; Rajab A; Mundlos S; Stricker S
    Hum Mol Genet; 2009 Nov; 18(21):4013-21. PubMed ID: 19640924
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.
    Afzal AR; Rajab A; Fenske CD; Oldridge M; Elanko N; Ternes-Pereira E; Tüysüz B; Murday VA; Patton MA; Wilkie AO; Jeffery S
    Nat Genet; 2000 Aug; 25(4):419-22. PubMed ID: 10932186
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.
    Schwabe GC; Tinschert S; Buschow C; Meinecke P; Wolff G; Gillessen-Kaesbach G; Oldridge M; Wilkie AO; Kömec R; Mundlos S
    Am J Hum Genet; 2000 Oct; 67(4):822-31. PubMed ID: 10986040
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome.
    van Bokhoven H; Celli J; Kayserili H; van Beusekom E; Balci S; Brussel W; Skovby F; Kerr B; Percin EF; Akarsu N; Brunner HG
    Nat Genet; 2000 Aug; 25(4):423-6. PubMed ID: 10932187
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B.
    Wang B; Sinha T; Jiao K; Serra R; Wang J
    Hum Mol Genet; 2011 Jan; 20(2):271-85. PubMed ID: 20962035
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Identification of a recurrent mutation in the ROR2 gene in a Chinese family with brachydactyly type B].
    Yang W; Tan FQ; Sun M; Zeng X; Liu J; Liu GY; Luo HY; Zhang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):61-3. PubMed ID: 14767912
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ROR-Family Receptor Tyrosine Kinases.
    Stricker S; Rauschenberger V; Schambony A
    Curr Top Dev Biol; 2017; 123():105-142. PubMed ID: 28236965
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Brachydactyly type B1: report of a family with de novo ROR2 mutation.
    Hamamy H; Saleh N; Oldridge M; Al-Hadidy A; Ajlouni K
    Clin Genet; 2006 Dec; 70(6):538-40. PubMed ID: 17101003
    [No Abstract]   [Full Text] [Related]  

  • 18. Dominant versus recessive traits conveyed by allelic mutations - to what extent is nonsense-mediated decay involved?
    Ben-Shachar S; Khajavi M; Withers MA; Shaw CA; van Bokhoven H; Brunner HG; Lupski JR
    Clin Genet; 2009 Apr; 75(4):394-400. PubMed ID: 19236432
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Novel Role for the BMP Antagonist Noggin in Sensitizing Cells to Non-canonical Wnt-5a/Ror2/Disheveled Pathway Activation.
    Bernatik O; Radaszkiewicz T; Behal M; Dave Z; Witte F; Mahl A; Cernohorsky NH; Krejci P; Stricker S; Bryja V
    Front Cell Dev Biol; 2017; 5():47. PubMed ID: 28523267
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Modulation of GDF5/BRI-b signalling through interaction with the tyrosine kinase receptor Ror2.
    Sammar M; Stricker S; Schwabe GC; Sieber C; Hartung A; Hanke M; Oishi I; Pohl J; Minami Y; Sebald W; Mundlos S; Knaus P
    Genes Cells; 2004 Dec; 9(12):1227-38. PubMed ID: 15569154
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.