全文获取类型
收费全文 | 2237篇 |
免费 | 143篇 |
国内免费 | 112篇 |
出版年
2023年 | 27篇 |
2022年 | 37篇 |
2021年 | 35篇 |
2020年 | 46篇 |
2019年 | 53篇 |
2018年 | 52篇 |
2017年 | 53篇 |
2016年 | 60篇 |
2015年 | 60篇 |
2014年 | 106篇 |
2013年 | 128篇 |
2012年 | 91篇 |
2011年 | 125篇 |
2010年 | 98篇 |
2009年 | 96篇 |
2008年 | 116篇 |
2007年 | 110篇 |
2006年 | 94篇 |
2005年 | 103篇 |
2004年 | 105篇 |
2003年 | 76篇 |
2002年 | 58篇 |
2001年 | 70篇 |
2000年 | 57篇 |
1999年 | 40篇 |
1998年 | 41篇 |
1997年 | 47篇 |
1996年 | 38篇 |
1995年 | 34篇 |
1994年 | 36篇 |
1993年 | 29篇 |
1992年 | 31篇 |
1991年 | 36篇 |
1990年 | 24篇 |
1989年 | 18篇 |
1988年 | 13篇 |
1987年 | 9篇 |
1986年 | 13篇 |
1985年 | 33篇 |
1984年 | 33篇 |
1983年 | 22篇 |
1982年 | 20篇 |
1981年 | 21篇 |
1980年 | 19篇 |
1979年 | 14篇 |
1978年 | 15篇 |
1977年 | 11篇 |
1976年 | 15篇 |
1975年 | 9篇 |
1974年 | 7篇 |
排序方式: 共有2492条查询结果,搜索用时 15 毫秒
11.
Yasuaki Kagotani Setsuji Hisano Yoshihiro Tsuruo Shigeo Daikoku Yasuhiko Okimura Kazuo Chihara 《Cell and tissue research》1990,262(1):47-52
Summary Certain populations of arginine vasopressin (AVP) neurons in the magnocellular paraventricular nucleus became immunoreactive for neuropeptide Y (NPY) when rats were treated with colchicine or monosodium glutamate (MSG). The co-storage of these peptides was examined by empooying a post-embedding electron-microscopic immunohistochemistry technique using goldlabeled antibodies to the two peptides. In colchicinetreated rats, the neuronal perikarya contained numerous secretory granules showing co-storage of the two peptides. The cells of the MSG-treated rats were characterized by having well-developed Golgi bodies with the granular structures also co-storing the two peptides, although the secretory granules in the perikarya were rather fewer than in the colchicine-treated rats. It is concluded that the destruction of the arcuate nucleus by MSG-treatment may potentiate the synthesis of NPY in AVP neurons, the synthesis of which is latent in intact animals. 相似文献
12.
