Mice with a null mutation of the TGF alpha gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation.
about
TRP channel regulates EGFR signaling in hair morphogenesis and skin barrier formationDistribution of mRNA for human epiregulin, a differentially expressed member of the epidermal growth factor familyAssociation of MSX1 and TGFB3 with nonsyndromic clefting in humansMammary ductal morphogenesis requires paracrine activation of stromal EGFR via ADAM17-dependent shedding of epithelial amphiregulinMechanisms underlying skin disorders induced by EGFR inhibitorsEGFR Signaling in Liver DiseasesHuman epidermal growth factor receptor signaling in acute lung injuryAsymmetric migration of human keratinocytes under mechanical stretch and cocultured fibroblasts in a wound repair modelAccelerated wound closure in vitro by fibroblasts from a subgroup of cleft lip/palate patients: role of transforming growth factor-αReversible interconversion and maintenance of mammary epithelial cell characteristics by the ligand-regulated EGFR system.Progress in corneal wound healingHeparin-binding EGF-like growth factor and ErbB signaling is essential for heart functionExcess biglycan causes eyelid malformation by perturbing muscle development and TGF-alpha signalingA new mutation Rim3 resembling Re(den) is mapped close to retinoic acid receptor alpha (Rara) gene on mouse chromosome 11Role of Gab1 in heart, placenta, and skin development and growth factor- and cytokine-induced extracellular signal-regulated kinase mitogen-activated protein kinase activationAngiopoietin-related growth factor (AGF) promotes epidermal proliferation, remodeling, and regenerationAcceleration of polycystic kidney disease progression in cpk mice carrying a deletion in the homeodomain protein Cux1Insights into the evolution of the ErbB receptor family and their ligands from sequence analysisThe Leydig cell MEK/ERK pathway is critical for maintaining a functional population of adult Leydig cells and for fertilityDistinct roles for ADAM10 and ADAM17 in ectodomain shedding of six EGFR ligandsEpidermal ADAM17 maintains the skin barrier by regulating EGFR ligand-dependent terminal keratinocyte differentiation.Selective roles for tumor necrosis factor alpha-converting enzyme/ADAM17 in the shedding of the epidermal growth factor receptor ligand family: the juxtamembrane stalk determines cleavage efficiency.Rhbdf2 mutations increase its protein stability and drive EGFR hyperactivation through enhanced secretion of amphiregulin.ADAM-17: the enzyme that does it all.The role of transforming growth factor alpha in rat craniofacial development and chondrogenesis.A strain-independent postnatal neurodegeneration in mice lacking the EGF receptorFrom wavy hair to naked proteins: the role of transforming growth factor alpha in health and disease.Molecular analysis of the Drosophila EGF receptor homolog reveals that several genetically defined classes of alleles cluster in subdomains of the receptor proteinFunctional characterization of cultured keratinocytes after acute cutaneous burn injury.ADAM10 mediates ectodomain shedding of the betacellulin precursor activated by p-aminophenylmercuric acetate and extracellular calcium influx.Saliva and growth factors: the fountain of youth resides in us all.Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l) gene.EGFR-mutated lung cancer: a paradigm of molecular oncology.Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables.EGF receptor transactivation mediated by the proteolytic production of EGF-like agonists.Hague (Hag). A new mouse hair mutation with an unstable semidominant allele.A mutation in the epidermal growth factor receptor in waved-2 mice has a profound effect on receptor biochemistry that results in impaired lactation.The epidermal growth factor receptor family: biology driving targeted therapeutics.Neuregulin-1-human epidermal receptor-2 signaling is a central regulator of pulmonary epithelial permeability and acute lung injury.The ADAM17-amphiregulin-EGFR axis in mammary development and cancer.
P2860
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P2860
Mice with a null mutation of the TGF alpha gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh-hant
name
Mice with a null mutation of t ...... develop corneal inflammation.
@en
Mice with a null mutation of t ...... develop corneal inflammation.
@nl
type
label
Mice with a null mutation of t ...... develop corneal inflammation.
@en
Mice with a null mutation of t ...... develop corneal inflammation.
@nl
prefLabel
Mice with a null mutation of t ...... develop corneal inflammation.
@en
Mice with a null mutation of t ...... develop corneal inflammation.
@nl
P2093
P1433
P1476
Mice with a null mutation of t ...... n develop corneal inflammation
@en
P2093
P304
P356
10.1016/0092-8674(93)90227-H
P407
P50
P577
1993-04-01T00:00:00Z