|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | 瞬时受体电位通道TRPV1、TRPA1和TRPM8拮抗剂在小鼠神经源性和神经病理性疼痛模型中的镇痛作用(英文)显示文摘目的:评价瞬时受体电位通道(TRP通道)TRPV1、TRPA1和TRPM8拮抗剂在小鼠神经源性、持续性和神经病理性疼痛模型中的作用。方法:通过辣椒素实验、异硫氰酸烯丙酯(AITC)实验和福尔马林实验,评估TRP通道拮抗剂在小鼠神经源性疼痛模型中的镇痛作用;通过建立紫杉醇诱导的小鼠神经病理性疼痛模型,对TRP通道拮抗剂的抗痛觉(冷、热、触觉)过敏效应进行评估;通过旋转法实验对小鼠的运动协调性进行评估。结论:TRP通道家族包含了不同的小鼠疼痛模型。TRP通道拮抗剂能减轻神经源性、持续性和神经病理性疼痛,但是其镇痛效果与疼痛模型有关。 | Kinga SALAT Barbara FILIPEK | 2015 | Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)2015，16，3： | 5 |
| 2 | Bevacizumab plus interferon alfa-2a for treatment of metastatic renal cell carcinoma: a randomised, double-blind phase III trial显示文摘 | Bernard Escudier Anna Pluzanska Piotr Koralewski Alain Ravaud Sergio Bracarda Cezary Szczylik Christine Chevreau Marek Filipek Bohuslav Melichar Emilio Bajetta Vera Gorbunova Jacques-Olivier Bay Istvan Bodrogi Agnieszka Jagiello-Gruszfeld Nicola Moore | 2007 | The Lancet . 2007 (9605)2007，，： | 2 |
| 3 | P30, a novel target of mouse calcyclin(S100A6) 显示文摘 | Filipek A Wojda U | 1996 | BiochemJ1996，320，2： | 2 |
| 4 | The screening and diagnosis of autistic spectrum disorders显示文摘 | Filipek PA Accaredo PJ Baranek GT | 1999 | Autism Dev Disord1999，29，6： | 1 |
| 5 | Molecular cloning and expression of a mouse brain cDNA encoding a novel protein target of calcyclin显示文摘 | Filipek A Kuznicki J | 1998 | J Neurochem1998，70，5： | 1 |
| 6 | Calcyclin (S100A6) binding protein (CacyBP) is highly expressed in brain neurons显示文摘 | Jastrzebska B Filipek A Nowicka D | 2000 | J Histochem Cytochem2000，48，9： | 1 |
| 7 | Involvement of $100A6 (calcyelin) and its binding partners in intracellular signaling pathways 显示文摘 | Filipek A Miehowski W Kuznieki J | 2008 | Advan Enzyme Regul2008，，： | 1 |
| 8 | Ca2+-dependent translocation of the calcyclin-binding protein in neurons and neuroblastoma NΒ-2a cells显示文摘 | Filipek A Jastrzebska B Nowotny M | 2002 | J Biol Chem2002，277，21： | 1 |
| 9 | S100A6 is transcrip- tionally regulated by 13-eatenin and interacts with a novel target, lamin A/C, in colorectal cancer cells 显示文摘 | Kilafaczyk E Graczyk A Filipek A | 2012 | Cell Calcium2012，51，6： | 1 |
| 10 | S100A6 and CacyBP/SIP-two proteins discovered in ehrlich ascites tumor cells that are potentially involved in the degradation of beta-catenin 显示文摘 | Filipek A | 2006 | Chemothera- py2006，52，1： | 1 |
| 11 | Etiopathogene- sis and management of high-degree myopia显示文摘 | Zejmo M Forminska-Kapuscik M Pieczara E Filipek E Mruk- wa-Kominek E Samochowiec-Donocik E | 2009 | Med Sci Monit2009，15，： | 1 |
| 12 | CacyBP/SIP,a calcyclin and Siah-1-interacting protein,binds EF-hand proteins of the S100 family显示文摘 | Filipek A Jastrzebska B Nowotny M | 2002 | J Biol Chem2002，277，28： | 1 |
| 13 | Language and other regression: Assessment and timing显示文摘 | Goldberg WA Osann K Filipek PA Laulhere T Jarvis K Modahl C | 2003 | J Autism and Dev Disord2003，33，6： | 1 |
| 14 | Age-dependent changes in neuronal distribution of CacyBP/SIP:comparison to tubulin and the tan protein 显示文摘 | Filipek A Schneider G Mietelska A | 2008 | J Neural Transm2008，115，9： | 1 |
| 15 | p30,a novel protein target of mouse calcyclin (S100A6)显示文摘 | Wojda U | 1996 | Biochem J1996，320，2： | 1 |
| 16 | Caleyelin (IOOAO) binding protein(CacyBP) is highly expressed in brain neurons 显示文摘 | Jastrzebska B Filipek A Nowieka D | 2000 | J Histochem Cytochem2000，48，9： | 1 |
| 17 | CacyBP/SIP,a calcyclin and Siah-1-interacting protein,binds EF-hand proteins of the S100 family显示文摘 | Jastrzebska B Nowotny M | 2002 | J Biol Chem2002，277，28： | 1 |
| 18 | Molecular cloning and expression of a mouse brain cDNA encoding a novel protein target of calcyclin 显示文摘 | Filipek A Kuzhicki J | 1998 | J Neurochem1998，70，5： | 1 |
| 19 | Calcyclin (S100A6) binding protein (CacyBP) is highly expressed in brain neurons显示文摘 | Filipek A Nowicka D | 2000 | J Histochem Cytochem2000，48，9： | 1 |
| 20 | Interaction of acidmine drainage with waters and sediments of west squaw creek in the westshasta mining district, california显示文摘 | FILIPEK L H NORDSTROM D K FICKLIN W H | 1987 | Environmental Science & Technology1987，21，4： | 1 |
您所在的机构暂未开通此部分的功能，请联系管理员