J. S. Lacroix A. Änggård T. Hökfelt M. M. T. O'Hare J. Fahrenkrug J. M. Lundberg 《Cell and tissue research》1990,259(1):119-128
Summary The occurrence of neuropeptide Y (NPY), vasoactive intestinal polypeptide (VIP) and peptide histidine isoleucine (PHI) in the sympathetic and parasympathetic innervation of the nasal mucosa was studied in various species including man. A dense network of NPY-immunoreactive (IR) fibres was present around arteries and arterioles in the nasal mucosa of all species studied. NPY was also located in nerves around seromucous glands in pig and guinea-pig, but not in rat, cat and man. The NPY-IR glandular innervation corresponded to about 20% of the NPY content of the nasal mucosa as revealed by remaining NPY content determined by radioimmunoassay after sympathectomy. These periglandular NPY-positive fibres had a distribution similar to the VIP-IR and PHI-IR nerves but not to the noradrenergic markers tyrosine hydroxylase (TH) or dopamine--hydroxylase (DBH). The NPY nerves around glands and some perivascular fibres were not influenced by sympathectomy and probably originated in the sphenopalatine ganglion where NPY-IR and VIP-IR ganglion cells were present. The venous sinusoids were innervated by NPY-positive fibres in all species except the cat. Dense NPY and DBH-positive innervation was seen around thick-walled vessels in the pig nasal mucosa; the latter may represent arterio-venous shunts. Double-labelling experiments using TH and DBH, and surgical sympathectomy revealed that the majority of NPY-IR fibres around blood vessels were probably noradrenergic. The NPY-positive perivascular nerves that remained after sympathectomy in the pig nasal mucosa also contained VIP/PHI-IR. The major nasal blood vessels, i.e. sphenopalatine artery and vein, were also densely innervated by NPY-IR fibres of sympathetic origin. Perivascular VIP-IR fibres were present around small arteries, arterioles, venous sinusoids and arterio-venous shunt vessels of the nasal mucosa whereas major nasal vessels received only single VIP-positive nerves. The trigeminal ganglion of the species studied contained only single TH-IR or VIP-IR but no NPY-positive ganglion cells. It is concluded that NPY in the nasal mucosa is mainly present in perivascular nerves of sympathetic origin. In some species, such as pig, glandular and perivascular parasympathetic nerves, probably of VIP/PHI nature, also contain NPY. 相似文献
13.
P. J. Skuce C. F. Johnston I. Fairweather D. W. Halton C. Shaw K. D. Buchanan 《Cell and tissue research》1990,261(3):573-581
Summary The presence and distribution of neuropeptides belonging to the pancreatic polypeptide family have been demonstrated by an indirect immunofluorescence technique in the nervous systems of adult male and female Schistosoma mansoni. Seven antisera of differing regional specificity to pancreatic polypeptide (PP), peptide YY (PYY) and neuropeptide Y (NPY) were employed on both whole-mount and cryostat-sectioned material. Positive immunoreactivity (IR) was obtained with all antisera except an N-terminally-directed antiserum to NPY. In the CNS, immunoreactivity was restricted to cell bodies and nerve fibres in the anterior ganglia, central commissure and dorsal and ventral nerve cords of both sexes, whereas, in the PNS, positive-IR was present in the plexuses innervating the subtegumental musculature and the oral and ventral suckers. Intense immunoreactivity was observed in a plexus of nerve fibres and cell bodies in the lining of the gynaecophoric canal and in fine nerve fibres innervating the dorsal tubercles of the male. In contrast, in the female, strong immunoreactivity was evident in nerve plexuses innervating the lining of the ovovitelline duct and in the wall of the ootype, but most notably in a cluster of cells in the region of Mehlis' gland. Results suggest that molecules with C-terminal homology to the PP-family are present in S. mansoni. These peptides would appear to be important regulatory molecules in the parasite's nervous system and may play a role in the control of egg production. 相似文献
14.
Neuropeptide Y (NPY) has been isolated from brain extracts of the rainbow trout (Oncorhynchus mykiss) and subjected to structural analyses. Plasma desorption mass spectroscopy estimated the molecular mass of the purified peptide as 4303.9 Da. Automated Edman degradation unequivocally established the sequence of a 36 amino acid residue peptide as: Tyr-Pro-Pro-Lys-Pro-Glu-Asn-Pro-Gly-Glu-Asp-Ala-Pro-Pro-Glu-Glu-Leu-Ala-Lys-Tyr-Tyr-Ala-Leu-Arg-His-Tyr-Ile-Asn-Leu-Ile-Thr-Arg-Gln-Arg-Tyr. The molecular mass calculated from this sequence (4304 Da) is consistent with that obtained by mass spectroscopy. The presence of a C-terminal amide was established by radioimmunoassay. Rainbow trout NPY is identical in primary structure to coho salmon (Oncorhynchus kisutch) pancreatic polypeptide (PP). These data may indicate that, in this group of salmonid fishes, a single member of the NPY/PP peptide family is expressed in both neurons and peripheral endocrine cells. 相似文献
15.
