全文获取类型
收费全文 | 836篇 |
免费 | 80篇 |
国内免费 | 1篇 |
专业分类
917篇 |
出版年
2022年 | 8篇 |
2021年 | 9篇 |
2019年 | 7篇 |
2018年 | 11篇 |
2016年 | 21篇 |
2015年 | 26篇 |
2014年 | 23篇 |
2013年 | 35篇 |
2012年 | 56篇 |
2011年 | 52篇 |
2010年 | 22篇 |
2009年 | 28篇 |
2008年 | 36篇 |
2007年 | 25篇 |
2006年 | 33篇 |
2005年 | 34篇 |
2004年 | 37篇 |
2003年 | 20篇 |
2002年 | 26篇 |
2001年 | 31篇 |
2000年 | 21篇 |
1999年 | 27篇 |
1998年 | 6篇 |
1996年 | 6篇 |
1994年 | 10篇 |
1992年 | 9篇 |
1991年 | 6篇 |
1990年 | 14篇 |
1989年 | 13篇 |
1988年 | 26篇 |
1987年 | 7篇 |
1986年 | 12篇 |
1985年 | 9篇 |
1984年 | 10篇 |
1983年 | 9篇 |
1981年 | 10篇 |
1980年 | 7篇 |
1979年 | 17篇 |
1978年 | 14篇 |
1977年 | 10篇 |
1976年 | 8篇 |
1975年 | 9篇 |
1974年 | 12篇 |
1973年 | 12篇 |
1972年 | 13篇 |
1971年 | 8篇 |
1970年 | 16篇 |
1969年 | 8篇 |
1967年 | 6篇 |
1965年 | 7篇 |
排序方式: 共有917条查询结果,搜索用时 15 毫秒
911.
912.
P Gerber 《In vitro》1974,10(5-6):247-252
913.
Absorption of radioactive lead (210Pb) was studied in an intestinal preparation from adult and young rats. Absorption was higher in the jejunal parts than in the duodenum or colon. Moreover, absorption in young rats was greater than in adults. No difference in absorption was found after loading with large amounts of lead. Maintaining the animals on a low calcium diet decreased rather than increased lead absorption. 相似文献
914.
F Thimm B Gerber 《European journal of applied physiology and occupational physiology》1988,58(1-2):112-119
In endurance trained (TR) and untrained (UTR) rats heart rate (HR) and respiratory rate (RR) were recorded during perfusion of the circulatorily isolated hind leg of the rat with exercise simulating modified tyrode solutions (TR:n = 10, UTR:n = 10; compare part I). During the 20 min test period and the preceding and succeeding periods of control perfusions with an unmodified tyrode solution, [lactate], pH, [K+], [Na+], PO2 and PCO2 were measured in the outflow of the femoral vein. In 3 experimental series: (1) hypoxic tyrode solution enriched with lactic acid (15 mmol.l-1), (2) normoxic solution with lactic acid, (3) hypoxic solution without lactic acid, were applied. The outflow parameters were cross correlated with both HR and RR. The analysis revealed a significant temporal relationship between [lactate], pH, PO2, PCO2 and [K+] and both HR and RR. In the trained rats no temporal correlation between either of the outflow and reflex parameters could be determined. This result was not due to low [lactate], but was also found during perfusion with lactic acid. In all 3 test conditions [lactate] in untrained individuals was best correlated with both HR and RR. Although the correlation peaks of the respiratory response, but not of the HR response were definitely lower in normoxic lactic and perfusion than in the two other experimental conditions, both inter- and intraindividual correlation analyses revealed a high degree of interdependence between respiratory and cardiac responses. 相似文献
915.
In chloroform solution, the D ,L -alternating stereo-co-oligopeptide HCO-L -Phe-(D -Phe-L -Phe)3-OMe (I) forms three major species, two of which are dimeric and one tetrameric. One of the two dimeric species gives a specific set of 1H-nmr signals at 25°C; the other, together with the tetrameric species, gives another set of resonance signals. In a carbon tetrachloride or cyclohexane solution at 25°C, I forms virtually only the tetrameric species. From the nmr data, it can be shown that the dimeric and tetrameric species, that are in rapid equilibrium with each other in chloroform solutions, are a right-handed ↑↑β5.6 helical dimer and the head-to-head (formyl-ends-to-formyl-ends) dimerization product of this dimer. It is suggested that the linear gramicidins may also form head-to-head dimers of parallel β helices, as observed for the model oligopeptide I. 相似文献
916.
A. Camuzat J. -M. Rozet H. Dollfus S. Gerber I. Perrault A. Munnich J. Kaplan J. Weissenbach 《Human genetics》1996,97(6):798-801
Leber’s congenital amaurosis (LCA) is an autosomal recessive disease responsible for congenital blindness. It is the earliest
and most severe inherited retinal dystrophy in human and its genetic heterogeneity has long been recognised. We have recently
reported on the first localisation of a disease gene (LCA1) to the short arm of chromosome 17 by homozygosity mapping in five
families of North African origin. Here, we refine the genetic mapping of LCA1 to chromosome 17p13 between loci D17S938 and
D17S1353 and provide strong support for the genetic heterogeneity of this condition (maximum likelihood for heterogeneity,
17.20 in lnL; heterogeneity versus homogeneity, P = 0.0002, heterogeneity versus no linkage, P < 0.0001)
Received: 23 October 1995 / Revised: 11 January 1996 相似文献
917.