Browse Items (22 total)
- Tags: gene
Knockdown Of Leptin A Expression Dramatically Alters Zebrafish Development
Tags: 2012, Akhter M, atlantic salmon, Auditory, bhlh genes, Bone, Brahmandam S, carp cyprinus-carpio, cell fate specification, central-nervous-system, Chen Y, Cloning, Dalman M, danio-rerio, differentiation, Endocrinology & Metabolism, gene, General and Comparative Endocrinology, Gregory A V, Journal Article or Conference Abstract Publication, Liu Q, Londraville R L, Lowe J, Metabolism, n-cadherin, Patel Y, Phelps D, Receptor, Riley C, sensory ganglia, Thakkar M, Visual, visual-system
One Multiplex Control For 29 Cystic Fibrosis Mutations
Evolutionary Changes Of The Importance Of Olfaction In Cetaceans Based On The Olfactory Marker Protein Gene
Exome Sequencing Reveals A Novel Wdr45 Frameshift Mutation And Inherited Polr3a Heterozygous Variants In A Female With A Complex Phenotype And Mixed Brain Mri Findings
Tags: 2015, 4H syndrome, accumulation, atp13a2 mutations, clinical spectrum, Demyelinating disease, diabetes-mellitus, European journal of medical genetics, gene, Genetics & Heredity, hallervorden-spatz-syndrome, hypogonadism, iron, Journal Article or Conference Abstract Publication, Khalifa M, Leukodystrophy, Naffaa L, NBIA, Neurodegeneration, POLR3A, spastic paraplegia spg35, WDR45, Whole Exome Sequencing
Congenital Hypomyelinating Neuropathy, Central Dysmyelination, And Waardenburg-hirschsprung Disease: Phenotypes Linked By Sox10 Mutation
Tags: 2002, Agamanolis D P, Annals of Neurology, Boerkoel C F, Crowe C, Department of Family & Community Medicine, expression, gene, Inoue K, Journal Article or Conference Abstract Publication, Lupski J R, NEOMED College of Medicine, Neurosciences & Neurology, Sawady J, Shilo K, transcription factor sox10
Hormonal-regulation Of Cholesterol-7-alpha-hydroxylase Messenger-rna Levels And Transcriptional Activity In Primary Rat Hepatocyte Cultures
Tags: 1992, bile-acid synthesis, Biochemistry & Molecular Biology, Chiang J Y L, chick-embryo hepatocytes, cholesterol 7-alpha-hydroxylase activity, circadian-rhythm, cyclic-amp, enzyme, gene, Gurley E C, Hylemon P B, Journal Article or Conference Abstract Publication, Journal of Biological Chemistry, Litz J S, Liver, malic, Metabolism, monolayer-cultures, Pandak W M, Stravitz R T, Vlahcevic Z R
Type Xxvii Collagen At The Transition Of Cartilage To Bone During Skeletogenesis
Tags: 2007, Bone, Bruckner P, Byers P H, Cartilage, chondrocyte, col27a1, COL27Al, endochondral, Endocrinology & Metabolism, expression, Fernandes R J, forms, gene, growth-plate, Hansen U, Hjorten R, ix, Jacquet R, Journal Article or Conference Abstract Publication, Krakow D, Landis W J, Pace J M, Sebald E, skeletogenesis, Telfer H E, type X-XVII collagen, Underwood R A, vertebrate fibrillar collagen, Wachsmann-Hogiu S, xi
Prevalence And Penetrance Of Zfpm2 Mutations And Deletions Causing Congenital Diaphragmatic Hernia
Tags: 2015, Ackerman K G, Andrews D, clinical genetics, Coletti C M, congenital diaphragmatic hernia, Darvishi K, defects, DNA copy number variation, Donahoe P K, Exome, fallot, FOG2, gene, Genetics & Heredity, High F A, Kashani A, Lage K, Lee C, Longoni M, Loscertales M, Maalouf F I, penetrance, Pober B R, Russell M K, tetralogy, Tracy A A, variants, Ward-Melver C, Woods S A, ZFPM2
Role Of Genetic Polymorphisms Of Ion Channels In The Pathophysiology Of Coronary Microvascular Dysfunction And Ischemic Heart Disease
Tags: 2013, artery-disease, Atherosclerosis, Atrial fibrillation, Basic research in cardiology, Canali E, Cardiovascular System & Cardiology, Chilian W M, Coronary microcirculation, De Marchis M L, dysfunction, Endothelial, Endothelium, Fedele F, gene, Genetic polymorphisms, Guadagni F, Ion Channels, Ischemic heart disease, k-atp channels, kir6.2, late sodium current, Logan S, Mancone M, nitric-oxide, Palmirotta R, sensitive potassium channels, Severino P, smooth-muscle, type-2 diabetes-mellitus, Vascular, Volterrani M
