Disease on EC 1.14.14.29 - 25/26-hydroxycholesterol 7alpha-hydroxylase
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25/26-hydroxycholesterol 7alpha-hydroxylase deficiency
25R,26-Hydroxycholesterol revisited: synthesis, metabolism, and biologic roles.
25/26-hydroxycholesterol 7alpha-hydroxylase deficiency
Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial.
25/26-hydroxycholesterol 7alpha-hydroxylase deficiency
Hippocampal 7?-Hydroxylated Neurosteroids Are Raised by Training and Bolster Remote Spatial Memory with Increase of the Spine Densities.
25/26-hydroxycholesterol 7alpha-hydroxylase deficiency
Mechanisms of disease: Inborn errors of bile acid synthesis.
25/26-hydroxycholesterol 7alpha-hydroxylase deficiency
Successful treatment of infantile oxysterol 7?-hydroxylase deficiency with oral chenodeoxycholic acid.
Adenocarcinoma
Regulation and expression of human CYP7B1 in prostate: overexpression of CYP7B1 during progression of prostatic adenocarcinoma.
Adrenoleukodystrophy
Case report of dysregulation of primary bile acid synthesis in a family with X-linked adrenoleukodystrophy.
Adrenoleukodystrophy
Exogenous Addition of 25-Hydroxycholesterol Reduces Level of Very Long-Chain Fatty Acids in X-Linked Adrenoleukodystrophy.
alpha-methylacyl-coa racemase deficiency
Mechanisms of disease: Inborn errors of bile acid synthesis.
Alzheimer Disease
Cholesterol 25-hydroxylase on chromosome 10q is a susceptibility gene for sporadic Alzheimer's disease.
Alzheimer Disease
Dehydroepiandrosterone 7-hydroxylase CYP7B: predominant expression in primate hippocampus and reduced expression in Alzheimer's disease.
Arthritis
DHEA metabolism in arthritis: a role for the p450 enzyme Cyp7b at the immune-endocrine crossroad.
Arthritis
Severity of murine collagen-induced arthritis correlates with increased CYP7B activity: enhancement of dehydroepiandrosterone metabolism by interleukin-1beta.
Arthritis, Experimental
CYP7B expression and activity in fibroblast-like synoviocytes from patients with rheumatoid arthritis: regulation by proinflammatory cytokines.
Arthritis, Experimental
Severity of murine collagen-induced arthritis correlates with increased CYP7B activity: enhancement of dehydroepiandrosterone metabolism by interleukin-1beta.
Arthritis, Rheumatoid
CYP7B expression and activity in fibroblast-like synoviocytes from patients with rheumatoid arthritis: regulation by proinflammatory cytokines.
Arthritis, Rheumatoid
DHEA metabolism in arthritis: a role for the p450 enzyme Cyp7b at the immune-endocrine crossroad.
Arthritis, Rheumatoid
Tumour necrosis factor-alpha stimulates dehydroepiandrosterone metabolism in human fibroblast-like synoviocytes: a role for nuclear factor-kappaB and activator protein-1 in the regulation of expression of cytochrome p450 enzyme 7b.
Ataxia
Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1.
Atherosclerosis
Increased 25-hydroxycholesterol concentrations in the lungs of patients with chronic obstructive pulmonary disease.
Atherosclerosis
The cholesterol metabolite 27-hydroxycholesterol promotes atherosclerosis via proinflammatory processes mediated by estrogen receptor alpha.
Breast Neoplasms
A potential role for the estrogen-metabolizing cytochrome P450 enzymes in human breast carcinogenesis.
Breast Neoplasms
Circulating 27-hydroxycholesterol and breast cancer tissue expression of CYP27A1, CYP7B1, LXR-?, and ER?: results from the EPIC-Heidelberg cohort.
Breast Neoplasms
Overexpression of G6PD is associated with high risks of recurrent metastasis and poor progression-free survival in primary breast carcinoma.
Breast Neoplasms
Recruitment of monocytes and epigenetic silencing of intratumoral CYP7B1 primarily contribute to the accumulation of 27-hydroxycholesterol in breast cancer.
Carcinoma, Hepatocellular
Transcriptional regulation of human oxysterol 7alpha-hydroxylase by sterol response element binding protein.
Central Nervous System Diseases
Reduced Plasma Levels of 25-Hydroxycholesterol and Increased Cerebrospinal Fluid Levels of Bile Acid Precursors in Multiple Sclerosis Patients.
Cerebellar Diseases
Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1.
Cholestasis
Successful treatment of infantile oxysterol 7?-hydroxylase deficiency with oral chenodeoxycholic acid.
Cholestasis
Transcriptional regulation of human oxysterol 7 alpha-hydroxylase gene (CYP7B1) by Sp1.
