B. F. Kase

发表

Characterization of an Acyl-CoA Thioesterase That Functions as a Major Regulator of Peroxisomal Lipid Metabolism*

M. Hunt, K. Solaas, B. F. Kase, 2002, The Journal of Biological Chemistry.

P. Ueland, H. Refsum, K. Meyer, 2004, The Journal of pediatrics.

A nine year follow-up study of patients with lymphoedema cholestasis syndrome 1 (LCS1/Aagenaes syndrome)

K. Retterstøl, B. F. Kase, K. Holven, 2018, Scandinavian journal of clinical and laboratory investigation.

attention, and behaviour high dose thyroxine treatment on adult memory, Congenital hypothyroidism: no adverse effects of

K. Sundet, S. Heyerdahl, B. F. Kase, 2006 .

Congenital hypothyroidism: influence of disease severity and L-thyroxine treatment on intellectual, motor, and school-associated outcomes in young adults.

K. Sundet, S. Heyerdahl, B. F. Kase, 2003, Pediatrics.

Linear growth in early treated children with congenital hypothyroidism

A. Larsson, S. Heyerdahl, B. F. Kase, 1997, Acta paediatrica.

New insights into bile acid amidation

M. Hunt, K. Solaas, B. F. Kase, 2005 .

Presence of choloyl- and chenodeoxycholoyl-coenzyme A thioesterase activity in human liver

O. Søreide, K. Solaas, B. F. Kase, 2000, Scandinavian journal of clinical and laboratory investigation.

Formation of chenodeoxycholic acid from 3 a , 7 a = di hydroxy-5 ~-cholestanoic acid by rat liver peroxisomes

J. I. Pedersen, K. Prydz, B. F. Kase, 2002 .

Role of liver peroxisomes in bile acid formation: inborn error of C27-steroid side chain cleavage in peroxisome deficiency (Zellweger syndrome).

B. F. Kase, 1989, Scandinavian journal of clinical and laboratory investigation.

In vivo and vitro studies on formation of bile acids in patients with Zellweger syndrome. Evidence that peroxisomes are of importance in the normal biosynthesis of both cholic and chenodeoxycholic acid.

B. Strandvik, J. I. Pedersen, I. Björkhem, 1985, The Journal of clinical investigation.

Sulphation of lithocholic acid in the colon-carcinoma cell line CaCo-2.

K. Prydz, S. O. Kolset, B. Halvorsen, 1999, The Biochemical journal.

Liver Peroxisomes and Bile Acid Formation

J. I. Pedersen, K. Prydz, I. Björkhem, 1987 .

Nutritional Consequences of Adhering to a Low Phenylalanine Diet for Late-Treated Adults with PKU : Low Phe Diet for Adults with PKU.

E. B. Løken, B. F. Kase, K. Motzfeldt, 2012, JIMD reports.

High pressure liquid chromatography solvent systems for studies of bile acid biosynthesis.

J. I. Pedersen, K. Prydz, B. F. Kase, 1988, Journal of lipid research.

Metabolism of prostaglandin F2 alpha in Zellweger syndrome. Peroxisomal beta-oxidation is a major importance for in vivo degradation of prostaglandins in humans.

I. Björkhem, U. Diczfalusy, B. F. Kase, 1991, The Journal of clinical investigation.

Differential Regulation of Cytosolic and Peroxisomal Bile Acid Amidation by Ppar ␣ Activation Favors the Formation of Unconjugated Bile Acids

K. Bamberg, M. Hunt, K. Solaas, 2022 .

Subcellular organization of bile acid amidation in human liver: a key issue in regulating the biosynthesis of bile salts.

K. Solaas, B. F. Kase, A. Ulvestad, 2000, Journal of lipid research.

In vitro formation of bile acids from di- and trihydroxy-5 beta-cholestanoic acid in human liver peroxisomes.

J. I. Pedersen, K. Prydz, I. Björkhem, 1986, Biochimica et biophysica acta.

Urinary excretion of dicarboxylic acids from patients with the Zellweger syndrome. Importance of peroxisomes in beta-oxidation of dicarboxylic acids.

B. Strandvik, J. I. Pedersen, I. Björkhem, 1984, Biochimica et biophysica acta.

Simple diagnosis of the Zellweger syndrome by gas-liquid chromatography of dimethylacetals.

I. Björkhem, R. Blomstrand, B. F. Kase, 1986, Journal of lipid research.

Peroxisomal chain-shortening of thromboxane B2: evidence for impaired degradation of thromboxane B2 in Zellweger syndrome.

U. Diczfalusy, E. Lund, B. F. Kase, 1993, Journal of lipid research.

Mechanism of peroxisomal 24-hydroxylation of 3α,7α,12α-trihydroxy-5β-cholestanoic acid in rat liver

J. I. Pedersen, I. Björkhem, B. F. Kase, 1984 .

Infantile Refsum's disease: A generalized peroxisomal disorder Case report with postmortem examination

S. Torp, A. Torvik, O. Skjeldal, 1988, Journal of the Neurological Sciences.

Peroxisomal dysfunction in a boy with neurologic symptoms and amaurosis (Leber disease): clinical and biochemical findings similar to those observed in Zellweger syndrome.

