Search Results - "Booms, P"

Reduction of relative centrifugal forces increases growth factor release within solid platelet-rich-fibrin (PRF)-based matrices: a proof of concept of LSCC (low speed centrifugation concept) by El Bagdadi, K., Kubesch, A., Yu, X., Al-Maawi, S., Orlowska, A., Dias, A., Booms, P., Dohle, E., Sader, R., Kirkpatrick, C. J., Choukroun, J., Ghanaati, S.

“…Purpose The present study evaluated the platelet distribution pattern and growth factor release (VEGF, TGF-β1 and EGF) within three PRF (platelet-rich-fibrin)…”
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Potential lack of “standardized” processing techniques for production of allogeneic and xenogeneic bone blocks for application in humans by Ghanaati, S., Barbeck, M., Booms, P., Lorenz, J., Kirkpatrick, C.J., Sader, R.A.

“…[Display omitted] In the present study, the structure of two allogeneic and three xenogeneic bone blocks, which are used in dental and orthopedic surgery, were…”
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Platelet-rich fibrin secretome induces three dimensional angiogenic activation in vitro by Herrera-Vizcaíno, C, Dohle, E, Al-Maawi, S, Booms, P, Sader, R, Kirkpatrick, C J, Choukroun, J, Ghanaati, S

“…Different tissue engineering techniques are used to support rapid vascularisation. A novel technique is the use of platelet-rich fibrin (PRF), an autologous…”
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The molecular genetics of Marfan syndrome and related disorders by Robinson, P N, Arteaga-Solis, E, Baldock, C, Collod-Béroud, G, Booms, P, De Paepe, A, Dietz, H C, Guo, G, Handford, P A, Judge, D P, Kielty, C M, Loeys, B, Milewicz, D M, Ney, A, Ramirez, F, Reinhardt, D P, Tiedemann, K, Whiteman, P, Godfrey, M

“…Marfan syndrome (MFS), a relatively common autosomal dominant hereditary disorder of connective tissue with prominent manifestations in the skeletal, ocular,…”
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Monocyte preseeding leads to an increased implant bed vascularization of biphasic calcium phosphate bone substitutes via vessel maturation by Barbeck, M., Unger, R. E., Booms, P., Dohle, E., Sader, R. A., Kirkpatrick, C. J., Ghanaati, S.

“…The present study analyzes the influence of the addition of monocytes to a biphasic bone substitute with two granule sizes (400–700 μm and 500–1000 μm). The…”
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Genetic variation in RYR1 and malignant hyperthermia phenotypes by Carpenter, D., Robinson, R.L., Quinnell, R.J., Ringrose, C., Hogg, M., Casson, F., Booms, P., Iles, D.E., Halsall, P.J., Steele, D.S., Shaw, M.-A., Hopkins, P.M.

“…Malignant hyperthermia (MH) is associated, in the majority of cases, with mutations in RYR1, the gene encoding the skeletal muscle ryanodine receptor. Our…”
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Assessing the pathogenicity of RYR1 variants in malignant hyperthermia by Merritt, A., Booms, P., Shaw, M.-A., Miller, D.M., Daly, C., Bilmen, J.G., Stowell, K.M., Allen, P.D., Steele, D.S., Hopkins, P.M.

“…Missense variants in the ryanodine receptor 1 gene (RYR1) are associated with malignant hyperthermia but only a minority of these have met the criteria for use…”
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P24 Biomaterial-based tissue-like constructs for assessing effects of vismodegib on soft and hard tissue by Booms, P, Ghanaati, S, Sader, R

“…This study is the first to show the effect of vismodegib on healthy and tumour cells. Such results are vey important when considering the resection margin…”
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Small-sized granules of biphasic bone substitutes support fast implant bed vascularization by Barbeck, M, Dard, M, Kokkinopoulou, M, Markl, J, Booms, P, Sader, Ra, Kirkpatrick, Cj, Ghanaati, S

