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1.
The isometric length-tension diagram for individual fibers and for whole muscle is considered, and it is proposed that the tensionp may be represented for any muscle whose fibers are parallel and not in series, in the form
$$p = f\left( x \right) + \beta \phi \left( {\alpha ,l,x} \right),$$  相似文献   

2.
Tests ofEpistomaria semi-marginata (D’ORBIGNY) are analysed; a complicated toothplate is present and the marginal foramen is homologised with that ofEpistomina, whereas the supplementary sutural foramina are connected with the toothplate also. The taxonomy of the Epistominidae can be established on the basis of the development of the toothplate inReinholdella, Epistomina, Epistomaria, Cushmanella, Pseudobulimina, Robertina andRobertinoides. Species with coarse pores, double septal walls, spaces between which form supplementary chambers closed ventrally by porous plates, and lacking a toothplate in the chambers do not belong toEpistomaria but are closely allied toGavelinella from the Upper Crateceous. They are joined in the genusEpistomaroides Uchio. Two of them,E. separans (LE CALVEZ) andE. punctata (SAID) are analysed in this paper. The type-species,E. polystomelloides has been analysed 1927 (Siboga I, p. 35–37, Tafel 16, Fig. 1–6).  相似文献   

3.
In this treatise the author describes two species from the Lias, and four from the Dogger. One liassic species is already known (Reinholdella macfadyeni [Ten Dam]) from the Upper Lias (Bifrons-Zone), England, the other one was found by Dr.Bartenstein in Luxemburg, Lias δ Grenze ε, and has been namedReinholdella pachyderma nov. spec. The species from the Dogger areReinholdella dreheri (Bartenstein) and three new species, viz.Reinholdella brandi nov. spec.,Reinholdella ornata nov. spec. andReinholdella epistominoides nov. spec. The genusReinholdella has obviously derived from the genusConorboides Hofker (1951) and the speciesR. epistominoides proves that the genusEpistomina is related withReinholdella. It may be thatReinholdella is related withAsterigerina; but the large gap in the Cretaceous, where noReinholdella is found nor any species ofAsterigerina, contradicts this view.  相似文献   

4.
This member of the vitamin-B complex is necessary in human diet to prevent soreness of mouth, lips and nose, and inflammation of the cornea. It is commercially produced from the fungi Ashbya gossypiiand Eremothecium ashbyii,and is used to enrich various foods and animal feedstuffs.  相似文献   

5.
E. Karrer 《Protoplasma》1933,18(1):475-489
Muscle belongs to a class of highly elastic gels typified by rubber. Results of studies of certain properties of gels seem applicable.
  1. 1.
    The change of fluidity with temperature is logarithmic: log φ=A?Q/TT is absolute temperature. The change of the constants with concentration and mastication suggests that rubber contains long filamentous molecules.  相似文献   

6.
The expressions of Wolfet al. (1951) and Renkin (1956) for the kinetics of artificial kidneys are generalized to include the effects of filtration. IfB is the bath volume,b the relevant volume of distribution,f the filtration rate,t the time, andA 0,B 0,b 0 representA, B, andb at timet=0, then the plasma concentrationA is given by
$$\frac{A}{{A_0 }} = \frac{{B_0 }}{{B_0 + b_0 }}e^{ - \frac{{\left( {B_0 + b_0 } \right)}}{{B_0 }}\frac{{D_f }}{{b_0 }}K\left( {ft} \right)t} + \frac{{b_0 }}{{B_0 + b_0 }}$$  相似文献   

