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 *

121 related articles for article (PubMed ID: 18591977)

  • 21. Outcome of intracytoplasmic sperm injection for a couple in which the man is carrier of CFTR p.[R74W;V201M;D1270N] and p.P841R mutations and his spouse a heterozygous carrier of p.F508del mutation of the cystic fibrosis transmembrane conductance regulator gene.
    Brugnon F; Bilan F; Heraud MC; Grizard G; Janny L; Creveaux I
    Fertil Steril; 2008 Nov; 90(5):2004.e23-6. PubMed ID: 18703181
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cystic fibrosis in a boy with meconium ileus and mild clinical phenotype associated with 2183AA-G/D1152H genotype.
    Yalçin E; Ozçelik U; Yilmaz E; Doğru D; Kiper N; Ferec C
    Turk J Pediatr; 2008; 50(4):383-5. PubMed ID: 19014055
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Single-dose lentiviral gene transfer for lifetime airway gene expression.
    Stocker AG; Kremer KL; Koldej R; Miller DS; Anson DS; Parsons DW
    J Gene Med; 2009 Oct; 11(10):861-7. PubMed ID: 19634193
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Old hopes and new horizons for treating cystic fibrosis.
    Featherstone C
    Lancet; 1996 Jun; 347(9014):1544. PubMed ID: 8684112
    [No Abstract]   [Full Text] [Related]  

  • 25. [Cystic fibrosis--review].
    Jonsdottir B; Bergsteinsson H; Baldursson O
    Laeknabladid; 2008 Dec; 94(12):831-7. PubMed ID: 19182319
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Drug pipeline: 1Q12.
    Mak C
    Nat Biotechnol; 2012 May; 30(5):383. PubMed ID: 22565954
    [No Abstract]   [Full Text] [Related]  

  • 27. Identification of a novel mutation of CFTR gene in a Korean patient with cystic fibrosis.
    Ko JM; Kim GH; Kim KM; Hong SJ; Yoo HW
    J Korean Med Sci; 2008 Oct; 23(5):912-5. PubMed ID: 18955805
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic heterogeneity and cystic fibrosis.
    Cutting GR
    Hum Mutat; 2009 Jul; 30(7):v. PubMed ID: 19551760
    [No Abstract]   [Full Text] [Related]  

  • 29. Phenotype expression in a case of adult cystic fibrosis caused by an extremely rare compound heterozygous genotype (2183AA>G/2789+5G>A).
    Capurso G; Sbrozzi-Vanni A; Piane M; Begini P; Panzuto F; Libi F; Margagnoni G; Capotondi C; Marignani M; Chessa L; Delle Fave G
    Pancreas; 2009 Jul; 38(5):599-601. PubMed ID: 19550280
    [No Abstract]   [Full Text] [Related]  

  • 30. Three novel mutations in the CFTR gene identified in Galician patients.
    Rana-Díez P; Colón C; Alonso-Fernández JR; Solar A; Barros-Tizón JC; Barros-Casas D; Sirvent J; Carracedo A; Barros F
    J Cyst Fibros; 2008 Nov; 7(6):520-2. PubMed ID: 18676185
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cystic fibrosis: refining the approach to newborn screening.
    Wilcken B
    J Pediatr; 2009 Nov; 155(5):605-6. PubMed ID: 19840611
    [No Abstract]   [Full Text] [Related]  

  • 32. Non-viral gene therapy lights up.
    Foubister V
    Drug Discov Today; 2005 Sep; 10(17):1133. PubMed ID: 16182202
    [No Abstract]   [Full Text] [Related]  

  • 33. CFTR H609R mutation in Ecuadorian patients with cystic fibrosis.
    Moya-Quiles MR; Glover G; Mondéjar-López P; Pastor-Vivero MD; Fernández-Sánchez A; Sánchez-Solís M
    J Cyst Fibros; 2009 Jul; 8(4):280-1. PubMed ID: 19457724
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Dynasore inhibits removal of wild-type and DeltaF508 cystic fibrosis transmembrane conductance regulator (CFTR) from the plasma membrane.
    Young A; Gentzsch M; Abban CY; Jia Y; Meneses PI; Bridges RJ; Bradbury NA
    Biochem J; 2009 Jul; 421(3):377-85. PubMed ID: 19442237
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Borderline sweat test: Utility and limits of genetic analysis for the diagnosis of cystic fibrosis.
    Seia M; Costantino L; Paracchini V; Porcaro L; Capasso P; Coviello D; Corbetta C; Torresani E; Magazzù D; Consalvo V; Monti A; Costantini D; Colombo C
    Clin Biochem; 2009 May; 42(7-8):611-6. PubMed ID: 19318035
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutation analysis of the CFTR gene in Slovak cystic fibrosis patients by DHPLC and subsequent sequencing: identification of four novel mutations.
    Kolesár P; Minárik G; Baldovic M; Ficek A; Kovács L; Kádasi L
    Gen Physiol Biophys; 2008 Dec; 27(4):299-305. PubMed ID: 19202204
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Innate immune activation and cystic fibrosis.
    Brennan S
    Paediatr Respir Rev; 2008 Dec; 9(4):271-9; quiz 279-80. PubMed ID: 19026368
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Phenotypic variability in a family with pancreatitis and cystic fibrosis sharing common mild CFTR mutation: report on CFTR mutations and their phenotypic variability.
    Alghisi F; Bella S; Lucidi V; Angioni A; Tomaiuolo AC; D'Apice MR; Gambardella S; Novelli G
    Pancreas; 2009 Jan; 38(1):109-10. PubMed ID: 19106752
    [No Abstract]   [Full Text] [Related]  

  • 39. Implication of the cystic fibrosis transmembrane conductance regulator gene in infertile family members of Indian CF patients.
    Sharma N; Singh M; Acharya N; Singh SK; Thapa BR; Kaur G; Prasad R
    Biochem Genet; 2008 Dec; 46(11-12):847-56. PubMed ID: 18810634
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification and characterization of CFTR gene mutations in Indian CF patients.
    Sharma N; Singh M; Kaur G; Thapa BR; Prasad R
    Ann Hum Genet; 2009 Jan; 73(1):26-33. PubMed ID: 18782298
    [TBL] [Abstract][Full Text] [Related]  

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