[HTML][HTML] Potential beneficial effects of butyrate in intestinal and extraintestinal diseases
RB Canani, M Di Costanzo, L Leone… - World journal of …, 2011 - ncbi.nlm.nih.gov
The multiple beneficial effects on human health of the short-chain fatty acid butyrate,
synthesized from non-absorbed carbohydrate by colonic microbiota, are well documented …
synthesized from non-absorbed carbohydrate by colonic microbiota, are well documented …
X‐linked adrenoleukodystrophy: pathology, pathophysiology, diagnostic testing, newborn screening and therapies
Adrenoleukodystrophy (ALD) is a rare X‐linked disease caused by a mutation of the
peroxisomal ABCD1 gene. This review summarizes our current understanding of the …
peroxisomal ABCD1 gene. This review summarizes our current understanding of the …
ABC transporters: human disease and pharmacotherapeutic potential
Adenosine triphosphate (ATP)-binding cassette (ABC) transporters are a 48-member
superfamily of membrane proteins that actively transport a variety of biological substrates …
superfamily of membrane proteins that actively transport a variety of biological substrates …
Mammalian ABC transporters in health and disease
P Borst, RO Elferink - Annual review of biochemistry, 2002 - annualreviews.org
▪ Abstract The ATP-binding cassette (ABC) transporters are a family of large proteins in
membranes and are able to transport a variety of compounds through membranes against …
membranes and are able to transport a variety of compounds through membranes against …
Adrenoleukodystrophy–neuroendocrine pathogenesis and redefinition of natural history
S Kemp, IC Huffnagel, GE Linthorst… - Nature Reviews …, 2016 - nature.com
X-Linked adrenoleukodystrophy (ALD) is a peroxisomal metabolic disorder with a highly
complex clinical presentation. ALD is caused by mutations in the ABCD1 gene, which leads …
complex clinical presentation. ALD is caused by mutations in the ABCD1 gene, which leads …
Biochemistry of mammalian peroxisomes revisited
RJA Wanders, HR Waterham - Annu. Rev. Biochem., 2006 - annualreviews.org
In this review, we describe the current state of knowledge about the biochemistry of
mammalian peroxisomes, especially human peroxisomes. The identification and …
mammalian peroxisomes, especially human peroxisomes. The identification and …
Peroxisomal ROS control cytosolic Mycobacterium tuberculosis replication in human macrophages
E Pellegrino, B Aylan, C Bussi, A Fearns… - Journal of Cell …, 2023 - rupress.org
Peroxisomes are organelles involved in many metabolic processes including lipid
metabolism, reactive oxygen species (ROS) turnover, and antimicrobial immune responses …
metabolism, reactive oxygen species (ROS) turnover, and antimicrobial immune responses …
Addison's disease 2001
S Ten, M New, N Maclaren - The Journal of Clinical …, 2001 - academic.oup.com
Whereas it is now more than 150 yr since T. Addison first described the clinical and
pathological features of adrenal failure, the disease remains underdiagnosed, leading to …
pathological features of adrenal failure, the disease remains underdiagnosed, leading to …
Clinical and experimental applications of sodium phenylbutyrate
T Iannitti, B Palmieri - Drugs in R & D, 2011 - Springer
Histone acetyltransferase and histone deacetylase are enzymes responsible for histone
acetylation and deacetylation, respectively, in which the histones are acetylated and …
acetylation and deacetylation, respectively, in which the histones are acetylated and …
X-linked adrenoleukodystrophy
HW Moser, A Mahmood, GV Raymond - Nature Clinical Practice …, 2007 - nature.com
Abstract X-linked adrenoleukodystrophy (X-ALD) is caused by a defect in the gene ABCD1,
which maps to Xq28 and codes for a peroxisomal membrane protein that is a member of the …
which maps to Xq28 and codes for a peroxisomal membrane protein that is a member of the …