[HTML][HTML] Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype
KK McKee, SC Crosson, S Meinen… - The Journal of …, 2017 - Am Soc Clin Investig
Mutations in laminin α2-subunit (Lmα2, encoded by LAMA2) are linked to approximately
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 …
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 …
Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype.
KK McKee, SC Crosson, S Meinen… - The Journal of …, 2017 - europepmc.org
Mutations in laminin α2-subunit (Lmα2, encoded by LAMA2) are linked to approximately
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 …
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 …
[引用][C] Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype
KK McKee, SC Crosson, S Meinen… - Journal of Clinical …, 2017 - cir.nii.ac.jp
Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype |
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 検索フォームへ …
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 検索フォームへ …
Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype
KK McKee, SC Crosson, S Meinen… - Journal of Clinical …, 2017 - researchwithrutgers.com
Abstract Mutations in laminin? 2-subunit (Lm? 2, encoded by LAMA2) are linked to
approximately 30% of congenital muscular dystrophy cases. Mice with a homozygous …
approximately 30% of congenital muscular dystrophy cases. Mice with a homozygous …
[PDF][PDF] Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype
KK McKee, SC Crosson, S Meinen, JR Reinhard… - scholar.archive.org
Laminin-211 (α2β1γ1 subunits, abbreviated herein as Lm211) is the major laminin of the
basement membrane (BM) of skeletal muscle and peripheral nerve Schwann cells …
basement membrane (BM) of skeletal muscle and peripheral nerve Schwann cells …
Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype
KK McKee, SC Crosson, S Meinen… - The Journal of …, 2017 - pubmed.ncbi.nlm.nih.gov
Mutations in laminin α2-subunit (Lmα2, encoded by LAMA2) are linked to approximately
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 …
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 …
Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype
KK McKee, SC Crosson, S Meinen… - Journal of Clinical …, 2017 - search.proquest.com
Mutations in laminin a2-subumt (Lmr/2, encoded by LAMA2) are linked to approximately
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation In Lama2 …
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation In Lama2 …
Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype
KK McKee, SC Crosson, S Meinen… - Journal of Clinical …, 2017 - go.gale.com
Mutations in laminin [alpha] 2-subunit (Lm [alpha] 2, encoded by LAMA2) are linked to
approximately 30% of congenital muscular dystrophy cases. Mice with a homozygous …
approximately 30% of congenital muscular dystrophy cases. Mice with a homozygous …
[HTML][HTML] Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype
KK McKee, SC Crosson, S Meinen… - The Journal of …, 2017 - ncbi.nlm.nih.gov
Mutations in laminin α2-subunit (Lmα2, encoded by LAMA2) are linked to approximately
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 …
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 …
Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype
KK McKee, SC Crosson, S Meinen… - Journal of Clinical …, 2017 - edoc.unibas.ch
Mutations in laminin α2-subunit (Lmα2, encoded by LAMA2) are linked to approximately
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 …
30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 …