UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 101

Sortiert nach

Human copper transporter 2 is localized in late endosomes and lysosomes and facilitates cellular copper uptake

Biochemical journal, 2007-10, Vol.407 (1), p.49-59

2007

Volltextzugriff (PDF)

A flippase‐independent function of ATP8B1, the protein affected in familial intrahepatic cholestasis type 1, is required for apical protein expression and microvillus formation in polarized epithelial cells

Hepatology (Baltimore, Md.), 2010-06, Vol.51 (6), p.2049-2060

2010

Volltextzugriff (PDF)

Liver-specific Commd1 knockout mice are susceptible to hepatic copper accumulation

PloS one, 2011-12, Vol.6 (12), p.e29183-e29183

2011

Volltextzugriff (PDF)

Reduced expression of ATP7B affected by Wilson disease–causing mutations is rescued by pharmacological folding chaperones 4‐phenylbutyrate and curcumin

Hepatology (Baltimore, Md.), 2009-12, Vol.50 (6), p.1783-1795

2009

Volltextzugriff (PDF)

Farnesoid X receptor activation inhibits inflammation and preserves the intestinal barrier in inflammatory bowel disease

Gut, 2011-04, Vol.60 (4), p.463-472

2011

Volltextzugriff (PDF)

Monitoring bile acid transport in single living cells using a genetically encoded Förster resonance energy transfer sensor

Hepatology (Baltimore, Md.), 2013-02, Vol.57 (2), p.740-752

2013

Volltextzugriff (PDF)

Raised hepatic bile acid concentrations during pregnancy in mice are associated with reduced farnesoid X receptor function

Hepatology (Baltimore, Md.), 2010-10, Vol.52 (4), p.1341-1349

2010

Volltextzugriff (PDF)

ATP8B1 is essential for maintaining normal hearing

Proceedings of the National Academy of Sciences - PNAS, 2009-06, Vol.106 (24), p.9709-9714

2009

Volltextzugriff (PDF)

The gene product Murr1 restricts HIV-1 replication in resting CD4 + lymphocytes

Nature, 2003-12, Vol.426 (6968), p.853-857

2003

Volltextzugriff (PDF)

Variation of Linker Length in Ratiometric Fluorescent Sensor Proteins Allows Rational Tuning of Zn(II) Affinity in the Picomolar to Femtomolar Range

Journal of the American Chemical Society, 2007-03, Vol.129 (12), p.3494-3495

2007

Volltextzugriff (PDF)

Cisplatin Rapidly Down-regulates Its Own Influx Transporter hCTR1 in Cultured Human Ovarian Carcinoma Cells

Clinical cancer research, 2004-10, Vol.10 (19), p.6744-6749

2004

Volltextzugriff (PDF)

The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression

Cellular and molecular life sciences : CMLS, 2012-01, Vol.69 (1), p.149-163

2012

Volltextzugriff (PDF)

Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis

Hepatology (Baltimore, Md.), 2006-01, Vol.43 (1), p.51-53

2006

Volltextzugriff (PDF)

Liver disease associated with canalicular transport defects: Current and future therapies

Journal of hepatology, 2010-02, Vol.52 (2), p.258-271

2010

Volltextzugriff (PDF)

Folding defects in P‐type ATP 8B1 associated with hereditary cholestasis are ameliorated by 4‐phenylbutyrate

Hepatology (Baltimore, Md.), 2010-01, Vol.51 (1), p.286-296

2010

Volltextzugriff (PDF)

The Copper Metabolism MURR1 domain protein 1 (COMMD1) modulates the aggregation of misfolded protein species in a client-specific manner

PloS one, 2014-04, Vol.9 (4), p.e92408-e92408

2014

Volltextzugriff (PDF)

D-serine in the developing human central nervous system

Annals of neurology, 2006-10, Vol.60 (4), p.476-480

2006

Volltextzugriff (PDF)

New developments in the regulation of intestinal copper absorption

Nutrition reviews, 2009-11, Vol.67 (11), p.658-672

2009

Volltextzugriff (PDF)

Increased concentrations of both NMDA receptor co-agonists d-serine and glycine in global ischemia: a potential novel treatment target for perinatal asphyxia

Amino acids, 2012-07, Vol.43 (1), p.355-363

2012

Volltextzugriff (PDF)

Two Mass-Spectrometric Techniques for Quantifying Serine Enantiomers and Glycine in Cerebrospinal Fluid: Potential Confounders and Age-Dependent Ranges

