144 research outputs found
A hollow cathode arc in neon: Simultaneous laser probing and molecularâbeam sampling of metastable atoms as a plasma diagnostic
The helium atom in a strong magnetic field
We investigate the electronic structure of the helium atom in a magnetic
field b etween B=0 and B=100a.u. The atom is treated as a nonrelativistic
system with two interactin g electrons and a fixed nucleus. Scaling laws are
provided connecting the fixed-nucleus Hamiltonia n to the one for the case of
finite nuclear mass. Respecting the symmetries of the electronic Ham iltonian
in the presence of a magnetic field, we represent this Hamiltonian as a matrix
with res pect to a two-particle basis composed of one-particle states of a
Gaussian basis set. The corresponding generalized eigenvalue problem is solved
numerically, providing in the present paper results for vanish ing magnetic
quantum number M=0 and even or odd z-parity, each for both singlet and triplet
spin symmetry. Total electronic energies of the ground state and the first few
excitations in each su bspace as well as their one-electron ionization energies
are presented as a function of the magnetic fie ld, and their behaviour is
discussed. Energy values for electromagnetic transitions within the M=0 sub
space are shown, and a complete table of wavelengths at all the detected
stationary points with respect to their field dependence is given, thereby
providing a basis for a comparison with observed ab sorption spectra of
magnetic white dwarfs.Comment: 21 pages, 4 Figures, acc.f.publ.in J.Phys.
Isotope shift in the electron affinity of chlorine
The specific mass shift in the electron affinity between ^{35}Cl and ^{37}Cl
has been determined by tunable laser photodetachment spectroscopy to be
-0.51(14) GHz. The isotope shift was observed as a difference in the onset of
the photodetachment process for the two isotopes. In addition, the electron
affinity of Cl was found to be 29138.59(22) cm^{-1}, giving a factor of 2
improvement in the accuracy over earlier measurements. Many-body calculations
including lowest-order correlation effects demonstrates the sensitivity of the
specific mass shift and show that the inclusion of higher-order correlation
effects would be necessary for a quantitative description.Comment: 16 pages, 6 figures, LaTeX2e, amsmat
The dog as an animal model for DISH?
Diffuse idiopathic skeletal hyperostosis (DISH) is a systemic disorder of the axial and peripheral skeleton in humans and has incidentally been described in dogs. The aims of this retrospective radiographic cohort study were to determine the prevalence of DISH in an outpatient population of skeletally mature dogs and to investigate if dogs can be used as an animal model for DISH. The overall prevalence of canine DISH was 3.8% (78/2041). The prevalence of DISH increased with age and was more frequent in male dogs, similar to findings in human studies. In the Boxer breed the prevalence of DISH was 40.6% (28/69). Dog breeds represent closed gene pools with a high degree of familiar relationship and the high prevalence in the Boxer may be indicative of a genetic origin of DISH. It is concluded that the Boxer breed may serve as an animal model for DISH in humans
Evidence for an ependymoma tumour suppressor gene in chromosome region 22pterâ22q11.2
Ependymomas are glial tumours of the brain and spinal cord. The most frequent genetic change in sporadic ependymoma is monosomy 22, suggesting the presence of an ependymoma tumour suppressor gene on that chromosome. Clustering of ependymomas has been reported to occur in some families. From an earlier study in a family in which four cousins developed an ependymoma, we concluded that an ependymoma-susceptibility gene, which is not the NF2 gene in 22q12, might be located on chromosome 22. To localize that gene, we performed a segregation analysis with chromosome 22 markers in this family. This analysis revealed that the susceptibility gene may be located proximal to marker D22S941 in 22pterâ22q11.2. Comparative genomic hybridization showed that monosomy 22 was the sole detectable genetic aberration in the tumour of one of the patients. Loss of heterozygosity studies in that tumour revealed that, in accordance to Knudsonâs two-hit theory of tumorigenesis, the lost chromosome 22 originated from the parent presumed to have contributed the wild-type allele of the susceptibility gene. Thus, our segregation and tumour studies collectively indicate that an ependymoma tumour suppressor gene may be present in region 22pterâ22q11.2. © 1999 Cancer Research Campaig
Modelling the neuropathology of lysosomal storage disorders through disease-specific human induced pluripotent stem cells
Mucopolysaccharidosis II (MPS II) is a lysosomal storage disorder (LSD), caused by iduronate 2-sulphatase (IDS)
enzyme dysfunction. The neuropathology of the disease is not well understood, although the neural symptoms
are currently incurable. MPS II-patient derived iPSC lines were established and differentiated to neuronal
lineage. The disease phenotype was confirmed by IDS enzyme and glycosaminoglycan assay. MPS II neuronal
precursor cells (NPCs) showed significantly decreased self-renewal capacity, while their cortical neuronal differentiation potential was not affected. Major structural alterations in the ER and Golgi complex, accumulation
of storage vacuoles, and increased apoptosis were observed both at protein expression and ultrastructural level
