ELOVL family member 6, elongation of very long chain fatty acids (Elovl6) is a microsomal enzyme, which regulates the elongation of C12-16 saturated and monounsaturated fatty acids. Elovl6 has been shown to be associated with various pathophysiologies including insulin resistance, atherosclerosis, and non-alcoholic steatohepatitis. To investigate a potential role of Elovl6 during bone development, we here examined a skeletal phenotype of Elovl6 knockout (Elovl6-/-) mice. The Elovl6-/- skeleton was smaller than that of controls, but exhibited no obvious patterning defects. Histological analysis revealed a reduced length of proliferating and an elongated length of hypertrophic chondrocyte layer, and decreased trabecular bone in Elovl6-/- mice...
The assembly and degradation of extracellular matrix (ECM) molecules are crucial processes during bo...
The differentiation of embryonic mesenchymal cells into chondrocytes and the subsequent formation of...
Mutations in the sulfate transporter gene, SCL26A2, lead to cartilage proteoglycan undersulfation re...
ELOVL family member 6, elongation of very long chain fatty acids (Elovl6) is a microsomal enzyme, wh...
<p>(A) Lack of <i>Elovl6</i> leads to the decreased number of BrdU-positive cells in proliferating c...
<p>(A) Lack of <i>Elovl6</i> significantly increases C16:0 and decreases C18:1 (n-9) in primary chon...
<p>(A) Knockdown of <i>Elovl6</i> significantly increases C16:0 and decreases C18:1 (n-9) in ATDC5 c...
The potential role of endogenously synthesized polyunsaturated fatty acids (PUFAs) is a highly overl...
SummaryDuring endochondral ossification, small, immature chondrocytes enlarge to form hypertrophic c...
<p>(A) The summary of microarray analysis of primary chondrocyte. The genes up-regulated in <i>Elovl...
Opsismodysplasia (OPS) is a rare but severe autosomal recessive skeletal chondrodysplasia caused by ...
Very long-chain fatty acids (VLCFAs), including polyunsaturated fatty acids (PUFAs), are essential l...
Objective: Chondrocytes in the growth plate at different stages of differentiation synthesize charac...
ELOVL6, a member of the elongation of very long-chain fatty acids (ELOVL) family, has recently been ...
AbstractL-Sox5 and Sox6 are highly identical Sry-related transcription factors coexpressed in cartil...
The assembly and degradation of extracellular matrix (ECM) molecules are crucial processes during bo...
The differentiation of embryonic mesenchymal cells into chondrocytes and the subsequent formation of...
Mutations in the sulfate transporter gene, SCL26A2, lead to cartilage proteoglycan undersulfation re...
ELOVL family member 6, elongation of very long chain fatty acids (Elovl6) is a microsomal enzyme, wh...
<p>(A) Lack of <i>Elovl6</i> leads to the decreased number of BrdU-positive cells in proliferating c...
<p>(A) Lack of <i>Elovl6</i> significantly increases C16:0 and decreases C18:1 (n-9) in primary chon...
<p>(A) Knockdown of <i>Elovl6</i> significantly increases C16:0 and decreases C18:1 (n-9) in ATDC5 c...
The potential role of endogenously synthesized polyunsaturated fatty acids (PUFAs) is a highly overl...
SummaryDuring endochondral ossification, small, immature chondrocytes enlarge to form hypertrophic c...
<p>(A) The summary of microarray analysis of primary chondrocyte. The genes up-regulated in <i>Elovl...
Opsismodysplasia (OPS) is a rare but severe autosomal recessive skeletal chondrodysplasia caused by ...
Very long-chain fatty acids (VLCFAs), including polyunsaturated fatty acids (PUFAs), are essential l...
Objective: Chondrocytes in the growth plate at different stages of differentiation synthesize charac...
ELOVL6, a member of the elongation of very long-chain fatty acids (ELOVL) family, has recently been ...
AbstractL-Sox5 and Sox6 are highly identical Sry-related transcription factors coexpressed in cartil...
The assembly and degradation of extracellular matrix (ECM) molecules are crucial processes during bo...
The differentiation of embryonic mesenchymal cells into chondrocytes and the subsequent formation of...
Mutations in the sulfate transporter gene, SCL26A2, lead to cartilage proteoglycan undersulfation re...