P. Booms

发表

Update of the UMD‐FBN1 mutation database and creation of an FBN1 polymorphism database

Gabor Matyas, Christophe Béroud, Claudine Junien, 2003, Human mutation.

Potential lack of "standardized" processing techniques for production of allogeneic and xenogeneic bone blocks for application in humans.

M. Barbeck, S. Ghanaati, J. Lorenz, 2014, Acta biomaterialia.

Epigenetic allele silencing and variable penetrance of malignant hyperthermia susceptibility.

R. Robinson, D. Carpenter, M. Shaw, 2009, British journal of anaesthesia.

Monocyte preseeding leads to an increased implant bed vascularization of biphasic calcium phosphate bone substitutes via vessel maturation.

M. Barbeck, S. Ghanaati, C. Kirkpatrick, 2016, Journal of biomedical materials research. Part A.

Scaffold vascularization in vivo driven by primary human osteoblasts in concert with host inflammatory cells.

Ronald E. Unger, C. James Kirkpatrick, Mike Barbeck, 2011, Biomaterials.

A low-speed centrifugation concept leads to cell accumulation and vascularization of solid platelet-rich fibrin: an experimental study in vivo

M. Barbeck, S. Ghanaati, C. Kirkpatrick, 2019, Platelets.

Multinucleated giant cells in the implant bed of bone substitutes are foreign body giant cells-New insights into the material-mediated healing process.

M. Barbeck, S. Ghanaati, C. Kirkpatrick, 2017, Journal of biomedical materials research. Part A.

Analysis of the in vitro degradation and the in vivo tissue response to bi-layered 3D-printed scaffolds combining PLA and biphasic PLA/bioglass components – Guidance of the inflammatory response as basis for osteochondral regeneration

T. Serra, M. Navarro, E. Engel, 2017, Bioactive materials.

Porcine Dermis and Pericardium-Based, Non-Cross-Linked Materials Induce Multinucleated Giant Cells After Their In Vivo Implantation: A Physiological Reaction?

M. Barbeck, S. Ghanaati, C. Kirkpatrick, 2015, The Journal of oral implantology.

Porcine Dermis-Derived Collagen Membranes Induce Implantation Bed Vascularization Via Multinucleated Giant Cells: A Physiological Reaction?

M. Barbeck, S. Ghanaati, C. Kirkpatrick, 2015, The Journal of oral implantology.

Advanced platelet-rich fibrin: a new concept for cell-based tissue engineering by means of inflammatory cells.

S. Ghanaati, C. Landes, J. Lorenz, 2014, The Journal of oral implantology.

Induction of Macrophage Chemotaxis by Aortic Extracts of the mgR Marfan Mouse Model and a GxxPG-Containing Fibrillin-1 Fragment

P. Robinson, S. Mundlos, M. Halushka, 2006, Circulation.

Mutations of FBN1 and genotype–phenotype correlations in Marfan syndrome and related fibrillinopathies

P. Robinson, T. Rosenberg, L. Neumann, 2002, Human mutation.

"Race for the Surface": Eukaryotic Cells Can Win.

E. Ivanova, V. K. Truong, R. Crawford, 2016, ACS applied materials & interfaces.

Effect of an inhaled neutral endopeptidase inhibitor, thiorphan, on airway responsiveness to leukotriene D4 in normal and asthmatic subjects.

P. Sterk, J. Sont, Z. Diamant, 1994, The European respiratory journal.

The determinants of airway hyperresponsiveness to hypertonic saline in atopic asthma in vivo. Relationship with sub‐populations of peripheral blood leucocytes

P. Sterk, J. Sont, P. Booms, 1993, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Differential effect of FBN1 mutations on in vitro proteolysis of recombinant fibrillin-1 fragments

P. Robinson, T. Rosenberg, C. Hagemeier, 2000, Human Genetics.

A novel de novo mutation in exon 14 of the fibrillin-1 gene associated with delayed secretion of fibrillin in a patient with a mild Marfan phenotype

P. Robinson, C. Hagemeier, P. Booms, 1997, Human Genetics.

Novel exon skipping mutation in the fibrillin‐1 gene: Two ‘hot spots’ for the neonatal Marfan syndrome

P. Robinson, C. Hagemeier, P. Booms, 1999, Clinical genetics.

Radiation Sensitization of Basal Cell and Head and Neck Squamous Cell Carcinoma by the Hedgehog Pathway Inhibitor Vismodegib

S. Ghanaati, Ö. Güllülü, S. Hehlgans, 2018, International journal of molecular sciences.

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

A. Ludolph, C. Münch, T. Meyer, 1998, Journal of neurology, neurosurgery, and psychiatry.

Genetic variation in RYR1 and malignant hyperthermia phenotypes.

R. Robinson, D. Carpenter, M. Shaw, 2009, British journal of anaesthesia.

Potential of FX06 to prevent disease progression in hospitalized non-intubated COVID-19 patients — the randomized, EU-wide, placebo-controlled, phase II study design of IXION

P. Meybohm, P. Kranke, C. V. D. van der Kallen, 2022, Trials.

The severity of breathlessness during challenges with inhaled methacholine and hypertonic saline in atopic asthmatic subjects. The relationship with deep breath-induced bronchodilation.

