BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 36829498)

  • 21. Tinkering with the inductive mesenchyme: Sostdc1 uncovers the role of dental mesenchyme in limiting tooth induction.
    Munne PM; Tummers M; Järvinen E; Thesleff I; Jernvall J
    Development; 2009 Feb; 136(3):393-402. PubMed ID: 19141669
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Balancing WNT signalling in early forebrain development: The role of LRP4 as a modulator of LRP6 function.
    Geng S; Paul F; Kowalczyk I; Raimundo S; Sporbert A; Mamo TM; Hammes A
    Front Cell Dev Biol; 2023; 11():1173688. PubMed ID: 37091972
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Truncating mutations in LRP4 lead to a prenatal lethal form of Cenani-Lenz syndrome.
    Lindy AS; Bupp CP; McGee SJ; Steed E; Stevenson RE; Basehore MJ; Friez MJ
    Am J Med Genet A; 2014 Sep; 164A(9):2391-7. PubMed ID: 24924585
    [TBL] [Abstract][Full Text] [Related]  

  • 24. BMP-2 controls alkaline phosphatase expression and osteoblast mineralization by a Wnt autocrine loop.
    Rawadi G; Vayssière B; Dunn F; Baron R; Roman-Roman S
    J Bone Miner Res; 2003 Oct; 18(10):1842-53. PubMed ID: 14584895
    [TBL] [Abstract][Full Text] [Related]  

  • 25. New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6.
    Whyte MP; McAlister WH; Zhang F; Bijanki VN; Nenninger A; Gottesman GS; Lin EL; Huskey M; Duan S; Dahir K; Mumm S
    Bone; 2019 Oct; 127():228-243. PubMed ID: 31085352
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Inhibition of Wnt signaling by Wise (Sostdc1) and negative feedback from Shh controls tooth number and patterning.
    Ahn Y; Sanderson BW; Klein OD; Krumlauf R
    Development; 2010 Oct; 137(19):3221-31. PubMed ID: 20724449
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel biallelic splice-site variant in the LRP4 gene causes sclerosteosis 2.
    Bukowska-Olech E; Sowińska-Seidler A; Szczałuba K; Jamsheer A
    Birth Defects Res; 2020 May; 112(9):652-659. PubMed ID: 32286743
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Synapse-specific Lrp4 mRNA enrichment requires Lrp4/MuSK signaling, muscle activity and Wnt non-canonical pathway.
    Jing H; Chen P; Hui T; Yu Z; Zhou J; Fei E; Wang S; Ren D; Lai X; Li B
    Cell Biosci; 2021 Jun; 11(1):105. PubMed ID: 34090516
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Wnt signaling in the murine diastema.
    Porntaveetus T; Ohazama A; Choi HY; Herz J; Sharpe PT
    Eur J Orthod; 2012 Aug; 34(4):518-24. PubMed ID: 21531785
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic Variants in Protein Tyrosine Phosphatase Non-Receptor Type 23 Are Responsible for Mesiodens Formation.
    Adisornkanj P; Chanprasit R; Eliason S; Fons JM; Intachai W; Tongsima S; Olsen B; Arold ST; Ngamphiw C; Amendt BA; Tucker AS; Kantaputra P
    Biology (Basel); 2023 Mar; 12(3):. PubMed ID: 36979085
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Interactions between Shh, Sostdc1 and Wnt signaling and a new feedback loop for spatial patterning of the teeth.
    Cho SW; Kwak S; Woolley TE; Lee MJ; Kim EJ; Baker RE; Kim HJ; Shin JS; Tickle C; Maini PK; Jung HS
    Development; 2011 May; 138(9):1807-16. PubMed ID: 21447550
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A common LRP4 haplotype is associated with bone mineral density and hip geometry in men-data from the Odense Androgen Study (OAS).
    Boudin E; Steenackers E; de Freitas F; Nielsen TL; Andersen M; Brixen K; Van Hul W; Piters E
    Bone; 2013 Apr; 53(2):414-20. PubMed ID: 23321396
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type I reveals candidate genes for cranio-facial development.
    Merello E; Tattini L; Magi A; Accogli A; Piatelli G; Pavanello M; Tortora D; Cama A; Kibar Z; Capra V; De Marco P
    Eur J Hum Genet; 2017 Aug; 25(8):952-959. PubMed ID: 28513615
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Lack of association between PAX6/SOSTDC1/FAM20B gene polymorphisms and mesiodens.
    Liu S; Li J; Xu J; Liao S; Chen Y; Zhang R; Tian R; Zhang K
    BMC Oral Health; 2019 May; 19(1):90. PubMed ID: 31133012
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The Lrp4R1170Q Homozygous Knock-In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans.
    Boudin E; Yorgan T; Fijalkowski I; Sonntag S; Steenackers E; Hendrickx G; Peeters S; De Maré A; Vervaet B; Verhulst A; Mortier G; D'Haese P; Schinke T; Van Hul W
    J Bone Miner Res; 2017 Aug; 32(8):1739-1749. PubMed ID: 28477420
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genetic alterations in mesiodens as revealed by targeted next-generation sequencing and gene co-occurrence network analysis.
    Kim YY; Hwang J; Kim HS; Kwon HJ; Kim S; Lee JH; Lee JH
    Oral Dis; 2017 Oct; 23(7):966-972. PubMed ID: 28415132
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Fork-shaped mandibular incisors as a novel phenotype of LRP5-associated disorder.
    Yamada M; Kubota K; Uchida A; Yagihashi T; Kawasaki M; Suzuki H; Uehara T; Takenouchi T; Kurosaka H; Kosaki K
    Am J Med Genet A; 2021 May; 185(5):1544-1549. PubMed ID: 33619830
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Opposing Roles of Wnt Inhibitors IGFBP-4 and Dkk1 in Cardiac Ischemia by Differential Targeting of LRP5/6 and β-catenin.
    Wo D; Peng J; Ren DN; Qiu L; Chen J; Zhu Y; Yan Y; Yan H; Wu J; Ma E; Zhong TP; Chen Y; Liu Z; Liu S; Ao L; Liu Z; Jiang C; Peng J; Zou Y; Qian Q; Zhu W
    Circulation; 2016 Dec; 134(24):1991-2007. PubMed ID: 27803037
    [TBL] [Abstract][Full Text] [Related]  

  • 39. DKK1 is a strong candidate for mesiodens and taurodontism.
    Kantaputra P; Jatooratthawichot P; Kottege N; Anthonappa RP; Kaewgahya M; Tongsima S; Ngamphiw C; Ketudat Cairns JR; Predes D; He X
    Clin Genet; 2023 Jun; 103(6):714-716. PubMed ID: 36601665
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis.
    Huybrechts Y; Boudin E; Hendrickx G; Steenackers E; Hamdy N; Mortier G; Martínez Díaz-Guerra G; Bracamonte MS; Appelman-Dijkstra NM; Van Hul W
    Genes (Basel); 2021 Dec; 13(1):. PubMed ID: 35052419
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.