J. I. Pedersen, I. Björkhem, B. F. Kase, 1986, The Journal of pediatrics.

Adrenoleukodystrophy. The chain shortening of erucic acid (22:1(n-9)) and adrenic acid (22:4(n-6)) is deficient in neonatal adrenoleukodystrophy and normal in X-linked adrenoleukodistrophy skin fibroblasts.

T. Hagve, B. F. Kase, B. Christophersen, 1989, Biochimica et biophysica acta.

Influence of human plasma or serum albumin on ADP- or vasopressin-induced calcium increases in human platelets.

B. F. Kase, O. S. Pedersen, K. L. Reichelt, 1994, Scandinavian journal of clinical and laboratory investigation.

Congenital hypothyroidism: no adverse effects of high dose thyroxine treatment on adult memory, attention, and behaviour

K. Sundet, S. Heyerdahl, B. F. Kase, 2005, Archives of Disease in Childhood.

Intellectual development in children with congenital hypothyroidism in relation to recommended thyroxine treatment.

Sverre O. Lie, S. Heyerdahl, B. F. Kase, 1991, The Journal of pediatrics.

Screening for serum total homocysteine in newborn children.

P. Ueland, A. Guttormsen, H. Refsum, 2004, Clinical chemistry.

Defective peroxisomal cleavage of the C27-steroid side chain in the cerebro-hepato-renal syndrome of Zellweger.

J. I. Pedersen, I. Björkhem, B. F. Kase, 1985, The Journal of clinical investigation.

Betwixt and between being healthy and ill: the stigma experienced by young adults with phenylketonuria

B. F. Kase, Lisbet Grut, I. Wiig, 2015 .

Differential regulation of cytosolic and peroxisomal bile acid amidation by PPARα activation favors the formation of unconjugated bile acids Published, JLR Papers in Press, March 16, 2004. DOI 10.1194/jlr.M300291-JLR200

K. Bamberg, M. Hunt, K. Solaas, 2004, Journal of Lipid Research.

Urinary Peptides in Rett Syndrome

K. Reichelt, M. L. G. Gardner, O. Skjeldal, 2002, Autism : the international journal of research and practice.

Evaluation of novel assays in clinical chemistry: quantification of plasma total homocysteine.

R. Clarke, P. Ueland, E. Nexo, 2000, Clinical chemistry.

Importance of peroxisomes in the formation of chenodeoxycholic acid in human liver. Metabolism of 3 alpha,7 alpha-dihydroxy-5 beta-cholestanoic acid in Zellweger syndrome.

J. I. Pedersen, I. Björkhem, B. F. Kase, 1991, Pediatric Research.

Importance of Peroxisomes in the Formation of Chenodeoxycholic Acid in Human Liver. Metabolism of 3α,7α-Dihydroxy-5β-cholestanoic Acid in Zellweger Syndrome

J. I. Pedersen, I. Björkhem, B. F. Kase, 1991, Pediatric Research.

Peroxisomal bile acid-CoA:amino-acid N-acyltransferase in rat liver.

I. Björkhem, B. F. Kase, 1989, The Journal of biological chemistry.

Subcellular localization of 3 alpha, 7 alpha-dihydroxy- and 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoyl-coenzyme A ligase(s) in rat liver.

J. I. Pedersen, K. Prydz, I. Björkhem, 1988, Journal of lipid research.

Role of peroxisomes in the biosynthesis of bile acids.

J. I. Pedersen, I. Björkhem, B. F. Kase, 1985, Scandinavian journal of clinical and laboratory investigation. Supplementum.

Conjugation of cholic acid with taurine and glycine by rat liver peroxisomes.

J. I. Pedersen, K. Prydz, I. Björkhem, 1986, Biochemical and biophysical research communications.

Formation of chenodeoxycholic acid from 3 alpha, 7 alpha-dihydroxy-5 beta-cholestanoic acid by rat liver peroxisomes.

J. I. Pedersen, K. Prydz, I. Björkhem, 1986, Journal of lipid research.

Metabolism of Prostaglandin F 2 st in Zellweger Syndrome Peroxisomal #-Oxidation Is of Major Importance for In Vivo Degradation of Prostaglandins in Humans

U. Diczfalusy, B. F. Kase, S. Alexson, 2013 .

Studies on the degradation of [U-3H]-phytanic acid and [U-3H]-pristanic acid in cultured fibroblasts from children with peroxisomal disorders.

I. Björkhem, B. F. Kase, Ingemar Björkhem, 1996, Scandinavian journal of clinical and laboratory investigation.