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 *

184 related articles for article (PubMed ID: 28400699)

  • 1. LADD syndrome with glaucoma is caused by a novel gene.
    Simpson A; Avdic A; Roos BR; DeLuca A; Miller K; Schnieders MJ; Scheetz TE; Alward WL; Fingert JH
    Mol Vis; 2017; 23():179-184. PubMed ID: 28400699
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lacrimo-auriculo-dento-digital syndrome: A novel mutation in a Korean family and review of literature.
    Ryu YH; Kyun Chae J; Kim JW; Lee S
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1412. PubMed ID: 32715658
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of a novel missence mutation in FGFR3 gene in an Iranian family with LADD syndrome by Next-Generation Sequencing.
    Talebi F; Ghanbari Mardasi F; Mohammadi Asl J; Bavarsad AH; Tizno S
    Int J Pediatr Otorhinolaryngol; 2017 Jun; 97():192-196. PubMed ID: 28483234
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dental issues in lacrimo-auriculo-dento-digital syndrome: An autosomal dominant condition with clinical and genetic variability.
    Hajianpour MJ; Bombei H; Lieberman SM; Revell R; Krishna R; Gregorsok R; Kao S; Milunsky JM
    J Am Dent Assoc; 2017 Mar; 148(3):157-163. PubMed ID: 28043400
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lacrimo-auriculo-dento-digital syndrome with AIRE mutation: A case report.
    Zhu H; Yu GY
    J Stomatol Oral Maxillofac Surg; 2022 Nov; 123(6):e988-e990. PubMed ID: 35870793
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interrogation of a lacrimo-auriculo-dento-digital syndrome protein reveals novel modes of fibroblast growth factor 10 (FGF10) function.
    Mikolajczak M; Goodman T; Hajihosseini MK
    Biochem J; 2016 Dec; 473(24):4593-4607. PubMed ID: 27742760
    [TBL] [Abstract][Full Text] [Related]  

  • 7. LADD syndrome is caused by FGF10 mutations.
    Milunsky JM; Zhao G; Maher TA; Colby R; Everman DB
    Clin Genet; 2006 Apr; 69(4):349-54. PubMed ID: 16630169
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasia.
    Wade EM; Parthasarathy P; Mi J; Morgan T; Wollnik B; Robertson SP; Cundy T
    Eur J Hum Genet; 2022 Apr; 30(4):480-484. PubMed ID: 33967277
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A requirement for Fgfr2 in middle ear development.
    Rigueur D; Roberts RR; Bobzin L; Merrill AE
    Genesis; 2019 Jan; 57(1):e23252. PubMed ID: 30253032
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Orodental Findings in Patients with Lacrimo-Auriculo-Dento-Digital Syndrome.
    Vicioni-Marques F; Meireles de Sousa SS; de Carvalho FK; de Oliveira SS; Paes Torres C; de Queiroz AM
    J Dent Child (Chic); 2019 Jan; 86(1):53-60. PubMed ID: 30992102
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinical diagnosis of familial Levy-Hollister syndrome].
    Vila Pérez D; Palanca Arias D; Gean Molins E; Palomeque Rico A
    An Pediatr (Barc); 2014 Feb; 80(2):114-6. PubMed ID: 23562527
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Thin central corneal thickness and early-onset glaucoma in lacrimo-auriculo-dento-digital syndrome.
    Tandon A; Tehrani S; Greiner MA; Fingert JH; Alward WL
    JAMA Ophthalmol; 2014 Jun; 132(6):782-4. PubMed ID: 24921174
    [No Abstract]   [Full Text] [Related]  

  • 13. Lacrimo-auriculo-dento-digital syndrome is caused by reduced activity of the fibroblast growth factor 10 (FGF10)-FGF receptor 2 signaling pathway.
    Shams I; Rohmann E; Eswarakumar VP; Lew ED; Yuzawa S; Wollnik B; Schlessinger J; Lax I
    Mol Cell Biol; 2007 Oct; 27(19):6903-12. PubMed ID: 17682060
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in different components of FGF signaling in LADD syndrome.
    Rohmann E; Brunner HG; Kayserili H; Uyguner O; Nürnberg G; Lew ED; Dobbie A; Eswarakumar VP; Uzumcu A; Ulubil-Emeroglu M; Leroy JG; Li Y; Becker C; Lehnerdt K; Cremers CW; Yüksel-Apak M; Nürnberg P; Kubisch C; Schlessinger J; van Bokhoven H; Wollnik B
    Nat Genet; 2006 Apr; 38(4):414-7. PubMed ID: 16501574
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Giant dacryocystocele and congenital alacrimia in lacrimo-auriculo-dento-digital syndrome.
    Santo RO; Golbert MB; Akaishi PM; Cruz AA; Cintra MB
    Ophthalmic Plast Reconstr Surg; 2013; 29(3):e67-8. PubMed ID: 23128532
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lacrimo-auriculo-dento-digital syndrome.
    Mathrawala NR; Hegde RJ
    J Indian Soc Pedod Prev Dent; 2011; 29(2):168-70. PubMed ID: 21911959
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
    Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel TP63 mutation in family with ADULT syndrome presenting with eczema and hypothelia.
    van Zelst-Stams WA; van Steensel MA
    Am J Med Genet A; 2009 Jul; 149A(7):1558-60. PubMed ID: 19530185
    [No Abstract]   [Full Text] [Related]  

  • 19. Case report: Presentation of lacrimo-auriculodento- digital (LADD) syndrome in a young female patient.
    McKenna GJ; Burke FM; Mellan K
    Eur Arch Paediatr Dent; 2009 Nov; 10 Suppl 1():35-9. PubMed ID: 19863897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. FGF10 missense mutations in aplasia of lacrimal and salivary glands (ALSG).
    Entesarian M; Dahlqvist J; Shashi V; Stanley CS; Falahat B; Reardon W; Dahl N
    Eur J Hum Genet; 2007 Mar; 15(3):379-82. PubMed ID: 17213838
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.