“…The present study investigated the influence of granule size of 2 biphasic bone substitutes (BoneCeramic® 400-700 μm and 500-1000 μm) on the induction of…”
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Collagen membranes induce different vascularization and cellular inflammatory response in relation to their origin – in vivo and clinical studies by Ghanaati, S, Lorenz, J, Barbeck, M, Teiler, A, Booms, P, Kirkpatrick, C, Sader, R

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Application of a three-dimensional collagen matrix for covering of cutaneous resection defects-preclinical and preliminary results from the first application in humans by Ghanaati, S, Lorenz, J, Barbeck, M, Teiler, A, Booms, P, Kirkpatrick, C, Sader, R

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Xenogeneic bone substitute materials-differences in processing techniques induce different extend of vascularization and foreign body giant cells: in vivo and clinical studies by Ghanaati, S, Lorenz, J, Barbeck, M, Teiler, A, Booms, P, Kirkpatrick, C, Sader, R

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Platelet rich fibrin-a promising approach for tissue regeneration in oral and maxillofacial surgery: preclinical and clinical studies by Ghanaati, S, Kubesch, A, Lorenz, J, Barbeck, M, Teiler, A, Booms, P, Kirkpatrick, C, Sader, R, Choukroun, J

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The molecular pathogenesis of the Marfan syndrome by Robinson, P N, Booms, P

“…The Marfan syndrome (MFS) is an autosomal dominant heritable disorder of connective tissue with highly variable clinical manifestations including aortic…”
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A fibrillin-1-fragment containing the elastin-binding-protein GxxPG consensus sequence upregulates matrix metalloproteinase-1: biochemical and computational analysis by Booms, Patrick, Ney, Andreas, Barthel, Frank, Moroy, Gautier, Counsell, Damian, Gille, Christoph, Guo, Gao, Pregla, Reinhard, Mundlos, Stefan, Alix, Alain J.P., Robinson, Peter N.

“…Mutations in the gene for fibrillin-1 cause Marfan syndrome (MFS), a common hereditary disorder of connective tissue. Recent findings suggest that proteolysis,…”
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Epigenetic allele silencing and variable penetrance of malignant hyperthermia susceptibility by Robinson, R.L., Carpenter, D., Halsall, P.J., Iles, D.E., Booms, P., Steele, D., Hopkins, P.M., Shaw, M.-A.

“…Tissue-specific monoallelic silencing of the RYR1 gene has been proposed as an explanation for variable penetrance of dominant RYR1 mutations in malignant…”
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Analysis of RYR1 Haplotype Profile in Patients with Malignant Hyperthermia by Carpenter, D., Morris, A., Robinson, R. L., Booms, P., Iles, D., Halsall, P. J., Steele, D., Hopkins, P. M., Shaw, M.‐A.

“…Summary This study represents a new approach to characterising patients at risk of malignant hyperthermia (MH) through the use of a recently published method…”
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Human Genome and Diseases:¶The molecular pathogenesis of the Marfan syndrome by Robinson, P.N., Booms, P.

“…The Marfan syndrome (MFS) is an autosomal dominant heritable disorder of connective tissue with highly variable clinical manifestations including aortic…”
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Differential effect of FBN1 mutations on in vitro proteolysis of recombinant fibrillin-1 fragments by BOOMS, P, TIECKE, F, ROSENBERG, T, HAGEMEIER, C, ROBINSON, P. N

“…Mutations in the fibrillin-1 gene (FBN1) cause Marfan syndrome (MFS), an autosomal dominant disorder of connective tissue with highly variable clinical…”
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The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia by Meyer, Thomas, Münch, Christoph, Völkel, Helge, Booms, Patrick, Ludolph, Albert C

“…OBJECTIVES To investigate if sequence alterations of the excitatory amino acid transporter gene EAAT2 (GLT-1) may be a contributory factor to the pathogenesis…”
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