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Search results 101 to 200 out of 713 for Cftr

Category restricted to Publication (x)

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Category: Publication
Type Details Score
Publication
First Author: van Heeckeren AM
Year: 2004
Journal: Am J Physiol Lung Cell Mol Physiol
Title: Role of Cftr genotype in the response to chronic Pseudomonas aeruginosa lung infection in mice.
Volume: 287
Issue: 5
Pages: L944-52
Publication
First Author: Ruan YC
Year: 2014
Journal: J Cell Sci
Title: CFTR interacts with ZO-1 to regulate tight junction assembly and epithelial differentiation through the ZONAB pathway.
Volume: 127
Issue: Pt 20
Pages: 4396-408
Publication
First Author: Pan J
Year: 2006
Journal: Am J Respir Cell Mol Biol
Title: Pulmonary neuroendocrine cells, airway innervation, and smooth muscle are altered in Cftr null mice.
Volume: 35
Issue: 3
Pages: 320-6
Publication  
First Author: Fang D
Year: 2010
Journal: Respir Res
Title: Increased plasma membrane cholesterol in cystic fibrosis cells correlates with CFTR genotype and depends on de novo cholesterol synthesis.
Volume: 11
Pages: 61
Publication
First Author: Dhooghe B
Year: 2013
Journal: PLoS One
Title: Correction of chloride transport and mislocalization of CFTR protein by vardenafil in the gastrointestinal tract of cystic fibrosis mice.
Volume: 8
Issue: 10
Pages: e77314
Publication
First Author: Ntimbane T
Year: 2016
Journal: Am J Physiol Endocrinol Metab
Title: CFTR silencing in pancreatic β-cells reveals a functional impact on glucose-stimulated insulin secretion and oxidative stress response.
Volume: 310
Issue: 3
Pages: E200-12
Publication
First Author: Kravtsov DV
Year: 2012
Journal: Traffic
Title: Myosin Ia is required for CFTR brush border membrane trafficking and ion transport in the mouse small intestine.
Volume: 13
Issue: 8
Pages: 1072-82
Publication
First Author: Yang A
Year: 2018
Journal: Cell Death Dis
Title: Homocysteine activates autophagy by inhibition of CFTR expression via interaction between DNA methylation and H3K27me3 in mouse liver.
Volume: 9
Issue: 2
Pages: 169
Publication
First Author: Bickford JS
Year: 2013
Journal: J Cyst Fibros
Title: Effect of allergy and inflammation on eicosanoid gene expression in CFTR deficiency.
Volume: 12
Issue: 3
Pages: 258-65
Publication  
First Author: Edlund A
Year: 2014
Journal: BMC Med
Title: CFTR and Anoctamin 1 (ANO1) contribute to cAMP amplified exocytosis and insulin secretion in human and murine pancreatic beta-cells.
Volume: 12
Pages: 87
Publication
First Author: Stalvey MS
Year: 2013
Journal: PLoS One
Title: Osteoblast CFTR inactivation reduces differentiation and osteoprotegerin expression in a mouse model of cystic fibrosis-related bone disease.
Volume: 8
Issue: 11
Pages: e80098
Publication
First Author: Chang CT
Year: 2005
Journal: J Physiol
Title: Vasopressin-stimulated CFTR Cl- currents are increased in the renal collecting duct cells of a mouse model of Liddle's syndrome.
Volume: 562
Issue: Pt 1
Pages: 271-84
Publication
First Author: Yang D
Year: 2009
Journal: J Clin Invest
Title: IRBIT coordinates epithelial fluid and HCO3- secretion by stimulating the transporters pNBC1 and CFTR in the murine pancreatic duct.
Volume: 119
Issue: 1
Pages: 193-202
Publication
First Author: Trapp S
Year: 2021
Journal: J Cell Mol Med
Title: Pancreatitis severity in mice with impaired CFTR function but pancreatic sufficiency is mediated via ductal and inflammatory cells-Not acinar cells.
Volume: 25
Issue: 10
Pages: 4658-4670
Publication
First Author: Veltman M
Year: 2016
Journal: Am J Physiol Lung Cell Mol Physiol
Title: Correction of lung inflammation in a F508del CFTR murine cystic fibrosis model by the sphingosine-1-phosphate lyase inhibitor LX2931.
