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1.
Aust Vet J ; 99(11): 469-472, 2021 Nov.
Article in English | MEDLINE | ID: mdl-34389980

ABSTRACT

This study aimed to clarify the effectiveness of foetal body weight estimation by measuring foetal coronet width using transrectal ultrasonography in beef cows during near-term pregnancy. A characteristic 'gull wing' pattern was obtained from the foetal coronet cross-section from the dewclaw side using ultrasonography. This pattern was matched to the bone surface of the distal part of the middle phalanx. Then, the relationship between coronet width and body weight at birth of 22 Japanese Brown calves was analysed and a high correlation coefficient of 0.8965 (P < 0.001) was obtained. In conclusion, the coronet width of the fetus is depicted as a 'gull wing' hyperechoic structure and can be measured by ultrasonography per rectum during near-term pregnancy. This technique may be a useful tool to identify high-risk cows with dystocia before calving. High foetal coronet values may predispose cattle to dystocia.


Subject(s)
Cattle Diseases , Dystocia , Animals , Body Weight , Cattle , Dystocia/diagnostic imaging , Dystocia/veterinary , Female , Fetal Weight , Pilot Projects , Pregnancy , Ultrasonography/veterinary
3.
Ultramicroscopy ; 176: 212-217, 2017 05.
Article in English | MEDLINE | ID: mdl-28089306

ABSTRACT

Electron energy-loss magnetic chiral dichroism (EMCD) spectroscopy, which is similar to the well-established X-ray magnetic circular dichroism spectroscopy (XMCD), can determine the quantitative magnetic parameters of materials with high spatial resolution. One of the major obstacles in quantitative analysis using the EMCD technique is the relatively poor signal-to-noise ratio (SNR), compared to XMCD. Here, in the example of a double perovskite Sr2FeMoO6, we predicted the optimal dynamical diffraction conditions such as sample thickness, crystallographic orientation and detection aperture position by theoretical simulations. By using the optimized conditions, we showed that the SNR of experimental EMCD spectra can be significantly improved and the error of quantitative magnetic parameter determined by EMCD technique can be remarkably lowered. Our results demonstrate that, with enhanced SNR, the EMCD technique can be a unique tool to understand the structure-property relationship of magnetic materials particularly in the high-density magnetic recording and spintronic devices by quantitatively determining magnetic structure and properties at the nanometer scale.

4.
Anim Genet ; 40(5): 763-5, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19456318

ABSTRACT

Two cases of hereditary bleeding disorder diagnosed as haemophilia A were recently observed in Japanese Brown cattle. We sequenced the entire coding region of the factor VIII gene of the affected animals to find a causative mutation. A nucleotide substitution of T to A resulting in an amino acid substitution of leucine to histidine (p.Leu2153His) was identified in a highly conserved residue in the C1 domain of factor VIII. Genotyping of 254 normal animals including the pedigree of the affected animals and randomly sampled animals of different breeds confirmed that the substitution is the causative mutation of cattle haemophilia A.


Subject(s)
Cattle Diseases/genetics , Factor VIII/genetics , Hemophilia A/veterinary , Mutation, Missense/genetics , Animals , Base Sequence , Cattle , Genotype , Hemophilia A/genetics , Japan , Molecular Sequence Data , Pedigree , Sequence Analysis, DNA/veterinary
5.
Phys Rev Lett ; 98(18): 187201, 2007 May 04.
Article in English | MEDLINE | ID: mdl-17501603

ABSTRACT

We have investigated the optical conductivity spectra of La2-2xSr1+2xMn2O7 (0.3

6.
Phys Rev Lett ; 96(2): 027201, 2006 Jan 20.
Article in English | MEDLINE | ID: mdl-16486622

ABSTRACT

Inelastic cold-neutron scattering on LaCoO3 provided evidence for a distinct low energy excitation at 0.6 meV coincident with the thermally induced magnetic transition. Coexisting strong ferromagnetic (FM) and weaker antiferromagnetic correlations that are dynamic follow the activation to the excited state, identified as the intermediate S = 1 spin triplet. This is indicative of dynamical orbital ordering favoring the observed magnetic interactions. With hole doping as in La(1-x)Sr(x)CoO3 , the FM correlations between Co spins become static and isotropically distributed due to the formation of FM droplets. The correlation length and condensation temperature of these droplets increase rapidly with metallicity due to the double exchange mechanism.

