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 *

289 related articles for article (PubMed ID: 28813618)

  • 1. Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis.
    Dinckan N; Du R; Petty LE; Coban-Akdemir Z; Jhangiani SN; Paine I; Baugh EH; Erdem AP; Kayserili H; Doddapaneni H; Hu J; Muzny DM; Boerwinkle E; Gibbs RA; Lupski JR; Uyguner ZO; Below JE; Letra A
    J Dent Res; 2018 Jan; 97(1):49-59. PubMed ID: 28813618
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia.
    Massink MP; Créton MA; Spanevello F; Fennis WM; Cune MS; Savelberg SM; Nijman IJ; Maurice MM; van den Boogaard MJ; van Haaften G
    Am J Hum Genet; 2015 Oct; 97(4):621-6. PubMed ID: 26387593
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis.
    Salvi A; Giacopuzzi E; Bardellini E; Amadori F; Ferrari L; De Petro G; Borsani G; Majorana A
    Int J Mol Med; 2016 Nov; 38(5):1338-1348. PubMed ID: 27665865
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
    Yu M; Wong SW; Han D; Cai T
    Oral Dis; 2019 Apr; 25(3):646-651. PubMed ID: 29969831
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis.
    Du R; Dinckan N; Song X; Coban-Akdemir Z; Jhangiani SN; Guven Y; Aktoren O; Kayserili H; Petty LE; Muzny DM; Below JE; Boerwinkle E; Wu N; Gibbs RA; Posey JE; Lupski JR; Letra A; Uyguner ZO
    Hum Genet; 2018 Sep; 137(9):689-703. PubMed ID: 30046887
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Role of WNT10A in failure of tooth development in humans and zebrafish.
    Yuan Q; Zhao M; Tandon B; Maili L; Liu X; Zhang A; Baugh EH; Tran T; Silva RM; Hecht JT; Swindell EC; Wagner DS; Letra A
    Mol Genet Genomic Med; 2017 Nov; 5(6):730-741. PubMed ID: 29178643
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing.
    Zhao K; Lian M; Zou D; Huang W; Zhou W; Shen Y; Wang F; Wu Y
    Oral Dis; 2019 Mar; 25(2):523-534. PubMed ID: 30417976
    [TBL] [Abstract][Full Text] [Related]  

  • 8.
    Su L; Lin B; Yu M; Liu Y; Sun S; Feng H; Liu H; Han D
    Int J Mol Sci; 2024 Sep; 25(19):. PubMed ID: 39408781
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functional Effects of
    Zeng Y; Baugh E; Akyalcin S; Letra A
    J Dent Res; 2021 Mar; 100(3):302-309. PubMed ID: 33034246
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel missense mutation of LRP6 identified by whole-exome sequencing in a Chinese family with non-syndromic tooth agenesis.
    Wang H; Liu Y; Zheng Y; Zhao X; Lin S; Zhang Q; Zhang X
    Orthod Craniofac Res; 2021 May; 24(2):233-240. PubMed ID: 32844563
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.
    Mostowska A; Biedziak B; Zadurska M; Dunin-Wilczynska I; Lianeri M; Jagodzinski PP
    Clin Genet; 2013 Nov; 84(5):429-40. PubMed ID: 23167694
    [TBL] [Abstract][Full Text] [Related]  

  • 12. WNT10A variants are associated with non-syndromic tooth agenesis in the general population.
    Song S; Zhao R; He H; Zhang J; Feng H; Lin L
    Hum Genet; 2014 Jan; 133(1):117-24. PubMed ID: 24043634
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Further evidence for the role of WNT10A, WNT10B and GREM2 as candidate genes for isolated tooth agenesis.
    Magruder S; Carter E; Williams MA; English J; Akyalcin S; Letra A
    Orthod Craniofac Res; 2018 Nov; 21(4):258-263. PubMed ID: 30246922
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deleterious Variants in
    Parveen A; Khan SA; Mirza MU; Bashir H; Arshad F; Iqbal M; Ahmad W; Wahab A; Fiaz A; Naz S; Ashraf F; Mobeen T; Aziz S; Ahmed SS; Muhammad N; Hassib NF; Mostafa MI; Gaboon NE; Gul R; Khan S; Froeyen M; Shoaib M; Wasif N
    Int J Mol Sci; 2019 Oct; 20(21):. PubMed ID: 31652981
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.
    Arte S; Parmanen S; Pirinen S; Alaluusua S; Nieminen P
    PLoS One; 2013; 8(8):e73705. PubMed ID: 23991204
    [TBL] [Abstract][Full Text] [Related]  

  • 16.
    Yu M; Fan Z; Wong SW; Sun K; Zhang L; Liu H; Feng H; Liu Y; Han D
    J Dent Res; 2021 Apr; 100(4):415-422. PubMed ID: 33164649
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in WNT10B Are Identified in Individuals with Oligodontia.
    Yu P; Yang W; Han D; Wang X; Guo S; Li J; Li F; Zhang X; Wong SW; Bai B; Liu Y; Du J; Sun ZS; Shi S; Feng H; Cai T
    Am J Hum Genet; 2016 Jul; 99(1):195-201. PubMed ID: 27321946
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies.
    Barbato E; Traversa A; Guarnieri R; Giovannetti A; Genovesi ML; Magliozzi MR; Paolacci S; Ciolfi A; Pizzi S; Di Giorgio R; Tartaglia M; Pizzuti A; Caputo V
    Arch Oral Biol; 2018 Jul; 91():96-102. PubMed ID: 29705498
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis.
    Ockeloen CW; Khandelwal KD; Dreesen K; Ludwig KU; Sullivan R; van Rooij IALM; Thonissen M; Swinnen S; Phan M; Conte F; Ishorst N; Gilissen C; RoaFuentes L; van de Vorst M; Henkes A; Steehouwer M; van Beusekom E; Bloemen M; Vankeirsbilck B; Bergé S; Hens G; Schoenaers J; Poorten VV; Roosenboom J; Verdonck A; Devriendt K; Roeleveldt N; Jhangiani SN; Vissers LELM; Lupski JR; de Ligt J; Von den Hoff JW; Pfundt R; Brunner HG; Zhou H; Dixon J; Mangold E; van Bokhoven H; Dixon MJ; Kleefstra T; Hoischen A; Carels CEL
    Genet Med; 2016 Nov; 18(11):1158-1162. PubMed ID: 26963285
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes : Analysis of a Turkish cohort.
    Keskin G; Karaer K; Uçar Gündoğar Z
    J Orofac Orthop; 2022 Oct; 83(Suppl 1):65-74. PubMed ID: 33725141
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.