马铃薯Y病毒外壳蛋白基因的克隆及序列分析 总被引:1,自引:0,他引:1
本文报道应用聚合酶链式反应(PCR)技术,在体外扩增马铃薯 Y 病毒外壳蛋白基因及其克隆和序列分析的结果。病毒 RNA 从马铃薯 Y 病毒感染的烟草叶片中提取,用合成的PCR 3引物及 AMV 逆转录酶合成了单链的 cDNA。利用 PCR 技术,经30个循玎的扩增。得到了一特异的0.8kb 片段。克隆后对此片段进行了限制性内切酶物理图谱分析,并测定了其全序列。实验结果证明,我们克隆到的是完整的马铃薯 Y 病毒的外壳蛋白基因。与国外报道的马铃薯 Y 病毒 N 株相比,其核苷酸序列及推测的氨基酸序列的同源率分别为97.8%和97%。将该基因导入马铃薯以期获得抗 Y 病毒马铃薯的工作正在进行。本文还对 PCR 技术用于扩增植物 RNA 病毒的方法以及用基因工程方法培育抗病毒作物新品种的可行性等进行了讨论。 相似文献
16.
Crystal structure of the Y52F/Y73F double mutant of phospholipase A2: increased hydrophobic interactions of the phenyl groups compensate for the disrupted hydrogen bonds of the tyrosines. 总被引:3,自引:1,他引:2 下载免费PDF全文
C. Sekharudu B. Ramakrishnan B. Huang R. T. Jiang C. M. Dupureur M. D. Tsai M. Sundaralingam 《Protein science : a publication of the Protein Society》1992,1(12):1585-1594
The enzyme phospholipase A2 (PLA2) catalyzes the hydrolysis of the sn-2 ester bond of membrane phospholipids. The highly conserved Tyr residues 52 and 73 in the enzyme form hydrogen bonds to the carboxylate group of the catalytic Asp-99. These hydrogen bonds were initially regarded as essential for the interfacial recognition and the stability of the overall catalytic network. The elimination of the hydrogen bonds involving the phenolic hydroxyl groups of the Tyr-52 and -73 by changing them to Phe lowered the stability but did not significantly affect the catalytic activity of the enzyme. The X-ray crystal structure of the double mutant Y52F/Y73F has been determined at 1.93 A resolution to study the effect of the mutation on the structure. The crystals are trigonal, space group P3(1)21, with cell parameters a = b = 46.3 A and c = 102.95 A. Intensity data were collected on a Siemens area detector, 8,024 reflections were unique with an R(sym) of 4.5% out of a total of 27,203. The structure was refined using all the unique reflections by XPLOR to a final R-factor of 18.6% for 955 protein atoms, 91 water molecules, and 1 calcium ion. The root mean square deviation for the alpha-carbon atoms between the double mutant and wild type was 0.56 A. The crystal structure revealed that four hydrogen bonds were lost in the catalytic network; three involving the tyrosines and one involving Pro-68. However, the hydrogen bonds of the catalytic triad, His-48, Asp-99, and the catalytic water, are retained. There is no additional solvent molecule at the active site to replace the missing hydroxyl groups; instead, the replacement of the phenolic OH groups by H atoms draws the Phe residues closer to the neighboring residues compared to wild type; Phe-52 moves toward His-48 and Asp-99 of the catalytic diad, and Phe-73 moves toward Met-8, both by about 0.5 A. The closing of the voids left by the OH groups increases the hydrophobic interactions compensating for the lost hydrogen bonds. The conservation of the triad hydrogen bonds and the stabilization of the active site by the increased hydrophobic interactions could explain why the double mutant has activity similar to wild type. The results indicate that the aspartyl carboxylate group of the catalytic triad can function alone without additional support from the hydrogen bonds of the two Tyr residues. 相似文献
17.
