Table of Contents
60 relations: ABL (gene), Adenomatous polyposis coli, Adenosine triphosphate, ALS, Alzheimer's disease, Androgen receptor, Apoptosis, ATPase, Autoimmune disease, Cell adhesion molecule, Cell cycle, Cell growth, Creutzfeldt–Jakob disease, Cyclin-dependent kinase, Cytokine, Dementia, Enzyme, Eukaryote, Frontotemporal dementia, Gene, Heart failure, Huntington's disease, ICAM-1, Interleukin 8, Ischemia, Lupus, Lysosome, Malignancy, MHC class I, MOS (gene), Muscular dystrophy, MYB (gene), Myc, NF-κB, Nitric oxide, Oncogene, P-selectin, P53, Parkinson's disease, Prostaglandin, Protease, Proteasome, Protein c-Fos, Proteolysis, Proto-oncogene tyrosine-protein kinase Src, PSMD1, PSMD2, PSMD4, RAF kinase, Retinoblastoma, ... Expand index (10 more) »
ABL (gene)
Tyrosine-protein kinase ABL1 also known as ABL1 is a protein that, in humans, is encoded by the ABL1 gene (previous symbol ABL) located on chromosome 9.
Adenomatous polyposis coli
Adenomatous polyposis coli (APC) also known as deleted in polyposis 2.5 (DP2.5) is a protein that in humans is encoded by the APC gene.
See PSMD7 and Adenomatous polyposis coli
Adenosine triphosphate
Adenosine triphosphate (ATP) is a nucleotide that provides energy to drive and support many processes in living cells, such as muscle contraction, nerve impulse propagation, and chemical synthesis.
See PSMD7 and Adenosine triphosphate
ALS
Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND) or Lou Gehrig's disease in the United States, is a rare, terminal neurodegenerative disorder that results in the progressive loss of both upper and lower motor neurons that normally control voluntary muscle contraction.
See PSMD7 and ALS
Alzheimer's disease
Alzheimer's disease (AD) is a neurodegenerative disease that usually starts slowly and progressively worsens, and is the cause of 60–70% of cases of dementia.
See PSMD7 and Alzheimer's disease
Androgen receptor
The androgen receptor (AR), also known as NR3C4 (nuclear receptor subfamily 3, group C, member 4), is a type of nuclear receptor that is activated by binding any of the androgenic hormones, including testosterone and dihydrotestosterone, in the cytoplasm and then translocating into the nucleus.
See PSMD7 and Androgen receptor
Apoptosis
Apoptosis (from falling off) is a form of programmed cell death that occurs in multicellular organisms and in some eukaryotic, single-celled microorganisms such as yeast.
ATPase
ATPases (Adenosine 5'-TriPhosphatase, adenylpyrophosphatase, ATP monophosphatase, triphosphatase, SV40 T-antigen, ATP hydrolase, complex V (mitochondrial electron transport), (Ca2+ + Mg2+)-ATPase, HCO3−-ATPase, adenosine triphosphatase) are a class of enzymes that catalyze the decomposition of ATP into ADP and a free phosphate ion or the inverse reaction.
See PSMD7 and ATPase
Autoimmune disease
An autoimmune disease is a condition that results from an anomalous response of the adaptive immune system, wherein it mistakenly targets and attacks healthy, functioning parts of the body as if they were foreign organisms.
See PSMD7 and Autoimmune disease
Cell adhesion molecule
Cell adhesion molecules (CAMs) are a subset of cell surface proteins that are involved in the binding of cells with other cells or with the extracellular matrix (ECM), in a process called cell adhesion.
See PSMD7 and Cell adhesion molecule
Cell cycle
The cell cycle, or cell-division cycle, is the sequential series of events that take place in a cell that causes it to divide into two daughter cells.
Cell growth
Cell growth refers to an increase in the total mass of a cell, including both cytoplasmic, nuclear and organelle volume.
Creutzfeldt–Jakob disease
Creutzfeldt–Jakob disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is a fatal neurodegenerative disease.
See PSMD7 and Creutzfeldt–Jakob disease
Cyclin-dependent kinase
Cyclin-dependent kinases (CDKs) are a predominant group of serine/threonine protein kinases involved in the regulation of the cell cycle and its progression, ensuring the integrity and functionality of cellular machinery.
