Found: 44
Select item for more details and to access through your institution.
Rankl genetic deficiency and functional blockade undermine skeletal stem and progenitor cell differentiation.
- Published in:
- Stem Cell Research & Therapy, 2024, v. 15, n. 1, p. 1, doi. 10.1186/s13287-024-03803-3
- By:
- Publication type:
- Article
Birefringence-induced phase delay enables Brillouin mechanical imaging in turbid media.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49419-2
- By:
- Publication type:
- Article
Interleukin-1β Polymorphisms Are Genetic Markers of Susceptibility to Periprosthetic Joint Infection in Total Hip and Knee Arthroplasty.
- Published in:
- Genes, 2024, v. 15, n. 5, p. 596, doi. 10.3390/genes15050596
- By:
- Publication type:
- Article
PBX1: a TALE of two seasons--key roles during development and in cancer.
- Published in:
- Frontiers in Cell & Developmental Biology, 2024, p. 1, doi. 10.3389/fcell.2024.1372873
- By:
- Publication type:
- Article
Genetic Deficiency of the Long Pentraxin 3 Affects Osteogenesis and Osteoclastogenesis in Homeostatic and Inflammatory Conditions.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 23, p. 16648, doi. 10.3390/ijms242316648
- By:
- Publication type:
- Article
The role of WNT and IL-1 signaling in osteoarthritis: therapeutic implications for platelet-rich plasma therapy.
- Published in:
- Frontiers in Aging Neuroscience, 2023, p. 1, doi. 10.3389/fragi.2023.1201019
- By:
- Publication type:
- Article
The role of WNT and IL-1 signaling in osteoarthritis: therapeutic implications for platelet-rich plasma therapy.
- Published in:
- Frontiers in Aging, 2023, p. 1, doi. 10.3389/fragi.2023.1201019
- By:
- Publication type:
- Article
Modulation of NBAS-Related Functions in the Early Response to SARS-CoV-2 Infection.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 2634, doi. 10.3390/ijms24032634
- By:
- Publication type:
- Article
Editorial: Regulation of osteoclast differentiation in autoimmune and inflammatory diseases.
- Published in:
- Frontiers in Immunology, 2023, v. 13, p. 1, doi. 10.3389/fimmu.2022.1125763
- By:
- Publication type:
- Article
The osteoblast secretome in Staphylococcus aureus osteomyelitis.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 01, doi. 10.3389/fimmu.2022.1048505
- By:
- Publication type:
- Article
Dipeptidyl Peptidase 3 Activity as a Promising Biomarker of Bone Fragility in Postmenopausal Women.
- Published in:
- Molecules, 2022, v. 27, n. 12, p. 3929, doi. 10.3390/molecules27123929
- By:
- Publication type:
- Article
Bone Marrow Niches and Tumour Cells: Lights and Shadows of a Mutual Relationship.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.884024
- By:
- Publication type:
- Article
3D Cocultures of Osteoblasts and Staphylococcus aureus on Biomimetic Bone Scaffolds as a Tool to Investigate the Host–Pathogen Interface in Osteomyelitis.
- Published in:
- Pathogens, 2021, v. 10, n. 7, p. 837, doi. 10.3390/pathogens10070837
- By:
- Publication type:
- Article
Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived From Structural and Functional Analysis of 14 ClC‐7 Mutants.
- Published in:
- Journal of Bone & Mineral Research, 2021, v. 36, n. 3, p. 531, doi. 10.1002/jbmr.4200
- By:
- Publication type:
- Article
The Long Pentraxin PTX3 in Bone Homeostasis and Pathology.
- Published in:
- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02628
- By:
- Publication type:
- Article
Absence of Dipeptidyl Peptidase 3 Increases Oxidative Stress and Causes Bone Loss.
- Published in:
- Journal of Bone & Mineral Research, 2019, v. 34, n. 11, p. 2133, doi. 10.1002/jbmr.3829
- By:
- Publication type:
- Article
The RANKL-RANK Axis: A Bone to Thymus Round Trip.
- Published in:
- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00629
- By:
- Publication type:
- Article
One Disease, Many Genes: Implications for the Treatment of Osteopetroses.
- Published in:
- Frontiers in Endocrinology, 2019, p. N.PAG, doi. 10.3389/fendo.2019.00085
- By:
- Publication type:
- Article
Mesenchymal Stromal Cell‐Seeded Biomimetic Scaffolds as a Factory of Soluble RANKL in Rankl‐Deficient Osteopetrosis.
- Published in:
- Stem Cells Translational Medicine, 2019, v. 8, n. 1, p. 22, doi. 10.1002/sctm.18-0085
- By:
- Publication type:
- Article
3D Bone Biomimetic Scaffolds for Basic and Translational Studies with Mesenchymal Stem Cells.
- Published in:
- International Journal of Molecular Sciences, 2018, v. 19, n. 10, p. 3150, doi. 10.3390/ijms19103150
- By:
- Publication type:
- Article
Genetics of Osteopetrosis.
- Published in:
- Current Osteoporosis Reports, 2018, v. 16, n. 1, p. 13, doi. 10.1007/s11914-018-0415-2
- By:
- Publication type:
- Article
Identification of new mutations in TCIRG1 as a cause of infantile malignant osteopetrosis in two Mexican patients.
