about
Role of PI 3-kinase and PIP3 in submandibular gland branching morphogenesis.Multiscale feature analysis of salivary gland branching morphogenesisPhosphatases in cell-matrix adhesion and migration.Systems analysis of salivary gland development and disease.The matrix reorganized: extracellular matrix remodeling and integrin signaling.Genetic modification and recombination of salivary gland organ cultures.TGFβ signaling promotes matrix assembly during mechanosensitive embryonic salivary gland restorationHeterotypic control of basement membrane dynamics during branching morphogenesis.The contribution of specific cell subpopulations to submandibular salivary gland branching morphogenesis.Core/shell nanofiber characterization by Raman scanning microscopy.Self-organization and branching morphogenesis of primary salivary epithelial cells.Regulation of rat prostate stromal cell myodifferentiation by androgen and TGF-beta1.A Novel Impedance Biosensor for Measurement of Trans-Epithelial Resistance in Cells Cultured on Nanofiber Scaffolds.RARα and RARγ reciprocally control K5+ progenitor cell expansion in developing salivary glands.Elastin-PLGA hybrid electrospun nanofiber scaffolds for salivary epithelial cell self-organization and polarization.FGF2-dependent mesenchyme and laminin-111 are niche factors in salivary gland organoids.Endothelial cell regulation of salivary gland epithelial patterning.Fibronectin requirement in branching morphogenesis.Development of Nanofiber Scaffolds for Engineering an Artificial Salivary GlandROCK inhibitor increases proacinar cells in adult salivary gland organoids
P50
Q30480198-409C0520-CDDB-4A95-9A43-D9253085A935Q34189753-1269C5EA-3749-4271-91FD-7BD9FB56CD8DQ35542014-64B23CD9-73EF-4DC7-928F-A2E3C0586BB0Q36099617-AD38FD31-E870-4113-9238-A643D350AA3DQ36571065-72D42A95-CA39-411B-AD4A-34F230F1FFBCQ36639600-02B7AF65-007B-45D2-8890-FEB4047E1E6BQ36983894-4D49BACB-489B-4698-8DED-5C75EB81C770Q38295055-AFFF4FD5-DCBD-4629-9D66-8302827DCEDBQ38364291-4C72D049-7BE8-4F3E-B271-AA845AFD63ACQ38922087-44BD2DC3-37E4-4654-A29A-B0E1F301BA20Q40236775-9203EAA0-45DC-4C3B-8133-10C6857C211AQ40595604-52EF1498-0D26-423C-8FB8-0074A7FDD1A8Q41663660-D53C0601-2D74-40FD-BE99-BA32EBC694E4Q42515535-F7A492EE-2040-47B2-AE13-DA05696D325BQ47802848-F73532FB-FF8B-4C1D-8641-C3FB1DC2FE25Q48183595-47C9AC50-8590-4FFF-9633-3FC0B98163BFQ48344075-F0B81EF4-0203-410E-903C-13D6C5053DBEQ52103932-0265DFE3-983F-4D49-B5EC-CD8802CFFBB5Q59756363-37415B8A-C46D-494E-8DE0-C57439CF6939Q91297711-A0DF630C-3E47-4197-A41C-A1881E53EEF2
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Melinda Larsen
@ast
Melinda Larsen
@en
Melinda Larsen
@es
Melinda Larsen
@nl
Melinda Larsen
@sl
type
label
Melinda Larsen
@ast
Melinda Larsen
@en
Melinda Larsen
@es
Melinda Larsen
@nl
Melinda Larsen
@sl
prefLabel
Melinda Larsen
@ast
Melinda Larsen
@en
Melinda Larsen
@es
Melinda Larsen
@nl
Melinda Larsen
@sl
P106
P31
P496
0000-0002-5026-2012