Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sara von Bahr"'
Publikováno v:
Journal of Lipid Research, Vol 44, Iss 8, Pp 1515-1522 (2003)
The mitochondrial sterol 27-hydroxylase (CYP27A1) is required for degradation of the C27-sterol side chain in bile acid biosynthesis. CYP27A1 seems, however, to have roles beyond this, as illustrated by patients with a deficient sterol 27-hydroxylase
Externí odkaz:
https://doaj.org/article/5766afb801ec443e9068d028deeed625
Autor:
Ingemar Björkhem, Lena Starck, Ulla Andersson, Dieter Lütjohann, Sara von Bahr, Irina Pikuleva, Amir Babiker, Ulf Diczfalusy
Publikováno v:
Journal of Lipid Research, Vol 42, Iss 3, Pp 366-371 (2001)
Infants with the cholesterol synthesis defect Smith-Lemli-Opitz syndrome (SLO) have reduced activity of the enzyme 7-dehydrocholesterol-7-reductase and accumulate 7-dehydrocholesterol, with the highest concentration in the brain. As a result of the g
Externí odkaz:
https://doaj.org/article/4f94ee2fa26640808e594ceb91475721
Autor:
Maria Olin, Elena Feinstein, Paolo Parini, Marjan Shafaati, Anita Lövgren-Sandblom, Ingemar Björkhem, Millicent Shafir, Anat Brafman, Maura Heverin, Lilian Larsson, Steve Meaney, Ulf Diczfalusy, Sara von Bahr
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 27:2191-2197
Objective— Characterization of cholesterol homeostasis in male mice with a genetic inactivation of 3β-hydroxysteroid-Δ 24 -reductase, causing replacement of almost all cholesterol with desmosterol. Methods and Results— There was an increase in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f4497c93fa9eeda496e72828ad8ff44
https://doi.org/10.1161/atvbaha.107.149823
https://doi.org/10.1161/atvbaha.107.149823
Autor:
Irina A. Pikuleva, Tomas Movin, Sara von Bahr, Nikos Papadogiannakis, Ulf Diczfalusy, Per Rönnow, Ingemar Björkhem
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 22:1129-1135
Objective — Tendon xanthomas are deposits of lipids and connective tissue commonly found in hypercholesterolemic patients. Macrophages are likely to be responsible for the lipid accumulation. Normolipidemic patients with the rare disease cerebroten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47b631d3e850e80c3511c509114deb17
https://doi.org/10.1161/01.atv.0000022600.61391.a5
https://doi.org/10.1161/01.atv.0000022600.61391.a5
Autor:
Jan Sjövall, Ingemar Björkhem, Sara von Bahr, Björn Fischler, Gunvor Alvelius, Ferdinand M. van't Hooft, Antal Nemeth
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 40(4)
BACKGROUND Inborn errors of bile acid synthesis are rare but potentially treatable causes of neonatal cholestasis. We here present a cholestatic infant with an ongoing cytomegalovirus infection who despite intensive treatment died of severe liver dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2741542b8f1ce0ebb3e3fd038cee048
https://pubmed.ncbi.nlm.nih.gov/15795599
https://pubmed.ncbi.nlm.nih.gov/15795599
Autor:
Ingemar Björkhem, Sven Bringman, Anna Strömsten, Masayumi Saeki, Sara von Bahr, Staffan Sahlin, Curt Einarsson
Publikováno v:
Journal of hepatology. 40(1)
Background/Aims : Cholesterolosis is characterized by accumulation of esterified cholesterol in human gallbladder mucosa. The present study aimed at investigating possible pathogenetic factors for cholesterolosis. The hypothesis was tested that a red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1f87f5c1e6d20322403777900d001bd
https://pubmed.ncbi.nlm.nih.gov/14672608
https://pubmed.ncbi.nlm.nih.gov/14672608
Autor:
Sara von Bahr
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition; Apr2005, Vol. 40 Issue 4, p481-486, 6p
Autor:
Sara von Bahr, Ulf Diczfalusy, Lena Starck, Ingemar Björkhem, Irina A. Pikuleva, Ulla Andersson, Dieter Lütjohann, Amir Babiker
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Journal of Lipid Research, Vol 42, Iss 3, Pp 366-371 (2001)
Scopus-Elsevier
Journal of Lipid Research, Vol 42, Iss 3, Pp 366-371 (2001)
Infants with the cholesterol synthesis defect Smith- Lemli-Opitz syndrome (SLO) have reduced activity of the enzyme 7-dehydrocholesterol-7-reductase and accumulate 7-dehydrocholesterol, with the highest concentration in the brain. As a result of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60f596db6cb3f0763c2b6fefaa9de2cf
http://europepmc.org/abstract/med/11254748
http://europepmc.org/abstract/med/11254748
