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 *

124 related articles for article (PubMed ID: 32308613)

  • 41. Identification of a Heterozygous Mutation in the
    Xiang Q; Yuan L; Cao Y; Xu H; Li Y; Deng H
    J Ophthalmol; 2019; 2019():2824179. PubMed ID: 30915236
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.
    Corden LD; Swensson O; Swensson B; Smith FJ; Rochels R; Uitto J; McLEAN WH
    Exp Eye Res; 2000 Jan; 70(1):41-9. PubMed ID: 10644419
    [TBL] [Abstract][Full Text] [Related]  

  • 43. The molecular genetics of the corneal dystrophies--current status.
    Klintworth GK
    Front Biosci; 2003 May; 8():d687-713. PubMed ID: 12700042
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy.
    Ha NT; Chau HM; Cung le X; Thanh TK; Fujiki K; Murakami A; Hiratsuka Y; Kanai A
    Invest Ophthalmol Vis Sci; 2003 Aug; 44(8):3310-6. PubMed ID: 12882775
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Genotype-phenotype analysis of Bietti crystalline dystrophy in a family with the CYP4V2 Ile111Thr mutation.
    García-García GP; López-Garrido MP; Martínez-Rubio M; Moya-Moya MA; Belmonte-Martínez J; Escribano J
    Cornea; 2013 Jul; 32(7):1002-8. PubMed ID: 23538635
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [The different opacity patterns of Lisch corneal dystrophy].
    Butros S; Lang GK; Alvarez de Toledo J; Teimann U; Rohrbach JM; Lisch W
    Klin Monbl Augenheilkd; 2006 Oct; 223(10):837-40. PubMed ID: 17063428
    [TBL] [Abstract][Full Text] [Related]  

  • 47. A corneal dystrophy associated with transforming growth factor beta-induced Gly623Asp mutation an amyloidogenic phenotype.
    Auw-Haedrich C; Agostini H; Clausen I; Reinhard T; Eberwein P; Schorderet DF; Gruenauer-Kloevekorn C
    Ophthalmology; 2009 Jan; 116(1):46-51. PubMed ID: 19019446
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Transforming growth factor β induced mutation-associated phenotype in a Chinese family exhibiting lattice corneal dystrophy.
    Qu C; Yu M; Guo X; Li J; Liu X; Shi Y; Gong B
    Biomed Rep; 2017 Oct; 7(4):314-318. PubMed ID: 29085627
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Identification of novel PIKFYVE gene mutations associated with Fleck corneal dystrophy.
    Gee JA; Frausto RF; Chung DW; Tangmonkongvoragul C; Le DJ; Wang C; Han J; Aldave AJ
    Mol Vis; 2015; 21():1093-100. PubMed ID: 26396486
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Mutation analysis of the TGFBI gene in Vietnamese with granular and Avellino corneal dystrophy.
    Cung le X; Ha NT; Chau HM; Thanh TK; Fujiki K; Murakami A; Hiratsuka Y; Kanai A
    Jpn J Ophthalmol; 2004; 48(1):12-6. PubMed ID: 14767644
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Development of a Corneal Bioluminescence Mouse for Real-Time In Vivo Evaluation of Gene Therapies.
    Fu DJ; Allen EHA; Hickerson RP; Leslie Pedrioli DM; McLean WHI
    Transl Vis Sci Technol; 2020 Dec; 9(13):44. PubMed ID: 33442498
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Spontaneous and inheritable R555Q mutation in the TGFBI/BIGH3 gene in two unrelated families exhibiting Bowman's layer corneal dystrophy.
    Zhao XC; Nakamura H; Subramanyam S; Stock LE; Gillette TE; Yoshikawa S; Ma X; Yee RW
    Ophthalmology; 2007 Nov; 114(11):e39-46. PubMed ID: 17980739
    [TBL] [Abstract][Full Text] [Related]  

  • 53. The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.
    Correa-Gomez V; Villalvazo-Cordero L; Zenteno JC
    Mol Vis; 2007 Sep; 13():1695-700. PubMed ID: 17893671
    [TBL] [Abstract][Full Text] [Related]  

  • 54. An unusual presentation of macular corneal dystrophy associated with uniparental isodisomy and a novel Leu173Pro mutation.
    Yellore VS; Sonmez B; Chen MC; Rayner SA; Thonar EJ; Aldave AJ
    Ophthalmic Genet; 2007 Sep; 28(3):169-74. PubMed ID: 17896316
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Imaging the microstructural abnormalities of meesmann corneal dystrophy by in vivo confocal microscopy.
    Patel DV; Grupcheva CN; McGhee CN
    Cornea; 2005 Aug; 24(6):669-73. PubMed ID: 16015084
    [TBL] [Abstract][Full Text] [Related]  

  • 56. A Mutation in
    Kim Y; You HJ; Park SH; Kim MS; Chae H; Park J; Jekarl DW; Kim J; Kwon A; Choi H; Kim Y; Paek AR; Lee A; Kim JM; Park SY; Kim Y; Joo K; Jung J; Chung SH; Mok JW; Kim M
    J Clin Med; 2019 Aug; 8(8):. PubMed ID: 31390831
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A novel mutation of the TGFBI gene found in a Vietnamese family with atypical granular corneal dystrophy.
    Ha NT; Cung le X; Chau HM; Thanh TK; Fujiki K; Murakami A; Kanai A
    Jpn J Ophthalmol; 2003; 47(3):246-8. PubMed ID: 12782158
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Schnyder corneal dystrophy and juvenile, systemic hypercholesteremia].
    Kohnen T; Pelton RW; Jones DB
    Klin Monbl Augenheilkd; 1997 Aug; 211(2):135-7. PubMed ID: 9379642
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Granular corneal dystrophy with homozygous mutations in the kerato-epithelin gene.
    Okada M; Yamamoto S; Watanabe H; Inoue Y; Tsujikawa M; Maeda N; Shimomura Y; Nishida K; Kinoshita S; Tano Y
    Am J Ophthalmol; 1998 Aug; 126(2):169-76. PubMed ID: 9727509
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Meesmann corneal dystrophy; a clinico-pathologic, ultrastructural and confocal scan report.
    Javadi MA; Rezaei-Kanavi M; Javadi A; Naghshgar N
    J Ophthalmic Vis Res; 2010 Apr; 5(2):122-6. PubMed ID: 22737341
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.