Zobrazeno 1 - 10
of 36
pro vyhledávání: '"William L. Ries"'
Autor:
Yuvaraj Sambandam, Sundaravadivel Balasubramanian, Kumaran Sundaram, Sakamuri V. Reddy, Balakrishnan Pillai, William L. Ries, Christina Voelkel-Johnson
Publikováno v:
Bone. 71:137-144
Receptor activator of nuclear factor kappa-B ligand (RANKL) is a critical osteoclastogenic factor expressed in bone marrow stromal/osteoblast lineage cells. Tumor necrosis factor (TNF) related apoptosis-inducing ligand (TRAIL) levels are elevated in
Autor:
William L. Ries, Yuvaraj Sambandam, Keith L. Kirkwood, Kumaran Sundaram, Sakamuri V. Reddy, Angen Liu
Publikováno v:
Oncogene
CXC chemokine ligand-13 (CXCL13) has been implicated in oral squamous cell carcinoma (OSCC) tumor progression and osteolysis. The tumor necrosis factor family member RANKL (receptor activator of NF-κB ligand), a critical bone resorbing osteoclastoge
Factors that affect postnatal bone growth retardation in the twitcher murine model of Krabbe disease
Autor:
Srinivasan Shanmugarajan, Gonzalo Arboleda, Inderjit Singh, William L. Ries, Miguel A. Contreras, Avtar K. Singh
Publikováno v:
Biochimica et Biophysica Acta-Molecular Basis of Disease
Biochimica et Biophysica Acta-Molecular Basis of Disease, Elsevier, 2010, 1802 (7-8), pp.601. ⟨10.1016/j.bbadis.2010.04.006⟩
Biochimica et Biophysica Acta-Molecular Basis of Disease, Elsevier, 2010, 1802 (7-8), pp.601. ⟨10.1016/j.bbadis.2010.04.006⟩
Krabbe disease is an inherited lysosomal disorder in which galactosylsphingosine (psychosine) accumulates mainly in the central nervous system. To gain insight into the possible mechanism(s) that may be participating in the inhibition of the postnata
Autor:
Eichi Tsuruga, Srinivasan Shanmugarajan, William L. Ries, Sakamuri V. Reddy, Bernard L. Maria, Kathryn J. Swoboda
Publikováno v:
The Journal of Pathology. 219:52-60
Spinal muscular atrophy (SMA) is characterized by degenerating lower motor neurons and an increased incidence of congenital bone fractures. Survival motor neuron (SMN) levels are significantly reduced due to deletions/mutations in the telomeric SMN1
Autor:
Parmita Pati, Srinivasan Shanmugarajan, D. Sudhaker Rao, William L. Ries, Sakamuri V. Reddy, Rimon F. Youssef
Publikováno v:
Journal of Cellular Biochemistry. 104:1500-1508
Paget's disease (PD) of bone is characterized by increased activity of large abnormal osteoclasts (OCLs) which contain paramyxoviral nuclear and cytoplasmic inclusions. MVNP gene expression has been shown to induce pagetic phenotype in OCLs. We previ
Autor:
William L. Ries, L. Lyndon Key, Sakamuri V. Reddy, Srinivasan Shanmugarajan, C Musselwhite, K Irie
Publikováno v:
The Journal of Pathology. 213:420-428
Regulatory mechanisms operative in bone-resorbing osteoclasts are complex. We previously defined the Ly-6 gene family member OIP-1/hSca as an inhibitor of osteoclastogenesis in vitro; however, a role in skeletal development is unknown. In this study,
Autor:
Masahiro Ito, Ivor J. Benjamin, Hiroshi Kajiya, William L. Ries, Hayato Ohshima, Sakamuri V. Reddy, Shin Ichi Kenmotsu
Publikováno v:
Journal of Cellular Biochemistry. 97:1362-1369
Heat Shock Proteins (HSP) are molecular chaperones activated upon cellular stress/stimuli. HSP gene expression is regulated by Heat Shock Factors (HSF). We have recently demonstrated a functional role for heat shock factor-2 (HSF-2) in fibroblast gro
Publikováno v:
Journal of Cellular Biochemistry. 84:645-654
Osteoclasts are the primary cells responsible for bone resorption. Osteoclast formation and bone resorption activities involve processes tightly controlled by a network of cytokines. The presence of interferon gamma (IFN-gamma) receptors on osteoclas
Publikováno v:
Journal of Interferon & Cytokine Research. 20:645-652
Interferon-gamma (IFN-gamma) treatment increases osteoclastic bone resorption in vivo in patients with malignant osteopetrosis (OP). The treatment effect was studied in vitro in osteoclasts generated by culturing peripheral white blood cells (PWBC) f
Publikováno v:
Molecular and Cellular Biochemistry. 199:15-24
Severe, malignant osteopetrosis is a disease characterized by osteoclasts that fail to resorb bone. Serious defects in the ability of white blood cells to eradicate infectious agents confound the clinical course. Defective superoxide generation by ne