榆中贝母(Fritillaria yuzhongensis)生长于马啣山的高山地带,全生育期约100 d左右,是一种生育期较短的类短命植物。在果实成熟时,种子的胚发育不全,具有后熟作用的特点,包括形态后熟和生理后热两个阶段;因此,需要一定时期的低温处理,才能完成后熟过程,以解除休眠,促使种子发芽。本试验表明:榆中贝母完成形态后熟过程的最佳温度是7℃左右,经过100d以上的低温处理才能使原胚发育成熟,继续在7℃低温下处理70d以上,才能完成生理后熟过程。榆中贝母种子休眠时间长,需要经过170d以上的低温处理,种子才能萌发。本试验结果为榆中贝母种子的萌发提出了适宜的温度范围和低温处理时间,为提高种子的出苗率和缩短栽培年限提供了科学依据。 相似文献
18.
N. Aste C. Viglietti-Panzica A. Fasolo C. Andreone H. Vaudry G. Pelletier G. C. Panzica 《Cell and tissue research》1991,265(2):219-230
Summary In the present study, we have demonstrated, by means of the biotin-avidin method, the widespread distribution of neuropeptide Y (NPY)-immunoreactive structures throughout the whole brain of the Japanese quail (Coturnix coturnix japonica). The prosencephalic region contained the highest concentration of both NPY-containing fibres and perikarya. Immunoreactive fibres were observed throughout, particularly within the paraolfactory lobe, the lateral septum, the nucleus taeniae, the preoptic area, the periventricular hypothalamic regions, the tuberal complex, and the ventrolateral thalamus. NPY-immunoreactive cells were represented by: a) small scattered perikarya in the telencephalic portion (i.e. archistriatal, neostriatal and hyperstriatal regions, hippocampus, piriform cortex); b) medium-sized cell bodies located around the nucleus rotundus, ventrolateral, and lateral anterior thalamic nuclei; c) small clustered cells within the periventricular and medial preoptic nuclei. The brainstem showed a less diffuse innervation, although a dense network of immunopositive fibres was observed within the optic tectum, the periaqueductal region, and the Edinger-Westphal, linearis caudalis and raphes nuclei. Two populations of large NPY-containing perikarya were detected: one located in the isthmic region, the other at the boundaries of the pons with the medulla. The wide distribution of NPY-immunoreactive structures within regions that have been demonstrated to play a role in the control of vegetative, endocrine and sensory activities suggests that, in birds, this neuropeptide is involved in the regulation of several aspects of cerebral functions.Abbreviations
AA
archistriatum anterius
-
AC
nucleus accumbens
-
AM
nucleus anterior medialis
-
APP
avian pancreatic polypeptide
-
CNS
centrai nervous system
-
CO
chiasma opticum
-
CP
commissura posterior
-
CPi
cortex piriformis
-
DIC
differential interferential contrast
-
DLAl
nucleus dorsolateralis anterior thalami, pars lateralis
-
DLAm
nucleus dorsolateralis anterior thalami, pars medialis
-
E
ectostriatum
-
EW
nucleus of Edinger-Westphal
-
FLM
fasciculus longitudinalis medialis
-
GCt
substantia grisea centralis
-
GLv
nucleus geniculatus lateralis, pars ventralis
-
HA
hyperstriatum accessorium
-
Hp
hippocampus
-
HPLC
high performance liquid chromatography
-
HV
hyperstriatum ventrale
-
IF
nucleus infundibularis
-
IO
nucleus isthmo-opticus
-
IP
nucleus interpeduncularis
-
IR
immunoreactive
-
LA
nucleus lateralis anterior thalami
-
LC
nucleus linearis caudalis
-
LFS
lamina frontalis superior
-
LH
lamina hyperstriatica
-
LHRH
luteinizing hormone-releasing hormone
-
LoC
locus coeruleus
-
LPO
lobus paraolfactorius
-
ME
eminentia mediana
-
N
neostriatum
-
NC
neostriatum caudale
-
NPY
neuropeptide Y
-
NIII
nervus oculomotorius
-
NV
nervus trigeminus
-
NVI
nervus facialis
-
NVIIIc
nervus octavus, pars cochlearis
-
nIV
nucleus nervi oculomotorii
-
nIX
nucleus nervi glossopharyngei
-
nBOR
nucleus opticus basalis (ectomamilaris)
-
nCPa
nucleus commissurae pallii
-
nST
nucleus striae terminalis
