All terms in MeSH

Label Id Description
Receptor Activity-Modifying Protein 1 D12.776.476.024.414.100
Receptor Activity-Modifying Proteins D12.776.476.024.414
Oncostatin M D12.644.276.374.562
Janus Kinase 2 D12.776.624.664.700.117
fms-Like Tyrosine Kinase 3 D12.776.624.664.700.114
G2 Phase D016195 [The period of the CELL CYCLE following DNA synthesis (S PHASE) and preceding M PHASE (cell division phase). The CHROMOSOMES are tetraploid in this point. ]
Microtubule Proteins D12.776.220.600
S Phase D016196 [Phase of the CELL CYCLE following G1 and preceding G2 when the entire DNA content of the nucleus is replicated. It is achieved by bidirectional replication at multiple sites along each chromosome. ]
Palliative Medicine D065126 [A branch of medicine concerned with preventing and relieving the suffering of patients in any stage of disease. Its focus is on comprehensive care and improving the quality of all areas of the patient's life. ]
Dopamine D2 Receptor Antagonists D065127 [Compounds and drugs that bind to and inhibit or block the activation of DOPAMINE D2 RECEPTORS. ]
Deoxyribonuclease HpaII D08.811.277.352.355.325.300.260.300
Dental High-Speed Equipment E06.186.376
Endothelin Receptor Antagonists D065128 [Compounds and drugs that bind to and inhibit or block the activation of ENDOTHELIN RECECPTORS. ]
Ammotherapy E02.056.020
Balneology E02.056
Pre-Exposure Prophylaxis D065129 [A method of disease prevention (abbreviated PrEP) which involves the administration of drugs to at-risk persons who have not been exposed to the disease-causing agent. ]
Carboplatin D016190 [An organoplatinum compound that possesses antineoplastic activity. ]
Receptors, Granulocyte Colony-Stimulating Factor D016188 [Receptors that bind and internalize GRANULOCYTE COLONY-STIMULATING FACTOR. Their MW is believed to be 150 kD. These receptors are found mainly on a subset of myelomonocytic cells. ]
KRIT1 Protein D12.776.624.664.700.119
Dystrophin D016189 [A muscle protein localized in surface membranes which is the product of the Duchenne/Becker muscular dystrophy gene. Individuals with Duchenne muscular dystrophy usually lack dystrophin completely while those with Becker muscular dystrophy have dystrophin of an altered size. It shares features with other cytoskeletal proteins such as SPECTRIN and alpha-actinin but the precise function of dystrophin is not clear. One possible role might be to preserve the integrity and alignment of the plasma membrane to the myofibrils during muscle contraction and relaxation. MW 400 kDa. ]