in the MPS II neuronal cells, which was more pronounced in GFAP + astrocytes, with increased LAMP2 expression but unchanged in their RAB7 compartment. Based on these finding we hypothesize that lysosomal
membrane protein (LMP) carrier vesicles have an initiating role in the formation of storage vacuoles leading to impaired lysosomal function. In conclusion, a novel human MPS II disease model was established for the first
time which recapitulates the in vitro neuropathology of the disorder, providing novel information on the disease
mechanism which allows better understanding of further lysosomal storage disorders and facilitates drug testing
and gene therapy approaches
Surgical outcome after spinal fractures in patients with ankylosing spondylitis
<p>Abstract</p> <p>Background</p> <p>Ankylosing spondylitis is a rheumatic disease in which spinal and sacroiliac joints are mainly affected. There is a gradual bone formation in the spinal ligaments and ankylosis of the spinal diarthroses which lead to stiffness of the spine.</p> <p>The diffuse paraspinal ossification and inflammatory osteitis of advanced Ankylosing spondylitis creates a fused, brittle spine that is susceptible to fracture. The aim of this study is to present the surgical experience of spinal fractures occurring in patients suffering from ankylosing spondylitis and to highlight the difficulties that exist as far as both diagnosis and surgical management are concerned.</p> <p>Methods</p> <p>Twenty patients suffering from ankylosing spondylitis were operated due to a spinal fracture. The fracture was located at the cervical spine in 7 cases, at the thoracic spine in 9, at the thoracolumbar junction in 3 and at the lumbar spine in one case. Neurological defects were revealed in 10 patients. In four of them, neurological signs were progressively developed after a time period of 4 to 15 days. The initial radiological study was negative for a spinal fracture in twelve patients. Every patient was assessed at the time of admission and daily until the day of surgery, then postoperatively upon discharge.</p> <p>Results</p> <p>Combined anterior and posterior approaches were performed in three patients with only posterior approaches performed on the rest. Spinal fusion was seen in 100% of the cases. No intra-operative complications occurred. There was one case in which superficial wound inflammation occurred. Loosening of posterior screws without loss of stability appeared in two patients with cervical injuries.</p> <p>Frankel neurological classification was used in order to evaluate the neurological status of the patients. There was statistically significant improvement of Frankel neurological classification between the preoperative and postoperative evaluation. 35% of patients showed improvement due to the operation performed.</p> <p>Conclusion</p> <p>The operative treatment of these injuries is useful and effective. It usually succeeds the improvement of the patients' neurological status. Taking into consideration the cardiovascular problems that these patients have, anterior and posterior stabilization aren't always possible. In these cases, posterior approach can be performed and give excellent results, while total operation time, blood loss and other possible complications are decreased.</p
Evaluation of National Surgical Practice for Lateral Lymph Nodes in Rectal Cancer in an Untrained Setting
Background: Involved lateral lymph nodes (LLNs) have been associated with increased local recurrence (LR) and ipsi-lateral LR (LLR) rates. However, consensus regarding the indication and type of surgical treatment for suspicious LLNs is lacking. This study evaluated the surgical treatment of LLNs in an untrained setting at a national level. Methods: Patients who underwent additional LLN surgery were selected from a national cross-sectional cohort study regarding patients undergoing rectal cancer surgery in 69 Dutch hospitals in 2016. LLN surgery consisted of either ânode-pickingâ (the removal of an individual LLN) or âpartial regional node dissectionâ (PRND; an incomplete resection of the LLN area). For all patients with primarily enlarged (â„7 mm) LLNs, those undergoing rectal surgery with an additional LLN procedure were compared to those undergoing only rectal resection. Results: Out of 3057 patients, 64 underwent additional LLN surgery, with 4-year LR and LLR rates of 26% and 15%, respectively. Forty-eight patients (75%) had enlarged LLNs, with corresponding recurrence rates of 26% and 19%, respectively. Node-picking (n = 40) resulted in a 20% 4-year LLR, and a 14% LLR after PRND (n = 8; p = 0.677). Multivariable analysis of 158 patients with enlarged LLNs undergoing additional LLN surgery (n = 48) or rectal resection alone (n = 110) showed no significant association of LLN surgery with 4-year LR or LLR, but suggested higher recurrence risks after LLN surgery (LR: hazard ratio [HR] 1.5, 95% confidence interval [CI] 0.7â3.2, p = 0.264; LLR: HR 1.9, 95% CI 0.2â2.5, p = 0.874). Conclusion: Evaluation of Dutch practice in 2016 revealed that approximately one-third of patients with primarily enlarged LLNs underwent surgical treatment, mostly consisting of node-picking. Recurrence rates were not significantly affected by LLN surgery, but did suggest worse outcomes. Outcomes of LLN surgery after adequate training requires further research.</p
Promoter methylation of DNA damage repair (DDR) genes in human tumor entities: RBBP8/CtIP is almost exclusively methylated in bladder cancer
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