Cholestasis, Intrahepatic
AKR1D1 and CYP7B1 mutations in patients with inborn errors of bile acid metabolism: Possibly underdiagnosed diseases.
Cholestasis, Intrahepatic
Successful treatment of infantile oxysterol 7?-hydroxylase deficiency with oral chenodeoxycholic acid.
Cholestasis, Intrahepatic
The Interaction of PPAR? and CYP7B1 with ER?, ? Impacted the Occurrence and Development of Intrahepatic Cholestasis in Pregnant Rats.
Cholestasis, Intrahepatic
[Interaction among peroxisome proliferators-activated receptor alpha, cytochrome P450 oxysterol 7?-hydroxylase and estrogen receptor and its association with intrahepatic cholestasis in pregnant rats].
Colitis
Cholesterol 25-hydroxylase protects against experimental colitis in mice by modulating epithelial gut barrier function.
Colonic Neoplasms
MicroRNA-17 induces epithelial-mesenchymal transition consistent with the cancer stem cell phenotype by regulating CYP7B1 expression in colon cancer.
Colorectal Neoplasms
Characterisation of the oxysterol metabolising enzyme pathway in mismatch repair proficient and deficient colorectal cancer.
Coronary Disease
The effect of CYP7B1 polymorphisms on the risk of coronary heart disease in Hainan Han population.
COVID-19
Cholesterol 25-hydroxylase expression following immune activation in response to SARS-CoV-2 infection.
COVID-19
Cholesterol 25-Hydroxylase inhibits SARS-CoV-2 and coronaviruses by depleting membrane cholesterol.
Demyelinating Diseases
EBI2 Is Temporarily Upregulated in MO3.13 Oligodendrocytes during Maturation and Regulates Remyelination in the Organotypic Cerebellar Slice Model.
Diabetes Mellitus, Type 2
Androgen receptor overexpression in prostate cancer in type 2 diabetes.
Gallstones
Protective Effects of Yinchenhao Decoction on Cholesterol Gallstone in Mice Fed a Lithogenic Diet by Regulating LXR, CYP7A1, CYP7B1, and HMGCR Pathways.
Genetic Diseases, Inborn
CYP7B1: one cytochrome P450, two human genetic diseases, and multiple physiological functions.
Glaucoma
Molecular Karyotyping of a Dysmorphic Girl from Saudi Arabia with CYP1B1-negative Primary Congenital Glaucoma.
Glioblastoma
On the role of 25-hydroxycholesterol synthesis by glioblastoma cell lines. Implications for chemotactic monocyte recruitment.
Hemochromatosis
Iron Overload Coordinately Promotes Ferritin Expression and Fat Accumulation in Caenorhabditis elegans.
Hepatitis C
Identification of Cholesterol 25-Hydroxylase as a Novel Host Restriction Factor and a Part of the Primary Innate Immune Responses against Hepatitis C Virus Infection.
Infections
Cholesterol 25-Hydroxylase inhibits bovine parainfluenza virus type 3 replication through enzyme activity-dependent and -independent ways.
Infections
Cholesterol 25-hydroxylase suppresses porcine deltacoronavirus infection by inhibiting viral entry.
Infections
Identification of Cholesterol 25-Hydroxylase as a Novel Host Restriction Factor and a Part of the Primary Innate Immune Responses against Hepatitis C Virus Infection.
Infections
Testosterone response of hepatic gene expression in female mice having acquired testosterone-unresponsive immunity to Plasmodium chabaudi malaria.
Infections
Variants in the CYP7B1 gene region do not affect natural resistance to HIV-1 infection.
Insulin Resistance
Hepatic insulin resistance directly promotes formation of cholesterol gallstones.
Insulin Resistance
Insulin resistance dysregulates CYP7B1 leading to oxysterol accumulation: a pathway for NAFL to NASH transition.
Iron Overload
Iron Overload Coordinately Promotes Ferritin Expression and Fat Accumulation in Caenorhabditis elegans.
Lipid Metabolism Disorders
Imperatae rhizoma-Hedyotis diffusa Willd. herbal pair alleviates nephrotic syndrome by integrating anti-inflammatory and hypolipidaemic effects.
Liver Diseases
25R,26-Hydroxycholesterol revisited: synthesis, metabolism, and biologic roles.
Liver Diseases
Bile Acid Synthesis Disorders in Japan: Long-Term Outcome and Chenodeoxycholic Acid Treatment.
Liver Diseases
Complete Recovery of Oxysterol 7?-Hydroxylase Deficiency by Living Donor Transplantation in a 4-Month-Old Infant: the First Korean Case Report and Literature Review.
Liver Diseases
Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease.
Liver Diseases
Neonatal cholestatic liver disease in an Asian patient with a homozygous mutation in the oxysterol 7alpha-hydroxylase gene.
