706 results on '"Hoffman, Hal M."'
Search Results
102. Author Correction: A guiding map for inflammation
103. Sa1586 YKL-40 REGULATES NEUTROPHILS RECRUITMENT VIA NLRP3 INFLAMMASOME DURING LIVER INFLAMMATION
104. Sa1585 NLRP3 INFLAMMASOME ACTIVATION IN NEUTROPHILS DRIVES HEPATIC STELLATE CELL ACTIVATION IN MURINE NON-ALCOHOLIC STEATOHEPATITIS
105. Fine structure mapping of CIAS1: identification of an ancestral haplotype and a common FCAS mutation, L353P
106. From NAFLD to NASH to cirrhosis —new insights into disease mechanisms
107. Divergence of IL-1, IL-18, and cell death in NLRP3 inflammasomopathies
108. Syndromes auto-inflammatoires
109. Contributeurs
110. The cardiac mechanical stretch sensor machinery involves a Z disk complex that is defective in a subset of human dilated cardiomyopathy
111. Contributors
112. Autoinflammatory Syndromes
113. Constitutive mutant NLRP3 expression in myeloid cells leads to spontaneous liver inflammation and fibrosis: 1946
114. Cold Urticaria, Immunodeficiency, and Autoimmunity Related to PLCG2 Deletions
115. Monogenic autoinflammatory disorders: Conceptual overview, phenotype, and clinical approach
116. Opportunistic Invasive Infection by Group A Streptococcus During Anti–Interleukin-6 Immunotherapy
117. Inhibition of the NLRP3 inflammasome prevents ovarian aging
118. ASK1 inhibition reduces cell death and hepatic fibrosis in an Nlrp3 mutant liver injury model
119. Autoinflammatory disease: New mouse models and therapies
120. Chapter 10 Episodic Autoinflammatory Disorders in Children
121. IL-1 and the inflammasome: IL-1-3
122. Role of the leucine-rich repeat domain of cryopyrin/NALP3 in monosodium urate crystal–induced inflammation in mice
123. Familial atypical cold urticaria: Description of a new hereditary disease
124. Therapy of autoinflammatory syndromes
125. Inflammasome-Mediated Disease Animal Models Reveal Roles for Innate but Not Adaptive Immunity
126. Recurrent febrile syndromes—what a rheumatologist needs to know
127. Mast Cell Adenosine Induced Calcium Mobilization Via Gi3 and Gq Proteins
128. Efficacy and Safety of Rilonacept (Interleukin-1 Trap) in Patients With Cryopyrin-Associated Periodic Syndromes: Results From Two Sequential Placebo-Controlled Studies
129. The Infevers Autoinflammatory Mutation Online Registry: Update With New Genes and Functions
130. The NLR Gene Family: A Standard Nomenclature
131. Insight into the inflammasome and caspase-activating mechanisms
132. NLRP3 inflammasome activation in hepatic stellate cells induces murine liver fibrosis
133. Treatment of patients with neonatal-onset multisystem inflammatory disease/chronic infantile neurologic, cutaneous, articular syndrome: Comment on the article by Matsubara et al
134. The clinical continuum of cryopyrinopathies: Novel CIAS1 mutations in North American patients and a new cryopyrin model
135. Response to IL-1-Receptor Antagonist in a Child with Familial Cold Autoinflammatory Syndrome
136. Anakinra for the treatment of neonatal-onset multisystem inflammatory disease
137. A Severe Case of Chronic Infantile Neurologic, Cutaneous, Articular Syndrome Treated With Biologic Agents
138. The spectrum of acquired and familial cold-induced urticaria/urticaria-like syndromes
139. Prevention of cold-associated acute inflammation in familial cold autoinflammatory syndrome by interleukin-1 receptor antagonist
140. Anakinra in mutation-negative NOMID/CINCA syndrome: comment on the articles by Hawkins et al and Hoffman and Patel
141. Genomic-Based Therapy: Targeting Interleukin-1 for Autoinflammatory Diseases
142. A large kindred with familial cold autoinflammatory syndrome
143. Familial cold autoinflammatory syndrome: Phenotype and genotype of an autosomal dominant periodic fever
144. Colaboradores
145. 99 - Patogenia de las enfermedades mediadas por inflamasomas
146. Vitamin D repletion ameliorates adipose tissue browning and muscle wasting in infantile nephropathic cystinosis‐associated cachexia
147. Mutations in topoisomerase IIβ result in a B cell immunodeficiency
148. Alternative splicing regulates stochastic NLRP3 activity
149. Partial Jacobsen syndrome phenotype in a patient with a de novo frameshift mutation in the ETS1 transcription factor
150. Choline Uptake and Metabolism Modulate Macrophage IL-1β and IL-18 Production
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.