7.
Starting from the basic flux equation, it is possible to obtain an integral form relating the current componentsI i at an arbitrary pointr 2 to the distribution of mobilities and concentrationsc i, potential forces\(\bar \mu \), and chemical productivityp i without any restrictive assumptions such as constant mobilities, constant field, steady state, or electrical neutrality. The equation is
$$\begin{gathered} I_i (r_2 ) = G_i (r_2 )\left[ {\Delta \bar \mu _i - \int_{r_1 }^{r_2 } {z_i } FA\left( {p_i - dc_i /dt} \right)\left( {\frac{1}{{G_i (r)}}} \right)dr} \right]; \hfill \\ G_i (r) = 1/\int_{r_1 }^r {\frac{{dr}}{{z_i^2 F^2 c_i u_i }}.} \hfill \\ \end{gathered} $$  相似文献   

8.
A sample of 12Mus (Leggada) triton Th. from the region of Bukavu (Democratic Republic of Congo) contains 5 ♂♂ and 7 ♀♀. 2N=32. All the autosomes are acrocentric. The sex-chromosomes of the ♂ are of the typeX—Y, theX beeing a big submetacentric (I.C.=0,4). Three ♀♀ possess two metacentricX, as expected. By four ♀♀, there is only one typicalX whose partner is acrocentric and as long as the long arm of a normalX. ThisX must have been arisen through the deletion of the short arm and is calledX ddc. The statistical analysis of the sample is compatible with this pattern:
$$\begin{array}{*{20}c} { \circ \circ } \\ { + + } \\ \end{array} \begin{array}{*{20}c} {X---X = 4/9} \\ {X---X_{dc} = 4/9} \\ {X_{dc} ---X_{dc} = 1/9} \\ \end{array} \begin{array}{*{20}c} { \nearrow \nearrow } \\ { \circ \circ } \\ \end{array} \begin{array}{*{20}c} {X---Y = 2/3} \\ {X_{dc} ---Y = 1/3} \\ \end{array} $$  相似文献   

9.
A polysaccharide was isolated from the opportunistic human pathogen Providencia alcalifaciens O45:H26 by extraction with aqueous phenol and studied by sugar and methylation analyses along with 1H and 13C NMR spectroscopy, including two-dimensional ROESY and H-detected 1H,13C HSQC experiments. The polysaccharide contains N-acetylglu-cosamine and N-acetylmuramic acid (D-GlcpNAc3Rlac) amidated with L-alanine and has the following structure:
$\to 4) - \beta - D - GlcpNAc - (1 \to 4) - \beta - D - GlcpNAc3(Rlac - L - Ala) - (1 \to .$
The polysaccharide possesses a remarkable structural similarity to the bacterial cell wall peptidoglycan. It is not unique to the strain studied but is common to strains of at least four P. alcalifaciens O-serogroups (O3, O24, O38, and O45). No evidence was obtained that the polysaccharide is associated with the LPS, and hence it might represent a bacterial capsule component.
  相似文献   

10.

Background

The Li-Fraumeni syndrome (LFS), an inherited rare cancer predisposition syndrome characterized by a variety of early-onset tumors, is caused by different highly penetrant germline mutations in the TP53 gene; each separate mutation has dissimilar functional and phenotypic effects, which partially clarifies the reported heterogeneity between LFS families. Increases in copy number variation (CNV) have been reported in TP53 mutated individuals, and are also postulated to contribute to LFS phenotypic variability. The Brazilian p.R337H TP53 mutation has particular functional and regulatory properties that differ from most other common LFS TP53 mutations, by conferring a strikingly milder phenotype.

Methods

We compared the CNV profiles of controls, and LFS individuals carrying either p.R337H or DNA binding domain (DBD) TP53 mutations by high resolution array-CGH.

Results

Although we did not find any significant difference in the frequency of CNVs between LFS patients and controls, our data indicated an increased proportion of rare CNVs per genome in patients carrying DBD mutations compared to both controls (p=0.0002***) and p.R337H (0.0156*) mutants.

Conclusions

The larger accumulation of rare CNVs in DBD mutants may contribute to the reported anticipation and severity of the syndrome; likewise the fact that p.R337H individuals do not present the same magnitude of rare CNV accumulation may also explain the maintenance of this mutation at relatively high frequency in some populations.
  相似文献   

11.
12.

