Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 90

1.

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis.

Sun L, Rommens JM, Corvol H, Li W, Li X, Chiang TA, Lin F, Dorfman R, Busson PF, Parekh RV, Zelenika D, Blackman SM, Corey M, Doshi VK, Henderson L, Naughton KM, O'Neal WK, Pace RG, Stonebraker JR, Wood SD, Wright FA, Zielenski J, Clement A, Drumm ML, Boëlle PY, Cutting GR, Knowles MR, Durie PR, Strug LJ.

Nat Genet. 2012 May;44(5):562-9. doi: 10.1038/ng.2221.

2.

Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities.

Li W, Soave D, Miller MR, Keenan K, Lin F, Gong J, Chiang T, Stephenson AL, Durie P, Rommens J, Sun L, Strug LJ.

Hum Genet. 2014 Feb;133(2):151-61. doi: 10.1007/s00439-013-1363-7. Epub 2013 Sep 22.

PMID:
24057835
3.

Variants in Solute Carrier SLC26A9 Modify Prenatal Exocrine Pancreatic Damage in Cystic Fibrosis.

Miller MR, Soave D, Li W, Gong J, Pace RG, Boëlle PY, Cutting GR, Drumm ML, Knowles MR, Sun L, Rommens JM, Accurso F, Durie PR, Corvol H, Levy H, Sontag MK, Strug LJ.

J Pediatr. 2015 May;166(5):1152-1157.e6. doi: 10.1016/j.jpeds.2015.01.044. Epub 2015 Mar 11.

4.

Association of the CLCA1 p.S357N variant with meconium ileus in European patients with cystic fibrosis.

van der Doef HP, Slieker MG, Staab D, Alizadeh BZ, Seia M, Colombo C, van der Ent CK, Nickel R, Witt H, Houwen RH.

J Pediatr Gastroenterol Nutr. 2010 Mar;50(3):347-9. doi: 10.1097/MPG.0b013e3181afce6c.

PMID:
20179644
5.

Is the hemochromatosis gene a modifier locus for cystic fibrosis?

Rohlfs EM, Shaheen NJ, Silverman LM.

Genet Test. 1998;2(1):85-8.

PMID:
10464603
6.

Lethal course of meconium ileus in preterm twins revealing a novel cystic fibrosis mutation (p.Cys524Tyr).

Puzik A, Morris-Rosendahl DJ, Rückauer KD, Otto C, Gessler P, Saueressig U, Hentschel R.

BMC Pediatr. 2014 Jan 17;14:13. doi: 10.1186/1471-2431-14-13.

7.

Association of clinical severity of cystic fibrosis with variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1 and SLC9A3).

Pereira SV, Ribeiro JD, Bertuzzo CS, Marson FAL.

Gene. 2017 Sep 20;629:117-126. doi: 10.1016/j.gene.2017.07.068. Epub 2017 Jul 27.

PMID:
28756021
8.

Clinical and genetic characteristics of meconium ileus in newborns with and without cystic fibrosis.

Gorter RR, Karimi A, Sleeboom C, Kneepkens CM, Heij HA.

J Pediatr Gastroenterol Nutr. 2010 May;50(5):569-72. doi: 10.1097/MPG.0b013e3181bb3427.

PMID:
20386322
9.

Analysis of risk factors for the development of liver disease associated with cystic fibrosis.

Colombo C, Apostolo MG, Ferrari M, Seia M, Genoni S, Giunta A, Sereni LP.

J Pediatr. 1994 Mar;124(3):393-9.

PMID:
8120708
10.

[Phenotypic variability of cystic fibrosis: case report of twins with F508/F508 mutation].

Hernández-Amaris MF, Gómez-Vásquez AM, Pachajua H H.

Rev Chil Pediatr. 2014 Jul;85(4):470-5. doi: 10.4067/S0370-41062014000400010. Spanish.

11.
12.

Is meconium ileus genetically determined or associated with a more severe evolution of cystic fibrosis?

De Braekeleer M, Allard C, Leblanc JP, Aubin G, Simard F.

J Med Genet. 1998 Mar;35(3):262-3. No abstract available.

13.

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 Jul-Aug;50(4):383-5.

PMID:
19014055
14.
15.

Loss of Slc26a9 anion transporter alters intestinal electrolyte and HCO3(-) transport and reduces survival in CFTR-deficient mice.

Liu X, Li T, Riederer B, Lenzen H, Ludolph L, Yeruva S, Tuo B, Soleimani M, Seidler U.

Pflugers Arch. 2015 Jun;467(6):1261-75. doi: 10.1007/s00424-014-1543-x. Epub 2014 Jun 27.

16.

Genetic modifiers of cystic fibrosis-related diabetes.

Blackman SM, Commander CW, Watson C, Arcara KM, Strug LJ, Stonebraker JR, Wright FA, Rommens JM, Sun L, Pace RG, Norris SA, Durie PR, Drumm ML, Knowles MR, Cutting GR.

Diabetes. 2013 Oct;62(10):3627-35. doi: 10.2337/db13-0510. Epub 2013 May 13.

17.

Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes.

Salvatore F, Scudiero O, Castaldo G.

Am J Med Genet. 2002 Jul 22;111(1):88-95. Review.

PMID:
12124743
18.

ATB(0)/SLC1A5 gene. Fine localisation and exclusion of association with the intestinal phenotype of cystic fibrosis.

Larriba S, Sumoy L, Ramos MD, Giménez J, Estivill X, Casals T, Nunes V.

Eur J Hum Genet. 2001 Nov;9(11):860-6.

19.

Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results.

Dorfman R, Li W, Sun L, Lin F, Wang Y, Sandford A, Paré PD, McKay K, Kayserova H, Piskackova T, Macek M, Czerska K, Sands D, Tiddens H, Margarit S, Repetto G, Sontag MK, Accurso FJ, Blackman S, Cutting GR, Tsui LC, Corey M, Durie P, Zielenski J, Strug LJ.

Hum Genet. 2009 Dec;126(6):763-78. doi: 10.1007/s00439-009-0724-8.

20.

Novel double mutant CF allele identified in a cystic fibrosis patient with meconium ileus.

Steffann J, Vidaud D, Bousquet S, Jullien M, Ninot A, Kaplan JC, Beldjord C, Bienvenu T.

Ann Genet. 1998;41(4):213-5. No abstract available.

PMID:
9881185

Supplemental Content

Support Center