Liver Diseases
Successful treatment of infantile oxysterol 7?-hydroxylase deficiency with oral chenodeoxycholic acid.
Liver Failure
CYP7B1: one cytochrome P450, two human genetic diseases, and multiple physiological functions.
Liver Failure
Human steroid and oxysterol 7?-hydroxylase CYP7B1: substrate specificity, azole binding and misfolding of clinically relevant mutants.
Liver Failure
Successful treatment of infantile oxysterol 7?-hydroxylase deficiency with oral chenodeoxycholic acid.
Melanoma
An Interferon-Driven Oxysterol-Based Defense against Tumor-Derived Extracellular Vesicles.
Neoplasms
27-Hydroxycholesterol promotes cell-autonomous, ER-positive breast cancer growth.
Neoplasms
Circulating 27-hydroxycholesterol and breast cancer tissue expression of CYP27A1, CYP7B1, LXR-?, and ER?: results from the EPIC-Heidelberg cohort.
Neoplasms
CYP7B expression and activity in fibroblast-like synoviocytes from patients with rheumatoid arthritis: regulation by proinflammatory cytokines.
Neoplasms
DHEA metabolism in arthritis: a role for the p450 enzyme Cyp7b at the immune-endocrine crossroad.
Neoplasms
Hyperglycemic Ins2AkitaLdlr-/- mice show severely elevated lipid levels and increased atherosclerosis: a model of type 1 diabetic macrovascular disease.
Neoplasms
MicroRNA-17 induces epithelial-mesenchymal transition consistent with the cancer stem cell phenotype by regulating CYP7B1 expression in colon cancer.
Neoplasms
Regulation and expression of human CYP7B1 in prostate: overexpression of CYP7B1 during progression of prostatic adenocarcinoma.
Neoplasms
Regulation of intercellular biomolecule transfer-driven tumor angiogenesis and responses to anticancer therapies.
Neoplasms
Tumour necrosis factor-alpha stimulates dehydroepiandrosterone metabolism in human fibroblast-like synoviocytes: a role for nuclear factor-kappaB and activator protein-1 in the regulation of expression of cytochrome p450 enzyme 7b.
Neurodegenerative Diseases
Comparative modeling of 25-hydroxycholesterol-7?-hydroxylase (CYP7B1): ligand binding and analysis of hereditary spastic paraplegia type 5 CYP7B1 mutations.
Neurodegenerative Diseases
CYP7B1: novel mutations and magnetic resonance spectroscopy abnormalities in hereditary spastic paraplegia type 5A.
Neurodegenerative Diseases
Estrogen-mediated regulation of steroid metabolism in rat glial cells; effects on neurosteroid levels via regulation of CYP7B1-mediated catalysis.
Neurodegenerative Diseases
mRNA as a Novel Treatment Strategy for Hereditary Spastic Paraplegia Type 5.
Obesity
Cholesterol 25-hydroxylase (CH25H) as a promoter of adipose tissue inflammation in obesity and diabetes.
Osteoarthritis
The CH25H-CYP7B1-ROR? axis of cholesterol metabolism regulates osteoarthritis.
Paramyxoviridae Infections
Cholesterol 25-Hydroxylase inhibits bovine parainfluenza virus type 3 replication through enzyme activity-dependent and -independent ways.
Paraplegia
Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients.
Paraplegia
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations.
Paraplegia
CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
Paraplegia
CYP7B1: one cytochrome P450, two human genetic diseases, and multiple physiological functions.
Paraplegia
Cytochrome P450s in the synthesis of cholesterol and bile acids - from mouse models to human diseases.
Paraplegia
Elevated hydroxycholesterols in Norwegian patients with hereditary spastic paraplegia SPG5.
Paraplegia
Plasma oxysterols: biomarkers for diagnosis and treatment in spastic paraplegia type 5.
Pneumonia
Cholesterol 25-hydroxylase promotes efferocytosis and resolution of lung inflammation.
Porcine Reproductive and Respiratory Syndrome
Cholesterol 25-Hydroxylase Inhibits Porcine Reproductive and Respiratory Syndrome Virus Replication through Enzyme Activity-Dependent and -Independent Mechanisms.
Porcine Reproductive and Respiratory Syndrome
Cholesterol 25-hydroxylase is an interferon-inducible factor that protects against porcine reproductive and respiratory syndrome virus infection.
Porcine Reproductive and Respiratory Syndrome
Porcine reproductive and respiratory syndrome virus E protein degrades porcine cholesterol 25-hydroxylase via the ubiquitin-proteasome pathway.
Prostatic Hyperplasia
CYP7B generates a selective estrogen receptor beta agonist in human prostate.
