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排序方式: 共有145条查询结果,搜索用时 171 毫秒
31.
Jos?C. Jansen Sharita Timal Monique van?Scherpenzeel Helen Michelakakis Dorothée Vicogne Angel Ashikov Marina Moraitou Alexander Hoischen Karin Huijben Gerry Steenbergen Marjolein?A.W. van?den?Boogert Francesco Porta Pier?Luigi Calvo Mersyni Mavrikou Giovanna Cenacchi Geert van?den?Bogaart Jody Salomon Adriaan?G. Holleboom Richard?J. Rodenburg Joost?P.H. Drenth Martijn?A. Huynen Ron?A. Wevers Eva Morava Fran?ois Foulquier Joris?A. Veltman Dirk?J. Lefeber 《American journal of human genetics》2016,98(2):322-330
Congenital disorders of glycosylation (CDGs) form a genetically and clinically heterogeneous group of diseases with aberrant protein glycosylation as a hallmark. A subgroup of CDGs can be attributed to disturbed Golgi homeostasis. However, identification of pathogenic variants is seriously complicated by the large number of proteins involved. As part of a strategy to identify human homologs of yeast proteins that are known to be involved in Golgi homeostasis, we identified uncharacterized transmembrane protein 199 (TMEM199, previously called C17orf32) as a human homolog of yeast V-ATPase assembly factor Vph2p (also known as Vma12p). Subsequently, we analyzed raw exome-sequencing data from families affected by genetically unsolved CDGs and identified four individuals with different mutations in TMEM199. The adolescent individuals presented with a mild phenotype of hepatic steatosis, elevated aminotransferases and alkaline phosphatase, and hypercholesterolemia, as well as low serum ceruloplasmin. Affected individuals showed abnormal N- and mucin-type O-glycosylation, and mass spectrometry indicated reduced incorporation of galactose and sialic acid, as seen in other Golgi homeostasis defects. Metabolic labeling of sialic acids in fibroblasts confirmed deficient Golgi glycosylation, which was restored by lentiviral transduction with wild-type TMEM199. V5-tagged TMEM199 localized with ERGIC and COPI markers in HeLa cells, and electron microscopy of a liver biopsy showed dilated organelles suggestive of the endoplasmic reticulum and Golgi apparatus. In conclusion, we have identified TMEM199 as a protein involved in Golgi homeostasis and show that TMEM199 deficiency results in a hepatic phenotype with abnormal glycosylation. 相似文献
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PROTEIN filaments are characteristic structural components of the assimilatory conducting elements of angiosperm plants (“P protein” of Cronshaw and Esau1). We have isolated filamentous structures from the phloem exudate of cut cucurbit stems2. The presence of the filaments could be clearly demonstrated after negative staining with the electron microscope. 相似文献
34.
Lock Hock Ngu Leo G. Nijtmans Felix DistelmaierHanka Venselaar Sjenet E. van Emst-de VriesMariël A.M. van den Brand Berendien J.M. StoltenborgLiesbeth T. Wintjes Peter H. WillemsLambertus P. van den Heuvel Jan A. SmeitinkRichard J.T. Rodenburg 《生物化学与生物物理学报:疾病的分子基础》2012,1822(2):168-175
In this study, we investigated the pathogenicity of a homozygous Asp446Asn mutation in the NDUFS2 gene of a patient with a mitochondrial respiratory chain complex I deficiency. The clinical, biochemical, and genetic features of the NDUFS2 patient were compared with those of 4 patients with previously identified NDUFS2 mutations. All 5 patients presented with Leigh syndrome. In addition, 3 out of 5 showed hypertrophic cardiomyopathy. Complex I amounts in the patient carrying the Asp446Asn mutation were normal, while the complex I activity was strongly reduced, showing that the NDUFS2 mutation affects complex I enzymatic function. By contrast, the 4 other NDUFS2 patients showed both a reduced amount and activity of complex I. The enzymatic defect in fibroblasts of the patient carrying the Asp446Asn mutation was rescued by transduction of wild type NDUFS2. A 3-D model of the catalytic core of complex I showed that the mutated amino acid residue resides near the coenzyme Q binding pocket. However, the KM of complex I for coenzyme Q analogs of the Asp446Asn mutated complex I was similar to the KM observed in other complex I defects and in controls. We propose that the mutation interferes with the reduction of coenzyme Q or with the coupling of coenzyme Q reduction with the conformational changes involved in proton pumping of complex I. 相似文献
35.
Jeroen L. A. Pennings Maria P. H. Koster Wendy Rodenburg Peter C. J. I. Schielen Annemieke de Vries 《PloS one》2009,4(11)
Background
To facilitate the experimental search for novel maternal serum biomarkers in prenatal Down Syndrome screening, we aimed to create a set of candidate biomarkers using a data mining approach.Methodology/Principal Findings
Because current screening markers are derived from either fetal liver or placental trophoblasts, we reasoned that new biomarkers can primarily be found to be derived from these two tissues. By applying a three-stage filtering strategy on publicly available data from different sources, we identified 49 potential blood-detectable protein biomarkers. Our set contains three biomarkers that are currently widely used in either first- or second-trimester screening (AFP, PAPP-A and fβ-hCG), as well as ten other proteins that are or have been examined as prenatal serum markers. This supports the effectiveness of our strategy and indicates the set contains other markers potentially applicable for screening.Conclusions/Significance
We anticipate the set will help support further experimental studies for the identification of new Down Syndrome screening markers in maternal blood. 相似文献36.