Volume: 311
Issue: 5
Pages: L1000-L1014
Publication
First Author: Morin G
Year: 2016
Journal: Am J Physiol Gastrointest Liver Physiol
Title: Vitamin D attenuates inflammation in CFTR knockdown intestinal epithelial cells but has no effect in cells with intact CFTR.
Volume: 310
Issue: 8
Pages: G539-49
Publication
First Author: Chappe V
Year: 2005
Journal: EMBO J
Title: Phosphorylation of CFTR by PKA promotes binding of the regulatory domain.
Volume: 24
Issue: 15
Pages: 2730-40
Publication
First Author: Baker JM
Year: 2007
Journal: Nat Struct Mol Biol
Title: CFTR regulatory region interacts with NBD1 predominantly via multiple transient helices.
Volume: 14
Issue: 8
Pages: 738-45
Publication  
First Author: Wu YZ
Year: 2010
Journal: Respir Res
Title: Cytosolic phospholipase A2alpha mediates Pseudomonas aeruginosa LPS-induced airway constriction of CFTR -/- mice.
Volume: 11
Pages: 49
Publication
First Author: Pelaseyed T
Year: 2013
Journal: Am J Physiol Cell Physiol
Title: Carbachol-induced MUC17 endocytosis is concomitant with NHE3 internalization and CFTR membrane recruitment in enterocytes.
Volume: 305
Issue: 4
Pages: C457-67
Publication
First Author: Kramer EL
Year: 2018
Journal: Am J Physiol Lung Cell Mol Physiol
Title: Subacute TGFβ expression drives inflammation, goblet cell hyperplasia, and pulmonary function abnormalities in mice with effects dependent on CFTR function.
Volume: 315
Issue: 3
Pages: L456-L465
Publication
First Author: Delaney SJ
Year: 1994
Journal: Genomics
Title: Alternative splicing of the first nucleotide binding fold of CFTR in mouse testes is associated with specific stages of spermatogenesis.
Volume: 20
Issue: 3
Pages: 517-8
Publication
First Author: Wellmerling JH
Year: 2019
Journal: Respir Res
Title: Reduced expression of the Ion channel CFTR contributes to airspace enlargement as a consequence of aging and in response to cigarette smoke in mice.
Volume: 20
Issue: 1
Pages: 200
Publication
First Author: Beumer W
Year: 2019
Journal: PLoS One
Title: Evaluation of eluforsen, a novel RNA oligonucleotide for restoration of CFTR function in in vitro and murine models of p.Phe508del cystic fibrosis.
Volume: 14
Issue: 6
Pages: e0219182
Publication
First Author: Dorin JR
Year: 1994
Journal: Mamm Genome
Title: Long-term survival of the exon 10 insertional cystic fibrosis mutant mouse is a consequence of low level residual wild-type Cftr gene expression.
Volume: 5
Issue: 8
Pages: 465-72
Publication
First Author: Davidson H
Year: 2000
Journal: Genome Res
Title: Genomic sequence analysis of Fugu rubripes CFTR and flanking genes in a 60 kb region conserving synteny with 800 kb of human chromosome 7.
Volume: 10
Issue: 8
Pages: 1194-203
Publication
First Author: Schütte A
Year: 2014
Journal: Proc Natl Acad Sci U S A
Title: Microbial-induced meprin β cleavage in MUC2 mucin and a functional CFTR channel are required to release anchored small intestinal mucus.
Volume: 111
Issue: 34
Pages: 12396-401
Publication
First Author: Dennis EA
Year: 2015
Journal: PLoS One
Title: The Effects of CFTR and Mucoid Phenotype on Susceptibility and Innate Immune Responses in a Mouse Model of Pneumococcal Lung Disease.
Volume: 10
Issue: 10
Pages: e0140335
Publication  
First Author: Martinovich KM
Year: 2022
Journal: Front Pharmacol
Title: Investigating the Implications of CFTR Exon Skipping Using a Cftr Exon 9 Deleted Mouse Model.
Volume: 13
Pages: 868863
Publication
First Author: Phua YL
Year: 2019
Journal: Am J Physiol Renal Physiol
Title: Loss of miR-17~92 results in dysregulation of Cftr in nephron progenitors.
