All individuals in MeSH

Label Id Description
tert-Butylhydroperoxide D020122 [A direct-acting oxidative stress-inducing agent used to examine the effects of oxidant stress on Ca(2+)-dependent signal transduction in vascular endothelial cells. It is also used as a catalyst in polymerization reactions and to introduce peroxy groups into organic molecules. ]
trans-1,4-Bis(2-chlorobenzaminomethyl)cyclohexane Dihydrochloride D001371 [An anti-cholesteremic agent that inhibits delta 7-reductase, delta 14 reductase, and sterol biosynthesis. ]
trans-Golgi Network D021601 [A network of membrane compartments, located at the cytoplasmic side of the GOLGI APPARATUS, where proteins and lipids are sorted for transport to various locations in the cell or cell membrane. ]
vif Gene Products, Human Immunodeficiency Virus D054320 [Proteins encoded by the VIF GENES of the HUMAN IMMUNODEFICIENCY VIRUS. ]
von Ebner Glands D054838 [Small tubulo-alveolar salivary glands located beneath the circumvallate and foliate papillae. ]
von Hippel-Lindau Disease D006623 [An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions. ]
von Willebrand Disease, Type 1 D056725 [A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR. ]
von Willebrand Disease, Type 2 D056728 [A subtype of von Willebrand disease that results from qualitative deficiencies of VON WILLEBRAND FACTOR. The subtype is divided into several variants with each variant having a distinctive pattern of PLATELET-interaction. ]
von Willebrand Disease, Type 3 D056729 [A subtype of von Willebrand disease that results from a total or near total deficiency of VON WILLEBRAND FACTOR. ]
von Willebrand Diseases D014842 [Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion. ]
von Willebrand Factor D014841 [A high-molecular-weight plasma protein, produced by endothelial cells and megakaryocytes, that is part of the factor VIII/von Willebrand factor complex. The von Willebrand factor has receptors for collagen, platelets, and ristocetin activity as well as the immunologically distinct antigenic determinants. It functions in adhesion of platelets to collagen and hemostatic plug formation. The prolonged bleeding time in VON WILLEBRAND DISEASES is due to the deficiency of this factor. ]
vpr Gene Products, Human Immunodeficiency Virus D054325 [Proteins encoded by the VPR GENES of the HUMAN IMMUNODEFICIENCY VIRUS. ]
zeta Carotene D024321 [A carotenoid produced in most carotenogenic organisms. It is one of several sequentially synthesized molecules that are precursors to BETA CAROTENE. ]
zeta-Crystallins D038226 [A group of crystallins that have been found in the lens (LENS, CRYSTALLINE) of certain species of VERTEBRATES including GUINEA PIGS; CAMELS; and LLAMAS. They are inactivated forms of NAD(P)H DEHYDROGENASE (QUINONE). ]
zeta-Globins D055543 [A member of the alpha-globin family. In humans, zeta-globin is encoded in the alpha-globin gene cluster located on CHROMOSOME 16. Two zeta-globin chains combine with two EPSILON GLOBIN chains to form the embryonic HEMOGLOBIN Gower 1. ]