See PSMD7 and Cyclin-dependent kinase
Cytokine
Cytokines are a broad and loose category of small proteins (~5–25 kDa) important in cell signaling.
Dementia
Dementia is a syndrome associated with many neurodegenerative diseases, characterized by a general decline in cognitive abilities that affects a person's ability to perform everyday activities.
Enzyme
Enzymes are proteins that act as biological catalysts by accelerating chemical reactions.
See PSMD7 and Enzyme
Eukaryote
The eukaryotes constitute the domain of Eukarya or Eukaryota, organisms whose cells have a membrane-bound nucleus.
Frontotemporal dementia
Frontotemporal dementia (FTD), also called frontotemporal degeneration disease or frontotemporal neurocognitive disorder, encompasses several types of dementia involving the progressive degeneration of the brain's frontal and temporal lobes.
See PSMD7 and Frontotemporal dementia
Gene
In biology, the word gene has two meanings.
See PSMD7 and Gene
Heart failure
Heart failure (HF), also known as congestive heart failure (CHF), is a syndrome caused by an impairment in the heart's ability to fill with and pump blood.
Huntington's disease
Huntington's disease (HD), also known as Huntington's chorea, is an incurable neurodegenerative disease that is mostly inherited.
See PSMD7 and Huntington's disease
ICAM-1
ICAM-1 (Intercellular Adhesion Molecule 1) also known as CD54 (Cluster of Differentiation 54) is a protein that in humans is encoded by the ICAM1 gene.
See PSMD7 and ICAM-1
Interleukin 8
Interleukin 8 (IL-8 or chemokine (C-X-C motif) ligand 8, CXCL8) is a chemokine produced by macrophages and other cell types such as epithelial cells, airway smooth muscle cells and endothelial cells.
Ischemia
Ischemia or ischaemia is a restriction in blood supply to any tissue, muscle group, or organ of the body, causing a shortage of oxygen that is needed for cellular metabolism (to keep tissue alive).
Lupus
Lupus, technically known as systemic lupus erythematosus (SLE), is an autoimmune disease in which the body's immune system mistakenly attacks healthy tissue in many parts of the body.
See PSMD7 and Lupus
Lysosome
A lysosome is a single membrane-bound organelle found in many animal cells.
Malignancy
Malignancy is the tendency of a medical condition to become progressively worse; the term is most familiar as a characterization of cancer.
MHC class I
MHC class I molecules are one of two primary classes of major histocompatibility complex (MHC) molecules (the other being MHC class II) and are found on the cell surface of all nucleated cells in the bodies of vertebrates.
MOS (gene)
Proto-oncogene serine/threonine-protein kinase mos is an enzyme that in humans is encoded by the MOS gene.
Muscular dystrophy
Muscular dystrophies (MD) are a genetically and clinically heterogeneous group of rare neuromuscular diseases that cause progressive weakness and breakdown of skeletal muscles over time.
See PSMD7 and Muscular dystrophy
MYB (gene)
Myb genes are part of a large gene family of transcription factors found in animals and plants.
Myc
Myc is a family of regulator genes and proto-oncogenes that code for transcription factors.
See PSMD7 and Myc
NF-κB
Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) is a family of transcription factor protein complexes that controls transcription of DNA, cytokine production and cell survival.
See PSMD7 and NF-κB
Nitric oxide
Nitric oxide (nitrogen oxide or nitrogen monoxide) is a colorless gas with the formula.
Oncogene
An oncogene is a gene that has the potential to cause cancer.
P-selectin
P-selectin is a type-1 transmembrane protein that in humans is encoded by the SELP gene.
P53
p53, also known as Tumor protein P53, cellular tumor antigen p53 (UniProt name), or transformation-related protein 53 (TRP53) is a regulatory protein that is often mutated in human cancers.
See PSMD7 and P53
Parkinson's disease
Parkinson's disease (PD), or simply Parkinson's, is a long-term neurodegenerative disease of mainly the central nervous system that affects both the motor and non-motor systems of the body.
See PSMD7 and Parkinson's disease
Prostaglandin
Prostaglandins (PG) are a group of physiologically active lipid compounds called eicosanoids that have diverse hormone-like effects in animals.
