- spastin
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spastin
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Spastin — Masse/Länge Primärstruktur 616 aa … Deutsch Wikipedia
Spastin — The human gene SPAST codes for the microtubule severing protein of the same name, commonly known as spastin [cite journal | author = Roll Mecak A, Vale RD | title = Structural basis of microtubule severing by the hereditary spastic paraplegia… … Wikipedia
Autosomal dominant hereditary spastic paraplegia — A degenerative disorder of nerves with progressive spasticity of the legs. Abbreviated as AD HSP. Spasticity is a state of increased muscle tone. Paraplegia refers to the legs (quadriplegia refers to both the arms and legs). In hereditary spastic … Medical dictionary
Hereditary spastic paraplegia, autosomal dominant — A degenerative disorder of nerves with progressive spasticity of the legs. Abbreviated as AD HSP. Spasticity is a state of increased muscle tone. Paraplegia refers to the legs (quadriplegia refers to both the arms and legs). In hereditary spastic … Medical dictionary
Spastic paraplegia, autosomal dominant — A degenerative disorder of nerves with progressive spasticity of the legs. Abbreviated as AD HSP. Spasticity is a state of increased muscle tone. Paraplegia refers to the legs (quadriplegia refers to both the arms and legs). In hereditary spastic … Medical dictionary
RTN1 — Reticulon 1, also known as RTN1, is a human gene.cite web | title = Entrez Gene: RTN1 reticulon 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=6252| accessdate = ] PBB Summary section title = summary… … Wikipedia
SPG7 — Spastic paraplegia 7, paraplegin (pure and complicated autosomal recessive), also known as SPG7, is a human gene.cite web | title = Entrez Gene: SPG7 spastic paraplegia 7, paraplegin (pure and complicated autosomal recessive)| url =… … Wikipedia
SPG20 — Spastic paraplegia 20, spartin (Troyer syndrome), also known as SPG20, is a human gene.cite web | title = Entrez Gene: SPG20 spastic paraplegia 20, spartin (Troyer syndrome)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
CHMP1B — Chromatin modifying protein 1B, also known as CHMP1B, is a human gene.cite web | title = Entrez Gene: CHMP1B chromatin modifying protein 1B| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=57132| accessdate … Wikipedia
БАКЛОФЕН — Действующее вещество ›› Баклофен* (Baclofen*) Латинское название Baclofen АТХ: ›› M03BX01 Баклофен Фармакологическая группа: Средства, влияющие на нервно мышечную передачу Состав и форма выпуска Таблетки1 табл.баклофен10 мг 25 мгвспомогательные… … Словарь медицинских препаратов
