Theodore M. Danoff

ORCID: 0000-0001-7012-9975
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About
Contact & Profiles
Research Areas
  • Hormonal and reproductive studies
  • Chemokine receptors and signaling
  • Mesenchymal stem cell research
  • Immunotherapy and Immune Responses
  • Pharmacological Effects and Assays
  • Renal Diseases and Glomerulopathies
  • Pharmacology and Obesity Treatment
  • T-cell and B-cell Immunology
  • Wound Healing and Treatments
  • Neonatal Respiratory Health Research
  • Cell death mechanisms and regulation
  • Hormonal Regulation and Hypertension
  • Cardiovascular Disease and Adiposity
  • Cardiovascular, Neuropeptides, and Oxidative Stress Research
  • Anesthesia and Sedative Agents
  • Immune Cell Function and Interaction
  • Acute Kidney Injury Research
  • Drug-Induced Adverse Reactions
  • Systemic Lupus Erythematosus Research
  • Eicosanoids and Hypertension Pharmacology
  • Monoclonal and Polyclonal Antibodies Research
  • Blood Pressure and Hypertension Studies
  • Sexual Differentiation and Disorders
  • Cell Adhesion Molecules Research
  • Renal and related cancers

Clarus Therapeutics (United States)
2018-2020

Torrance Memorial Medical Center
2020

Aventura Hospital and Medical Center
2020

University of New Haven
2020

New York Proton Center
2020

University of Pennsylvania
1997-2015

Endo Pharmaceuticals (United States)
2013-2014

GlaxoSmithKline (United States)
2002-2010

GlaxoSmithKline (United Kingdom)
2003-2008

California University of Pennsylvania
2002

Interstitial fibroblasts are principal effector cells of organ fibrosis in kidneys, lungs, and liver. While some view adult tissues as nothing more than primitive mesenchymal surviving embryologic development, they differ from their unique expression fibroblast-specific protein-1 (FSP1). This difference raises questions about origin. Using bone marrow chimeras transgenic reporter mice, we show here that interstitial kidney derive two sources. A small number FSP1(+), CD34(-) migrate to normal...

10.1172/jci15518 article EN Journal of Clinical Investigation 2002-08-01

Interstitial fibroblasts are principal effector cells of organ fibrosis in kidneys, lungs, and liver. While some view adult tissues as nothing more than primitive mesenchymal surviving embryologic development, they differ from their unique expression fibroblast-specific protein-1 (FSP1). This difference raises questions about origin. Using bone marrow chimeras transgenic reporter mice, we show here that interstitial kidney derive two sources. A small number FSP1+, CD34– migrate to normal...

10.1172/jci0215518 article EN Journal of Clinical Investigation 2002-08-01

We performed subtractive and differential hybridization for transcript comparison between murine fibroblasts isogenic epithelium, observed only a few novel intracellular genes which were relatively specific fibroblasts. One such gene encodes filament-associated, calcium-binding protein, fibroblast-specific protein 1 (FSP1). The promoter/enhancer region driving this is active in but not mesangial cells or embryonic endoderm. During development, FSP1 first detected by situ after day 8.5 as...

10.1083/jcb.130.2.393 article EN The Journal of Cell Biology 1995-07-15

Abstract Background Cardiovascular diseases and their associated risk factors remain the main cause of mortality in western societies. In order to assess prevalence cardiovascular (CVRFs) Caucasian population Lausanne, Switzerland, we conducted a population-based study (Colaus Study). A secondary aim CoLaus will be determine new genetic determinants with CVRFs. Methods Single-center, cross-sectional including random sample 6,188 extensively phenotyped subjects (3,251 women 2,937 men) aged 35...

10.1186/1471-2261-8-6 article EN cc-by BMC Cardiovascular Disorders 2008-03-17

A seamless plasticity exists among cells shifting between epithelial and mesenchymal phenotypes during early development again later, in adult tissues, following wound repair or organ remodeling response to injury. Fsp1, a gene encoding fibroblast-specific protein associated with cell morphology motility, is expressed epithelial-mesenchymal transformations (EMT) vivo. In the current study, we identified several cytokines that induce Fsp1 cultured cells. combination of these factors, however,...

10.1152/ajprenal.1997.273.4.f563 article EN AJP Renal Physiology 1997-10-01

OBJECTIVE— Pharmacological use of peroxisome proliferator–activated receptor (PPAR)δ agonists and transgenic overexpression PPARδ in mice suggest amelioration features the metabolic syndrome through enhanced fat oxidation skeletal muscle. We hypothesize a similar mechanism operates humans. RESEARCH DESIGN AND METHODS— The agonist (10 mg o.d. GW501516), comparator PPARα (20 μg GW590735), placebo were given double-blind, randomized, three-parallel group, 2-week study to six healthy moderately...

10.2337/db07-1318 article EN Diabetes 2007-11-17

Interstitial fibroblasts are principal effector cells of organ fibrosis in kidneys, lungs, and liver. While some view adult tissues as nothing more than primitive mesenchymal surviving embryologic development, they differ from their unique expression fibroblast-specific protein-1 (FSP1). This difference raises questions about origin. Using bone marrow chimeras transgenic reporter mice, we show here that interstitial kidney derive two sources. A small number FSP1+, CD34– migrate to normal...