Background

Amyloid plaques and neurofibrillary tangles (NFTs) are the defining pathological hallmarks of Alzheimer’s disease (AD). Increasing the quantity of the O-linked N-acetylglucosamine (O-GlcNAc) post-translational modification of nuclear and cytoplasmic proteins slows neurodegeneration and blocks the formation of NFTs in a tauopathy mouse model. It remains unknown, however, if O-GlcNAc can influence the formation of amyloid plaques in the presence of tau pathology.

Results

We treated double transgenic TAPP mice, which express both mutant human tau and amyloid precursor protein (APP), with a highly selective orally bioavailable inhibitor of the enzyme responsible for removing O-GlcNAc (OGA) to increase O-GlcNAc in the brain. We find that increased O-GlcNAc levels block cognitive decline in the TAPP mice and this effect parallels decreased β-amyloid peptide levels and decreased levels of amyloid plaques.

Conclusions

This study indicates that increased O-GlcNAc can influence β-amyloid pathology in the presence of tau pathology. The findings provide good support for OGA as a promising therapeutic target to alter disease progression in Alzheimer disease.
  相似文献   

13.
Seven hitherto unrecognizedSalmonella types are described.S.leiden (13, 22, 36 : z 38),S. enschede (35 : z 10 : l,w) andS. hillegersberg (9, 46 : z 35 : 1,5) were isolated from patients in the Netherlands.S. lawra (44 : k : e,n,z 15) was isolated from a healthy student in Ghana.S. overvecht (30 : a : 1,2),S. woerden (17 : c : z 39) andS. odijk (30 : a : z 39) were isolated from animals kept in zoological gardens in the Netherlands.  相似文献   

14.

Background

Frontotemporal lobar degeneration (FTLD) consists of a clinically and neuropathologically heterogeneous group of syndromes affecting the frontal and temporal lobes of the brain. Mutations in microtubule-associated protein tau (MAPT), progranulin (PGRN) and charged multi-vesicular body protein 2B (CHMP2B) are associated with familial forms of the disease. The prevalence of these mutations varies between populations. The H1 haplotype of MAPT has been found to be closely associated with tauopathies and with sporadic FTLD. Our aim was to investigate MAPT mutations and haplotype frequencies in a clinical series of patients with FTLD in Northern Finland.

Methods

MAPT exons 1, 2 and 9–13 were sequenced in 59 patients with FTLD, and MAPT haplotypes were analysed in these patients, 122 patients with early onset Alzheimer's disease (eoAD) and 198 healthy controls.

Results

No pathogenic mutations were found. The H2 allele frequency was 11.0% (P = 0.028) in the FTLD patients, 9.8% (P = 0.029) in the eoAD patients and 5.3% in the controls. The H2 allele was especially clustered in patients with a positive family history (P = 0.011) but did not lower the age at onset of the disease. The ApoE4 allele frequency was significantly increased in the patients with eoAD and in those with FTLD.

Conclusion

We conclude that although pathogenic MAPT mutations are rare in Northern Finland, the MAPT H2 allele may be associated with increased risks of FTLD and eoAD in the Finnish population.
  相似文献   

15.

Background and aims

Intraspecific aggregation of plant individuals can promote species coexistence by delaying competitive exclusions. However, such impacts may differ among species with contrasting spatial architecture and rely on the spatial distribution of resources.

Methods

We grew a phalanx clonal plant Carex neurocarpa (with aggregated ramets) and a guerilla one Bolboschoenus planiculmis (with diffused ramets) in monocultures or in 1:1 mixtures with an even or a clustered distribution pattern of the two species in homogeneous or heterogeneous soils.

