411 results on '"Economides, Aris N."'
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52. NMIHBA results from hypomorphic PRUNE1 variants that lack short-chain exopolyphosphatase activity
53. Twisted gastrulation, a bone morphogenetic protein agonist/antagonist, is not required for post-natal skeletal function
54. The BMP antagonist noggin regulates cranial suture fusion
55. Cytokine traps: multi-component, high-affinity blockers of cytokine action
56. Structural basis of BMP signalling inhibition by the cystine knot protein Noggin
57. Activin A forms a non-signaling complex with ACVR1 and type II Activin/BMP receptors via its finger 2 tip loop
58. Author response: Activin A forms a non-signaling complex with ACVR1 and type II Activin/BMP receptors via its finger 2 tip loop
59. Targeted delivery of acid alpha-glucosidase corrects skeletal muscle phenotypes in Pompe disease mice
60. Effects of BMP7 produced by group 2 innate lymphoid cells on adipogenesis
61. Functional modeling of NMIHBA-causingPRUNE1variants reveals a requirement for its exopolyphosphatase activity
62. Connective Tissue Growth Factor Is Required for Skeletal Development and Postnatal Skeletal Homeostasis in Male Mice
63. Nephroblastoma Overexpressed (Nov) Inactivation Sensitizes Osteoblasts to Bone Morphogenetic Protein-2, But Nov Is Dispensable for Skeletal Homeostasis
64. The novel Cer-like protein Caronte mediates the establishment of embryonic left-right asymmetry
65. Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injury
66. Morphogenesis of digits in the avian limb is controlled by FGFs, TGFbetas, and Noggin through BMP signaling
67. Skeletal Overexpression of Gremlin Impairs Bone Formation and Causes Osteopenia
68. Designer Cytokines: Targeting Actions to Cells of Choice
69. IN VIVO SOMATIC CELL GENE TRANSFER OF AN ENGINEERED NOGGIN MUTEIN PREVENTS BMP4-INDUCED HETEROTOPIC OSSIFICATION
70. Bone Morphogenetic Proteins, Their Antagonists, and the Skeleton
71. STRUCTURAL BASIS OF BMP SIGNALING INHIBITION BY NOGGIN, A NOVEL TWELVE-MEMBERED CYSTINE KNOT PROTEIN
72. Bone Morphogenetic Proteins Induce Gremlin, a Protein That Limits Their Activity in Osteoblasts*
73. Noncoding RNA transcription targets AID to divergently transcribed loci in B cells
74. The finger 2 tip loop of Activin A is required for the formation of its non-signaling complex with ACVR1 and type II Bone Morphogenetic Protein receptors
75. Multifunctional Alleles: A novel method for the generation of “All-In-One” null and conditional alleles
76. The cortico-striatal circuit regulates sensorimotor gating via Disc1/Huntingtin-mediated Bdnf transport
77. Comparative Transcriptomics Identifies Novel Genes and Pathways Involved in Post-Traumatic Osteoarthritis Development and Progression
78. Next-generation antibody-guided enzyme replacement therapy in Pompe disease mice
79. Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injury
80. Canonical and noncanonical Wnts use a common mechanism to activate completely unrelated coreceptors
81. The Expansion of Heterotopic Bone in Fibrodysplasia Ossificans Progressiva Is Activin A-Dependent
82. MAPPIN: a method for annotating, predicting pathogenicity and mode of inheritance for nonsynonymous variants
83. Sustained Notch2 signaling in osteoblasts, but not in osteoclasts, is linked to osteopenia in a mouse model of Hajdu-Cheney syndrome
84. Profiling copy number variation and disease associations from 50,726 DiscovEHR Study exomes
85. Engineering tissue specific delivery of enzymes for lysosomal disease treatment
86. Two tissue-resident progenitor lineages drive distinct phenotypes of heterotopic ossification
87. Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1pathogenic alleles worldwide
88. Global molecular changes in a tibial compression induced ACL rupture model of post‐traumatic osteoarthritis
89. Palovarotene Inhibits Heterotopic Ossification and Maintains Limb Mobility and Growth in Mice With the Human ACVR1R206H Fibrodysplasia Ossificans Progressiva (FOP) Mutation
90. Severity and Frequency of Proximal Tubule Injury Determines Renal Prognosis
91. ISDN2014_0036: REMOVED: Craniofacial development is fine tuned by Sox2
92. The Bulk of Autotaxin Activity Is Dispensable for Adult Mouse Life
93. Context-dependent functions of angiopoietin 2 are determined by the endothelial phosphatase VEPTP.
94. ACVR1R206Hreceptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A
95. RNA Exosome-Regulated Long Non-Coding RNA Transcription Controls Super-Enhancer Activity
96. Abstract 661: Tie2 Deficiency Leads to Lymphatic Defects and Resistance to High-fat Diet Induced Obesity
97. Elimination of BMP7 from the developing limb mesenchyme leads to articular cartilage degeneration and synovial inflammation with increased age
98. Removal of SOST or blocking its product sclerostin rescues defects in the periodontitis mouse model
99. microTSS: accurate microRNA transcription start site identification reveals a significant number of divergent pri-miRNAs
100. Sox2 acts as a rheostat of epithelial to mesenchymal transition during neural crest development
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