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1.
J Genet ; 96(5): 783-794, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29237887
2.
Eur Cell Mater ; 20: 45-57, 2010 Jul 21.
Article in English | MEDLINE | ID: mdl-20648425

ABSTRACT

Dexamethasone (Dex) is used widely to induce differentiation in human mesenchymal stem cells (hMSCs); however, using a pharmaceutical agent to stimulate hMSC differentiation is not the best choice for engineered tissue transplantation due to potential side-effects. The goal of the present study was to investigate the effects of dynamic compressive loading on differentiation and mineralized matrix production of hMSCs in 3D polyurethane scaffolds, using a loading regimen previously shown to stimulate mineralised matrix production of mature bone cells (MLO-A5). hMSCs were seeded in polyurethane scaffolds and cultured in standard culture media with or without Dex. Cell-seeded scaffolds were compressed at 5% global strain for 2 h on day 9 and then every 5 days in a media-filled sterile chamber. Samples were tested for mRNA expression of alkaline phosphatase (ALP), osteopontin (OPN), collagen type 1 (col 1) and runt-related transcription factor-2 (RUNX-212 h) after the first loading, cell viability by MTS assay and alkaline phosphatase activity at day 12 of culture and cell viability, collagen content by Sirius red and calcium content by alizarin red at day 24 of culture. Neither Dex nor loading had significant effects on cell viability. Collagen content was significantly higher (p<0.01) in the loaded group compared with the non-loaded group in all conditions. There was no difference in ALP activity or the amount of collagen and calcium produced between the non-loaded group supplemented with Dex and the loaded group without Dex. We conclude that dynamic loading has the ability to stimulate osteogenic differentiation of hMSC in the absence of glucocorticoids.


Subject(s)
Bone Marrow Cells/cytology , Calcification, Physiologic , Dexamethasone/pharmacology , Glucocorticoids/pharmacology , Mesenchymal Stem Cells/cytology , Alkaline Phosphatase/genetics , Alkaline Phosphatase/metabolism , Bone Marrow Cells/drug effects , Bone Marrow Cells/metabolism , Calcification, Physiologic/drug effects , Cell Differentiation , Cell Survival , Cells, Cultured , Collagen Type I/metabolism , Core Binding Factor alpha Subunits/metabolism , Extracellular Matrix/metabolism , Humans , Mechanical Phenomena , Mesenchymal Stem Cells/drug effects , Mesenchymal Stem Cells/metabolism , Osteopontin/metabolism , RNA, Messenger/metabolism , Tissue Engineering
3.
Eye (Lond) ; 23(3): 640-4, 2009 Mar.
Article in English | MEDLINE | ID: mdl-18327160

ABSTRACT

PURPOSE: To establish the contemporary aetiology of adult superior oblique palsy (SOP). MATERIALS AND METHODS: A retrospective consecutive case series of 150 persons diagnosed with SOP between 1 January 1999 and 31 May 2005 at a neuro-ophthalmology centre in the West Midlands, the United Kingdom. Interrogating two different hospital databases identified all cases. A case note review was performed on all participants to determine demographics and aetiology based on diagnostic criteria, neuroimaging used, and outcome. RESULTS: We identified 133 unilateral isolated, 7 unilateral associated with other cranial nerve involvement, and 10 bilateral cases of SOP. Eighty-six were acquired, 51 congenital, and 13 undetermined. Of the unilateral isolated cases, 38.3% were considered to be congenital, 29.3% followed trauma, 23.3% were presumed to be vasculopathic in origin, and no cause could be established in 7.5%. All presumed microvascular-associated palsies resolved within 6 months of presentation. Unilateral SOPs associated with other cranial nerve palsies were commonly caused by trauma (71.4%), followed by tumour and undetermined causes (both 14.3%). Trauma was the most frequent cause of bilateral SOP (50%), followed by tumours and undetermined causes (both 20%), with congenital causes being uncommon (10%). CONCLUSION: We present a contemporary aetiological spectrum for adult SOP, with the lowest incidence of undetermined cases published in the medical literature. Neuroimaging did not change the management for the vast majority of cases and should be prompted by atypical presentations.