Results

After 16 months, shoot biomass and ramet number were greater in mixtures than in monocultures in C. neurocarpa, but smaller in B. planiculmis. However, the growth of neither C. neurocarpa nor B. planiculmis differed between even and clustered mixtures. Soil nutrient heterogeneity did not significantly affect the growth of either species, but increased relative yield of B. planiculmis and decreased that of C. neurocarpa.

Conclusions

The relative importance of intra- vs. interspecific competition depends on the spatial architecture of plants, and soil nutrient heterogeneity slows down competitive exclusion by decreasing differences in competitive ability between plants. However, our results do not support the idea that intraspecific aggregation of individuals alters competitive interactions between species.
  相似文献   

16.

Background

Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum have been considered as pathogens in animals and humans. The role of wild cervids in the epidemiology is not clear. We analyzed questing Ixodes ricinus ticks collected in spring for these pathogens from sites with high (Fjelløyvær and Strøm) and low density (Tjore, Hinnebu and Jomfruland) of wild cervids to study the spread of the pathogens in questing ticks.

Methods

For detection of Anaplasma phagocytophilum a 77-bp fragment in the msp 2 gene was used. Detection of Borrelia burgdorferi sensu lato was performed using the FL6 and FL7 primers according to sequences of conserved regions of the fla gene. The Osp A gene located on the linear 49-kb plasmid was used as target in multiplex PCR for genotyping. Genospecies-specific primers were used in the PCR for Borrelia burgdorferi sensu stricto, B. afzelii and B. garinii.

Results

Infection rates with Borrelia spp. were significantly lower at Fjelløyvær and Strøm compared to Tjore and Hinnebu; Fjelløyvær vs. Tjore (χ2 = 20.27, p < 0.0001); Fjelløyvær vs. Hinnebu (χ2 = 24.04, p < 0.0001); Strøm vs. Tjore (χ2 = 11.47, p = 0.0007) and Strøm vs. Hinnebu (χ2 = 16.63, p < 0.0001). The Borrelia genospecies were dominated by. B. afzelii (82%) followed by B. garinii (9.7%) and B. burgdorferi sensu stricto (6.9%). B. burgdorferi s.s. was only found on the island of Jomfruland. The infection rate of Anaplasma phagocytophilum showed the following figures; Fjelløyvær vs Hinnebu (χ2 = 16.27, p = 0.0001); Strøm vs. Tjore (χ2 = 13.16, p = 0.0003); Strøm vs. Hinnebu (χ2 = 34.71, p < 0.0001); Fjelløyvær vs. Tjore (χ2 = 3.19, p = 0.0742) and Fjelløyvær vs. Støm (χ2 = 5.06, p = 0.0245). Wild cervids may serve as a reservoir for A. phagocytophilum. Jomfruland, with no wild cervids but high levels of migrating birds and rodents, harboured both B. burgdorferi s.l. and A. phagocytophilum in questing I. ricinus ticks. Birds and rodents may play an important role in maintaining the pathogens on Jomfruland.

Conclusion

The high abundance of roe deer and red deer on the Norwegian islands of Fjelløyvær and Strøm may reduce the infection rate of Borrelia burgdorferi sensu lato in host seeking Ixodes ricinus, in contrast to mainland sites at Hinnebu and Tjore with moderate abundance of wild cervids. The infection rate of Anaplasma phagocytophilum showed the opposite result with a high prevalence in questing ticks in localities with a high density of wild cervids compared to localities with lower density.
  相似文献   

17.

Introduction

Congenital dysplasia of the hip is an abnormal seating of the femoral head in the acetabulum, mainly caused by shallow acetabulum and lax joint capsule. Genetic factors play a considerable role in the pathogenesis of congenital dysplasia of the hip. The gene growth differentiate factor 5 (GDF5) has been implicated in skeletal development and joint morphogenesis in humans and mice. A functional single nucleotide polymorphism (SNP) in the 5'-untranslated region of GDF5 (rs143383) was reported to be associated with osteoarthritis susceptibility. As a key regulator in morphogenesis of skeletal components and soft tissues in and around the joints, GDF5 may be involved in the aetiology and pathogenesis of congenital dysplasia of the hip. Our objective is to evaluate if the GDF5 SNP is associated with congenital dysplasia of the hip in people of Han Chinese origin.