Volume: 316
Issue: 5
Pages: F993-F1005
Publication
First Author: Ostedgaard LS
Year: 2011
Journal: Proc Natl Acad Sci U S A
Title: Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- mice.
Volume: 108
Issue: 7
Pages: 2921-6
Publication
First Author: McHugh DR
Year: 2018
Journal: PLoS One
Title: A G542X cystic fibrosis mouse model for examining nonsense mutation directed therapies.
Volume: 13
Issue: 6
Pages: e0199573
Publication
First Author: Ratcliff R
Year: 1993
Journal: Nat Genet
Title: Production of a severe cystic fibrosis mutation in mice by gene targeting.
Volume: 4
Issue: 1
Pages: 35-41
Publication
First Author: Hyde SC
Year: 1993
Journal: Nature
Title: Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy.
Volume: 362
Issue: 6417
Pages: 250-5
Publication
First Author: Wang G
Year: 2011
Journal: J Biol Chem
Title: The inhibition mechanism of non-phosphorylated Ser768 in the regulatory domain of cystic fibrosis transmembrane conductance regulator.
Volume: 286
Issue: 3
Pages: 2171-82
Publication
First Author: Xue X
Year: 2014
Journal: Am J Respir Cell Mol Biol
Title: Synthetic aminoglycosides efficiently suppress cystic fibrosis transmembrane conductance regulator nonsense mutations and are enhanced by ivacaftor.
Volume: 50
Issue: 4
Pages: 805-16
Publication
First Author: Kelly J
Year: 2022
Journal: Sci Rep
Title: Alterations of mucosa-attached microbiome and epithelial cell numbers in the cystic fibrosis small intestine with implications for intestinal disease.
Volume: 12
Issue: 1
Pages: 6593
Publication
First Author: Cuthbert AW
Year: 1994
Journal: Br J Pharmacol
Title: Chloride secretion in response to guanylin in colonic epithelial from normal and transgenic cystic fibrosis mice.
Volume: 112
Issue: 1
Pages: 31-6
Publication
First Author: Bijvelds MJ
Year: 2005
Journal: Am J Physiol Gastrointest Liver Physiol
Title: Fat absorption in cystic fibrosis mice is impeded by defective lipolysis and post-lipolytic events.
Volume: 288
Issue: 4
Pages: G646-53
Publication
First Author: Bronckers A
Year: 2010
Journal: Bone
Title: The cystic fibrosis transmembrane conductance regulator (CFTR) is expressed in maturation stage ameloblasts, odontoblasts and bone cells.
Volume: 46
Issue: 4
Pages: 1188-96
Publication
First Author: Wallace HL
Year: 2013
Journal: Physiol Rep
Title: Abnormal tracheal smooth muscle function in the CF mouse.
Volume: 1
Issue: 6
Pages: e00138
Publication
First Author: Goddard CA
Year: 2000
Journal: Am J Physiol Cell Physiol
Title: Genistein activates CFTR-mediated Cl(-) secretion in the murine trachea and colon.
Volume: 279
Issue: 2
Pages: C383-92
Publication
First Author: Werner A
Year: 2004
Journal: J Lipid Res
Title: No indications for altered essential fatty acid metabolism in two murine models for cystic fibrosis.
Volume: 45
Issue: 12
Pages: 2277-86
Publication  
First Author: Cuthbert AW
Year: 1995
Journal: J Physiol
Title: The genetic advantage hypothesis in cystic fibrosis heterozygotes: a murine study.
Volume: 482 ( Pt 2)
Pages: 449-54
Publication  
First Author: Tan X
Year: 2022
Journal: Int J Mol Sci
Title: The NHE3 Inhibitor Tenapanor Prevents Intestinal Obstructions in CFTR-Deleted Mice.
Volume: 23
Issue: 17
Publication
First Author: Bronckers AL
Year: 2015
Journal: Eur J Oral Sci
Title: Composition of mineralizing incisor enamel in cystic fibrosis transmembrane conductance regulator-deficient mice.
Volume: 123
Issue: 1
Pages: 9-16
Publication
First Author: French PJ
Year: 1996
Journal: J Clin Invest
Title: A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.
