Irregular bladder smooth muscle actin-gamma 2 expression in ACTG2  mutation-associated Megacystis Microcolon Intestinal Hypoperistalsis  Syndrome (MMIHS): A case report

Irregular bladder smooth muscle actin-gamma 2 expression in ACTG2 mutation-associated Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (MMIHS): A case report

4.7
(236)
Write Review
More
$ 25.99
Add to Cart
In stock
Description

Overexpression constructs and HISMC validation. (A) CMV promoter

Quantitative analysis of V5 antibody-and phalloidin-stained HISMCs

ACTG2 Gene - GeneCards, ACTH Protein

ACTG2 R257C does not affect radial collagen gel contraction. (A

Compound heterozygous variants in MYH11 underlie autosomal

ACTG2 Gene - GeneCards, ACTH Protein

The defining pathology of the new clinical and histopathologic

MYL9 deficiency is neonatal lethal in mice due to abnormalities in

Heterozygous De Novo and Inherited Mutations in the Smooth Muscle

Chronic intestinal pseudo‐obstruction in a child harboring a

High-resolution iris and retinal imaging in multisystemic smooth

PDF) Irregular bladder smooth muscle actin-gamma2 expression in