[HTML][HTML] Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice
R Rouf, EG MacFarlane, E Takimoto, R Chaudhary… - Jci Insight, 2017 - ncbi.nlm.nih.gov
Among children with the most severe presentation of Marfan syndrome (MFS), an inherited
disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is …
disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is …
[PDF][PDF] Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice
R Rouf, EG MacFarlane, E Takimoto, R Chaudhary… - researchgate.net
Heterozygous mutations in the gene encoding fibrillin-1 (FBN1) cause Marfan syndrome
(MFS), a systemic connective tissue disorder characterized by manifestations in the ocular …
(MFS), a systemic connective tissue disorder characterized by manifestations in the ocular …
Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice
R Rouf, EG MacFarlane, E Takimoto… - JCI …, 2017 - pure.johnshopkins.edu
Among children with the most severe presentation of Marfan syndrome (MFS), an inherited
disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is …
disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is …
[PDF][PDF] Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice
R Rouf, EG MacFarlane, E Takimoto, R Chaudhary… - academia.edu
Heterozygous mutations in the gene encoding fibrillin-1 (FBN1) cause Marfan syndrome
(MFS), a systemic connective tissue disorder characterized by manifestations in the ocular …
(MFS), a systemic connective tissue disorder characterized by manifestations in the ocular …
Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice.
R Rouf, EG MacFarlane, E Takimoto, R Chaudhary… - JCI Insight, 2017 - europepmc.org
Among children with the most severe presentation of Marfan syndrome (MFS), an inherited
disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is …
disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is …
Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice
R Rouf, EG MacFarlane, E Takimoto… - JCI …, 2017 - pubmed.ncbi.nlm.nih.gov
Among children with the most severe presentation of Marfan syndrome (MFS), an inherited
disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is …
disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is …
[HTML][HTML] Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice
R Rouf, EG MacFarlane, E Takimoto… - JCI …, 2020 - Am Soc Clin Investig
Heterozygous mutations in the gene encoding fibrillin-1 (FBN1) cause Marfan syndrome
(MFS), a systemic connective tissue disorder characterized by manifestations in the ocular …
(MFS), a systemic connective tissue disorder characterized by manifestations in the ocular …
[引用][C] Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice
R Rouf, EG MacFarlane, E Takimoto, R Chaudhary… - JCI Insight, 2017 - cir.nii.ac.jp
Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice |
CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォーム …
CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォーム …
[PDF][PDF] Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice
R Rouf, EG MacFarlane, E Takimoto, R Chaudhary… - researchgate.net
Heterozygous mutations in the gene encoding fibrillin-1 (FBN1) cause Marfan syndrome
(MFS), a systemic connective tissue disorder characterized by manifestations in the ocular …
(MFS), a systemic connective tissue disorder characterized by manifestations in the ocular …
Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice.
R Rouf, EG MacFarlane, E Takimoto, R Chaudhary… - JCI Insight, 2017 - europepmc.org
Among children with the most severe presentation of Marfan syndrome (MFS), an inherited
disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is …
disorder of connective tissue caused by a deficiency of extracellular fibrillin-1, heart failure is …