|
Syntaxin 1
|
D050827 |
[A neuronal cell membrane protein that combines with SNAP-25 and SYNAPTOBREVIN 2 to form a SNARE complex that leads to EXOCYTOSIS.
] |
|
Syntaxin 16
|
D051438 |
[A ubiquitously expressed member of the syntaxin subfamily of SNARE proteins that localizes to the GOLGI APPARATUS.
] |
|
Syntenins
|
D053676 |
[Intracellular signaling adaptor proteins that play a role in the coupling of SYNDECANS to CYTOSKELETAL PROTEINS.
] |
|
Synteny
|
D026801 |
[The presence of two or more genetic loci on the same chromosome. Extensions of this original definition refer to the similarity in content and organization between chromosomes, of different species for example.
, The similarity between chromosome segments or chromosomes in the linear arrangement of genes (GENE ORDER) or genetic markers.
] |
|
Synthetic Biology
|
D058615 |
[A field of biological research combining engineering in the formulation, design, and building (synthesis) of novel biological structures, functions, and systems.
] |
|
Synthetic Drugs
|
D000076742 |
[Legal or illegal drugs created using SYNTHETIC CHEMISTRY TECHNIQUES.
] |
|
Synthetic Lethal Mutations
|
D000072020 |
[Mutations in genes which lead to cell or organism death when occurring in combination with mutations in one or more other genes.
] |
|
Synucleinopathies
|
D000080874 |
[Neurodegenerative disorders involving deposition of abnormal ALPHA-SYNUCLEIN in dopaminergic neurons and glial cells in the brain. Pathological aggregations of alpha-synuclein proteins results in LEWY BODIES and Lewy neurites; melanin granules in the SUBSTANTIA NIGRA and LOCUS COERULEUS; and glial cytoplasmic inclusions. Synucleinopathies are associated with mutation in the ALPHA-SYNUCLEIN (SNCA) gene on chromosome 4. PARKINSON DISEASE; LEWY BODY DISEASE with dementia; and MULTIPLE SYSTEM ATROPHY are prominent examples of synucleinopathy.
] |
|
Synucleins
|
D051843 |
[A family of homologous proteins of low MOLECULAR WEIGHT that are predominately expressed in the BRAIN and that have been implicated in a variety of human diseases. They were originally isolated from CHOLINERGIC FIBERS of TORPEDO.
] |
|
Syphilis
|
D013587 |
[A contagious venereal disease caused by the spirochete TREPONEMA PALLIDUM.
] |
|
Syphilis Serodiagnosis
|
D013588 |
[Serologic tests for syphilis.
] |
|
Syphilis, Cardiovascular
|
D013589 |
[Cardiovascular manifestations of SYPHILIS, an infection of TREPONEMA PALLIDUM. In the late stage of syphilis, sometimes 20-30 years after the initial infection, damages are often seen in the blood vessels including the AORTA and the AORTIC VALVE. Clinical signs include syphilitic aortitis, aortic insufficiency, or aortic ANEURYSM.
] |
|
Syphilis, Congenital
|
D013590 |
[Syphilis acquired in utero and manifested by any of several characteristic tooth (Hutchinson's teeth) or bone malformations and by active mucocutaneous syphilis at birth or shortly thereafter. Ocular and neurologic changes may also occur.
] |
|
Syphilis, Cutaneous
|
D013591 |
[Cutaneous lesions arising from infection with Treponema pallidum. In the primary stage, 18-21 days following infection, one or more chancres appear. If untreated, the subsequent stages of the disease appear as syphilids. These eruptions are superficial, nondestructive, exanthematic, transient, macular roseolas that may later be maculopapular or papular polymorphous or scaly, pustular, pigmented eruptions.(Arnold, Odom, and James, Andrew's Diseases of the Skin, 8th ed, p409)
] |
|
Syphilis, Latent
|
D013592 |
[The stage of syphilis that occurs following the primary (CHANCRE) and secondary stages. The patient is asymptomatic at the latent stage but remains seropositive for the SPIROCHETE.
] |
|
Syria
|
D013593 |
[Country in the Middle East, bordering the Mediterranean Sea, between Lebanon and Turkey. The capital is Damascus.
] |
|
Syringa
|
D031662 |
[A plant genus of the family OLEACEAE. Oleuropein has been identified in the stem bark.
] |
|
Syringes
|
D013594 |
[Instruments used for injecting or withdrawing fluids. (Stedman, 25th ed)
] |
|
Syringoma
|
D018252 |
[A benign tumor of the sweat glands which is usually multiple and results from malformation of sweat ducts. It is uncommon and more common in females than in males. It is most likely to appear at adolescence, and further lesions may develop during adult life. It does not appear to be hereditary. (Rook et al., Textbook of Dermatology, 4th ed, pp2407-8)
] |
|
Syringomyelia
|
D013595 |
[Longitudinal cavities in the spinal cord, most often in the cervical region, which may extend for multiple spinal levels. The cavities are lined by dense, gliogenous tissue and may be associated with SPINAL CORD NEOPLASMS; spinal cord traumatic injuries; and vascular malformations. Syringomyelia is marked clinically by pain and PARESTHESIA, muscular atrophy of the hands, and analgesia with thermoanesthesia of the hands and arms, but with the tactile sense preserved (sensory dissociation). Lower extremity spasticity and incontinence may also develop. (From Adams et al., Principles of Neurology, 6th ed, p1269)
] |