Methods

The GDF5 SNP was genotyped in 338 children with congenital dysplasia of the hip and 622 control subjects.

Results

The SNP was significantly associated with congenital dysplasia of the hip (p = 0.0037; odds ration (OR) = 1.40; 95% confidence interval (CI) = 1.11 to 1.75). A significant difference was detected in female samples when stratified by gender (p = 0.0053; OR = 1.46; 95% CI = 1.21 to 1.91), and in hip dislocation when stratified by severity (p = 0.0078; OR = 1.43; 95% CI = 1.11 to 1.85).

Conclusions

Our results indicate that GDF5 is important in the aetiology of congenital dysplasia of the hip. To the authors' knowledge this is the first time that a definite association with the congenital dysplasia of the hip susceptibility has been detected.
  相似文献   

18.
19.

Background

Chronic inflammation appears to play a role in the pathogenesis of vascular dementia. Given the association between Chlamydia pneumoniae and stroke, the possibility exists that previous exposure to C. pneumoniae may play a role in vascular dementia. The objective of this study was to determine if there was an association between serological evidence of C. pneumoniae infection or inflammatory markers with vascular dementia.

Methods

28 case-patients with vascular dementia at a geriatric clinic and 24 caregiver-controls were tested for C. pneumoniae IgG and IgA antibodies. The association between vascular dementia and C. pneumoniae titres as well as inflammatory markers was estimated by using both conditional logistic regression and stratified logistic regression.

Results

When matched cases were compared to controls, there was no significant difference in elevated C. pneumoniae specific IgG antibodies (titre ≥ 1:32), odds ratio [OR] 1.3 (95% confidence intervals [CI] 0.3 to 6.0), p = 0.71, or in elevated C. pneumoniae specific IgA antibodies (titre ≥ 1:16), OR 2.0 (95%CI 0.5 to 8.0), p = 0.33 indicative of past or persistent C. pneumoniae infection. Similarly, no difference in high IgG or IgA antibody levels (IgG titre ≥ 1:512 or IgA titre ≥ 1:64) between the two groups, indicative of recent C. pneumoniae infection, was found, OR 0.4 (95%CI 0.1 to 2.1), p = 0.27. For C-reactive protein (CRP), the mean difference between 18 matched pairs (case – control) was – 3.33 mg/L. There was no significant difference between cases and controls when comparing log transformed values, OR 0.03 (95%CI 0.00 to 2.89), p = 0.13 or comparing CRP values above or below the median, OR 0.8 (95%CI 0.2 to 3.4), p = 0.71. For fibrinogen, the mean difference between pairs (case – control) was -0.07 g/L. There was no statistical difference between cases and controls when comparing log transformed values, OR 0.6 (95%CI 0.0 to 31.2), p = 0.79 or between fibrinogen values above and below the median, OR = 0.5 (95%CI 0.1 to 2.0), p = 0.50.

Conclusion

We found no evidence for a significant association between C. pneumoniae infection, inflammatory markers such as CRP and fibrinogen, and vascular dementia.
  相似文献   

20.
The potential distribution about a kernleiter is determined according to Weber's method. It is shown that the distribution reduces to the solution of a telegrapher's equation when the volume of the external medium is small. The velocity of propagation as a function of the external volume is determined approximately. This involves the solution of the equation
$$\frac{{\left[ {Y_0 (k\xi )} \right]^\prime }}{{\left[ {J_0 (k\xi )} \right]^\prime }} = \frac{{\left[ {\xi ^{ - a} Y_0 (\xi )} \right]^\prime }}{{\left[ {\xi ^{ - a} J_0 (\xi )} \right]^\prime }}$$  相似文献   

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