全文获取类型
收费全文 | 6214篇 |
免费 | 298篇 |
国内免费 | 31篇 |
专业分类
耳鼻咽喉 | 38篇 |
儿科学 | 158篇 |
妇产科学 | 176篇 |
基础医学 | 819篇 |
口腔科学 | 105篇 |
临床医学 | 402篇 |
内科学 | 1736篇 |
皮肤病学 | 73篇 |
神经病学 | 511篇 |
特种医学 | 227篇 |
外科学 | 981篇 |
综合类 | 19篇 |
一般理论 | 1篇 |
预防医学 | 118篇 |
眼科学 | 118篇 |
药学 | 389篇 |
中国医学 | 6篇 |
肿瘤学 | 666篇 |
出版年
2023年 | 34篇 |
2022年 | 55篇 |
2021年 | 148篇 |
2020年 | 60篇 |
2019年 | 106篇 |
2018年 | 129篇 |
2017年 | 116篇 |
2016年 | 120篇 |
2015年 | 122篇 |
2014年 | 164篇 |
2013年 | 197篇 |
2012年 | 337篇 |
2011年 | 384篇 |
2010年 | 187篇 |
2009年 | 156篇 |
2008年 | 298篇 |
2007年 | 345篇 |
2006年 | 347篇 |
2005年 | 304篇 |
2004年 | 357篇 |
2003年 | 270篇 |
2002年 | 289篇 |
2001年 | 162篇 |
2000年 | 201篇 |
1999年 | 147篇 |
1998年 | 73篇 |
1997年 | 46篇 |
1996年 | 50篇 |
1995年 | 36篇 |
1994年 | 51篇 |
1993年 | 55篇 |
1992年 | 111篇 |
1991年 | 117篇 |
1990年 | 121篇 |
1989年 | 115篇 |
1988年 | 104篇 |
1987年 | 97篇 |
1986年 | 81篇 |
1985年 | 59篇 |
1984年 | 51篇 |
1983年 | 56篇 |
1982年 | 27篇 |
1981年 | 18篇 |
1980年 | 18篇 |
1979年 | 44篇 |
1978年 | 16篇 |
1977年 | 31篇 |
1974年 | 15篇 |
1973年 | 18篇 |
1969年 | 16篇 |
排序方式: 共有6543条查询结果,搜索用时 46 毫秒
71.
Significant association between nonsyndromic oral clefts and arylhydrocarbon receptor nuclear translocator (ARNT) 总被引:1,自引:0,他引:1
Kayano S Suzuki Y Kanno K Aoki Y Kure S Yamada A Matsubara Y 《American journal of medical genetics. Part A》2004,(1):40-44
The etiology of nonsyndromic oral clefts (cleft lip, cleft palate, or cleft lip and palate) is still controversial, but is considered to involve both genetic and environmental factors. One of suspected environmental factors is 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) found in tobacco, herbicides, contaminated soil, and food. TCDD administered during organogenesis in mice causes a high incidence of CP in fetuses. There is ample evidence that aryl hydrocarbon receptor (AHR), AHR nuclear translocator (ARNT), and cytochrome P450 1A1 (CYP1A1) are involved in TCDD metabolism. We assessed whether there is any association in the Japanese population of nonsyndromic oral clefts with single nucleotide polymorphisms (SNPs) in the AHR, ARNT, and CYP1A1 genes using transmission disequilibrium test (TDT) and case-control study. We identified and investigated three SNPs in ARNT; 567G/C (V189V), IVS12-19T/G, and 2117C/T (P706L). Two amino acid substitutions, R554L in AHR and I462V in CYP1A1, were also investigated. In the TDT, the C allele of ARNT 567G/C was preferentially transmitted to patients (P = 0.033). When a haplotype consisting of 567G/C and IVS12-19T/G in ARNT was considered, the preferential transmission of the CT (567C-IVS12-19T) haplotype was observed (P = 0.0012). In a case-control study, a significant association of IVS12-19T/G in ARNT was observed (P = 0.021). The SNPs studied in AHR and CYP1A1 were not associated with the disease. Our results suggest that ARNT is involved in the development of nonsyndromic oral clefts in the Japanese population. 相似文献
72.
Aberrant transcription of FHIT gene in intrahepatic cholangiocellular carcinomas induced by N-nitrosobis(2-oxopropyl)amine in hamsters. 总被引:1,自引:0,他引:1
73.