-
OM
tractus occipitomesencephalicus
-
OS
nucleus olivaris superior
-
PA
palaeostriatum augmentatum
-
PBS
phosphate-buffered saline
-
POA
nucleus praeopticus anterior
-
POM
nucleus praeopticus medialis
-
POP
nucleus praeopticus periventricularis
-
PP
pancreatic polypeptide
-
PYY
polypeptide YY
-
PVN
nucleus paraventricularis magnocellularis
-
PVO
organum paraventriculare
-
R
nucleus raphes
-
ROT
nucleus rotundus
-
RP
nucleus reticularis pontis caudalis
-
Rpc
nucleus reticularis parvocellularis
-
RPgc
nucleus reticularis pontis caudalis, pars gigantocellularis
-
RPO
nucleus reticularis pontis oralis
-
SCd
nucleus subcoeruleus dorsalis
-
SCv
nucleus subcoeruleus ventralis
-
SCNm
nucleus suprachiasmaticus, pars medialis
-
SCNl
nucleus suprachiasmaticus, pars lateralis
-
SL
nucleus septalis lateralis
-
SM
nucleus septalis medialis
-
Ta
nucleus tangentialis
-
TeO
tectum opticum
-
Tn
nucleus taeniae
-
TPc
nucleus tegmenti pedunculo-pontinus, pars compacta
-
TSM
tractus septo-mesencephalicus
-
TV
nueleus tegmenti ventralis
-
VeL
nucleus vestibularis lateralis
-
VLT
nucleus ventrolateralis thalami
-
VMN
nucleus ventromedialis hypothalami
A preliminary report of this study was presented at the 15th Conference of European Comparative Endocrinologists, Leuven, Belgium, September 1990 相似文献
19.
Summary Applying a double-immunofluorescence technique, the porcine ovary is demonstrated to receive two populations of NPY-immunoreactive nerve fibres originating from the inferior mesenteric ganglion: one with colocalized tyrosine hydroxylase and supplying predominantly the ovarian vasculature, and a second, solely NPY-immunoreactive and almost exclusively associated with growing follicles. A third group of tyrosine hydroxylase-and dopamine--hydroxylase-positive, but NPY-negative nerve fibres is associated with ovarian blood vessels and, to a minor extent, with ovarian follicles. As revealed by retrograde tracing, the vast majority of postganglionic neurons projecting to the ovary is located in a discrete area of the ganglion, suggesting a somatotopic organization of the porcine inferior mesenteric ganglion. Moreover, the finding indicate that three subpopulations of postganglionic sympathetic neurons with different chemical codes supply different target components of the porcine ovary. The physiological relevance of the described neurons in the nervous control of ovarian functions remains to be elucidated.A portion of these results has been presented in abstract form (Majewski et al. 1991) 相似文献
20.
Summary The opioidergic, sympathetic and neuropeptide Y-positive innervation of the sphincter of Oddi (common bile duct sphincter and pancreatic duct sphincter), as well as other segments of the extrahepatic biliary tree was studied in the monkey by use of immunohistochemistry. Methionine-enkephalin-positive nerves were seen to innervate the smooth muscle of all portions of the sphincter of Oddi and also local ganglion cells. No methionine-enkephalin-positive nerves could be detected in the common bile duct, pancreatic duct or gallbladder. Tyrosine hydroxylase-positive nerves occurred between smooth muscle bundles and also ran to local ganglion cells as well as along the common bile duct. Neuropeptide Y-positive nerves were observed within smooth muscle of the sphincter of Oddi (all portions), common bile duct, pancreatic duct and gallbladder. No evidence of any differential innervation of the pancreatic duct and common bile duct sphincters could be detected with these markers. 相似文献