Volume: 98
Issue: 6
Pages: 1304-12
Publication
First Author: Bodewes FA
Year: 2012
Journal: Am J Physiol Gastrointest Liver Physiol
Title: Ursodeoxycholate modulates bile flow and bile salt pool independently from the cystic fibrosis transmembrane regulator (Cftr) in mice.
Volume: 302
Issue: 9
Pages: G1035-42
Publication
First Author: Du M
Year: 2002
Journal: J Mol Med (Berl)
Title: Aminoglycoside suppression of a premature stop mutation in a Cftr-/- mouse carrying a human CFTR-G542X transgene.
Volume: 80
Issue: 9
Pages: 595-604
Publication
First Author: Sheppard DN
Year: 1999
Journal: Physiol Rev
Title: Structure and function of the CFTR chloride channel.
Volume: 79
Issue: 1 Suppl
Pages: S23-45
Publication
First Author: Singh AK
Year: 2009
Journal: J Clin Invest
Title: Differential roles of NHERF1, NHERF2, and PDZK1 in regulating CFTR-mediated intestinal anion secretion in mice.
Volume: 119
Issue: 3
Pages: 540-50
Publication
First Author: Bachmann O
Year: 2003
Journal: J Physiol
Title: Expression and regulation of the Na+-K+-2Cl- cotransporter NKCC1 in the normal and CFTR-deficient murine colon.
Volume: 549
Issue: Pt 2
Pages: 525-36
Publication
First Author: Trezise AE
Year: 1997
Journal: Hum Mol Genet
Title: Co-ordinate regulation of the cystic fibrosis and multidrug resistance genes in cystic fibrosis knockout mice.
Volume: 6
Issue: 4
Pages: 527-37
Publication
First Author: Jalali R
Year: 2014
Journal: Cell Tissue Res
Title: NBCe1 (SLC4A4) a potential pH regulator in enamel organ cells during enamel development in the mouse.
Volume: 358
Issue: 2
Pages: 433-42
Publication
First Author: Guilbault C
Year: 2007
Journal: Am J Respir Cell Mol Biol
Title: Cystic fibrosis mouse models.
Volume: 36
Issue: 1
Pages: 1-7
Publication
First Author: Zheng W
Year: 2009
Journal: FASEB J
Title: Hypoxia inducible factor-1 (HIF-1)-mediated repression of cystic fibrosis transmembrane conductance regulator (CFTR) in the intestinal epithelium.
Volume: 23
Issue: 1
Pages: 204-13
Publication  
First Author: Bronckers AL
Year: 2017
Journal: Bone
Title: Magnesium, pH regulation and modulation by mouse ameloblasts exposed to fluoride.
Volume: 94
Pages: 56-64
Publication
First Author: Grubb BR
Year: 2012
Journal: Am J Physiol Lung Cell Mol Physiol
Title: Transgenic hCFTR expression fails to correct β-ENaC mouse lung disease.
Volume: 302
Issue: 2
Pages: L238-47
Publication  
First Author: Al-Ansari S
Year: 2018
Journal: Front Physiol
Title: The Importance of Connexin 43 in Enamel Development and Mineralization.
Volume: 9
Pages: 750
Publication
First Author: Ikpa PT
Year: 2020
Journal: Cell Mol Gastroenterol Hepatol
Title: Impaired Intestinal Farnesoid X Receptor Signaling in Cystic Fibrosis Mice.
Volume: 9
Issue: 1
Pages: 47-60
Publication
First Author: Xiao F
Year: 2012
Journal: J Physiol
Title: Rescue of epithelial HCO3- secretion in murine intestine by apical membrane expression of the cystic fibrosis transmembrane conductance regulator mutant F508del.
Volume: 590
Issue: 21
Pages: 5317-34
Publication
First Author: van der Mark VA
Year: 2016
Journal: Biochim Biophys Acta
Title: The phospholipid flippase ATP8B1 mediates apical localization of the cystic fibrosis transmembrane regulator.
Volume: 1863
Issue: 9
Pages: 2280-8
Publication
First Author: MacVinish LJ
Year: 1997
Journal: Am J Physiol
Title: Normalization of ion transport in murine cystic fibrosis nasal epithelium using gene transfer.
Volume: 273
Issue: 2 Pt 1
Pages: C734-40
Publication
First Author: Ghosal S
Year: 2000
Journal: Eur Respir J
Title: Sodium channel blockers and uridine triphosphate: effects on nasal potential difference in cystic fibrosis mice.
