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81.
82.
Background
In many areas of medical research, a bivariate analysis is desirable because it simultaneously tests two response variables that are of equal interest and importance in two populations. Several parametric and nonparametric bivariate procedures are available for the location problem but each of them requires a series of stringent assumptions such as specific distribution, affine-invariance or elliptical symmetry. 相似文献83.
Cathepsins L and B are lysosomal cysteine proteinases whose activities and cellular location are altered in many types of cancers and cancer cell lines. Cathepsins L and B play an unspecified role in cancer invasion and metastasis. The purpose of our study was to determine whether cathepsins L and B are important for the ability of two prostate cancer cell lines, PC3 and DU 145, to invade the basement membrane-like preparation, Matrigel®. Exposure of PC3 and DU145 to the irreversible cysteine proteinase inhibitor, E64, decreases the invasive ability of DU145, but not PC3. PC3 and DU145 were treated with the phorbol ester analogue, phorbol 12-myristate 13-acetate (PMA), a known tumor promoter that activates protein kinase C and contributes to the metastatic phenotype. PMA increased secreted cathepsin L+B activity and the invasive ability of PC3 and DU145; co-exposure to E64 and PMA decreased both cathepsin L+B activity and invasion. We conclude that DU145 requires cathepsin L+B activity more than PC3 for the invasion of the Matrigel®. When the amount of secreted cathepsin L+B activity is increased by PMA treatment, however, PC3 becomes dependent on cathepsin L+B for invasion. Our study demonstrates that modulation of the amount of secreted cathepsin L+B activity influences the invasive phenotype of PC3 and DU145. 相似文献
84.
P. Scartezzini Aliana Egeo Stefano Colella Prisca Fumagalli Patrizio Arrigo Dean Nizetic Roberto Taramelli Alberto Rasore-Quartino 《Human genetics》1997,99(3):387-392
The identification and functional characterization of genes on chromosome 21 is a necessary step to understand the pathogenesis
of the various phenotypic anomalies that affect Down syndrome patients. Using direct cDNA selection we have identified a new
gene, SH3BGR, that maps to 21q22.3, proximal to HMG14, and is differentially expressed in heart and skeletal muscle. SH3BGR
encodes a novel protein that is characterized by the presence of a proline-rich region containing the consensus sequence for
a SH3-binding domain and by an acidic carboxyl-terminal region containing a glutamic acid-rich domain predicted to assume
a coiled coil. The presence of two functional domains involved in protein-protein interactions suggests that SH3BGR could
be part of a multimeric complex. Its overexpression might alter specific functions of muscular tissue and therefore take part
in the pathophysiology of muscular hypotonia in Down syndrome.
Received: 12 August 1996 / Revised: 22 October 1996 相似文献
85.
86.
FOXOs support the metabolic requirements of normal and tumor cells by promoting IDH1 expression
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87.
The Notch pathway contributes to self-renewal of tumor-initiating cell and inhibition of normal colonic epithelial cell differentiation. Deregulated expression of Notch1 and Jagged1 is observed in colorectal cancer. Hairy/enhancer of split (HES) family, the most characterized targets of Notch, involved in the development of many cancers. In this study, we explored the role of Hes1 in the tumorigenesis of colorectal cancer. Knocking down Hes1 induced CRC cell senescence and decreased the invasion ability, whereas over-expression of Hes1 increased STAT3 phosphorylation activity and up-regulated MMP14 protein level. We further explored the expression of Hes1 in human colorectal cancer and found high Hes1 mRNA expression is associated with poor prognosis in CRC patients. These findings suggest that Hes1 regulates the invasion ability through the STAT3-MMP14 pathway in CRC cells and high Hes1 expression is a predictor of poor prognosis of CRC. 相似文献
88.
Ali Ebrahim Eivind Almaas Eugen Bauer Aarash Bordbar Anthony P Burgard Roger L Chang Andreas Dräger Iman Famili Adam M Feist Ronan MT Fleming Stephen S Fong Vassily Hatzimanikatis Markus J Herrgård Allen Holder Michael Hucka Daniel Hyduke Neema Jamshidi Sang Yup Lee Nicolas Le Novère Joshua A Lerman Nathan E Lewis Ding Ma Radhakrishnan Mahadevan Costas Maranas Harish Nagarajan Ali Navid Jens Nielsen Lars K Nielsen Juan Nogales Alberto Noronha Csaba Pal Bernhard O Palsson Jason A Papin Kiran R Patil Nathan D Price Jennifer L Reed Michael Saunders Ryan S Senger Nikolaus Sonnenschein Yuekai Sun Ines Thiele 《Molecular systems biology》2015,11(10)
89.
Bruscoli S Velardi E Di Sante M Bereshchenko O Venanzi A Coppo M Berno V Mameli MG Colella R Cavaliere A Riccardi C 《The Journal of biological chemistry》2012,287(2):1242-1251
Correct function of spermatogonia is critical for the maintenance of spermatogenesis throughout life, but the cellular pathways regulating undifferentiated spermatogonia proliferation, differentiation, and survival are only partially known. We show here that long glucocorticoid-induced leucine zipper (L-GILZ) is highly expressed in spermatogonia and primary spermatocytes and controls spermatogenesis. Gilz deficiency in knock-out (gilz KO) mice leads to a complete loss of germ cell lineage within first cycles of spermatogenesis, resulting in male sterility. Spermatogenesis failure is intrinsic to germ cells and is associated with increased proliferation and aberrant differentiation of undifferentiated spermatogonia and with hyperactivity of Ras signaling pathway as indicated by an increase of ERK and Akt phosphorylation. Spermatogonia differentiation does not proceed beyond the prophase of the first meiotic division due to massive apoptosis associated with accumulation of unrepaired chromosomal damage. These results identify L-GILZ as a novel important factor for undifferentiated spermatogonia function and spermatogenesis. 相似文献
90.
MT Butcher JW Hermanson NG Ducharme LM Mitchell LV Soderholm JE Bertram 《Comparative biochemistry and physiology. Part A, Molecular & integrative physiology》2009,152(1):100-114
The forelimb digital flexors of the horse display remarkable diversity in muscle architecture despite each muscle-tendon unit having a similar mechanical advantage across the fetlock joint. We focus on two distinct muscles of the digital flexor system: short compartment deep digital flexor (DDF(sc)) and the superficial digital flexor (SDF). The objectives were to investigate force-length behavior and work performance of these two muscles in vivo during locomotion, and to determine how muscle architecture contributes to in vivo function in this system. We directly recorded muscle force (via tendon strain gauges) and muscle fascicle length (via sonomicrometry crystals) as horses walked (1.7 m s(-1)), trotted (4.1 m s(-1)) and cantered (7.0 m s(-1)) on a motorized treadmill. Over the range of gaits and speeds, DDF(sc) fascicles shortened while producing relatively low force, generating modest positive net work. In contrast, SDF fascicles initially shortened, then lengthened while producing high force, resulting in substantial negative net work. These findings suggest the long fibered, unipennate DDF(sc) supplements mechanical work during running, whereas the short fibered, multipennate SDF is specialized for economical high force and enhanced elastic energy storage. Apparent in vivo functions match well with the distinct architectural features of each muscle. 相似文献