7.
Phys Rev Lett ; 97(23): 235501, 2006 Dec 08.
Article in English | MEDLINE | ID: mdl-17280211

ABSTRACT

The perovskite LaCoO3 evolves from a nonmagnetic Mott insulator to a spin cluster ferromagnet (FM) with the substitution of Sr2+ for La3+ in La1-xSrxCoO3. The clusters increase in size and number with x and the charge percolation through the clusters leads to a metallic state. Using elastic neutron scattering on La1-xSrxCoO3 single crystals, we show that an incommensurate spin superstructure coexists with the FM spin clusters. The incommensurability increases continuously with x, with the intensity rising in the insulating phase and dropping in the metallic phase as it directly competes with the commensurate FM, itinerant clusters. The spin incommensurability arises from local order of Co3+-Co4+ clusters but no long-range static or dynamic spin stripes develop. The coexistence and competition of the two magnetic phases explain the residual resistivity at low temperatures in samples with metalliclike transport.

8.
Phys Rev Lett ; 92(2): 027202, 2004 Jan 16.
Article in English | MEDLINE | ID: mdl-14753965

ABSTRACT

Optical spectroscopy was used to determine nearest-neighbor spin correlations in pyrochlore molybdates R2Mo2O7 (R=Y, Sm, and Nd), which exhibit ferromagnetic metal to spin-glass insulator transition as the R ion size decreases. Using an analysis based on the orbitally degenerate Hubbard model, we could estimate important physical parameters, such as the effective on-site Coulomb energy U(eff) and the Hund rule exchange coupling J(H). We demonstrated experimentally and theoretically that the effective superexchange interaction between the Mo ions depends on J(H)/U(eff), which determines the phase boundary of the magnetic ground states.

9.
Nat Mater ; 2(10): 653-5, 2003 Oct.
Article in English | MEDLINE | ID: mdl-12970759

ABSTRACT

The silicon clathrates--materials composed of metal-doped Si(20) dodecahedra--were identified as the first superconductors based on pure silicon networks. The mechanism of superconductivity in these materials can be obtained by studying their phonon modes, as modified by isotope substitution, and specific-heat measurements. Here, we present experimental studies that provide strong evidence that superconductivity in Ba(8)Si(46) is explained in the framework of phonon-mediated Bardeen-Cooper-Schriefer theory. Analyses using the McMillan approximation of the Eliashberg equation indicate that the superconducting mechanism is in the medium coupling regime, but at the high-end limit. The large density of states at the Fermi level, which arises from hybridization of the Si(20) cluster and Ba orbitals, is responsible for the unexpectedly high superconducting temperature. The temperature evolution of the specific heat unambiguously shows that this is an s-wave symmetry superconductor.

10.
Phys Rev Lett ; 91(4): 047201, 2003 Jul 25.
Article in English | MEDLINE | ID: mdl-12906691

ABSTRACT

We have observed magnetic diffuse signals of the bilayer manganite La1.1Sr1.9Mn2O7 by neutron scattering. Even at the low temperature, 20 K, there is a diffuse signal, which is much stronger than that observed in the high temperatures, 144 and 288 K. This signal cannot be characterized by a bilayer structure as observed at 144 K nor by a monolayer structure as at 288 K, but by a high degeneracy of a canted spin structure. Thus, an observation of this diffuse signal is the direct evidence for the establishment of the canted spin structure in La1.1Sr1.9Mn2O7.

11.
Phys Rev Lett ; 90(9): 096404, 2003 Mar 07.
Article in English | MEDLINE | ID: mdl-12689246

ABSTRACT

The relationship between charge and spin degrees of freedom in a geometrically frustrated system, AlV2-xCrxO4 spinel, is investigated. Upon Cr doping, the charge-ordered phase of AlV2O4 is rapidly suppressed and a charge-disordered phase grows up instead. It is found that the magnetic ground state is a spin-glass state dominated by geometrical frustration for both phases, but larger spin entropy remains down to low temperatures in the charge-ordered phase, possibly owing to its two-dimensional character.

12.
Phys Rev Lett ; 91(25): 255502, 2003 Dec 19.
Article in English | MEDLINE | ID: mdl-14754125

ABSTRACT

The charge density distribution has been determined for a transition metal cyanide, RbMn[Fe(CN)(6)], by means of the maximum entropy-Rietveld method combined with the highly angularly resolved synchrotron radiation x-ray powder diffraction at SPring-8 BL02B2. We directly observed a charge transfer from the Mn site to the Fe site in the low-temperature phase. On the basis of a local density approximation calculation, we discuss the origin for the anisotropic bonding electron distribution around the Mn3+ ion in the low-temperature phase.

13.
Anim Genet ; 33(5): 351-5, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12354143

ABSTRACT

Fibroblast growth factor receptor 3 (FGFR3) is one of the four distinct membrane-spanning tyrosine kinase receptors for fibroblast growth factors. The FGFR3 is a negative regulator of endochondral ossification and mutations in the FGFR3 gene have been found in patients of human hereditary diseases with chondrodysplastic phenotypes. Recently, we mapped the locus responsible for hereditary chondrodysplastic dwarfism in Japanese brown cattle to the distal region of bovine chromosome 6 close to the FGFR3 gene, suggesting that FGFR3 was a positional candidate gene for this disorder. In the present study, we isolated complementary DNA (cDNA) clones containing the entire coding region of the bovine FGFR3 gene. Comparison of the nucleotide sequence between affected and normal animals revealed no disease-specific differences in the deduced amino acid sequences. We further refined the localization of FGFR3 by radiation hybrid mapping, which is distinct from that of the disease locus. Therefore we conclude that bovine chondrodysplastic dwarfism in Japanese brown cattle is not caused by mutation in the FGFR3 gene.


