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Search results 401 to 459 out of 459 for Abcb1b

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0.021s
Type Details Score
Publication  
First Author: Venglovecz V
Year: 2018
Journal: Front Physiol
Title: The Importance of Aquaporin 1 in Pancreatitis and Its Relation to the CFTR Cl- Channel.
Volume: 9
Pages: 854
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: 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: Bodewes FA
Year: 2015
Journal: PLoS One
Title: Cholic acid induces a Cftr dependent biliary secretion and liver growth response in mice.
Volume: 10
Issue: 2
Pages: e0117599
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: Khan D
Year: 2019
Journal: Sci Rep
Title: Short-term CFTR inhibition reduces islet area in C57BL/6 mice.
Volume: 9
Issue: 1
Pages: 11244
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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: Berczeli O
Year: 2018
Journal: Invest Ophthalmol Vis Sci
Title: Novel Insight Into the Role of CFTR in Lacrimal Gland Duct Function in Mice.
Volume: 59
Issue: 1
Pages: 54-62
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: 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: Valverde MA
Year: 1993
Journal: Pflugers Arch
Title: Inactivation of the murine cftr gene abolishes cAMP-mediated but not Ca(2+)-mediated secretagogue-induced volume decrease in small-intestinal crypts.
Volume: 425
Issue: 5-6
Pages: 434-8
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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: Manson AL
Year: 1997
Journal: EMBO J
Title: Complementation of null CF mice with a human CFTR YAC transgene.
Volume: 16
Issue: 14
Pages: 4238-49
Genotype
Symbol: Cftr/Cftr
Background: involves: 129S/SvEv
Zygosity: hm
Has Mutant Allele: true
Strain
Attribute String: congenic, mutant strain, targeted mutation
Strain
Attribute String: targeted mutation, mutant strain, congenic
Genotype
Symbol: Abcb1a/Abcb1a Abcb1b/Abcb1b
Background: involves: 129P2/OlaHsd * FVB
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Abcb1a/Abcb1a Abcb1b/Abcb1b
Background: FVBTac.129P2-Abcb1b Abcb1a
Zygosity: cx
Has Mutant Allele: true
Publication
First Author: Ibold B
Year: 2019
Journal: Lipids Health Dis
Title: Abcc6 deficiency in mice leads to altered ABC transporter gene expression in metabolic active tissues.
Volume: 18
Issue: 1
Pages: 2
Publication
First Author: Binder AK
Year: 2013
Journal: Endocrinology
Title: The absence of ER-β results in altered gene expression in ovarian granulosa cells isolated from in vivo preovulatory follicles.
Volume: 154
Issue: 6
Pages: 2174-87
Publication
First Author: Singh AK
Year: 2010
Journal: Am J Physiol Cell Physiol
Title: The switch of intestinal Slc26 exchangers from anion absorptive to HCOFormula secretory mode is dependent on CFTR anion channel function.
Volume: 298
Issue: 5
Pages: C1057-65
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
HT Experiment
Series Id: GSE44651
Experiment Type: transcription profiling by array
Study Type: WT vs. Mutant
Source: ArrayExpress
Strain
Attribute String: targeted mutation, mutant strain, congenic
Genotype
Symbol: Abcb1a/Abcb1a Abcb1b/Abcb1b Abcc2/Abcc2
Background: FVB.129P2-Abcb1b Abcb1a Abcc2
Zygosity: cx
Has Mutant Allele: true
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: 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: Reynaert I
Year: 2000
Journal: Mol Reprod Dev
Title: Morphological changes in the vas deferens and expression of the cystic fibrosis transmembrane conductance regulator (CFTR) in control, deltaF508 and knock-out CFTR mice during postnatal life.
Volume: 55
Issue: 2
Pages: 125-35
Strain
Attribute String: transgenic, mutant strain, targeted mutation, congenic
Strain
Attribute String: congenic, mutant strain, targeted mutation, transgenic
Strain
Attribute String: targeted mutation, mutant strain, congenic
Strain
Attribute String: mutant strain, targeted mutation, deletion
Genotype
Symbol: Abcb1a/Abcb1a Abcb1b/Abcb1b Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr/?
Background: FVB.Cg-Abcb1b Abcb1a Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Abcb1a/Abcb1a Abcb1b/Abcb1b Tg(Thy1-APPDutch)#Jckr/?
Background: FVB.Cg-Abcb1b Abcb1a Tg(Thy1-APPDutch)#Jckr
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Abcb1a/Abcb1a Abcb1b/Abcb1b Cyp3a13/Cyp3a13 Del(5Cyp3a57-Cyp3a59)2Nki/Del(5Cyp3a57-Cyp3a59)2Nki
Background: FVB.129P2-Abcb1a Abcb1b Cyp3a13 Del(5Cyp3a57-Cyp3a59)2Nki
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Abcb1a/Abcb1a Abcb1b/Abcb1b Abcc2/Abcc2 Cyp3a13/Cyp3a13 Del(5Cyp3a57-Cyp3a59)2Nki/Del(5Cyp3a57-Cyp3a59)2Nki
Background: involves: 129P2/OlaHsd
Zygosity: cx
Has Mutant Allele: true