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 *

148 related articles for article (PubMed ID: 21110105)

  • 1. Cystic fibrosis Δf508 mutation screening in Brazilian women with altered fertility.
    Brunoro GV; Wolfgramm EV; Louro ID; Degasperi II; Busatto VC; Perrone AM; Batitucci MC
    Mol Biol Rep; 2011 Oct; 38(7):4343-6. PubMed ID: 21110105
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prevalence of ΔF508 mutation in the cystic fibrosis transmembrane conductance regulator gene among cystic fibrosis patients from a Brazilian referral center.
    Bieger AM; Marson FA; Bertuzzo CS
    J Pediatr (Rio J); 2012; 88(6):531-4. PubMed ID: 23064458
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detections.
    Comeau AM; Parad RB; Dorkin HL; Dovey M; Gerstle R; Haver K; Lapey A; O'Sullivan BP; Waltz DA; Zwerdling RG; Eaton RB
    Pediatrics; 2004 Jun; 113(6):1573-81. PubMed ID: 15173476
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Potentiators (specific therapies for class III and IV mutations) for cystic fibrosis.
    Patel S; Sinha IP; Dwan K; Echevarria C; Schechter M; Southern KW
    Cochrane Database Syst Rev; 2015 Mar; (3):CD009841. PubMed ID: 25811419
    [TBL] [Abstract][Full Text] [Related]  

  • 5. CF gene and cystic fibrosis transmembrane conductance regulator expression in autosomal dominant polycystic kidney disease.
    Persu A; Devuyst O; Lannoy N; Materne R; Brosnahan G; Gabow PA; Pirson Y; Verellen-Dumoulin C
    J Am Soc Nephrol; 2000 Dec; 11(12):2285-2296. PubMed ID: 11095651
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Application of multiplex ARMS and SSCP/HD analysis in molecular diagnosis of cystic fibrosis in Indian patients.
    Ashavaid TF; Kondkar AA; Dherai AJ; Raghavan R; Udani SV; Udwadia ZF; Desai D
    Mol Diagn; 2005; 9(2):59-66. PubMed ID: 16137181
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CFTR DeltaF508 mutation detection from dried blood samples in the first trimester of pregnancy: a possible routine prenatal screening strategy for cystic fibrosis?
    Konialis CP; Hagnefelt B; Kazamia C; Karapanou S; Pangalos C
    Fetal Diagn Ther; 2007; 22(1):41-4. PubMed ID: 17003555
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prospective analysis of cystic fibrosis transmembrane regulator mutations in adults with bronchiectasis or pulmonary nontuberculous mycobacterial infection.
    Ziedalski TM; Kao PN; Henig NR; Jacobs SS; Ruoss SJ
    Chest; 2006 Oct; 130(4):995-1002. PubMed ID: 17035430
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Frequency of the deltaF508 mutation in 108 cystic fibrosis patients in Sao Paulo: comparison with reported Brazilian data.
    Okay TS; Oliveira WP; Raiz-Júnior R; Rodrigues JC; Del Negro GM
    Clinics (Sao Paulo); 2005 Apr; 60(2):131-4. PubMed ID: 15880249
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Population screening of F508del (DeltaF508), the most frequent mutation in the CFTR gene associated with cystic fibrosis in Argentina.
    Roqué M; Godoy CP; Castellanos M; Pusiol E; Mayorga LS
    Hum Mutat; 2001 Aug; 18(2):167. PubMed ID: 11462248
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening.
    Bobadilla JL; Macek M; Fine JP; Farrell PM
    Hum Mutat; 2002 Jun; 19(6):575-606. PubMed ID: 12007216
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Low frequency of the deltaAF508 mutation of the CFTR gene in a highly admixed population in Bahia, Brazil.
    Moura Costa FM; Santana MA; Lemos AC; Galvão-Castro B; Acosta AX
    Hum Biol; 2007 Jun; 79(3):293-7. PubMed ID: 18078202
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Regulation of cystic fibrosis transmembrane conductance regulator by microRNA-145, -223, and -494 is altered in ΔF508 cystic fibrosis airway epithelium.
    Oglesby IK; Chotirmall SH; McElvaney NG; Greene CM
    J Immunol; 2013 Apr; 190(7):3354-62. PubMed ID: 23436935
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease.
    Bonadia LC; de Lima Marson FA; Ribeiro JD; Paschoal IA; Pereira MC; Ribeiro AF; Bertuzzo CS
    Gene; 2014 May; 540(2):183-90. PubMed ID: 24583165
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cystic fibrosis and fertility.
    Ahmad A; Ahmed A; Patrizio P
    Curr Opin Obstet Gynecol; 2013 Jun; 25(3):167-72. PubMed ID: 23429570
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spectrum of CFTR gene mutations in Iranian Azeri Turkish patients with cystic fibrosis.
    Bonyadi M; Omrani O; Rafeey M; Bilan N
    Genet Test Mol Biomarkers; 2011; 15(1-2):89-92. PubMed ID: 21198395
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular diagnosis of cystic fibrosis in Indian patients--a preliminary report.
    Ashavaid TF; Dherai AJ; Kondkar AA; Raghavan R; Udani SV; Udwadia ZF; Desai D
    J Assoc Physicians India; 2003 Apr; 51():345-8. PubMed ID: 12723646
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inhibition of acinar apoptosis occurs during acute pancreatitis in the human homologue DeltaF508 cystic fibrosis mouse.
    DiMagno MJ; Lee SH; Owyang C; Zhou SY
    Am J Physiol Gastrointest Liver Physiol; 2010 Aug; 299(2):G400-12. PubMed ID: 20522641
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Can correcting the ΔF508-CFTR proteostasis-defect rescue CF lung disease?
    Valle CW; Vij N
    Curr Mol Med; 2012 Aug; 12(7):860-71. PubMed ID: 22697346
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis.
    Mickle JE; Macek M; Fulmer-Smentek SB; Egan MM; Schwiebert E; Guggino W; Moss R; Cutting GR
    Hum Mol Genet; 1998 Apr; 7(4):729-35. PubMed ID: 9499426
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.