Subject(s)
Trochlear Nerve Diseases/etiology , Adolescent , Adult , Age Distribution , Aged , Aged, 80 and over , Brain Neoplasms/complications , Humans , Hypertension/complications , Middle Aged , Orbital Neoplasms/complications , Prognosis , Retrospective Studies , Trochlear Nerve Diseases/congenital , Trochlear Nerve Diseases/diagnosis , Trochlear Nerve Injuries , Young Adult
4.
J Environ Qual ; 34(5): 1682-6, 2005.
Article in English | MEDLINE | ID: mdl-16091621

ABSTRACT

Applications of animal manures have increased soil test P values in many parts of the USA and thus increased the risk that soil P will be transferred to surface water and decrease water quality. To continue farming these areas, landowners need tools to reduce the risk of P losses. A field experiment was conducted near Kurten, TX, on a Zulch fine sandy loam (thermic Udertic Paleustalfs) with Bray-1 P values exceeding 3000 mg P kg(-1) soil (dry wt.) in the A(p) horizon to evaluate the effectiveness of soil amendments for reducing soil test P values. Soils were amended annually from 1999 to 2001 with 1.5 and 5.0 Mg gypsum ha(-1), 1.4 Mg alum ha(-1), or 24.4 Mg ha(-1) of waste paper product high in Al alone or in combination with 1.5 Mg gypsum ha(-1) and/or 1.4 Mg alum ha(-1). These treatments supplied a maximum of 225 and 1163 kg ha(-1) yr(-1) of Al and Ca, respectively. Soil Bray-1 P and dissolved reactive P levels were monitored from 1999 to 2004. None of the soil amendment treatments affected Bray-1 P values. Only annual additions of 5.0 Mg gypsum ha(-1) from 1999 to 2001 significantly reduced soil dissolved reactive P. Dissolved reactive P levels reached minimal levels after two applications of 5.0 Mg gypsum ha(-1) but increased in 2003 and 2004. These results indicate that soil dissolved reactive P levels can be reduced if sufficient amounts of gypsum were added to supply Ca in amounts similar to the soil test P values.


Subject(s)
Environmental Pollutants/analysis , Manure , Phosphorus/analysis , Soil/analysis , Agriculture/methods , Alum Compounds/chemistry , Calcium Sulfate/chemistry , Phosphorus/chemistry , Texas
5.
Clin Genet ; 63(1): 1-9, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12519363

ABSTRACT

Common disorders are, by definition, the major cause of ill health and death. Most can be modified by avoiding or shielding an environment, as in sunburn and coeliac disease, by replacing some deficient substance, as in diabetes or myxoedema, or by empirical methods of evident effect as in schizophrenia and depressive illness. As expected, all show an increased incidence in relatives and the identification of the more influential loci involved may define unexpected links in the metabolic map: these may be amenable to therapy, or, in autoimmune disorders and asthma, define precipitating factors by sequencing the receptor involved. The major investment in trawling the genotype for influential loci has been by affected sib-pairs with parents (ASPs). Over a hundred major studies have been published with very limited success. No substantial study of normal sib-pairs has been undertaken, making this family of surveys one of the largest undertaken in the absence of controls. Possible reasons for this limited success and the many suggestive false positives are considered.


Subject(s)
Multifactorial Inheritance/genetics , Siblings , False Positive Reactions , Haplotypes , Humans , Models, Biological
6.
7.
Ann Hum Genet ; 63(Pt 2): 101-24, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10738523

