Ikuti
Gali Guterman-Ram
Gali Guterman-Ram
Head of Bone research center, Rambam Health Care Campus
Email yang diverifikasi di rambam.health.gov.il
Judul
Dikutip oleh
Dikutip oleh
Tahun
Osteogenesis Imperfecta: Mechanisms and signaling pathways connecting classical and rare OI types
JCM Milena Jovanovic, Gali Guterman-Ram
Endocrine Reviews, 2021
124*2021
Osteoclast fusion is initiated by a small subset of RANKL-stimulated monocyte progenitors, which can fuse to RANKL-unstimulated progenitors
N Levaot, A Ottolenghi, M Mann, G Guterman-Ram, Z Kam, B Geiger
Bone 79, 21-28, 2015
732015
A dual-specific macrophage colony-stimulating factor antagonist of c-FMS and αvβ3 integrin for osteoporosis therapy
Y Zur, L Rosenfeld, CA Keshelman, N Dalal, G Guterman-Ram, ...
PLoS Biology 16 (8), e2002979, 2018
282018
Perturbed bone composition and integrity with disorganized osteoblast function in zinc receptor/Gpr39‐deficient mice
M Jovanovic, FN Schmidt, G Guterman‐Ram, H Khayyeri, S Hiram‐Bab, ...
The FASEB Journal 32 (5), 2507-2518, 2018
242018
High content of Langerhans cells in malignant lymphoma—incidence and significance
D Benharroch, G Guterman, I Levy, R Shaco-Levy
Virchows Archiv 457, 63-67, 2010
232010
Streptococcus pneumoniae Cell-Wall-Localized Phosphoenolpyruvate Protein Phosphotransferase Can Function as an Adhesin: Identification of Its Host Target …
Y Mizrachi Nebenzahl, K Blau, T Kushnir, M Shagan, M Portnoi, A Cohen, ...
PLoS One 11 (3), e0150320, 2016
222016
Alterations of bone material properties in growing Ifitm5/BRIL p. S42 knock-in mice, a new model for atypical type VI osteogenesis imperfecta
G Hedjazi, G Guterman-Ram, S Blouin, V Schemenz, W Wagermaier, ...
Bone 162, 116451, 2022
172022
Schlafen2 mutation in mice causes an osteopetrotic phenotype due to a decrease in the number of osteoclast progenitors
I Omar, G Guterman-Ram, D Rahat, Y Tabach, M Berger, N Levaot
Scientific reports 8 (1), 13005, 2018
172018
Pea Protein‐Rich Scaffolds Support 3D Bovine Skeletal Muscle Formation for Cultivated Meat Application
S David, I Ianovici, G Guterman Ram, Y Shaulov Dvir, N Lavon, ...
Advanced Sustainable Systems 8 (6), 2300499, 2024
92024
Dual‐specificity tyrosine phosphorylation‐regulated kinase 2 regulates osteoclast fusion in a cell heterotypic manner
G Guterman‐Ram, M Pesic, A Orenbuch, T Czeiger, A Aflalo, N Levaot
Journal of cellular physiology 233 (1), 617-629, 2018
72018
Placenta‐Derived Mesenchymal Stromal‐Like Cells Promote 3D‐Engineered Muscle Tissue Differentiation and Vessel Network Maturation
A Tsukerman, M Machour, M Shuhmaher, EO Fischer, H Shoyhet, ...
Small Science 4 (11), 2400228, 2024
12024
Atypical type VI Osteogenesis Imperfecta mouse models the intersection of IFITM5 and SERPINF1 pathways in patients
G Guterman-Ram, G Hedjazi, C Stephan, S Blouin, J Zwerina, KM Kozloff, ...
Bone Reports 14, 100805, 2021
12021
Bone tissue in murine atypical type VI osteogenesis imperfecta has changes in vascular pores and matrix organization, plus classic OI hypermineralization
G Hedjazi, G Guterman-Ram, S Blouin, P Roschger, V Schemenz, ...
Bone Reports 13, 100335, 2020
12020
New Ifitm5 S42L mouse model for atypical type VI OI connects types V and VI Osteogenesis Imperfecta
G Guterman-Ram, G Hedjazi, C Stephan, S Blouin, P Roschger, ...
Bone Reports 13, 100650, 2020
12020
Rational design of 3D-printed scaffolds for breast tissue engineering using structural analysis
SL Kracoff-Sella, I Goldfracht, A Silverstein, S Landau, L Debbi, ...
Biofabrication, 2025
2025
Novel murine model of atypical type VI osteogenesis imperfecta has altered matrix mineralization, osteocyte canalicular network and disordered collagen orientation
G Hedjazi, G Guterman-Ram, S Blouin, MA Hartmann, V Schemenz, ...
JOURNAL OF BONE AND MINERAL RESEARCH 37, 169-169, 2022
2022
Atypical type VI Osteogenesis Imperfecta mouse models the intersection of IFITM5 and SERPINF1 pathways in patients
G Guterman-Ram, G Hedjazi, C Stephan, S Blouin, J Zwerina, KM Kozloff, ...
JOURNAL OF BONE AND MINERAL RESEARCH 37, 170-170, 2022
2022
Novel murine model of atypical type VI osteogenesis imperfecta has altered osteocyte canalicular network, disordered collagen orientation along with hypermineralization of bone …
G Hedjazi, G Guterman-Ram, S Blouin, MA Hartmann, V Schemenz, ...
Bone Reports 14, 100806, 2021
2021
New Ifitm5 S42L mouse model for atypical type VI Osteogenesis Imperfecta recapitulates patient phenotype.
GG Ram, G Hedjazi, C Stephan, S Blouin, V Schemenz, W Wagermaier, ...
JOURNAL OF BONE AND MINERAL RESEARCH 35, 299-299, 2020
2020
New mouse model with Ifitm5 S42L connects types V and VI osteogenesis imperfecta
GG Ram, JC Marini, G Hedjazi, S Blouin, P Roschger, K Klaushofer, ...
JOURNAL OF BONE AND MINERAL RESEARCH 34, 123-123, 2019
2019
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