Shoji M Kanai M Matsubara E Tomidokoro Y Shizuka M Ikeda Y Ikeda M Harigaya Y Okamoto K Hirai S 《Neurobiology of aging》2001,22(2):209-215
Decreased levels of cerebrospinal fluid (CSF) Abeta42 is a diagnostic marker of Alzheimer's disease. To clarify the biological basis of this marker, the physiological alterations of CSF Abeta40 and Abeta42 by aging were studied. CSF samples from 92 normal subjects between 8 and 89 years old were measured using a specific ELISA for Abeta40 and Abeta42(43). High concentrations of Abeta40 and Abeta42(43) in the young group, under 29 years old, changed to be at low concentrations in the adult group between 30 and 59 years old. Subsequently, the levels increased again with age. Third order regression analysis showed a significant correlation between the levels of Abeta40 and age (Y = - 169 X(3) + 3.1X(2)- 0.02X + 4135; P < 0.034) and between the levels of Abeta42(43) and age (Y = - 46 X(3) + 0.9 X(2)- 0.005X + 992; P < 0.005). The levels of CSF Abeta40 and Abeta42(43) were physiologically regulated to show a U-shaped natural course in normal aging. These findings suggested that the physiological increase of Abeta42(43) over 59 years of age is selectively inhibited in Alzheimer's disease. 相似文献
74.
75.
Role of apoptosis controlled by cytochrome c released from mitochondria for luteal function in human granulosa cells 总被引:1,自引:0,他引:1
Makino A Ozaki Y Matsubara H Sato T Ikuta K Nishizawa Y Suzumori K 《American journal of reproductive immunology (New York, N.Y. : 1989)》2005,53(3):144-152
PROBLEM: The aim of this study was to investigate the relationship between apoptosis by the mitochondrial pathway and luteal function in human granulosa cells. METHOD OF STUDY: Granulosa cells were obtained by ultrasound-guided follicular aspiration from patients undergoing in vitro fertilization and embryo transfer. After the addition of RU486, cells were stained with a mitochondria-specific fluorescent dye, MitoTracker Red CM x Ros. Using flow cytometry and National Institute of Health image, the mitochondrial fluorescent area was measured. After staining with Hoechst 33258 dye, the number of apoptotic bodies per 1000 cells were counted at random on photomicrographs. Homogenates were used for sodium dodecyl sulphate-polyacrylamide gel electrophoresis and Western blot analysis using antibodies against cytochrome c or caspase-3. RESULTS: The incidence of apoptotic bodies increased and the mitochondrial membrane potential decreased time dependently. The opposite effect was observed dose dependently with RU486 treatment. Western blot analysis showed increased cytochrome c expression, after treatment with 1-2 microg/mL of RU486 which then decreased with 5-10 microg/mL of RU486. Caspase-3 expression increased dose dependently with RU486. CONCLUSIONS: These results suggest that the activation of caspase-3 caused by cytochrome c released from mitochondria plays an important role in apoptosis-related luteal function in human granulosa cells. 相似文献
76.
Tochigi M Umekage T Kato C Marui T Otowa T Hibino H Otani T Kohda K Kato N Sasaki T 《Psychiatric genetics》2005,15(1):67-69
A number of studies have observed associations between the serotonin 2A (5-HT2A) receptor and mental disorders. Here, we investigated correlations between polymorphisms (-1438G/A and 102T/C) of the 5-HT2A gene and personality traits in healthy Japanese volunteers (n = 239). The personality traits were evaluated using the Revised NEO Personality Inventory (NEO PI-R). The -1438G/A and 102T/C were in complete linkage disequilibrium. There was a tendency for associations between the genotype and the scores for Agreeableness, Conscientiousness and Neuroticism of the NEO PI-R (P = 0.028, 0.039 and 0.062, respectively; analysis of variance, uncorrected for multiple testing). Subjects with the A/A of -1438G/A (or T/T of 102T/C) appeared to be lower in Neuroticism and higher in Conscientiousness than the rest of the subjects. However, the results were statistically non-significant after Bonferroni's correction for multiple testing of the five scales of the NEO PI-R. Thus, the present study provided no evidence for statistically significant associations between the 5-HT2A polymorphisms and the personality traits. 相似文献
77.