- Published in:
- Revista Alergia de Mexico, 2018, v. 65, n. 1, p. 108, doi. 10.29262/ram.v65i1.314
- By:
- Publication type:
- Article
The scavenging chemokine receptor ACKR2 has a significant impact on acute mortality rate and early lesion development after traumatic brain injury.
- Published in:
- PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0188305
- By:
- Publication type:
- Article
Murine Rankl<sup>−/−</sup> Mesenchymal Stromal Cells Display an Osteogenic Differentiation Defect Improved by a RANKL-Expressing Lentiviral Vector.
- Published in:
- Stem Cells, 2017, v. 35, n. 5, p. 1365, doi. 10.1002/stem.2574
- By:
- Publication type:
- Article
Synonymous Mutations Add a Layer of Complexity in the Diagnosis of Human Osteopetrosis.
- Published in:
- Journal of Bone & Mineral Research, 2017, v. 32, n. 1, p. 99, doi. 10.1002/jbmr.2929
- By:
- Publication type:
- Article
Quantitation of the Rank-Rankl Axis in Primary Biliary Cholangitis.
- Published in:
- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0159612
- By:
- Publication type:
- Article
The Endocrine Role of the Skeleton.
- Published in:
- International Journal of Endocrinology, 2015, v. 2015, p. 1, doi. 10.1155/2015/265151
- By:
- Publication type:
- Article
As Little as Needed: The Extraordinary Case of a Mild Recessive Osteopetrosis Owing to a Novel Splicing Hypomorphic Mutation in the TCIRG1 Gene.
- Published in:
- Journal of Bone & Mineral Research, 2014, v. 29, n. 7, p. 1646, doi. 10.1002/jbmr.2203
- By:
- Publication type:
- Article
Severe Combined Immunodeficiency in Serbia and Montenegro Between Years 1986 and 2010: A Single-Center Experience.
- Published in:
- Journal of Clinical Immunology, 2014, v. 34, n. 3, p. 304, doi. 10.1007/s10875-014-9991-9
- By:
- Publication type:
- Article
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient.
- Published in:
- 2012
- By:
- Publication type:
- journal article
A Homozygous Contiguous Gene Deletion in Chromosome 16p13.3 Leads to Autosomal Recessive Osteopetrosis in a Jordanian Patient.
- Published in:
- Calcified Tissue International, 2012, v. 91, n. 4, p. 250, doi. 10.1007/s00223-012-9631-4
- By:
- Publication type:
- Article
Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locus.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 5, p. 1106, doi. 10.1002/ajmg.a.33826
- By:
- Publication type:
- Article
Infantile malignant, autosomal recessive osteopetrosis: the rich and the poor.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Clinical Vignette: Characterization of a Novel Alu-Alu Recombination-Mediated Genomic Deletion in the TCIRGJ Gene in Five Osteopetrotic Patients.
- Published in:
- Journal of Bone & Mineral Research, 2009, v. 24, n. 1, p. 162, doi. 10.1359/jbmr.080818
- By:
- Publication type:
- Article
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL.
- Published in:
- Nature Genetics, 2007, v. 39, n. 8, p. 960, doi. 10.1038/ng2076
- By:
- Publication type:
- Article
RAG-dependent primary immunodeficiencies.
- Published in:
- Human Mutation, 2006, v. 27, n. 12, p. 1174, doi. 10.1002/humu.20408
- By:
- Publication type:
- Article
Damaging-agent sensitivity of Artemis-deficient cell lines.
- Published in:
- European Journal of Immunology, 2005, v. 35, n. 4, p. 1250, doi. 10.1002/eji.200425555
- By:
- Publication type:
- Article
TCIRG1-dependent recessive osteopetrosis: Mutation analysis, functional identification of the splicing defects, and in vitro rescue by U1 snRNA.
- Published in:
- Human Mutation, 2004, v. 24, n. 3, p. 225, doi. 10.1002/humu.20076
- By:
- Publication type:
- Article
Chloride Channel ClCN7 Mutations Are Responsible for Severe Recessive, Dominant, and Intermediate Osteopetrosis.
- Published in:
- Journal of Bone & Mineral Research, 2003, v. 18, n. 10, p. 1740, doi. 10.1359/jbmr.2003.18.10.1740
- By:
- Publication type:
- Article
The mutational spectrum of human malignant autosomal recessive osteopetrosis.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1767, doi. 10.1093/hmg/10.17.1767
- By:
- Publication type:
- Article
The mutational spectrum of human malignant autosomal recessive osteopetrosis.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 16, p. 1767, doi. 10.1093/hmg/10.17.1767
- By:
- Publication type:
- Article
The genetic and biochemical basis of Omenn syndrome.
- Published in:
- Immunological Reviews, 2000, v. 178, n. 1, p. 64, doi. 10.1034/j.1600-065x.2000.17818.x
- By:
- Publication type:
- Article
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis.
- Published in:
- Nature Genetics, 2000, v. 25, n. 3, p. 343, doi. 10.1038/77131
- By:
- Publication type:
- Article
Prenatal diagnosis of RAG-deficient Omenn syndrome.
- Published in:
- 2000
- By:
- Publication type:
- journal article