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 *

287 related articles for article (PubMed ID: 34404380)

  • 1. Unique three-site compound heterozygous mutation in the WFS1 gene in Wolfram syndrome.
    Ren Z; Yi J; Zhong M; Wang Y; Liu Q; Wang X; Liu D; Ren W
    BMC Endocr Disord; 2021 Aug; 21(1):166. PubMed ID: 34404380
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel mutations and the ophthalmologic characters in Chinese patients with Wolfram Syndrome.
    Zhang Y; Feng L; Kong X; Wu J; Chen Y; Tian G
    Orphanet J Rare Dis; 2019 Aug; 14(1):190. PubMed ID: 31391115
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The novel compound heterozygous mutations, V434del and W666X, in WFS1 gene causing the Wolfram syndrome in a Chinese family.
    Hong J; Zhang YW; Zhang HJ; Jia HY; Zhang Y; Ding XY; Zhou DY; Chen HP; Jiang XH; Cui B; Li XY; Ning G
    Endocrine; 2009 Apr; 35(2):151-7. PubMed ID: 19160074
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular characterization of WFS1 in patients with Wolfram syndrome.
    van ven Ouweland JM; Cryns K; Pennings RJ; Walraven I; Janssen GM; Maassen JA; Veldhuijzen BF; Arntzenius AB; Lindhout D; Cremers CW; Van Camp G; Dikkeschei LD
    J Mol Diagn; 2003 May; 5(2):88-95. PubMed ID: 12707373
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Wolfram syndrome in the Japanese population; molecular analysis of WFS1 gene and characterization of clinical features.
    Matsunaga K; Tanabe K; Inoue H; Okuya S; Ohta Y; Akiyama M; Taguchi A; Kora Y; Okayama N; Yamada Y; Wada Y; Amemiya S; Sugihara S; Nakao Y; Oka Y; Tanizawa Y
    PLoS One; 2014; 9(9):e106906. PubMed ID: 25211237
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A novel mutation of WFS1 gene in Chinese patients with Wolfram syndrome].
    Fang QC; Jia WP; Zhang R; Li Q; Hu C; Shao XY; Chai HQ; Lu HJ; Xiang KS
    Zhonghua Yi Xue Za Zhi; 2005 Sep; 85(35):2468-71. PubMed ID: 16321270
    [TBL] [Abstract][Full Text] [Related]  

  • 7. c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness.
    Safarpour Lima B; Ghaedi H; Daftarian N; Ahmadieh H; Jamshidi J; Khorrami M; Noroozi R; Sohrabifar N; Assarzadegan F; Hesami O; Taghavi S; Ahmadifard A; Atakhorrami M; Rahimi-Aliabadi S; Shahmohammadibeni N; Alehabib E; Andarva M; Darvish H; Emamalizadeh B
    Eur J Med Genet; 2016 Feb; 59(2):65-9. PubMed ID: 26773575
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel mutation of WFS1 gene leading to increase ER stress and cell apoptosis is associated an autosomal dominant form of Wolfram syndrome type 1.
    Gong Y; Xiong L; Li X; Su L; Xiao H
    BMC Endocr Disord; 2021 Apr; 21(1):76. PubMed ID: 33879153
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.
    Young TL; Ives E; Lynch E; Person R; Snook S; MacLaren L; Cater T; Griffin A; Fernandez B; Lee MK; King MC
    Hum Mol Genet; 2001 Oct; 10(22):2509-14. PubMed ID: 11709538
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ophthalmic, systemic, and genetic characteristics of patients with Wolfram syndrome.
    Ustaoglu M; Onder F; Karapapak M; Taslidere H; Guven D
    Eur J Ophthalmol; 2020 Sep; 30(5):1099-1105. PubMed ID: 30957632
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment?
    Ghirardello S; Dusi E; Castiglione B; Fumagalli M; Mosca F
    Ital J Pediatr; 2014 Sep; 40():76. PubMed ID: 25255707
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report.
    Li M; Liu J; Yi H; Xu L; Zhong X; Peng F
    BMC Pediatr; 2018 Mar; 18(1):116. PubMed ID: 29549887
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cataract as a phenotypic marker for a mutation in WFS1, the Wolfram syndrome gene.
    Titah SM; Meunier I; Blanchet C; Lopez S; Rondouin G; Lenaers G; Amati-Bonneau P; Reynier P; Paquis-Flucklinger V; Hamel CP
    Eur J Ophthalmol; 2012; 22(2):254-8. PubMed ID: 21623591
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular characterization of WFS1 in an Iranian family with Wolfram syndrome reveals a novel frameshift mutation associated with early symptoms.
    Sobhani M; Tabatabaiefar MA; Rajab A; Kajbafzadeh AM; Noori-Daloii MR
    Gene; 2013 Oct; 528(2):309-13. PubMed ID: 23845777
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial Wolfram syndrome due to compound heterozygosity for two novel WFS1 mutations.
    Zenteno JC; Ruiz G; Pérez-Cano HJ; Camargo M
    Mol Vis; 2008 Jul; 14():1353-7. PubMed ID: 18660851
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of unsuspected Wolfram syndrome cases through clinical assessment and WFS1 gene screening in type 1 diabetes mellitus patients.
    Blanco-Aguirre ME; la Parra DR; Tapia-Garcia H; Gonzalez-Rodriguez J; Welschen D; Arroyo-Yllanes ME; Escudero I; Nuñez-Hernandez JA; Medina-Bravo P; Zenteno JC
    Gene; 2015 Jul; 566(1):63-7. PubMed ID: 25895475
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of novel mutations of the WFS1 gene in Brazilian patients with Wolfram syndrome.
    Gasparin MR; Crispim F; Paula SL; Freire MB; Dalbosco IS; Manna TD; Salles JE; Gasparin F; Guedes A; Marcantonio JM; Gambini M; Salim CP; Moisés RS
    Eur J Endocrinol; 2009 Feb; 160(2):309-16. PubMed ID: 19042979
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rapidly progressive renal disease as part of Wolfram syndrome in a large inbred Turkish family due to a novel WFS1 mutation (p.Leu511Pro).
    Yuca SA; Rendtorff ND; Boulahbel H; Lodahl M; Tranebjærg L; Cesur Y; Dogan M; Yilmaz C; Akgun C; Acikgoz M
    Eur J Med Genet; 2012 Jan; 55(1):37-42. PubMed ID: 21968327
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.
    Sobhani M; Tabatabaiefar MA; Ghafouri-Fard S; Rajab A; Hojjat A; Kajbafzadeh AM; Noori-Daloii MR
    BMC Med Genet; 2020 Jan; 21(1):13. PubMed ID: 31937257
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Significant expressivity of Wolfram syndrome: phenotypic assessment of two known and one novel mutation in the WFS1 gene in three Iranian families.
    Sobhani M; Tabatabaiefar MA; Rajab A; Kajbafzadeh AM; Noori-Daloii MR
    Mol Biol Rep; 2014 Nov; 41(11):7499-505. PubMed ID: 25173644
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.