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 *

176 related articles for article (PubMed ID: 26490182)

  • 1. A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract.
    Behnam M; Imagawa E; Chaleshtori AR; Ronasian F; Salehi M; Miyake N; Matsumoto N
    J Hum Genet; 2016 Feb; 61(2):177-9. PubMed ID: 26490182
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataract.
    Smaoui N; Beltaief O; BenHamed S; M'Rad R; Maazoul F; Ouertani A; Chaabouni H; Hejtmancik JF
    Invest Ophthalmol Vis Sci; 2004 Aug; 45(8):2716-21. PubMed ID: 15277496
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations.
    Forshew T; Johnson CA; Khaliq S; Pasha S; Willis C; Abbasi R; Tee L; Smith U; Trembath RC; Mehdi SQ; Moore AT; Maher ER
    Hum Genet; 2005 Sep; 117(5):452-9. PubMed ID: 15959809
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan.
    Sajjad N; Goebel I; Kakar N; Cheema AM; Kubisch C; Ahmad J
    BMC Med Genet; 2008 Nov; 9():99. PubMed ID: 19014451
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel HSF4 mutation causes congenital total white cataract in a Chinese family.
    Ke T; Wang QK; Ji B; Wang X; Liu P; Zhang X; Tang Z; Ren X; Liu M
    Am J Ophthalmol; 2006 Aug; 142(2):298-303. PubMed ID: 16876512
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract.
    Bu L; Jin Y; Shi Y; Chu R; Ban A; Eiberg H; Andres L; Jiang H; Zheng G; Qian M; Cui B; Xia Y; Liu J; Hu L; Zhao G; Hayden MR; Kong X
    Nat Genet; 2002 Jul; 31(3):276-8. PubMed ID: 12089525
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Functional analysis of HSF4 mutations found in patients with autosomal recessive congenital cataracts.
    Merath K; Ronchetti A; Sidjanin DJ
    Invest Ophthalmol Vis Sci; 2013 Oct; 54(10):6646-54. PubMed ID: 24045990
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel HSF4 mutation in a Chinese family with autosomal dominant congenital cataract.
    Liu L; Zhang Q; Zhou LX; Tang ZH
    J Huazhong Univ Sci Technolog Med Sci; 2015 Apr; 35(2):316-318. PubMed ID: 25877371
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract.
    Cohen D; Bar-Yosef U; Levy J; Gradstein L; Belfair N; Ofir R; Joshua S; Lifshitz T; Carmi R; Birk OS
    Invest Ophthalmol Vis Sci; 2007 May; 48(5):2208-13. PubMed ID: 17460281
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DNA-binding and transcriptional activities of human HSF4 containing mutations that associate with congenital and age-related cataracts.
    Enoki Y; Mukoda Y; Furutani C; Sakurai H
    Biochim Biophys Acta; 2010 Sep; 1802(9):749-53. PubMed ID: 20670914
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice.
    Talamas E; Jackson L; Koeberl M; Jackson T; McElwee JL; Hawes NL; Chang B; Jablonski MM; Sidjanin DJ
    Genomics; 2006 Jul; 88(1):44-51. PubMed ID: 16595169
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family.
    Jiao X; Khan SY; Kaul H; Butt T; Naeem MA; Riazuddin S; Hejtmancik JF; Riazuddin SA
    PLoS One; 2019; 14(12):e0225010. PubMed ID: 31815953
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation screening of HSF4 in 150 age-related cataract patients.
    Shi Y; Shi X; Jin Y; Miao A; Bu L; He J; Jiang H; Lu Y; Kong X; Hu L
    Mol Vis; 2008; 14():1850-5. PubMed ID: 18941546
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation.
    Chograni M; Chaabouni M; Mâazoul F; Bouzid H; Kraiem A; Chaabouni HB
    BMC Ophthalmol; 2011 Nov; 11():35. PubMed ID: 22103961
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family.
    Berry V; Pontikos N; Moore A; Ionides ACW; Plagnol V; Cheetham ME; Michaelides M
    Eye (Lond); 2018 Apr; 32(4):806-812. PubMed ID: 29243736
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel HSF4 gene mutation causes autosomal-dominant cataracts in a Chinese family.
    Lv H; Huang C; Zhang J; Liu Z; Zhang Z; Xu H; You Y; Hu J; Li X; Wang W
    G3 (Bethesda); 2014 Mar; 4(5):823-8. PubMed ID: 24637349
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutations in HSF4 cause congenital cataracts in Chinese families.
    Cao Z; Zhu Y; Liu L; Wu S; Liu B; Zhuang J; Tong Y; Chen X; Xie Y; Nie K; Lu C; Ma X; Yang J
    BMC Med Genet; 2018 Aug; 19(1):150. PubMed ID: 30143024
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataracts.
    Berry V; Ionides A; Pontikos N; Moore AT; Quinlan RA; Michaelides M
    Eye (Lond); 2022 Aug; 36(8):1694-1701. PubMed ID: 34345029
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel connexin46 (GJA3) mutation in autosomal dominant congenital nuclear pulverulent cataract.
    Li Y; Wang J; Dong B; Man H
    Mol Vis; 2004 Sep; 10():668-71. PubMed ID: 15448617
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family.
    Chograni M; Alkuraya FS; Ourteni I; Maazoul F; Lariani I; Chaabouni HB
    Clin Genet; 2015 Sep; 88(3):283-7. PubMed ID: 25358429
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.