ABSTRACT

A meeting on chromosome 9 was held on Tuesday, 27 October 1998 in Denver, with 38 participants (see appendix). Since the last meeting several of the positional cloning efforts on chromosome 9q have come to fruition, and the most detailed discussion was on 9p. Dr Ian Dunham from the Sanger Centre explained the strategy to be used for sequencing chromosome 9, and encouraged collaboration in the preparatory mapping. He indicated that some priority could be given to those regions where people in the field had a strong interest and could identify relevant PAC clones. At this short meeting it was clearly not possible to construct a comprehensive map of chromosome 9, and it was decided that efforts should be made to maintain links to sources of information on the chromosome 9 web page (http:@www.gene.ucl.ac.uk/chr9/). The discussions at the meeting are summarized in four sections: 9p, 9cen-q31, 9q32-9q34 and comparative mapping. Many of the posters presented at the meeting were also presented at the ASHG meeting (28-31 October 1998). They are listed here and are published in The American Journal of Human Genetics, vol. 63 (supplement). Abstracts for posters presented only at this meeting are appended to this report.


Subject(s)
Chromosomes, Human, Pair 9/genetics , Animals , Chromosome Mapping , Genetic Diseases, Inborn/genetics , Humans , Mice , Microsatellite Repeats
8.
Ann Hum Genet ; 62(Pt 5): 365-77, 1998 Sep.
Article in English | MEDLINE | ID: mdl-10088034

ABSTRACT

Penrose's sib-pair papers (1935-1953) are discussed in relation to recent applications. His essential contribution that parental typing was an inefficient addition to sib-pair data for linkage detection remains. Parents now have even less to offer with contemporary markers in the detection of linkage, although not the enumeration of haplotypes. Attention is drawn to two little known papers by Penrose on multifactorial disease, and it is suggested that this term should replace polygenic in relation to family analyses. The convention established by Penrose, both as author and editor, of raw data being published alongside its analysis, which later fell into disuse on grounds of sheer bulk, can now be remedied by the Internet, and has been for the largest set of sib-pair data on diabetes (Davies et al. Nature 371 (1994), 130-136). This is essential if the contributions to the identity and location of alleles possibly relevant to common disorders, none of which are likely to be more than suggestive in any single study, can be combined to assess consistency and joint evidence. Attention is drawn to a third little known paper by Penrose of high relevance to the strategy of familial investigations in multifactorial disorders. All five of the Penrose papers discussed here can be viewed at http:/(/)www.gene.ucl.ac.uk/anhumgen/.


Subject(s)
Genetic Linkage , Genetics/history , Nuclear Family , England , Female , History, 20th Century , Humans , Male , Models, Statistical , Multifactorial Inheritance , Pedigree
9.
Ann Hum Genet ; 61(Pt 4): 351-64, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9365787

ABSTRACT

Affected sib pairs with typed but unaffected parents, conveniently termed foursomes, have become a major source of information on genetic susceptibility to common disease. So far most methods of analysis have been based on extensions of the single locus analyses developed, and successfully applied, to the mendelian disorders. However, unifactorial methods are not suited to multifactorial disorders. The power of methods of detecting linkage in the presence of more than one locus with one or more susceptibility alleles is considered. The relevance of familial clustering to predicting the presence of loci with susceptibility or resistance alleles sufficiently frequent and effective to have an appreciable influence on population incidence is discussed. The mathematical problem of clustering due to numerous alleles of small effect was resolved by Pearson in 1901 in relation to claims that the mendelian model of an allele at a single locus determining a distinct phenotype was necessary to explain the familial concentrations that had been observed in several species. The apparent inconsistency between the mendelian and polygenic models was resolved by Fisher's demonstration in 1918 that there was no essential difference between these two extreme forms of phenotypic determination. Although constant penetrance models are unrealistic, and no longer necessary since Pearson's analysis, the assumption is implicit in most recent analyses and has the advantage of simplicity in providing a lower limit on the sample sizes necessary.