Volume: 15
Issue: 1
Pages: 146-50
Publication
First Author: Colledge WH
Year: 1992
Journal: Lancet
Title: Cystic fibrosis mouse with intestinal obstruction.
Volume: 340
Issue: 8820
Pages: 680
Publication
First Author: Du M
Year: 2008
Journal: Proc Natl Acad Sci U S A
Title: PTC124 is an orally bioavailable compound that promotes suppression of the human CFTR-G542X nonsense allele in a CF mouse model.
Volume: 105
Issue: 6
Pages: 2064-9
Publication
First Author: Navarro P
Year: 1995
Journal: Mol Immunol
Title: The complete cDNA and deduced amino acid sequence of equine IgE.
Volume: 32
Issue: 1
Pages: 1-8
Publication
First Author: Braun J
Year: 2010
Journal: J Cyst Fibros
Title: Quantitative expression analyses of candidates for alternative anion conductance in cystic fibrosis mouse models.
Volume: 9
Issue: 5
Pages: 351-64
Publication
First Author: Liu X
Year: 2015
Journal: Pflugers Arch
Title: Loss of Slc26a9 anion transporter alters intestinal electrolyte and HCO3(-) transport and reduces survival in CFTR-deficient mice.
Volume: 467
Issue: 6
Pages: 1261-75
Publication
First Author: Sørensen MV
Year: 2010
Journal: J Physiol
Title: Adrenaline-induced colonic K+ secretion is mediated by KCa1.1 (BK) channels.
Volume: 588
Issue: Pt 10
Pages: 1763-77
Publication  
First Author: Wilke M
Year: 2011
Journal: J Cyst Fibros
Title: Mouse models of cystic fibrosis: phenotypic analysis and research applications.
Volume: 10 Suppl 2
Pages: S152-71
Publication
First Author: Gibson-Corley KN
Year: 2016
Journal: J Pathol
Title: Pancreatic pathophysiology in cystic fibrosis.
Volume: 238
Issue: 2
Pages: 311-20
Publication
First Author: Du M
Year: 2009
Journal: J Biol Chem
Title: Poly-L-aspartic acid enhances and prolongs gentamicin-mediated suppression of the CFTR-G542X mutation in a cystic fibrosis mouse model.
Volume: 284
Issue: 11
Pages: 6885-92
Publication
First Author: Skals M
Year: 2010
Journal: J Biol Chem
Title: Escherichia coli alpha-hemolysin triggers shrinkage of erythrocytes via K(Ca)3.1 and TMEM16A channels with subsequent phosphatidylserine exposure.
Volume: 285
Issue: 20
Pages: 15557-65
Publication
First Author: Bronckers AL
Year: 2015
Journal: J Dent Res
Title: Ameloblast Modulation and Transport of Cl⁻, Na⁺, and K⁺ during Amelogenesis.
Volume: 94
Issue: 12
Pages: 1740-7
Publication
First Author: Zhou L
Year: 1994
Journal: Science
Title: Correction of lethal intestinal defect in a mouse model of cystic fibrosis by human CFTR.
Volume: 266
Issue: 5191
Pages: 1705-8
Publication
First Author: Hasty P
Year: 1995
Journal: Somat Cell Mol Genet
Title: Severe phenotype in mice with termination mutation in exon 2 of cystic fibrosis gene.
Volume: 21
Issue: 3
Pages: 177-87
Publication
First Author: Gabriel SE
Year: 1994
Journal: Science
Title: Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model.
Volume: 266
Issue: 5182
Pages: 107-9
Publication
First Author: Snouwaert JN
Year: 1992
Journal: Science
Title: An animal model for cystic fibrosis made by gene targeting.
Volume: 257
Issue: 5073
Pages: 1083-8
Publication
First Author: Delaney SJ
Year: 1993
Journal: Nat Genet
Title: Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels.
Volume: 4
Issue: 4
Pages: 426-31
Publication
First Author: Shah VS
Year: 2016
Journal: Science
Title: Airway acidification initiates host defense abnormalities in cystic fibrosis mice.