Prostatic Intraepithelial Neoplasia
Regulation and expression of human CYP7B1 in prostate: overexpression of CYP7B1 during progression of prostatic adenocarcinoma.
Prostatic Neoplasms
A functional C-G polymorphism in the CYP7B1 promoter region and its different distribution in Orientals and Caucasians.
Prostatic Neoplasms
Regulation and expression of human CYP7B1 in prostate: overexpression of CYP7B1 during progression of prostatic adenocarcinoma.
Prostatic Neoplasms
Regulation of steroid hydroxylase CYP7B1 by androgens and estrogens in prostate cancer LNCaP cells.
Pseudorabies
Cholesterol 25-hydroxylase acts as a host restriction factor on pseudorabies virus replication.
Pulmonary Disease, Chronic Obstructive
Cholesterol metabolism promotes B-cell positioning during immune pathogenesis of chronic obstructive pulmonary disease.
Pulmonary Disease, Chronic Obstructive
Increased 25-hydroxycholesterol concentrations in the lungs of patients with chronic obstructive pulmonary disease.
Rabies
Cholesterol 25-hydroxylase suppresses rabies virus infection by inhibiting viral entry.
Spastic Paraplegia, Hereditary
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia.
Spastic Paraplegia, Hereditary
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations.
Spastic Paraplegia, Hereditary
Comparative modeling of 25-hydroxycholesterol-7?-hydroxylase (CYP7B1): ligand binding and analysis of hereditary spastic paraplegia type 5 CYP7B1 mutations.
Spastic Paraplegia, Hereditary
CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjects.
Spastic Paraplegia, Hereditary
CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
Spastic Paraplegia, Hereditary
CYP7B1: novel mutations and magnetic resonance spectroscopy abnormalities in hereditary spastic paraplegia type 5A.
Spastic Paraplegia, Hereditary
Elevated hydroxycholesterols in Norwegian patients with hereditary spastic paraplegia SPG5.
Spastic Paraplegia, Hereditary
Exome Sequencing Reveals a Novel Homozygous Frameshift Mutation in the CYP7B1 Gene in a Japanese Patient with SPG5.
Spastic Paraplegia, Hereditary
Generation of induced pluripotent stem cells (iPSCs) from a hereditary spastic paraplegia patient carrying a homozygous R486C mutation in CYP7B1 (SPG5).
Spastic Paraplegia, Hereditary
Generation of induced pluripotent stem cells (iPSCs) from a hereditary spastic paraplegia patient carrying a homozygous Y275X mutation in CYP7B1 (SPG5).
Spastic Paraplegia, Hereditary
Identification of 7?,24-dihydroxy-3-oxocholest-4-en-26-oic and 7?,25-dihydroxy-3-oxocholest-4-en-26-oic acids in human cerebrospinal fluid and plasma.
Spastic Paraplegia, Hereditary
Liver disease in infancy caused by oxysterol 7?-hydroxylase deficiency: successful treatment with chenodeoxycholic acid.
Spastic Paraplegia, Hereditary
mRNA as a Novel Treatment Strategy for Hereditary Spastic Paraplegia Type 5.
Spastic Paraplegia, Hereditary
Mutational analysis of the CYP7B1, PNPLA6 and C19orf12 genes in autosomal recessive hereditary spastic paraplegia.
Spastic Paraplegia, Hereditary
Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia.
Spastic Paraplegia, Hereditary
Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1.
Spastic Paraplegia, Hereditary
Successful treatment of infantile oxysterol 7?-hydroxylase deficiency with oral chenodeoxycholic acid.
Spinal Cord Injuries
Macrophage Migration Inhibitory Factor Promotes Chemotaxis of Astrocytes through Regulation of Cholesterol 25-Hydroxylase Following Rat Spinal Cord Injury.
Vaccinia
Cyp7b, a novel brain cytochrome P450, catalyzes the synthesis of neurosteroids 7alpha-hydroxy dehydroepiandrosterone and 7alpha-hydroxy pregnenolone.
Virus Diseases
Activation of liver X receptor plays a central role in antiviral actions of 25-hydroxycholesterol.
Virus Diseases
Cholesterol 25-hydroxylase is an interferon-inducible factor that protects against porcine reproductive and respiratory syndrome virus infection.
Virus Diseases
Cholesterol 25-hydroxylase suppresses rabies virus infection by inhibiting viral entry.
Virus Diseases
Identification of Cholesterol 25-Hydroxylase as a Novel Host Restriction Factor and a Part of the Primary Innate Immune Responses against Hepatitis C Virus Infection.
Xanthomatosis, Cerebrotendinous
Cholestenoic acids regulate motor neuron survival via liver X receptors.
Xanthomatosis, Cerebrotendinous
Mechanisms of disease: Inborn errors of bile acid synthesis.
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