10.1172/jci200215518 article EN Journal of Clinical Investigation 2002-08-01

Abstract Context A novel formulation of oral testosterone (T) undecanoate (TU) was evaluated in a phase 3 clinical trial. Objective Determine efficacy, short-term safety, and alignment new TU with current US approval standards for T replacement therapy. Design Randomized, active-controlled, open-label study. Setting Patients Academic private practice sites; enrolled patients were clinically hypogonadal men 18 to 65 years old. Methods randomized 3:1 TU, as prescribed (JATENZO®; n = 166) or...

10.1210/clinem/dgaa238 article EN cc-by The Journal of Clinical Endocrinology & Metabolism 2020-05-08

We developed a new mouse model of human anti-glomerular basement membrane (GBM) disease to better characterize the genetic determinants cell-mediated injury. While all major histocompatibility complex (MHC) haplotypes (H-2a, k, s, b, and d) immunized with alpha3 NC1 domains type IV collagen produce anti-alpha3(IV) antibodies that cross-react Goodpasture [anti-GBM/anti-alpha3(IV) NC1] autoantibodies, only few strains nephritis lung hemorrhage associated syndrome. Crescentic glomerulonephritis...

10.1172/jci119764 article EN Journal of Clinical Investigation 1997-11-01

Background. The chemokine receptor, CCR5, and its three high-affinity ligands, macrophage inflammatory protein- (MIP) 1α, MIP-1β, regulated on activation normal T cell expressed secreted (RANTES), are by infiltrating mononuclear cells during the rejection of clinical experimental organ allografts, although significance these molecules in pathogenesis has not been established. Methods. We studied intragraft events four allograft models. First, we cardiac transplants fully MHC-mismatched mice...

10.1097/00007890-200110150-00003 article EN Transplantation 2001-10-01

Increased blood flow and vascular permeability of early diabetes have been associated with increased nitric oxide formation in diabetic rats, but the specific synthase responsible is unknown. We examined modulation induction activity inducible NOS isoform by high glucose concentration a murine macrophage cell line, RAW 264.7, glomerular mesangial cells. Culturing both types led to significant increases nitrite production mRNA encoding iNOS upon stimulation LPS plus interferon-γ as compared...

10.1006/bbrc.1995.1156 article EN cc-by-nc-nd Biochemical and Biophysical Research Communications 1995-02-01

Fas ligand (FasL) and belong to a recently described family of cytokines receptors with similarities tumor necrosis factor (TNF) its receptors. Upon engagement by specific antibodies or FasL, transduces signal for apoptosis in permissive cells. Although occurs during renal development following injury mature cells, the factors responsible programmed cell death are uncertain. We have studied expression cells vitro endotoxemia mice. Several types, including glomerular mesangial tubular...

10.1152/ajprenal.1996.271.6.f1193 article EN AJP Renal Physiology 1996-12-01

Progressive tissue fibrosis can compromise epithelial function resulting in organ failure. Appreciating evidence suggests that fibroblasts provide fibrogenic collagens during such injury. We further tested this notion by attempting to reduce the physiologic consequences of through selective killing at sites Here, we report conditional reduction using coding sequence for herpesvirus thymidine kinase (ΔTK) put under control a cell-specific promoter from gene encoding fibroblast-specific...

10.1006/mthe.2000.0251 article EN cc-by-nc-nd Molecular Therapy 2001-02-01

Type IV collagen has recently emerged as a family composed of five known chains (alpha 1-alpha 5), each which contains carboxyl-terminal noncollagenous domain (NC1) approximately 230 amino acids. The NC1 the alpha 3(IV) chain is probable target for autoantibodies in patients with Goodpasture syndrome (GP), evidenced from studies employing bovine type collagen. In present experiments, specificity GP antibodies domains human was determined by using recombinant antigen. cDNAs encoding were...

10.1016/s0021-9258(18)52887-8 article EN cc-by Journal of Biological Chemistry 1993-04-01

RANTES is a member of the C-C subfamily chemokines that functions as proinflammatory chemoattractant for CD4+ T cells, monocytes, and eosinophils, an activator basophils to release histamine. Like other members chemokine superfamily, has been implicated in number chronic inflammatory autoimmune processes based on its function pattern regulation. To begin study transcriptional regulation RANTES, we have determined genomic organization gene encoding small inducible cytokine A5 (Scya5)...

10.4049/jimmunol.152.3.1182 article EN The Journal of Immunology 1994-02-01

Gonadotropin-releasing hormone agonist (GnRHa)-stimulated luteinizing (LH) is the standard hormonal assessment for both diagnosis and therapeutic monitoring of children with central precocious puberty (CPP). Use unstimulated (random) LH levels may be helpful in has gained popularity GnRHa therapy despite lack validation against stimulated values. The objective this investigation was to assess suitability random pubertal suppression during treatment.Data from a multi-year, multicenter,...

10.1186/1687-9856-2013-20 article EN International Journal of Pediatric Endocrinology 2013-12-01
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