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 *

167 related articles for article (PubMed ID: 18484629)

  • 21. Novel FAM83H mutations in patients with amelogenesis imperfecta.
    Xin W; Wenjun W; Man Q; Yuming Z
    Sci Rep; 2017 Jul; 7(1):6075. PubMed ID: 28729668
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Effects of Fam83h truncation mutation on enamel developmental defects in male C57/BL6J mice.
    Zheng X; Huang W; He Z; Li Y; Li S; Song Y
    Bone; 2023 Jan; 166():116595. PubMed ID: 36272714
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The gain-of-function FAM83H mutation caused hypocalcification amelogenesis imperfecta in a Chinese family.
    Zheng Y; Lu T; Chen J; Li M; Xiong J; He F; Gan Z; Guo Y; Zhang L; Xiong F
    Clin Oral Investig; 2021 May; 25(5):2915-2923. PubMed ID: 33009625
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Exclusion of candidate genes in seven Turkish families with autosomal recessive amelogenesis imperfecta.
    Becerik S; Cogulu D; Emingil G; Han T; Hart PS; Hart TC
    Am J Med Genet A; 2009 Jul; 149A(7):1392-8. PubMed ID: 19530186
    [TBL] [Abstract][Full Text] [Related]  

  • 25. LAMB3 mutations causing autosomal-dominant amelogenesis imperfecta.
    Kim JW; Seymen F; Lee KE; Ko J; Yildirim M; Tuna EB; Gencay K; Shin TJ; Kyun HK; Simmer JP; Hu JC
    J Dent Res; 2013 Oct; 92(10):899-904. PubMed ID: 23958762
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Enamelin and autosomal-dominant amelogenesis imperfecta.
    Hu JC; Yamakoshi Y
    Crit Rev Oral Biol Med; 2003; 14(6):387-98. PubMed ID: 14656895
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary.
    Kida M; Ariga T; Shirakawa T; Oguchi H; Sakiyama Y
    J Dent Res; 2002 Nov; 81(11):738-42. PubMed ID: 12407086
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Tooth ultrastructure changes induced by a nonsense mutation in the FAM83H gene: insights into the diversity of amelogenesis imperfecta.
    Tan L; Guo Y; Zhong MM; Zhao YQ; Zhao J; Aimee DM; Feng Y; Ye Q; Hu J; Ou-Yang ZY; Chen NX; Su XL; Zhang Q; Liu Q; Yuan H; Wang MY; Feng YZ; Zhang FY
    Clin Oral Investig; 2023 Oct; 27(10):6111-6123. PubMed ID: 37615776
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Novel ENAM and LAMB3 mutations in Chinese families with hypoplastic amelogenesis imperfecta.
    Wang X; Zhao Y; Yang Y; Qin M
    PLoS One; 2015; 10(3):e0116514. PubMed ID: 25769099
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Phenotype and enamel ultrastructure characteristics in patients with ENAM gene mutations g.13185-13186insAG and 8344delG.
    Pavlic A; Petelin M; Battelino T
    Arch Oral Biol; 2007 Mar; 52(3):209-17. PubMed ID: 17125728
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Amelogenesis imperfecta: A novel FAM83H mutation and characteristics of periodontal ligament cells.
    Nowwarote N; Theerapanon T; Osathanon T; Pavasant P; Porntaveetus T; Shotelersuk V
    Oral Dis; 2018 Nov; 24(8):1522-1531. PubMed ID: 29949226
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Immunochemical and biochemical characteristics of enamel proteins in hypocalcified amelogenesis imperfecta.
    Takagi Y; Fujita H; Katano H; Shimokawa H; Kuroda T
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 1998 Apr; 85(4):424-30. PubMed ID: 9574951
    [TBL] [Abstract][Full Text] [Related]  

  • 33. MMP20 hemopexin domain mutation in amelogenesis imperfecta.
    Lee SK; Seymen F; Kang HY; Lee KE; Gencay K; Tuna B; Kim JW
    J Dent Res; 2010 Jan; 89(1):46-50. PubMed ID: 19966041
    [TBL] [Abstract][Full Text] [Related]  

  • 34. WDR72 models of structure and function: a stage-specific regulator of enamel mineralization.
    Katsura KA; Horst JA; Chandra D; Le TQ; Nakano Y; Zhang Y; Horst OV; Zhu L; Le MH; DenBesten PK
    Matrix Biol; 2014 Sep; 38():48-58. PubMed ID: 25008349
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The mineral composition and enamel ultrastructure of hypocalcified amelogenesis imperfecta.
    Wright JT; Duggal MS; Robinson C; Kirkham J; Shore R
    J Craniofac Genet Dev Biol; 1993; 13(2):117-26. PubMed ID: 8325967
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.
    Hart PS; Becerik S; Cogulu D; Emingil G; Ozdemir-Ozenen D; Han ST; Sulima PP; Firatli E; Hart TC
    Clin Genet; 2009 Apr; 75(4):401-4. PubMed ID: 19220331
    [No Abstract]   [Full Text] [Related]  

  • 37. A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).
    Mårdh CK; Bäckman B; Holmgren G; Hu JC; Simmer JP; Forsman-Semb K
    Hum Mol Genet; 2002 May; 11(9):1069-74. PubMed ID: 11978766
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Analysis of amelogenesis imperfecta with abnormal tooth eruption caused by FAM83H mutation].
    Mao SY; Duan XH
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2023 Sep; 58(9):933-937. PubMed ID: 37659852
    [No Abstract]   [Full Text] [Related]  

  • 39. ENAM mutations in autosomal-dominant amelogenesis imperfecta.
    Kim JW; Seymen F; Lin BP; Kiziltan B; Gencay K; Simmer JP; Hu JC
    J Dent Res; 2005 Mar; 84(3):278-82. PubMed ID: 15723871
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.
    Hu JC; Chan HC; Simmer SG; Seymen F; Richardson AS; Hu Y; Milkovich RN; Estrella NM; Yildirim M; Bayram M; Chen CF; Simmer JP
    PLoS One; 2012; 7(12):e52052. PubMed ID: 23251683
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.