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 *

133 related articles for article (PubMed ID: 35327733)

  • 1. A Recurrent
    Alvarez C; Aragón MA; Lee Y; Gutiérrez S; Méndez P; García DA; Otero L; Kim JW
    Children (Basel); 2022 Mar; 9(3):. PubMed ID: 35327733
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ultrastructural analyses of deciduous teeth affected by hypocalcified amelogenesis imperfecta from a family with a novel Y458X FAM83H nonsense mutation.
    El-Sayed W; Shore RC; Parry DA; Inglehearn CF; Mighell AJ
    Cells Tissues Organs; 2010; 191(3):235-9. PubMed ID: 20160442
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of a Novel
    Song JS; Lee Y; Shin TJ; Hyun HK; Kim YJ; Kim JW
    Children (Basel); 2022 Mar; 9(3):. PubMed ID: 35327801
    [TBL] [Abstract][Full Text] [Related]  

  • 4. FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta.
    Kim JW; Lee SK; Lee ZH; Park JC; Lee KE; Lee MH; Park JT; Seo BM; Hu JC; Simmer JP
    Am J Hum Genet; 2008 Feb; 82(2):489-94. PubMed ID: 18252228
    [TBL] [Abstract][Full Text] [Related]  

  • 5.
    Wang SK; Zhang H; Hu CY; Liu JF; Chadha S; Kim JW; Simmer JP; Hu JCC
    J Dent Res; 2021 Mar; 100(3):293-301. PubMed ID: 33034243
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation.
    Haubek D; Gjørup H; Jensen LG; Juncker I; Nyegaard M; Børglum AD; Poulsen S; Hertz JM
    Int J Paediatr Dent; 2011 Nov; 21(6):407-12. PubMed ID: 21702852
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Missense Mutation in Fam83H Gene in Iranian Patients with Amelogenesis Imperfecta.
    Pourhashemi SJ; Ghandehari Motlagh M; Meighani G; Ebrahimi Takaloo A; Mansouri M; Mohandes F; Mirzaii M; Khoshzaban A; Moshtaghi F; Abedkhojasteh H; Heidari M
    Iran J Public Health; 2014 Dec; 43(12):1680-7. PubMed ID: 26171361
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Age-related dental phenotypes and tooth characteristics of FAM83H-associated hypocalcified amelogenesis imperfecta.
    Sriwattanapong K; Nitayavardhana I; Theerapanon T; Thaweesapphithak S; Chantarawaratit PO; Garuyakich R; Phokaew C; Porntaveetus T; Shotelersuk V
    Oral Dis; 2022 Apr; 28(3):734-744. PubMed ID: 33486840
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular characterization of amelogenesis imperfecta in Chinese patients.
    Song YL; Wang CN; Zhang CZ; Yang K; Bian Z
    Cells Tissues Organs; 2012; 196(3):271-9. PubMed ID: 22414746
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta.
    Hyun HK; Lee SK; Lee KE; Kang HY; Kim EJ; Choung PH; Kim JW
    Int Endod J; 2009 Nov; 42(11):1039-43. PubMed ID: 19825039
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta.
    Hart PS; Wright JT; Savage M; Kang G; Bensen JT; Gorry MC; Hart TC
    Eur J Oral Sci; 2003 Aug; 111(4):326-31. PubMed ID: 12887398
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel missense mutation of the FAM83H gene causes retention of amelogenin and a mild clinical phenotype of hypocalcified enamel.
    Urzúa B; Martínez C; Ortega-Pinto A; Adorno D; Morales-Bozo I; Riadi G; Jara L; Plaza A; Lefimil C; Lozano C; Reyes M
    Arch Oral Biol; 2015 Sep; 60(9):1356-67. PubMed ID: 26142250
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Amelogenesis imperfecta: genotype-phenotype studies in 71 families.
    Wright JT; Torain M; Long K; Seow K; Crawford P; Aldred MJ; Hart PS; Hart TC
    Cells Tissues Organs; 2011; 194(2-4):279-83. PubMed ID: 21597265
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel
    Lee Y; Zhang H; Seymen F; Kim YJ; Kasimoglu Y; Koruyucu M; Simmer JP; Hu JC; Kim JW
    J Pers Med; 2022 Jan; 12(2):. PubMed ID: 35207639
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. The Enamel Phenotype in Homozygous Fam83h Truncation Mice.
    Wang SK; Hu Y; Smith CE; Yang J; Zeng C; Kim JW; Hu JC; Simmer JP
    Mol Genet Genomic Med; 2019 Jun; 7(6):e724. PubMed ID: 31060110
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.