Regulation of cholesterol 7 alpha-hydroxylase gene (CYP7A1) transcription by the liver orphan receptor (LXR alpha)
Tags: 2001, Bile acid synthesis, BILE acids, Chiang J Y L, coup-tfii, cytochrome P450, dietary-cholesterol, expression, gene, Gene Regulation, Genetics & Heredity, hepg2 cells, Journal Article or Conference Abstract Publication, Kimmel R, Ligands, Nuclear Receptor, Nuclear Receptors, pathway, promoter, reverse cholesterol transport, Signaling, Stroup D, x-receptor
Regulation of human sterol 27-hydroxylase gene (CYP27A1) by bile acids and hepatocyte nuclear factor 4 alpha (HNF4 alpha)
Tags: 2003, alpha-fetoprotein transcription factor, Bile acid synthesis, cerebrotendinous xanthomatosis, Chen W L, Chiang J Y L, cholesterol 7-alpha-hydroxylase, cholic-acid, Down-Regulation, factor 4-alpha, Farnesoid X receptor, gene, Genetics & Heredity, hepatocytes, heterodimer partner, Journal Article or Conference Abstract Publication, Liver, negative feedback-regulation, Nuclear Receptor, rat, Small, transcriptional regulation, x-receptor
Hormonal regulation of cholesterol 7 alpha-hydroxylase specific activity, mRNA levels, and transcriptional activity in vivo in the rat
Tags: 1997, bile-acid biosynthesis, Biochemistry & Molecular Biology, Chiang J Y L, Cholesterol, cholesterol 7 alpha-hydroxylase, cultures, gene, gene cyp7, Glucocorticoid, hepatic cholesterol, hepatocyte cultures, Heuman D M, Hylemon P B, Journal Article, Journal of lipid research, Liver, messenger-rna levels, monolayer-cultures, Pandak W M, primary, protein-kinase-c, Redford K, regulation, sterol 27-hydroxylase, Stravitz R T, thyroid, thyroid-hormone, Vlahcevic Z R
CONSISTENT CHROMOSOME-ABNORMALITIES IN SQUAMOUS-CELL CARCINOMA OF THE VULVA
Tags: 1991, bowenoid papulosis, Cancer, Carey T E, colorectal carcinomas, DNA, Gasser K M, gene, Genes Chromosomes & Cancer, Genetics & Heredity, Grenman R, Grenman S E, Hopkins M P, identification, Journal Article, neoplasia, oncology, Prostate, Roberts J A, Schwartz D R, Tumor, tumorigenic expression, Vandyke D L, wilms, Worsham M J
Reduced Paneth cell alpha-defensins in ileal Crohn's disease
Tags: 2005, Bacteria, Bevins C L, Chu H T, expression, Feathers R W, Fellermann K, Ganz T, gene, human intestinal defensin, inflammatory bowel disease, Innate, Innate immunity, Intestine, Journal Article, Lima H, Linzmeier R, mechanisms, microflora, mutations, Nuding S, Peptides, Petras R E, Porter E, Proceedings of the National Academy of Sciences of the United States of America, Salzman N H, Schaeffeler E, Schwab M, Science & Technology - Other Topics, Shen B, Stange E F, Wehkamp J, Weichenthal M
The antiviral xanthate compound D609 inhibits herpes simplex virus type 1 replication and protein phosphorylation
The Ras-related protein AGS1/RASD1 suppresses cell growth
Tags: 2004, activation, AGS1, Apoptosis, binding protein, Biochemistry & Molecular Biology, Brown K D, Cancer, Cell Biology, Cismowski M J, coupled receptors, Dexras1, G protein, gene, Genetics &, Heredity, hormone, identification, Integration, Journal Article, Lanier S M, Oncogene, oncology, RASD1, signal-transduction, Vaidyanathan G, Vincent T S, Wang G S
Hepatic Forkhead Box Protein A3 Regulates ApoA-I (Apolipoprotein A-I) Expression, Cholesterol Efflux, and Atherogenesis
Tags: 2019, activation, and vascular biology, Arteriosclerosis, Arteriosclerosis, thrombosis, and vascular biology, Atherosclerosis, Cardiovascular System & Cardiology, cholesterol efflux, Department of Integrative Medical Sciences, fatty-acids, FOXA3, gene, Hematology, high-density-lipoprotein, increased, Jadhav Kavita, Li Yuanyuan, Liver, Macrophages, mice lacking, NEOMED College of Medicine, nuclear factor 3-gamma, September 2019 Update, Thrombosis, transport, Xu Yanyong, Yin Liya, Zhang Yanqiao, Zhu Yingdong