Clinical chemistry (Baltimore, Md.), 2008-09, Vol.54 (9), p.1443-1450

2008

Volltextzugriff (PDF)

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

Hepatology (Baltimore, Md.), 2004-07, Vol.40 (1), p.27-38

2004

Volltextzugriff (PDF)

Transcription Factor Sp1 Plays an Important Role in the Regulation of Copper Homeostasis in Mammalian Cells

Molecular pharmacology, 2008-09, Vol.74 (3), p.705-713

2008

Volltextzugriff (PDF)

Ratiometric Fluorescent Sensor Proteins with Subnanomolar Affinity for Zn(II) Based on Copper Chaperone Domains

Journal of the American Chemical Society, 2006-08, Vol.128 (33), p.10754-10762

2006

Volltextzugriff (PDF)

Posttranslational regulation of copper transporters

Journal of biological inorganic chemistry, 2010, Vol.15 (1), p.37-46

2010

Volltextzugriff (PDF)

Cu,Zn Superoxide Dismutase Maturation and Activity Are Regulated by COMMD1

The Journal of biological chemistry, 2010-09, Vol.285 (37), p.28991-29000

2010

Volltextzugriff (PDF)

1 – 25 von 101

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(101)
Mit Volltextzugriff
(98)

Publikationsform

Artikel
(101)

Sprache

Englisch
(101)
Japanisch
(35)

Erscheinungsjahr

n.n

Thema

Science & Technology
(79)
Life Sciences & Biomedicine
(72)
Humans
(71)
Animals
(35)
Biological And Medical Sciences
(31)
Medical Sciences
(28)
Biochemistry & Molecular Biology
(24)
Copper - Metabolism
(24)
Mice
(21)
Copper
(19)
Gastroenterology & Hepatology
(18)
Adenosine Triphosphatases - Genetics
(16)
Mutation
(16)
Adaptor Proteins, Signal Transducing
(14)
Female
(14)
Gastroenterology. Liver. Pancreas. Abdomen
(14)
Homeostasis
(14)
Molecular Sequence Data
(14)
Male
(13)
Amino Acid Sequence
(12)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Human copper transporter 2 is localized in late endosomes and lysosomes and facilitates cellular copper uptake

A flippase‐independent function of ATP8B1, the protein affected in familial intrahepatic cholestasis type 1, is required for apical protein expression and microvillus formation in polarized epithelial cells

Liver-specific Commd1 knockout mice are susceptible to hepatic copper accumulation

Reduced expression of ATP7B affected by Wilson disease–causing mutations is rescued by pharmacological folding chaperones 4‐phenylbutyrate and curcumin

Farnesoid X receptor activation inhibits inflammation and preserves the intestinal barrier in inflammatory bowel disease

Monitoring bile acid transport in single living cells using a genetically encoded Förster resonance energy transfer sensor

Raised hepatic bile acid concentrations during pregnancy in mice are associated with reduced farnesoid X receptor function

ATP8B1 is essential for maintaining normal hearing

The gene product Murr1 restricts HIV-1 replication in resting CD4 + lymphocytes

Variation of Linker Length in Ratiometric Fluorescent Sensor Proteins Allows Rational Tuning of Zn(II) Affinity in the Picomolar to Femtomolar Range

Cisplatin Rapidly Down-regulates Its Own Influx Transporter hCTR1 in Cultured Human Ovarian Carcinoma Cells

The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression

Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis

Liver disease associated with canalicular transport defects: Current and future therapies

Folding defects in P‐type ATP 8B1 associated with hereditary cholestasis are ameliorated by 4‐phenylbutyrate

The Copper Metabolism MURR1 domain protein 1 (COMMD1) modulates the aggregation of misfolded protein species in a client-specific manner

D-serine in the developing human central nervous system

New developments in the regulation of intestinal copper absorption

Increased concentrations of both NMDA receptor co-agonists d-serine and glycine in global ischemia: a potential novel treatment target for perinatal asphyxia

Two Mass-Spectrometric Techniques for Quantifying Serine Enantiomers and Glycine in Cerebrospinal Fluid: Potential Confounders and Age-Dependent Ranges

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

Transcription Factor Sp1 Plays an Important Role in the Regulation of Copper Homeostasis in Mammalian Cells

Ratiometric Fluorescent Sensor Proteins with Subnanomolar Affinity for Zn(II) Based on Copper Chaperone Domains

Posttranslational regulation of copper transporters

Cu,Zn Superoxide Dismutase Maturation and Activity Are Regulated by COMMD1

Suchergebnisse filtern