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101. Design of primers for direct sequencing of nine coding exons in the human ACVR1 gene.

102. Oncogene-Induced Senescence Limits the Progression of Pancreatic Neoplasia through Production of Activin A.

103. ALK7 Promotes Vascular Smooth Muscle Cells Phenotypic Modulation by Negative Regulating PPARγ Expression.

104. Fibrodysplasia ossificans progressiva as a form of pseudodystonia.

105. Functional characterization of a unique mutant of ALK2, p.K400E, that is associated with a skeletal disorder, diffuse idiopathic skeletal hyperostosis.

106. Therapeutic Efficacy of Immune Stimulatory Thymidine Kinase and fms-like Tyrosine Kinase 3 Ligand (TK/Flt3L) Gene Therapy in a Mouse Model of High-Grade Brainstem Glioma.

107. Patients with ACVR1 R206H mutations have an increased prevalence of cardiac conduction abnormalities on electrocardiogram in a natural history study of Fibrodysplasia Ossificans Progressiva.

108. BMP signaling plays a role in anterior-neural/head development, but not organizer activity, in the gastropod Crepidula fornicata.

109. Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin.

110. Activin A forms a non-signaling complex with ACVR1 and type II Activin/BMP receptors via its finger 2 tip loop.

111. Prophylactic treatment of rapamycin ameliorates naturally developing and episode -induced heterotopic ossification in mice expressing human mutant ACVR1.

112. Targeting ALK2: An Open Science Approach to Developing Therapeutics for the Treatment of Diffuse Intrinsic Pontine Glioma.

113. Structure-based design of small bicyclic peptide inhibitors of Cripto-1 activity.

114. Differential kinase activity of ACVR1 G328V and R206H mutations with implications to possible TβRI cross-talk in diffuse intrinsic pontine glioma.

115. Fibrodysplasia ossificans progressiva-a rare disease with distinctive features yet still a diagnostic challenge: A case report.

116. CFIm25-regulated lncRNA acv3UTR promotes gastric tumorigenesis via miR-590-5p/YAP1 axis.

117. Recent perspectives of molecular aberrations in pediatric high-grade glioma.

118. KLF10 is upregulated in osteoarthritis and inhibits chondrocyte proliferation and migration by upregulating Acvr1 and suppressing inhbb expression.

119. Mutant ACVR1 Arrests Glial Cell Differentiation to Drive Tumorigenesis in Pediatric Gliomas.

120. Serum osteocalcin level is associated with the mortality in Chinese patients with Fibrodysplasia ossificans progressiva aged ≤18 years at diagnosis.

121. Methods for the reliable induction of heterotopic ossification in the conditional Alk2 Q207D mouse.

122. Role of Signal Transduction Pathways and Transcription Factors in Cartilage and Joint Diseases.

123. Skeletal malformations and developmental arthropathy in individuals who have fibrodysplasia ossificans progressiva.

124. New candidate genes for ST-elevation myocardial infarction.

125. Increased activity of mesenchymal ALK2-BMP signaling causes posteriorly truncated microglossia and disorganization of lingual tissues.

126. HLA-B27 alters BMP/TGFβ signalling in Drosophila , revealing putative pathogenic mechanism for spondyloarthritis.

127. Fibrodysplasia ossificans progressiva: lessons learned from a rare disease.

128. A set of microRNAs coordinately controls tumorigenesis, invasion, and metastasis.

129. Blockade of ALK4/5 signaling suppresses cadmium- and erastin-induced cell death in renal proximal tubular epithelial cells via distinct signaling mechanisms.

130. ACVR1 Function in Health and Disease.

131. Fostering open collaboration in drug development for paediatric brain tumours.

132. Metalloprotease-Dependent Attenuation of BMP Signaling Restricts Cardiac Neural Crest Cell Fate.

133. Genome-wide association analysis of hippocampal volume identifies enrichment of neurogenesis-related pathways.

134. Inhibition of phosphatidylinositol 3-kinase α (PI3Kα) prevents heterotopic ossification.

135. Molecular characterization of known and novel ACVR1 variants in phenotypes of aberrant ossification.

136. ALK4-SMAD2/3-SMAD4 signaling mediates the activin A-induced suppression of PTX3 in human granulosa-lutein cells.

137. SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells†.

138. Severe digital malformations in a rare variant of fibrodysplasia ossificans progressiva.

139. Identification of the Identical Human Mutation in ACVR1 in 2 Cats With Fibrodysplasia Ossificans Progressiva.

140. Crosstalk between BMP and Notch Induces Sox2 in Cerebral Endothelial Cells.

141. Activin a promotes myofibroblast differentiation of endometrial mesenchymal stem cells via STAT3-dependent Smad/CTGF pathway.

142. ALK2 inhibitors display beneficial effects in preclinical models of ACVR1 mutant diffuse intrinsic pontine glioma.

143. Limb specific Acvr1-knockout during embryogenesis in mice exhibits great toe malformation as seen in Fibrodysplasia Ossificans Progressiva (FOP).

144. Integrative Genomics Analysis Identifies ACVR1B as a Candidate Causal Gene of Emphysema Distribution.

145. ACVR1 R206H cooperates with H3.1K27M in promoting diffuse intrinsic pontine glioma pathogenesis.

146. ACVR1C/SMAD2 signaling promotes invasion and growth in retinoblastoma.

147. MicroRNA-454 contributes to sustaining the proliferation and invasion of trophoblast cells through inhibiting Nodal/ALK7 signaling in pre-eclampsia.

148. Bone Morphogenetic Protein 9 Regulates Early Lymphatic-Specified Endothelial Cell Expansion during Mouse Embryonic Stem Cell Differentiation.

149. Heterotopic Ossification in Mouse Models of Fibrodysplasia Ossificans Progressiva.

150. An Adult Zebrafish Model of Fibrodysplasia Ossificans Progressiva.

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