Homozygosity for a mutation affecting the catalytic domain of tyrosyl-tRNA synthetase (YARS) causes multisystem disease
Tags: 2019, Adult, Antonellis Anthony, Baras Aris, Biochemistry & Molecular Biology, Brigatti Karlla W, Carson Vincent J, Catalytic Domain, Child, Demczko Matthew M, Female, Fox Michael D, Furuya Katryn N, gene, Genetic Diseases, Genetic Predisposition to Disease, Genetics & Heredity, Gonzaga-Jauregui Claudia, Griffin Laurie B, Hearing Loss, Heterozygote, Homozygote, Human molecular genetics, Humans, impairment, Inborn, Infant, Jinks Robert N, Kandula Vinay V R, lactic-acidosis, Loss of Function Mutation, Male, Martinez Erick D, mechanisms, Miles Lili, Mutation, myopathy, NEOMED College of Medicine Student, NEOMED Student Publications, Newborn, onset, Overton John D, Pedigree, Phenotype, phenotypic variability, Poskitt Laura, Preschool, Puffenberger Erik G, Radhakrishnan Kadakkal, recessive mutations, Reid Jeffrey G, Sensorineural, September 2019 Update, Severity of Illness Index, Strauss Kevin A, swiss-model, Tyrosine-tRNA Ligase, variant, Wenger Olivia K, Whole Exome Sequencing, Williams Katie B, Yeasts, Yoder Mark A
Transcriptional regulation of human oxysterol 7 alpha-hydroxylase gene (CYP7B1) by Sp1.
Tags: 2001, Base Sequence, Binding, Binding Sites/genetics, Cell Line, Chiang J Y, Competitive, CpG Islands/genetics, Cultured, Cytochrome P-450 Enzyme System/*genetics/metabolism, Cytochrome P450 Family 7, Department of Integrative Medical Sciences, DNA/genetics, Enzymologic, gene, Gene Expression Regulation, Genetic, Humans, Luciferases/genetics/metabolism, Molecular Sequence Data, Mutagenesis, NEOMED College of Medicine, Nucleic Acid/genetics, Protein Binding, Recombinant Fusion Proteins/genetics/metabolism, Regulatory Sequences, Sequence Deletion, Site-Directed, Sp1 Transcription Factor/metabolism/*physiology, Steroid Hydroxylases/*genetics/metabolism, Transcription, Transfection, Tumor Cells, Wu Z
Regulation of cholesterol 7alpha-hydroxylase gene (CYP7A1) transcription by the liver orphan receptor (LXRalpha).
Tags: 2001, Animals, Binding Sites, Cells, Chiang J Y, Cholesterol 7-alpha-Hydroxylase/drug effects/*genetics/metabolism, Cricetinae, Cultured, Department of Integrative Medical Sciences, gene, Gene Expression Regulation/drug effects, Genetic, Humans, Hydroxycholesterols, Kimmel R, Liver/physiology, Lovastatin/pharmacology, Luciferases/genetics/metabolism, Mevalonic Acid/metabolism/pharmacology, NEOMED College of Medicine, Nicotinic Acids/pharmacology, Organ Specificity, Polyisoprenyl Phosphates/pharmacology, Rats, Receptors, Response Elements, Retinoic Acid/genetics/metabolism, Retinoid X Receptors, Species Specificity, Steroid/genetics/*metabolism, Stroup D, Tetrahydronaphthalenes/pharmacology, Transcription, Transcription Factors/genetics/metabolism, Transfection
Regulation of human sterol 27-hydroxylase gene (CYP27A1) by bile acids and hepatocyte nuclear factor 4alpha (HNF4alpha).
Tags: *DNA-Binding Proteins, 2003, Base Sequence, Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, Bile Acids and Salts/*pharmacology, Binding Sites/genetics, Cell Line, Chen Wenling, Chenodeoxycholic Acid/pharmacology, Chiang John Y L, Cholestanetriol 26-Monooxygenase, Cloning, Cultured, Cytoplasmic and Nuclear/genetics/metabolism, Department of Integrative Medical Sciences, DNA, DNA/chemistry/genetics, Dose-Response Relationship, Drug, gene, Gene Expression Regulation/drug effects, Genetic/*genetics, Hepatocyte Nuclear Factor 4, Humans, Luciferases/genetics/metabolism, Molecular, Molecular Sequence Data, Mutagenesis, Mutation, NEOMED College of Medicine, Phosphoproteins/genetics/*metabolism, Promoter Regions, Receptors, Recombinant Fusion Proteins/genetics/metabolism, Response Elements/genetics, Sequence Analysis, Site-Directed, Steroid Hydroxylases/*genetics, Transcription Factors/genetics/*metabolism, Transfection, Tumor Cells