scholarly article | Q13442814 |
P50 | author | Renato V. Iozzo | Q37371755 |
Reuven Bergman | Q117264463 | ||
P2093 | author name string | Dina Ron | |
Ifat Sher | |||
Eri Arikawa-Hirasawa | |||
Yoshihiko Yamada | |||
Simona Zisman-Rozen | |||
Dirk Breitkreutz | |||
John M Whitelock | |||
Nicole Maas-Szabowski | |||
Norbert E Fusenig | |||
Liat Eliahu | |||
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Human KGF is FGF-related with properties of a paracrine effector of epithelial cell growth | Q24295049 | ||
Heparan sulfate chains of perlecan are indispensable in the lens capsule but not in the kidney | Q24540314 | ||
Antisense targeting of perlecan blocks tumor growth and angiogenesis in vivo | Q24564477 | ||
Suppression of autocrine and paracrine functions of basic fibroblast growth factor by stable expression of perlecan antisense cDNA | Q24646731 | ||
Perlecan maintains the integrity of cartilage and some basement membranes | Q24680954 | ||
Fibroblast growth factors, their receptors and signaling | Q28140520 | ||
Organotypic keratinocyte cocultures in defined medium with regular epidermal morphogenesis and differentiation | Q28143290 | ||
The Ki-67 protein: from the known and the unknown | Q28143714 | ||
The protein core of the proteoglycan perlecan binds specifically to fibroblast growth factor-7 | Q28145823 | ||
Perlecan is essential for cartilage and cephalic development | Q28146148 | ||
The C‐Terminal Domain V of Perlecan Promotes β1 Integrin‐Mediated Cell Adhesion, Binds Heparin, Nidogen and Fibulin‐2 and Can be Modified by Glycosaminoglycans | Q28259215 | ||
Impaired angiogenesis, delayed wound healing and retarded tumor growth in perlecan heparan sulfate-deficient mice | Q28272282 | ||
The N‐terminal globular domain of the laminin α1 chain binds to α1β1 and α2β1 integrins and to the heparan sulfate‐containing domains of perlecan | Q28278214 | ||
Keratinocyte growth factor/fibroblast growth factor 7, a homeostatic factor with therapeutic potential for epithelial protection and repair | Q28278567 | ||
Alternative splicing generates an isoform of the human Sef gene with altered subcellular localization and specificity | Q28312213 | ||
Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line | Q29547520 | ||
Serial cultivation of strains of human epidermal keratinocytes: the formation of keratinizing colonies from single cells | Q29614425 | ||
Functions of cell surface heparan sulfate proteoglycans | Q29618521 | ||
Heparan sulfate: lessons from knockout mice | Q30689506 | ||
Epidermal cell lineage | Q33678380 | ||
Life without perlecan has its problems | Q33783384 | ||
FGFs, heparan sulfate and FGFRs: complex interactions essential for development | Q33828280 | ||
Carcinogenesis in mouse and human cells: parallels and paradoxes | Q33846175 | ||
Epidermal differentiation, apoptosis, and senescence: common pathways? | Q33855465 | ||
Cellular functions of proteoglycans--an overview. | Q34211741 | ||
Nrf2 transcription factor, a novel target of keratinocyte growth factor action which regulates gene expression and inflammation in the healing skin wound | Q34283835 | ||
Heparan sulfate proteoglycans: intricate molecules with intriguing functions. | Q34310368 | ||
Heparan sulfate proteoglycans: heavy hitters in the angiogenesis arena | Q34328750 | ||
Extracellular matrix and keratinocyte migration. | Q34419124 | ||
Heparan sulfate proteoglycans and cancer. | Q34441253 | ||
Science, medicine and the future: healing chronic wounds | Q34499583 | ||
Role of integrins in regulating epidermal adhesion, growth and differentiation | Q34764924 | ||
Perlecan and tumor angiogenesis | Q35562693 | ||
Perlecan is required to inhibit thrombosis after deep vascular injury and contributes to endothelial cell-mediated inhibition of intimal hyperplasia | Q35799754 | ||
Endothelial cell-derived heparan sulfate binds basic fibroblast growth factor and protects it from proteolytic degradation | Q36219245 | ||
Sequestration and release of basic fibroblast growth factor | Q36463376 | ||
Dyssegmental dysplasias: clinical, radiographic, and morphologic evidence of heterogeneity | Q39775578 | ||
Basement membrane (type IV) collagen | Q40553053 | ||
Epidermal tissue regeneration and stromal interaction in HaCaT cells is initiated by TGF-alpha | Q40644434 | ||
Vitamin D enhances mitogenesis mediated by keratinocyte growth factor receptor in keratinocytes | Q40645723 | ||
Mutations uncouple human fibroblast growth factor (FGF)-7 biological activity and receptor binding and support broad specificity in the secondary receptor binding site of FGFs. | Q40915825 | ||
Human perlecan immunopurified from different endothelial cell sources has different adhesive properties for vascular cells. | Q40947660 | ||
Epidermal differentiation and basement membrane formation by HaCaT cells in surface transplants | Q41042865 | ||
Identification of glypican as a dual modulator of the biological activity of fibroblast growth factors | Q41110684 | ||
Involvement of heparan sulfate and related molecules in sequestration and growth promoting activity of fibroblast growth factor | Q41140266 | ||
Supramolecular assembly of basement membranes | Q41147111 | ||
Epidermis generated in vitro: practical considerations and applications | Q41156888 | ||
A role for the perlecan protein core in the activation of the keratinocyte growth factor receptor | Q41895425 | ||
Keratinocyte growth factor inhibits cross-linked envelope formation and nucleosomal fragmentation in cultured human keratinocytes | Q42517338 | ||
Mutual induction of growth factor gene expression by epidermal-dermal cell interaction | Q42769779 | ||