P. Sterk, J. Sont, P. Booms, 1995, American journal of respiratory and critical care medicine.

Assessing the pathogenicity of RYR1 variants in malignant hyperthermia.

P. Allen, P. Hopkins, K. Stowell, 2017, British journal of anaesthesia.

Influence of concentration and preparation of platelet rich fibrin on human bone marrow mononuclear cells (in vitro)

I. Marzi, S. Ghanaati, S. Al-Maawi, 2018, Platelets.

Bipolar clamping improves the sensitivity of mutation detection by temperature gradient gel electrophoresis

P. Robinson, P. Nürnberg, P. Booms, 1998, Electrophoresis.

Vismodegib hedgehog-signaling inhibition and treatment of basal cell carcinomas as well as keratocystic odontogenic tumors in Gorlin syndrome

S. Ghanaati, R. Sader, P. Booms, 2015, Annals of maxillofacial surgery.

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)

S. Ghanaati, S. Al-Maawi, P. Booms, 2017, European Journal of Trauma and Emergency Surgery.

Platelet-rich fibrin secretome induces three dimensional angiogenic activation in vitro.

S. Ghanaati, S. Al-Maawi, P. Booms, 2019, European cells & materials.

Reduction of the relative centrifugal force influences cell number and growth factor release within injectable PRF-based matrices

S. Ghanaati, C. Kirkpatrick, R. Miron, 2017, Journal of Materials Science: Materials in Medicine.

Small-sized granules of biphasic bone substitutes support fast implant bed vascularization

J. Markl, M. Barbeck, S. Ghanaati, 2015, Biomatter.

PTCH-1 and MDM2 expression in ameloblastoma from a West African sub-population: implication for chemotherapeutics

R. Sader, M. Barbeck, S. Ghanaati, 2015, The Pan African medical journal.

Analysis of RYR1 Haplotype Profile in Patients with Malignant Hyperthermia

R. Robinson, D. Carpenter, M. Shaw, 2009, Annals of human genetics.

TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies

Flemming Skovby, Christian Hagemeier, P. Robinson, 2002, Human mutation.

Clustering of mutations associated with mild Marfan-like phenotypes in the 3' region of FBN1 suggests a potential genotype-phenotype correlation.

P. Robinson, T. Rosenberg, C. Nienaber, 2000, American journal of medical genetics.

The molecular genetics of Marfan syndrome and related disorders

P. Robinson, D. Milewicz, D. Judge, 2006, Journal of Medical Genetics.

A fibrillin-1-fragment containing the elastin-binding-protein GxxPG consensus sequence upregulates matrix metalloproteinase-1: biochemical and computational analysis.

P. Robinson, S. Mundlos, C. Gille, 2006, Journal of molecular and cellular cardiology.

RGD-containing fibrillin-1 fragments upregulate matrix metalloproteinase expression in cell culture: A potential factor in the pathogenesis of the Marfan syndrome

P. Robinson, S. Mundlos, F. Barthel, 2004, Human Genetics.

Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype–phenotype correlations in FBN1 exons 24–40

Flemming Skovby, Christian Hagemeier, P. Robinson, 2001, European Journal of Human Genetics.

Human Genome and Diseases:¶The molecular pathogenesis of the Marfan syndrome

P. Robinson, P. Booms, 2001, Cellular and Molecular Life Sciences CMLS.

A RYR1 mutation associated with recessive congenital myopathy and dominant malignant hyperthermia in Asian families

Azzam Ismail, R. Robinson, D. Carpenter, 2009, Muscle & nerve.

Calcium-dependent self-association of the C-type lectin domain of versican.

Gao Guo, P. Robinson, M. Mörgelin, 2006, The international journal of biochemistry & cell biology.

Protective effect of inhaled budesonide against unlimited airway narrowing to methacholine in atopic patients with asthma.

A. Zwinderman, A. Zwinderman, P. Sterk, 1997, The Journal of allergy and clinical immunology.

Histological and histomorphometrical analysis of a silica matrix embedded nanocrystalline hydroxyapatite bone substitute using the subcutaneous implantation model in Wistar rats

M. Barbeck, S. Ghanaati, S. Stübinger, 2010, Biomedical materials.

Collagen membranes induce different vascularization and cellular inflammatory response in relation to their origin – in vivo and clinical studies

M. Barbeck, S. Ghanaati, C. Kirkpatrick, 2015 .

The molecular pathogenesis of the Marfan syndrome.

P. Robinson, P. Booms, 2001, Cellular and molecular life sciences : CMLS.

The molecular genetics of Marfan syndrome and related disorders

D. Milewicz, D. Judge, H. Dietz, 2006, Journal of Medical Genetics.

The Molecular Genetics of Marfan Syndrome and Related Disorders the Fibrillin-ltbp Gene Family

D. Milewicz, G. Collod-Béroud, A. De Paepe, 2022 .

The Journal of Macro Trends in Health and Medicine A Strategy for DNA Sequencing of CASQ 1 reveals no mutations associated with malignant hyperthermia

M. Shaw, P. Hopkins, D. Fiszer, 2016 .