Antoni Caimari Paula Oliver Wendy Rodenburg Jaap Keijer Andreu Palou 《The Journal of nutritional biochemistry》2010,21(11):1127-1133
Peripheral blood mononuclear cells (PBMC) are easily obtainable cells from blood whose gene expression profiles have been proven to be highly robust in distinguishing a disease state from healthy state. Sterol metabolism is of physiological importance, and although its nutritional response in liver has been described, it is poorly studied in PBMC. To examine if PBMC sterol metabolism reflects diet-induced physiological responses, we analysed the whole genome gene expression response of PBMC and focused on sterol metabolism-related genes affected by different feeding conditions (ad libitum feeding, fasting, and refeeding) in normoweight (control) rats and in diet-induced (cafeteria) obese rats.Our results of microarray analysis show that, in control rats, 21 genes involved in sterol metabolism were regulated by the different feeding conditions, whereas in cafeteria-obese rats, only seven genes showed a changed expression. Most of the genes identified were classified into three pathways: sterol biosynthesis, cholesterol transport and uptake and sterol signaling. The expression profile of these genes was similar to that previously described for liver, decreasing in response to fasting conditions and recovering the levels found in fed animals after 6-h-refeeding. In addition, our data and the comparable expression pattern of sterol metabolism-related genes between PBMC and liver suggest similar sterol regulatory element-binding protein-mediated regulatory mechanisms in response to feeding conditions in both tissues.In conclusion, the expression of genes involved in sterol metabolism is highly controlled by feeding conditions in PBMC of control rats, but this control is impaired in cafeteria-obese animals. The pathophysiological significance of this impairment requires further investigation. 相似文献
37.
Background
Epistatic interactions of multiple single nucleotide polymorphisms (SNPs) are now believed to affect individual susceptibility to common diseases. The detection of such interactions, however, is a challenging task in large scale association studies. Ant colony optimization (ACO) algorithms have been shown to be useful in detecting epistatic interactions.Findings
AntEpiSeeker, a new two-stage ant colony optimization algorithm, has been developed for detecting epistasis in a case-control design. Based on some practical epistatic models, AntEpiSeeker has performed very well.Conclusions
AntEpiSeeker is a powerful and efficient tool for large-scale association studies and can be downloaded from http://nce.ads.uga.edu/~romdhane/AntEpiSeeker/index.html. 相似文献38.
Willemsen M Rodenburg RJ Teszas A van den Heuvel L Kosztolanyi G Morava E 《Mitochondrion》2006,6(3):155-159
Biochemical analysis was performed in muscle tissue and in fibroblasts of four unrelated females consecutively diagnosed with a 'de novo' point mutation in the PDHA1 gene. Pyruvate dehydrogenase E1 subunit deficiency was confirmed in the muscle sample of all patients, however, in three out of four cases the activity of the pyruvate dehydrogenase complex in fibroblasts showed a normal activity. A skewed inactivation was confirmed of the maternal X chromosome in fibroblasts in all children. Due to the possibility of a skewed X inactivation pattern enzyme measurements in fibroblasts are not always reliable for the diagnosis of a PDHc defect in females. Based on the overlapping features of PDHc deficiency with those of the disorders of the oxidative phosphorylation we suggest performing a fresh muscle biopsy for detailed biochemical analysis in females with a suspected pyruvate dehydrogenase deficiency, followed by molecular genetic analysis of the PDHA1 gene. 相似文献
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40.
The threshold for rotation about the yaw axis was determined for constant acceleration stimuli as a function of their duration in the range from 3 to 25 s. From the torsion-swing model the following theoretical equation can be derived: 1 $$a_{{\text{thr}}} = {C \mathord{\left/ {\vphantom {C {\left[ {1 - \exp \left( { - {{t_s } \mathord{\left/ {\vphantom {{t_s } {\tau _1 }}} \right. \kern-\nulldelimiterspace} {\tau _1 }}} \right)} \right]}}} \right. \kern-\nulldelimiterspace} {\left[ {1 - \exp \left( { - {{t_s } \mathord{\left/ {\vphantom {{t_s } {\tau _1 }}} \right. \kern-\nulldelimiterspace} {\tau _1 }}} \right)} \right]}}$$ , where a thr=acceleration amplitude at threshold, t s =duration of the acceleration, τ1=time constant, C=threshold for very long stimuli. According to this formula the Mulder product (i.e. the product of the threshold acceleration amplitude and the duration of the stimulus) is constant for durations up to 0.3 τ1. The best fit of this theoretical function to the somatosensory data is found for τ1=14.5 s, and C=0.220/s 2. The time within the Mulder product is constant (about 5s) is doubtless due to the mechanics of the semicircular canals. For the oculogyral data a lower value of τ1 is found. We do not have any explanation for this lower value. 相似文献