Subject(s)
Genetic Linkage , Models, Genetic , Nuclear Family , Penetrance , Disease Susceptibility , Humans , Matched-Pair Analysis
10.
Nature ; 381(6577): 17, 1996 May 02.
Article in English | MEDLINE | ID: mdl-8609976
12.
Cytogenet Cell Genet ; 69(3-4): 175-8, 1995.
Article in English | MEDLINE | ID: mdl-7698005

ABSTRACT

Families from the linkage panel of Centre d'Etude du Polymorphisme Humain have been used to generate a linkage map containing 68 loci; 13 genes, 33 di- and 4 tetranucleotide repeats, one oligonucleotide ligation assay (OLA), and 17 RFLPs. This map integrates markers from several previous maps, and has undergone further error checking. 43 loci have been placed with odds of 1000:1 or greater, five with odds of 100:1, with an average interval of 3.5 cM. An additional 20 loci have been placed within defined intervals.


Subject(s)
Chromosome Mapping , Chromosomes, Human, Pair 14 , Genetic Linkage , Genetic Markers , Humans , Polymorphism, Restriction Fragment Length
13.
Nature ; 373(6510): 98, 1995 Jan 12.
Article in English | MEDLINE | ID: mdl-7880281
14.
Curr Opin Genet Dev ; 4(6): 861-7, 1994 Dec.
Article in English | MEDLINE | ID: mdl-7888756

ABSTRACT

The mammals all have similar amounts of DNA, usually distributed over 40-60 chromosomes. Most of the differences in karyotype are related to fixation of less than 100 reciprocal translocations which have occurred over less than 100 million years. This allows the genome mapping of the main laboratory and farmyard species to help, and to be helped by, mapping of the human genome.


Subject(s)
Chromosome Mapping/methods , Genome , Mammals/genetics , Animals , Cattle , Chromosomes, Artificial, Yeast , Genetic Linkage , Genome, Human , Humans , Marsupialia , Mice , Monotremata , Sheep , Species Specificity , Swine
16.
Ann Hum Genet ; 58(2): 145-50, 1994 05.
Article in English | MEDLINE | ID: mdl-7979158

ABSTRACT

The problem of detecting linkage between two loci expressed as similar phenotypes and two or more marker loci from a set of families is discussed and a solution advanced. The term amphigenic is suggested for such conditions.


Subject(s)
Genetic Linkage , Genetic Markers , Humans , Lod Score , Phenotype
17.
J Med Genet ; 31(1): 1-19, 1994 Jan.
Article in English | MEDLINE | ID: mdl-8151633

ABSTRACT

Details are given of 214 loci known to be associated with human hereditary disease, which have been mapped on both human and mouse chromosomes. Forty two of these have pathological variants in both species; in general the mouse variants are similar in their effects to the corresponding human ones, but exceptions include the Dmd/DMD and Hprt/HPRT mutations which cause little, if any, harm in mice. Possible reasons for phenotypic differences are discussed. In most pathological variants the gene product seems to be absent or greatly reduced in both species. The extensive data on conserved segments between human and mouse chromosomes are used to predict locations in the mouse of over 50 loci of medical interest which are mapped so far only on human chromosomes. In about 80% of these a fairly confident prediction can be made. Some likely homologies between mapped mouse loci and unmapped human ones are also given. Sixty six human and mouse proto-oncogene and growth factor gene homologies are also listed; those of confirmed location are all in known conserved segments. A survey of 18 mapped human disease loci and chromosome regions in which the manifestation or severity of pathological effects is thought to be the result of genomic imprinting shows that most of the homologous regions in the mouse are also associated with imprinting, especially those with homologues on human chromosomes 11p and 15q. Useful methods of accelerating the production of mouse models of human hereditary disease include (1) use of a supermutagen, such as ethylnitrosourea (ENU), (2) targeted mutagenesis involving ES cells, and (3) use of gene transfer techniques, with production of 'knockout mutations'.