Shinichiro Nanko Akira Ueki Mineko Hattori Xiao Y. Dai Tsukasa Sasaki Rimmei Fukuda Kazuhiko Ikeda Hajime Kazamatsuri 《American journal of medical genetics. Part A》1994,54(4):361-364
Parkinson's disease is thought to be caused by a combination of unknown environmental, genetic, and degenerative factors. Evidence from necropsy brain samples and pharmacokinetics suggests involvement of dopamine receptors in the pathogenesis or pathophysiology of Parkinson's disease. Genetic association studies between Parkinson's disease and dopamine D2, D3 and D4 receptor gene polymorphisms were conducted. The polymorphism was examined in 71 patients with Parkinson's disease and 90 controls. There were no significant differences between two groups in allele frequencies at the D2, D3, and D4 dopamine receptor loci. Our findings do not support the hypothesis that susceptibility to Parkinson's disease is associated with the dopamine receptor polymorphisms examined. © 1994 Wiley-Liss, Inc. 相似文献
78.
Melanocytes in the nasal cavity and paranasal sinus. Incidence and distribution in Japan 总被引:1,自引:0,他引:1
Random, nonselected tissue specimens from 99 Japanese-20 cylindrically cut nasal blocks removed during autopsy (A.C., Autopsy Cases) and 79 cases removed during surgery, consisting of 32 chronic sinusitis cases (C.S.) and 47 nasal polyp cases (N.P.)-were examined histopathologically and electronmicroscopically with respect to distribution and frequency of melanocytes in the nasal cavity and paranasal sinus. Malignant melanoma cases were excluded. The overall incidence of positive cases for melanocytes revealed 21.2% (21 of 99 cases), with an incidence ratio of male to female of 0.9:1.0. Melanocytes were found beginning in the under 19 age group with incidence increasing proportionately with age. Peak incidence was in the 50-year age group at 50%. Melanocytes and melanotic cell foci were distributed in the stroma of the propria mucosa beneath the pseudostratified columnar epithelium and focused around the nasal and paranasal glands and sinuses. In 2 of the 21 cases positive for stromal melanocytes, intraepithelial melanocytes with dendritic processes were found. The histogenesis of malignant melanoma arising from the nasal cavity and paranasal sinus are also discussed in this study. 相似文献
79.
Isao Nakanishi Shogo Katsuda Yoshikatsu Okada Yoshio Oda Fujitsugu Matsubara 《Pathology international》1986,36(2):261-267
Confronting cisternae of the endoplasmic reticulum recognized in tumor cells of 7 cases of osteosarcoma were presented. They were found in the mitotic cells as well as in the cytoplasms of interphase cells. The more the mitotic cells were observed in 1 μm-thick sections, the more frequently those membranous structures were encountered in the corresponding ultrathin sections. In the interphase cells, such structures were located around Golgi apparatus or close to the nucleus. Occasionally, they were composed of a pair of closely apposed cisternae of the nuclear membrane and the rough endoplasmic reticulum. These results seem to indicate that the nuclear envelope which is disrupted and reformed during mitosis in rapidly proliferating cells takes part in the formation of the confronting cisternae of the endoplasmic reticulum. 相似文献
80.
Yasuo Harigaya Yasushi Tomidokoro Masaki Ikeda Atsushi Sasaki Takeshi Kawarabayashi Etsuro Matsubara Mitsuyasu Kanai Takaomi C. Saido Steven G. Younkin Mikio Shoji 《Neuroscience letters》2006
To clarify how Aβ deposits start in the brain, we examined the early to late stages of senile plaques and amyloid angiopathy in APPsw mice. All types of human senile plaques were observed in the mouse brains. The premature forms of cored plaques appeared first in the cerebral cortex of mice at 7–8 months old. Then, amyloid angiopathy emerged, followed by diffuse plaques consisting of Aβ1–42. Modifications of the N-terminus of Aβ were late phase phenomena. The premature forms of cored plaques were composed of central Aβ1–40 amyloid cores, surrounding amorphous Aβ1–42 deposits, and accumulation of Aβ1–42 in some peripheral cells. These cells were incorporated in amyloid cores, and these plaques developed to large cored plaques composed of Aβ1–40 and Aβ1–42. The size and number of cored plaques were increased with age. These findings indicate different evolution paths for cored plaques and diffuse plaques, and suggest the presence of a pathway that initiates with the intracellular accumulation of Aβ1–42 and leads to the development of classic plaques in human brain tissues. 相似文献