Subject(s)
Cattle Diseases/genetics , Dwarfism/veterinary , Osteochondrodysplasias/veterinary , Protein-Tyrosine Kinases , Receptors, Fibroblast Growth Factor/genetics , Animals , Base Sequence , Cattle , Chromosome Mapping , DNA, Complementary/genetics , Dwarfism/genetics , Humans , Mutation , Osteochondrodysplasias/genetics , Receptor, Fibroblast Growth Factor, Type 3 , Reverse Transcriptase Polymerase Chain Reaction , Species Specificity
14.
Phys Rev Lett ; 89(1): 016403, 2002 Jul 01.
Article in English | MEDLINE | ID: mdl-12097058

ABSTRACT

We systematically investigated optical properties of Nd1-xSrxMnO3 single crystals ( x = 0.40, 0.50, 0.55, and 0.65). They are similar in their spin-orbital (SO) disordered states at room temperature. At low temperature, the crystals enter into various SO ordered states, i.e., F-, CE-, A-, and C-type orderings, and their mid-infrared absorptions become quite different. The remarkable variation can be explained by polaron dynamics which depend on the ordering patterns. This SO pattern dependent polaron model can also explain the pseudo CE-type ordering case, demonstrating that this scheme can explain the carrier dynamics in complex SO configurations.

15.
J Vet Med Sci ; 63(12): 1335-7, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11789614

ABSTRACT

Atlanto-occipital fusion in a Japanese Brown calf was examined morphologically, paying special attention to skeletal changes. At the craniovertebral junction, the basal occipital bone fused to the cranial extremity of the ventral arch of the atlas with the rudiment of the atlantal centrum. The dens was not formed at the axis. These changes suggest that a hypocentrum and a centrum of the atlas derived from the first cervical sclerotome had failed to separate the occipital base from the proatlantal sclerotome including the apical element of the dens. Although a developmental disturbance at the cervical and thoracic vertebrae was also associated, critical neurological signs such as ataxia and paralysis were absent.


Subject(s)
Atlanto-Occipital Joint/abnormalities , Cattle/abnormalities , Animals , Fatal Outcome , Female
16.
Phys Rev Lett ; 85(20): 4353-6, 2000 Nov 13.
Article in English | MEDLINE | ID: mdl-11060636

ABSTRACT

We present elastic and quasielastic neutron scattering measurements characterizing peculiar short-range charge-orbital and spin order in the layered perovskite material La1.5Sr0.5CoO4. We find that below T(c) approximately 750 K holes introduced by Sr doping lose mobility and enter a statically ordered charge glass phase with loosely correlated checkerboard arrangement of empty and occupied d(3z(2)-r(2)) orbitals ( Co3+ and Co2+). The dynamics of the resultant mixed spin system is governed by the anisotropic nature of the crystal-field Hamiltonian and the peculiar exchange pattern produced by the orbital order. It undergoes a spin freezing transition at a much lower temperature, T(s) less, similar30 K.

17.
Phys Rev Lett ; 85(18): 3914-7, 2000 Oct 30.
Article in English | MEDLINE | ID: mdl-11041959

ABSTRACT

The temperature variation of the resistivity rho and specific heat C have been measured for prototypical half-metallic ferromagnets, R0. 6Sr 0.4MnO3, by controlling the one-electron bandwidth W. We have found variations in the temperature scalings of rho from approximately T2 ( R = La, and Nd) to approximately T3 ( R = Sm), and have interpreted the T3 law in terms of the anomalous single-magnon scattering process in the half-metallic system.

18.
J Vet Med Sci ; 61(10): 1147-52, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10563294

ABSTRACT

Thirteen anomalous calves with clefts of the face were morphologically examined, and craniofacial skeletons were studied in detail. According to the type and site of the cleft, four groups could be distinguished: median cleft lip and jaw (CLJ); median cleft lip, jaw, and palate (CLJP); lateral CLJ; and cleft palate (CP), including unilateral and bilateral type. Craniofacial skeletal abnormalities were observed in several bones at the roof, wall, and floor of the nasal cavity and at the boundary portion between the nasal and cranial cavities. Fissure formation at the cranial sutures, partial absence of the nasal process of the incisive bone, and opening of the bony palate were characteristic changes in median CLJ and CLJP, lateral CLJ, and CP, respectively. Furthermore, various associated changes were recognized in the median and paramedian skeletal elements of the face and other organs. The morphological changes of craniofacial skeletons with various types of clefts of the face depended on the site and degree of the cleft formation and reflected developmental errors of the facial embryonic segments. These changes would suggest disorders of the correlated development of facial processes and of other fetal organs of the face. For these conditions, etiologically hereditary cases were negative.