Subject(s)
Genetic Diseases, Inborn/genetics , Animals , Chromosome Mapping , Genetic Variation , Humans , Mice , Proto-Oncogene Mas , Proto-Oncogenes , Species Specificity
18.
J Neurol Sci ; 116(2): 193-200, 1993 Jun.
Article in English | MEDLINE | ID: mdl-8336166

ABSTRACT

Skeletal muscle function of 15 patients with myotonic dystrophy (dystrophia myotonica, DM) was investigated using 31P magnetic resonance spectroscopy to evaluate bioenergetics and intracellular pH at rest and during exercise and recovery. Results from DM patients, normal controls and mitochondrial myopathy patients were compared in order to assess the possible contribution of abnormal mitochondrial metabolism to muscle dysfunction in DM. In resting DM muscle, intracellular pH (pHi) was normal, but there were significant elevations in the concentration ratios of Pi/ATP, phosphomonoesters/ATP and phosphodiesters/ATP. In patients with the most severe exercise intolerance the phosphocreatine/ATP ratio was also reduced. Resting muscle of 11 mitochondrial myopathy patients showed similar changes to those of the most exercise-intolerant DM patients. In exercising DM muscle, energy stores were rapidly depleted as in mitochondrial myopathy. Muscle acidified in all subjects, but in DM the decrease in pHi was less than in normal muscle. Recovery half-times for phosphocreatine, Pi and ADP were normal in DM but slow in mitochondrial myopathy. The initial rate of phosphocreatine repletion after exercise was rapid in DM, consistent with high [ADP], but slow in mitochondrial myopathy in spite of elevated [ADP]. Because recovery is an oxidative process, we conclude that there was no decrease in the oxidative capacity of the muscles in this group of DM patients. In the subjects in whom it could be measured, the rate of recovery of intracellular pH was greater in the 3 DM patients (0.14, 0.15 and 0.16 U/min) than in the 7 normal controls (0.08-0.12 U/min, mean 0.10). The results do not rule out a minor abnormality in glycogenolysis, but they suggest that the failure to acidify normally during exercise is probably due to rapid proton efflux.


Subject(s)
Energy Metabolism/physiology , Muscles/metabolism , Myotonic Dystrophy/metabolism , Adenosine Diphosphate/metabolism , Adult , Exercise/physiology , Female , Forearm/physiology , Humans , Hydrogen-Ion Concentration , Magnetic Resonance Spectroscopy , Male , Middle Aged , Mitochondrial Myopathies/metabolism , Phosphates/metabolism , Phosphocreatine/metabolism , Rest/physiology
20.
Eur Respir J ; 6(4): 467-76, 1993 Apr.
Article in English | MEDLINE | ID: mdl-8491295

ABSTRACT

The purpose of this study was to determine the cellular events occurring 6 h after bronchial inhalation challenge, in a group of pigeon breeders. Twelve subjects agreed to undergo challenge, either with nebulized pigeon serum (Ps) (n = 10), or with saline (n = 2). The development of characteristic symptoms was used to detect a positive response in combination with monitoring tests (white blood cell count (WBC), body temperature, and spirometry). An initial bronchoalveolar lavage (BAL) was performed before inhalation challenge, and a further BAL on the previously spared right middle lobe subsegment or lingula 6 h after challenge. Paired bronchoalveolar lavage fluid (BALF) samples were analysed for urea, albumin, total and differential WBC, interleukin-1 and interleukin-2. There was a significant increase in total cells, lymphocytes, T-lymphocytes, and neutrophils; numbers.ml-1 of BALF in responders. A monitoring score reflecting severity of patient response correlated with an increase in all cell types (p < 0.05). In conclusion, responders developed both a BALF lymphocytic and neutrophilic "alveolitis" following inhalation challenge, the degree of BALF "alveolitis" correlating with the severity of patient response.


Subject(s)
Bird Fancier's Lung/diagnosis , Bronchoalveolar Lavage Fluid , Columbidae/immunology , Adult , Albumins/analysis , Animals , Bird Fancier's Lung/pathology , Bronchial Provocation Tests , Bronchoalveolar Lavage Fluid/chemistry , Bronchoalveolar Lavage Fluid/cytology , Enzyme-Linked Immunosorbent Assay , Forced Expiratory Volume , Humans , Interleukin-1/analysis , Interleukin-2/analysis , Middle Aged , Time Factors , Urea/analysis , Vital Capacity
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