Terminology Service < Semantic Lookup Platform

All terms in MESH

Label	Id	Description
GPR173 protein, mouse	C578985
TUBB1 protein, human	C578986
3,4'-dihydroxystilbene	C578987
Yuwen02f1	C578988
PON2 protein, mouse	C578990
HMX3 protein, human	C578991
Arg-Pro-Phe-His-Leu-Leu-Val-Tyr-AMC	C000605929
Gemini of Coiled Bodies	D055531	[Small, punctate nuclear structures found in close proximity to COILED BODIES. They are enriched with SMN COMPLEX PROTEINS and may play a role in the processing of SMALL NUCLEAR RIBONUCLEOPROTEINS.]
Intranuclear Space	D042581	[The area within the CELL NUCLEUS.]
2-(4-(hexyloxy)benzyl)-1-methylquinuclidin-1-ium	C000605930
Molecular Chaperones	D018832	[A family of cellular proteins that mediate the correct assembly or disassembly of polypeptides and their associated ligands. Although they take part in the assembly process, molecular chaperones are not components of the final structures.]
RNA-Binding Proteins	D016601	[Proteins that bind to RNA molecules. Included here are RIBONUCLEOPROTEINS and other proteins whose function is to bind specifically to RNA.]
Brca1 protein, mouse	C000605931
Survival of Motor Neuron 1 Protein	D055533	[An SMN complex protein that contains a TUDOR DOMAIN and is essential for the function of the SMN protein complex. In humans, the protein is encoded by a single gene found near the inversion TELOMERE of a large inverted region of CHROMOSOME 5. Mutations in the gene coding for survival of motor neuron 1 protein may result in SPINAL MUSCULAR ATROPHIES OF CHILDHOOD.]
NB-360	C000605932
Bulbo-Spinal Atrophy, X-Linked	D055534	[An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.]
Muscular Atrophy, Spinal	D009134	[A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)]
Genetic Diseases, X-Linked	D040181	[Genetic diseases that are linked to gene mutations on the X CHROMOSOME in humans (X CHROMOSOME, HUMAN) or the X CHROMOSOME in other species. Included here are animal models of human X-linked diseases.]
GCN1 protein, human	C000605933
Morgellons Disease	D055535	[An unexplained illness which is characterized by skin manifestations including non-healing lesions, itching, and the appearance of fibers.]