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排序方式: 共有440条查询结果,搜索用时 15 毫秒
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A P Rodionov V V Lyskovtsev N A Ignatova E A Tolmacheva E K Grigor'eva G F Belinskiaia B V She?nberg 《Farmakologiia i toksikologiia》1990,53(3):40-43
The pharmacokinetics and pharmacodynamics of bonnecor were studied simultaneously in animals with experimental arrhythmia. It was shown that irrespective of the animal species and individual features of the drug elimination kinetics the level of bonnecor concentration correlated with the antiarrhythmic effect. The data on the excretion of bonnecor and its metabolites in the urine in the dog and man were obtained. The decrease of bioavailability at oral administration of bonnecor was demonstrated to be related to its intensive conversion in metabolite M-I. 相似文献
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Vinod Dasa James R.B. Eastwood Michal Podgorski Heewon Park Christopher Blackstock Tetyana Antoshchenko Piotr Rogala Tadeusz Bieganski S. Michal Jazwinski Malwina Czarny‐Ratajczak 《American journal of medical genetics. Part A》2019,179(4):534-541
Mutations in the COMP, COL9A1, COL9A2, COL9A3, MATN3, and SLC26A2 genes cause approximately 70% of multiple epiphyseal dysplasia (MED) cases. The genetic changes involved in the etiology of the remaining cases are still unknown, suggesting that other genes contribute to MED development. Our goal was to identify a mutation causing an autosomal dominant form of MED in a large multigenerational family. Initially, we excluded all genes known to be associated with autosomal dominant MED by using microsatellite and SNP markers. Follow‐up with whole‐exome sequencing analysis revealed a mutation c.2032G>A (p.Gly678Arg) in the COL2A1 gene (NCBI Reference Sequence: NM_001844.4), which co‐segregated with the disease phenotype in this family, manifested by severe hip dysplasia and osteoarthritis. One of the affected family members had a double‐layered patella, which is frequently seen in patients with autosomal recessive MED caused by DTDST mutations and sporadically in the dominant form of MED caused by COL9A2 defect. 相似文献
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Mikael F. Forsgren Patrik Nasr Markus Karlsson Nils Dahlström Bengt Norén Simone Ignatova 《Scandinavian journal of gastroenterology》2020,55(7):848-859
Abstract
Background and aims
Accurate biomarkers for quantifying liver fibrosis are important for clinical practice and trial end-points. We compared the diagnostic performance of magnetic resonance imaging (MRI), including gadoxetate-enhanced MRI and 31P-MR spectroscopy, with fibrosis stage and serum fibrosis algorithms in a clinical setting. Also, in a subset of patients, MR- and transient elastography (MRE and TE) was evaluated when available. 相似文献7.
Zemlyanova M. A. Zaitseva N. V. Ignatova A. M. Stepankov M. S. Toropov L. I. Kol’dibekova Yu. V. 《Bulletin of experimental biology and medicine》2021,170(5):665-668
Bulletin of Experimental Biology and Medicine - In female Wistar rats, we studied the effects of daily 20-day administration of intragastric suspension of nanosized calcium oxide on hematological... 相似文献
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