Protease
A protease (also called a peptidase, proteinase, or proteolytic enzyme) is an enzyme that catalyzes proteolysis, breaking down proteins into smaller polypeptides or single amino acids, and spurring the formation of new protein products.
Proteasome
Proteasomes are protein complexes which degrade ubiquitin-tagged proteins by proteolysis, a chemical reaction that breaks peptide bonds.
Protein c-Fos
Protein c-Fos is a proto-oncogene that is the human homolog of the retroviral oncogene v-fos.
Proteolysis
Proteolysis is the breakdown of proteins into smaller polypeptides or amino acids.
Proto-oncogene tyrosine-protein kinase Src
Proto-oncogene tyrosine-protein kinase Src, also known as proto-oncogene c-Src, or simply c-Src (cellular Src; pronounced "sarc", as it is short for sarcoma), is a non-receptor tyrosine kinase protein that in humans is encoded by the SRC gene.
See PSMD7 and Proto-oncogene tyrosine-protein kinase Src
PSMD1
26S proteasome non-ATPase regulatory subunit 1, also as known as 26S Proteasome Regulatory Subunit Rpn2 (systematic nomenclature), is a protein that in humans is encoded by the PSMD1 gene.
See PSMD7 and PSMD1
PSMD2
26S proteasome non-ATPase regulatory subunit 2, also as known as 26S Proteasome Regulatory Subunit Rpn1 (systematic nomenclature), is an enzyme that in humans is encoded by the PSMD2 gene.
See PSMD7 and PSMD2
PSMD4
26S proteasome non-ATPase regulatory subunit 4, also as known as 26S Proteasome Regulatory Subunit Rpn10 (systematic nomenclature), is an enzyme that in humans is encoded by the PSMD4 gene.
See PSMD7 and PSMD4
RAF kinase
RAF kinases are a family of three serine/threonine-specific protein kinases that are related to retroviral oncogenes.
Retinoblastoma
Retinoblastoma (Rb) is a rare form of cancer that rapidly develops from the immature cells of a retina, the light-detecting tissue of the eye.
Rheumatoid arthritis
Rheumatoid arthritis (RA) is a long-term autoimmune disorder that primarily affects joints.
See PSMD7 and Rheumatoid arthritis
Sjögren syndrome
Sjögren syndrome or Sjögren's syndrome (SjS, SS) is a long-term autoimmune disease that primarily affects the body's exocrine glands, particularly the lacrimal and salivary glands.
See PSMD7 and Sjögren syndrome
STAT3
Signal transducer and activator of transcription 3 (STAT3) is a transcription factor which in humans is encoded by the STAT3 gene.
See PSMD7 and STAT3
Transcription factor
In molecular biology, a transcription factor (TF) (or sequence-specific DNA-binding factor) is a protein that controls the rate of transcription of genetic information from DNA to messenger RNA, by binding to a specific DNA sequence.
See PSMD7 and Transcription factor
Transcription factor Jun
Transcription factor Jun is a protein that in humans is encoded by the JUN gene.
See PSMD7 and Transcription factor Jun
Tumor necrosis factor
Tumor necrosis factor (TNF, cachexin, or cachectin; formerly known as tumor necrosis factor alpha, TNFα or TNF-α) is a cytokine and member of the TNF superfamily, which consists of various transmembrane proteins with a homologous TNF domain.
See PSMD7 and Tumor necrosis factor
Ubiquitin
Ubiquitin is a small (8.6 kDa) regulatory protein found in most tissues of eukaryotic organisms, i.e., it is found ''ubiquitously''.
VCAM-1
Vascular cell adhesion protein 1 also known as vascular cell adhesion molecule 1 (VCAM-1) or cluster of differentiation 106 (CD106) is a protein that in humans is encoded by the VCAM1 gene.
See PSMD7 and VCAM-1
Ventricular hypertrophy
Ventricular hypertrophy (VH) is thickening of the walls of a ventricle (lower chamber) of the heart.
See PSMD7 and Ventricular hypertrophy
Von Hippel–Lindau tumor suppressor
The Von Hippel–Lindau tumor suppressor also known as pVHL is a protein that, in humans, is encoded by the VHL gene.
See PSMD7 and Von Hippel–Lindau tumor suppressor
References
Also known as PSMD7 (gene).