Subject(s)
Cattle/abnormalities , Cleft Lip/veterinary , Cleft Palate/veterinary , Craniofacial Abnormalities/veterinary , Animals , Antibodies, Viral/blood , Cattle/embryology , Cleft Lip/embryology , Cleft Lip/pathology , Cleft Palate/embryology , Cleft Palate/pathology , Cranial Sutures/abnormalities , Cranial Sutures/embryology , Craniofacial Abnormalities/embryology , Craniofacial Abnormalities/pathology , Face/abnormalities , Face/embryology , Female , Male , Nasal Cavity/abnormalities , Nasal Cavity/embryology
19.
Mamm Genome ; 10(6): 597-600, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10341093

ABSTRACT

A hereditary chondrodysplastic dwarfism caused by an autosomal recessive gene has been reported in a population of Japanese Brown cattle. Affected calves show an insufficiency of endochondral ossification at the long bones of the limbs. In the present study, we mapped the locus responsible for the disease (bcd) by linkage analysis, using microsatellite markers and a single paternal half-sib pedigree obtained from commercial herds. Linkage analysis revealed a significant linkage between the bcd locus and marker loci on the distal region of bovine Chromosome (Chr) 6. The bcd locus was mapped in the interval between microsatellite markers BM9257 and BP7 or BMS511 with a recombination fraction of 0.05 and 0.06, and a lod score of 8.6 and 10.1, respectively. A comparison of genetic maps between bovine Chr 6 and human Chr 4 or mouse Chr 5 indicates possible candidate genes including FGFR3 and BMP3 genes, which are responsible for human chondrodysplasias and associated with bone morphogenesis, respectively.


Subject(s)
Cattle Diseases/genetics , Chromosome Mapping , Dwarfism/veterinary , Osteochondrodysplasias/veterinary , Protein-Tyrosine Kinases , Animals , Bone Morphogenetic Protein 3 , Bone Morphogenetic Proteins/genetics , Cattle , Chromosomes, Human , Dwarfism/genetics , Female , Genetic Linkage , Growth Substances/genetics , Humans , Male , Mice , Microsatellite Repeats , Osteochondrodysplasias/genetics , Pedigree , Receptor, Fibroblast Growth Factor, Type 3 , Receptors, Fibroblast Growth Factor/genetics
20.
Diabetes Res Clin Pract ; 36(1): 11-8, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9187410

ABSTRACT

Increased plasma plasminogen activator inhibitor type 1 (PAI-1), coagulation factor VII (FVII) and fibrinogen levels have been recognized as risk factors for cardiovascular disease. Because a substantially high incidence of cardiovascular disease has been reported in diabetic patients with nephropathy compared with those without nephropathy, we measured plasma levels of PAI-1, FVII activity and fibrinogen in non-insulin-dependent diabetic patients (NIDDM) with normoalbuminuria (without nephropathy), microalbuminuria (incipient nephropathy) and macroalbuminuria (overt nephropathy). PAI-1 and FVII levels were significantly increased in NIDDM with overt nephropathy compared with NIDDM without nephropathy. Fibrinogen levels were comparable between the patients with normo-, micro- and macro-albuminuria. Univariate regression analysis indicated that PAI-1 and FVII levels were significantly correlated with the albumin excretion rate (AER) in urine. PAI-1, FVII and fibrinogen levels were significantly correlated with the degree of insulin resistance estimated by the steady state plasma glucose concentration (SSPG) during the continuous infusion of glucose, insulin and octreotide. PAI-1 levels were correlated with plasma triglyceride (TG) levels. Multiple regression analysis revealed that AER was significantly associated with PAI-1 and FVII levels, whereas TG lost significant correlation with PAI-1 when AER, SSPG and plasma TG were entered as independent variables. SSPG retained an independent correlation with fibrinogen, PAI-1 and FVII levels. These results suggest that elevated plasma levels of PAI-1 and FVII in NIDDM patients with nephropathy are directly associated with renal damage, whereas insulin resistance widely regulates hemostatic components in NIDDM patients, irrespective of the presence of nephropathy.


Subject(s)
Albuminuria/urine , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/urine , Factor VII/analysis , Plasminogen Activator Inhibitor 1/blood , Blood Glucose/analysis , Diabetes Mellitus, Type 2/physiopathology , Female , Homeostasis , Humans , Insulin Resistance , Male , Middle Aged , Osmolar Concentration , Triglycerides/blood
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