Volume: 351
Issue: 6272
Pages: 503-7
Publication
First Author: Gee HY
Year: 2011
Journal: Cell
Title: Rescue of ΔF508-CFTR trafficking via a GRASP-dependent unconventional secretion pathway.
Volume: 146
Issue: 5
Pages: 746-60
Publication
First Author: Bruscia EM
Year: 2006
Journal: Proc Natl Acad Sci U S A
Title: Assessment of cystic fibrosis transmembrane conductance regulator (CFTR) activity in CFTR-null mice after bone marrow transplantation.
Volume: 103
Issue: 8
Pages: 2965-70
Publication
First Author: Sellers ZM
Year: 2013
Journal: J Cyst Fibros
Title: Left ventricular and aortic dysfunction in cystic fibrosis mice.
Volume: 12
Issue: 5
Pages: 517-24
Publication
First Author: Colledge WH
Year: 1995
Journal: Nat Genet
Title: Generation and characterization of a delta F508 cystic fibrosis mouse model.
Volume: 10
Issue: 4
Pages: 445-52
Publication
First Author: Delaney SJ
Year: 1996
Journal: EMBO J
Title: Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations.
Volume: 15
Issue: 5
Pages: 955-63
Publication
First Author: Oceandy D
Year: 2002
Journal: Hum Mol Genet
Title: Gene complementation of airway epithelium in the cystic fibrosis mouse is necessary and sufficient to correct the pathogen clearance and inflammatory abnormalities.
Volume: 11
Issue: 9
Pages: 1059-67
Publication
First Author: Zeiher BG
Year: 1995
Journal: J Clin Invest
Title: A mouse model for the delta F508 allele of cystic fibrosis.
Volume: 96
Issue: 4
Pages: 2051-64
Publication
First Author: Muchekehu RW
Year: 2010
Journal: J Physiol
Title: A new role for bicarbonate secretion in cervico-uterine mucus release.
Volume: 588
Issue: Pt 13
Pages: 2329-42
Publication
First Author: Paradis J
Year: 2010
Journal: J Cyst Fibros
Title: Osteopenia in Cftr-deltaF508 mice.
Volume: 9
Issue: 4
Pages: 239-45
Publication
First Author: Xu WM
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Cystic fibrosis transmembrane conductance regulator is vital to sperm fertilizing capacity and male fertility.
Volume: 104
Issue: 23
Pages: 9816-21
Publication
First Author: Alton EW
Year: 1993
Journal: Nat Genet
Title: Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice.
Volume: 5
Issue: 2
Pages: 135-42
Publication
First Author: Bazett M
Year: 2014
Journal: J Cyst Fibros
Title: Airway hyperresponsiveness in FVB/N delta F508 cystic fibrosis transmembrane conductance regulator mice.
Volume: 13
Issue: 4
Pages: 378-83
Publication
First Author: Kent G
Year: 1996
Journal: Pediatr Res
Title: Phenotypic abnormalities in long-term surviving cystic fibrosis mice.
Volume: 40
Issue: 2
Pages: 233-41
Publication
First Author: Dif F
Year: 2004
Journal: Bone
Title: Severe osteopenia in CFTR-null mice.
Volume: 35
Issue: 3
Pages: 595-603
Publication
First Author: Clarke LL
Year: 1992
Journal: Science
Title: Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis.
Volume: 257
Issue: 5073
Pages: 1125-8
Publication
First Author: Arquitt CK
Year: 2002
Journal: J Dent Res
Title: Cystic fibrosis transmembrane regulator gene (CFTR) is associated with abnormal enamel formation.
Volume: 81
Issue: 7
Pages: 492-6
Publication
First Author: Egan ME
Year: 2004
Journal: Science
Title: Curcumin, a major constituent of turmeric, corrects cystic fibrosis defects.
Volume: 304
Issue: 5670
Pages: 600-2
Publication
First Author: Liu Z
Year: 2017
Journal: Cell Death Differ
Title: CFTR-β-catenin interaction regulates mouse embryonic stem cell differentiation and embryonic development.
Volume: 24
Issue: 1
Pages: 98-110
Publication
First Author: Whitsett JA
Year: 1992
Journal: Nat Genet
Title: Human cystic fibrosis transmembrane conductance regulator directed to respiratory epithelial cells of transgenic mice.
Volume: 2
Issue: 1
Pages: 13-20