Christiane Albrecht

Summary

Country: Germany

Publications

  1. ncbi request reprint Two novel missense mutations in ABCA1 result in altered trafficking and cause severe autosomal recessive HDL deficiency
    Christiane Albrecht
    MRC Clinical Sciences Centre, Hammersmith Hospital, Faculty of Medicine, Imperial College, Du Cane Road, London W12 ONN, UK
    Biochim Biophys Acta 1689:47-57. 2004
  2. ncbi request reprint The ABCA subfamily--gene and protein structures, functions and associated hereditary diseases
    Christiane Albrecht
    Physiology Weihenstephan, Technical University Munich, Freising, Germany
    Pflugers Arch 453:581-9. 2007
  3. ncbi request reprint A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome
    Christiane Albrecht
    Medical Research Council Clinical Sciences Centre, Faculty of Medicine, Imperial College, Hammersmith Hospital Campus, London, United Kingdom
    Blood 106:542-9. 2005
  4. ncbi request reprint Degradation of Cry1Ab protein from genetically modified maize in the bovine gastrointestinal tract
    Bodo Lutz
    Physiology Weihenstephan, Technical University Munich, Weihenstephaner Berg 3, D 85350 Freising, Germany
    J Agric Food Chem 53:1453-6. 2005
  5. doi request reprint Differential expression of ABC transporters and their regulatory genes during lactation and dry period in bovine mammary tissue
    Carolin Farke
    Physiology Weihenstephan, Technical University Munich, 85354 Freising, Germany
    J Dairy Res 75:406-14. 2008
  6. pmc Type 2 diabetes is associated with reduced ATP-binding cassette transporter A1 gene expression, protein and function
    Dipesh C Patel
    Division of Medicine, Imperial College London, London, United Kingdom
    PLoS ONE 6:e22142. 2011
  7. doi request reprint Sensitive and highly specific quantitative real-time PCR and ELISA for recording a potential transfer of novel DNA and Cry1Ab protein from feed into bovine milk
    Patrick Guertler
    Physiology Weihenstephan, Technische Universitat Munchen, Weihenstephaner Berg 3, 85350, Freising, Germany
    Anal Bioanal Chem 393:1629-38. 2009
  8. doi request reprint A novel enzyme immunoassay specific for ABCA1 protein quantification in human tissues and cells
    Vijay Paul
    Physiology Weihenstephan, Technical University Munich, Weihenstephaner Berg 3, 85350 Freising, Germany
    J Lipid Res 49:2259-67. 2008
  9. ncbi request reprint Accelerated exposure of phosphatidylserine on lymphocyte populations from patients with systemic lupus erythematosus or rheumatoid arthritis
    Christiane Albrecht
    MRC CSC, Membrane Transport Biology, London, UK
    Thromb Haemost 93:989-92. 2005
  10. ncbi request reprint Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients
    Theodosios Kyriakou
    Human Genetics Division, School of Medicine, University of Southampton, UK
    Hum Mol Genet 16:1412-22. 2007

Collaborators

Detail Information

Publications11

  1. ncbi request reprint Two novel missense mutations in ABCA1 result in altered trafficking and cause severe autosomal recessive HDL deficiency
    Christiane Albrecht
    MRC Clinical Sciences Centre, Hammersmith Hospital, Faculty of Medicine, Imperial College, Du Cane Road, London W12 ONN, UK
    Biochim Biophys Acta 1689:47-57. 2004
    ..Both mutations prevent normal trafficking of ABCA1, thereby explaining their inability to mediate apoA1-dependent lipid efflux...
  2. ncbi request reprint The ABCA subfamily--gene and protein structures, functions and associated hereditary diseases
    Christiane Albrecht
    Physiology Weihenstephan, Technical University Munich, Freising, Germany
    Pflugers Arch 453:581-9. 2007
    ..The objective of this review is to summarize the literature for this subfamily of ABC transporter proteins, excluding ABCA1 and ABCA4, which will be discussed in other chapters of this issue...
  3. ncbi request reprint A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome
    Christiane Albrecht
    Medical Research Council Clinical Sciences Centre, Faculty of Medicine, Imperial College, Hammersmith Hospital Campus, London, United Kingdom
    Blood 106:542-9. 2005
    ..These data identify a mutation in ABCA1 that contributes to the defective PS translocation phenotype in our patient with SS...
  4. ncbi request reprint Degradation of Cry1Ab protein from genetically modified maize in the bovine gastrointestinal tract
    Bodo Lutz
    Physiology Weihenstephan, Technical University Munich, Weihenstephaner Berg 3, D 85350 Freising, Germany
    J Agric Food Chem 53:1453-6. 2005
    ..It was concluded that Cry1Ab protein is degraded during digestion in cattle. To avoid misinterpretation, samples tested positive for Cry1Ab protein by ELISA should be reassessed by another technique...
  5. doi request reprint Differential expression of ABC transporters and their regulatory genes during lactation and dry period in bovine mammary tissue
    Carolin Farke
    Physiology Weihenstephan, Technical University Munich, 85354 Freising, Germany
    J Dairy Res 75:406-14. 2008
    ..The current mRNA expression analysis of transporters in the mammary gland is the prerequisite for elucidating novel molecular mechanisms underlying cholesterol and lipid transfer into milk...
  6. pmc Type 2 diabetes is associated with reduced ATP-binding cassette transporter A1 gene expression, protein and function
    Dipesh C Patel
    Division of Medicine, Imperial College London, London, United Kingdom
    PLoS ONE 6:e22142. 2011
    ....
  7. doi request reprint Sensitive and highly specific quantitative real-time PCR and ELISA for recording a potential transfer of novel DNA and Cry1Ab protein from feed into bovine milk
    Patrick Guertler
    Physiology Weihenstephan, Technische Universitat Munchen, Weihenstephaner Berg 3, 85350, Freising, Germany
    Anal Bioanal Chem 393:1629-38. 2009
    ....
  8. doi request reprint A novel enzyme immunoassay specific for ABCA1 protein quantification in human tissues and cells
    Vijay Paul
    Physiology Weihenstephan, Technical University Munich, Weihenstephaner Berg 3, 85350 Freising, Germany
    J Lipid Res 49:2259-67. 2008
    ..37 +/- 0.82 vs. 17.03 +/- 4.25 microg/g tissue; P < 0.01). The novel ELISA enables the quantification of ABCA1 protein in human tissues and confirms previous semiquantitative immunoblot results...
  9. ncbi request reprint Accelerated exposure of phosphatidylserine on lymphocyte populations from patients with systemic lupus erythematosus or rheumatoid arthritis
    Christiane Albrecht
    MRC CSC, Membrane Transport Biology, London, UK
    Thromb Haemost 93:989-92. 2005
  10. ncbi request reprint Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients
    Theodosios Kyriakou
    Human Genetics Division, School of Medicine, University of Southampton, UK
    Hum Mol Genet 16:1412-22. 2007
    ..A trend towards higher symptom onset age in 825I allele carriers was observed. The data indicate an influence of common ABCA1 functional polymorphisms on age of symptom onset in CAD patients...
  11. ncbi request reprint Characterisation of lymphocyte responses to Ca2+ in Scott syndrome
    James I Elliott
    Thromb Haemost 91:412-5. 2004