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: 35243551)

  • 21. Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.
    Cherkaoui Jaouad I; El Alloussi M; Chafai El Alaoui S; Laarabi FZ; Lyahyai J; Sefiani A
    BMC Oral Health; 2015 Jan; 15():14. PubMed ID: 25636655
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta.
    Kim YJ; Seymen F; Koruyucu M; Kasimoglu Y; Gencay K; Shin TJ; Hyun HK; Lee ZH; Kim JW
    Oral Dis; 2016 May; 22(4):297-302. PubMed ID: 26762616
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genes and related proteins involved in amelogenesis imperfecta.
    Stephanopoulos G; Garefalaki ME; Lyroudia K
    J Dent Res; 2005 Dec; 84(12):1117-26. PubMed ID: 16304440
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Phenotype and Variant Spectrum in the LAMB3 Form of Amelogenesis Imperfecta.
    Smith CEL; Poulter JA; Brookes SJ; Murillo G; Silva S; Brown CJ; Patel A; Hussain H; Kirkham J; Inglehearn CF; Mighell AJ
    J Dent Res; 2019 Jun; 98(6):698-704. PubMed ID: 30905256
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20.
    Nikolopoulos G; Smith CEL; Poulter JA; Murillo G; Silva S; Lamb T; Berry IR; Brown CJ; Day PF; Soldani F; Al-Bahlani S; Harris SA; O'Connell MJ; Inglehearn CF; Mighell AJ
    Hum Mutat; 2021 May; 42(5):567-576. PubMed ID: 33600052
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Enamelin maps to human chromosome 4q21 within the autosomal dominant amelogenesis imperfecta locus.
    Dong J; Gu TT; Simmons D; MacDougall M
    Eur J Oral Sci; 2000 Oct; 108(5):353-8. PubMed ID: 11037750
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta.
    Smith CE; Whitehouse LL; Poulter JA; Brookes SJ; Day PF; Soldani F; Kirkham J; Inglehearn CF; Mighell AJ
    Eur J Hum Genet; 2017 Aug; 25(8):1015-1019. PubMed ID: 28513613
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry.
    Urzúa B; Ortega-Pinto A; Morales-Bozo I; Rojas-Alcayaga G; Cifuentes V
    Biochem Genet; 2011 Feb; 49(1-2):104-21. PubMed ID: 21127961
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening tool.
    Hentschel J; Tatun D; Parkhomchuk D; Kurth I; Schimmel B; Heinrich-Weltzien R; Bertzbach S; Peters H; Beetz C
    Gene; 2016 Sep; 590(1):1-4. PubMed ID: 27259663
    [TBL] [Abstract][Full Text] [Related]  

  • 31. ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta.
    Wang SK; Choi M; Richardson AS; Reid BM; Lin BP; Wang SJ; Kim JW; Simmer JP; Hu JC
    Hum Mol Genet; 2014 Apr; 23(8):2157-63. PubMed ID: 24305999
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Dental management of amelogenesis imperfecta patients: a primer on genotype-phenotype correlations.
    Ng FK; Messer LB
    Pediatr Dent; 2009; 31(1):20-30. PubMed ID: 19320256
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients.
    Mårdh CK; Bäckman B; Simmons D; Golovleva I; Gu TT; Holmgren G; MacDougall M; Forsman-Semb K
    Eur J Oral Sci; 2001 Feb; 109(1):8-13. PubMed ID: 11330937
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A mutation in the enamelin gene in a mouse model.
    Seedorf H; Klaften M; Eke F; Fuchs H; Seedorf U; Hrabe de Angelis M
    J Dent Res; 2007 Aug; 86(8):764-8. PubMed ID: 17652207
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Analyses of
    Kim YJ; Kang J; Seymen F; Koruyucu M; Gencay K; Shin TJ; Hyun HK; Lee ZH; Hu JC; Simmer JP; Kim JW
    Front Physiol; 2017; 8():229. PubMed ID: 28473773
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Detection of a novel mutation in X-linked amelogenesis imperfecta.
    Kindelan SA; Brook AH; Gangemi L; Lench N; Wong FS; Fearne J; Jackson Z; Foster G; Stringer BM
    J Dent Res; 2000 Dec; 79(12):1978-82. PubMed ID: 11201048
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. Novel FAM20A mutations in hypoplastic amelogenesis imperfecta.
    Cho SH; Seymen F; Lee KE; Lee SK; Kweon YS; Kim KJ; Jung SE; Song SJ; Yildirim M; Bayram M; Tuna EB; Gencay K; Kim JW
    Hum Mutat; 2012 Jan; 33(1):91-4. PubMed ID: 21990045
    [TBL] [Abstract][Full Text] [Related]  

  • 40. ENAM mutations with incomplete penetrance.
    Seymen F; Lee KE; Koruyucu M; Gencay K; Bayram M; Tuna EB; Lee ZH; Kim JW
    J Dent Res; 2014 Oct; 93(10):988-92. PubMed ID: 25143514
    [TBL] [Abstract][Full Text] [Related]  

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