Expression of mouse telomerase reverse transcriptase during development, differentiation and proliferation | Q42830375 | ||
Comparison of gene expression profiles in human keratinocyte mono-layer cultures, reconstituted epidermis and normal human skin; transcriptional effects of retinoid treatments in reconstituted human epidermis | Q43959137 | ||
Non-viral liposomal keratinocyte growth factor (KGF) cDNA gene transfer improves dermal and epidermal regeneration through stimulation of epithelial and mesenchymal factors | Q45888073 | ||
Apoptosis of endothelial cells triggers a caspase-dependent anti-apoptotic paracrine loop active on VSMC. | Q51025323 | ||
Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene | Q52137443 | ||
There is binding of collagen IV to beta 1 integrin during early skin basement membrane assembly | Q52533549 | ||
Dynamics of Basement Membrane Formation by Keratinocyte–Fibroblast Interactions in Organotypic Skin Culture | Q53435976 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | keratinocyte | Q1473931 |
P304 | page(s) | 5178-5187 | |
P577 | publication date | 2005-11-02 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Targeting perlecan in human keratinocytes reveals novel roles for perlecan in epidermal formation | |
P478 | volume | 281 |
Q30392738 | A current view of perlecan in physiology and pathology: A mosaic of functions |
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Q80926113 | Basement membranes in skin are differently affected by lack of nidogen 1 and 2 |
Q34016825 | Basement membranes in skin: unique matrix structures with diverse functions? |
Q90367099 | Corneal epithelial basement membrane: Structure, function and regeneration |
Q38325054 | Different domains in nidogen‐1 and nidogen‐2 drive basement membrane formation in skin organotypic cocultures |
Q99238544 | Distribution and Function of Glycosaminoglycans and Proteoglycans in the Development, Homeostasis and Pathology of the Ocular Surface |
Q37020797 | Diverse cell signaling events modulated by perlecan. |
Q40147464 | Downregulation of Sef, an inhibitor of receptor tyrosine kinase signaling, is common to a variety of human carcinomas |
Q48634415 | Effects of growth differentiation factor-9 and FSH on in vitro development, viability and mRNA expression in bovine preantral follicles |
Q36481790 | Endorepellin affects angiogenesis by antagonizing diverse vascular endothelial growth factor receptor 2 (VEGFR2)-evoked signaling pathways: transcriptional repression of hypoxia-inducible factor 1α and VEGFA and concurrent inhibition of nuclear fact |
Q33718473 | Endorepellin evokes autophagy in endothelial cells |
Q24312922 | Endorepellin laminin-like globular 1/2 domains bind Ig3-5 of vascular endothelial growth factor (VEGF) receptor 2 and block pro-angiogenic signaling by VEGFA in endothelial cells |
Q36578668 | Endostatin and endorepellin: A common route of action for similar angiostatic cancer avengers |
Q35588817 | Epithelial basement membrane proteins perlecan and nidogen-2 are up-regulated in stromal cells after epithelial injury in human corneas |
Q26783509 | Fibroblast heterogeneity and its implications for engineering organotypic skin models in vitro |
Q42517779 | Functional redundancy of extracellular matrix protein 1 in epidermal differentiation. |
Q47978307 | Gene expression in the lamellar dermis-epidermis during the developmental phase of carbohydrate overload-induced laminitis in the horse |
Q47381829 | Glycosaminoglycans of Abdominal Skin After Massive Weight Loss in Post-bariatric Female Patients |
Q29619329 | Heparan sulphate proteoglycans fine-tune mammalian physiology |
Q41504553 | Heparanase Inhibitors Facilitate the Assembly of the Basement Membrane in Artificial Skin |
Q28242715 | Heparin inhibits melanosome uptake and inflammatory response coupled with phagocytosis through blocking PI3k/Akt and MEK/ERK signaling pathways in human epidermal keratinocytes |
Q42491092 | Influence of heparan sulfate chains in proteoglycan at the dermal-epidermal junction on epidermal homeostasis |
Q40048806 | Integrin alpha2beta1 is the required receptor for endorepellin angiostatic activity |
Q34569918 | Lack of nidogen-1 and -2 prevents basement membrane assembly in skin-organotypic coculture |
Q42693930 | Laminin deposition in the extracellular matrix: a complex picture emerges |
Q37049108 | Perlecan expression influences the keratin 15-positive cell population fate in the epidermis of aging skin |
Q24653433 | Perlecan regulates developmental angiogenesis by modulating the VEGF-VEGFR2 axis. |
Q37271840 | Polyamines release the let-7b-mediated suppression of initiation codon recognition during the protein synthesis of EXT2. |
Q21710680 | Proteoglycan form and function: A comprehensive nomenclature of proteoglycans |
Q34467680 | Proteoglycans in Normal and Healing Skin |
Q36787608 | Proteoglycans in cancer biology, tumour microenvironment and angiogenesis |
Q30433703 | Rac1 is essential for basement membrane-dependent epiblast survival |
Q42124126 | Skin Basement Membrane: The Foundation of Epidermal Integrity—BM Functions and Diverse Roles of Bridging Molecules Nidogen and Perlecan |
Q89736179 | Small Leucine-Rich Proteoglycans in Skin Wound Healing |
Q39304062 | Superficial dermal fibroblasts enhance basement membrane and epidermal barrier formation in tissue-engineered skin: implications for treatment of skin basement membrane disorders |
Q37208901 | The corneal epithelial basement membrane: structure, function, and disease. |
Q36967337 | The molecular basis of lipoid proteinosis: mutations in extracellular matrix protein 1. |
Q38888282 | The role of heparan sulphate in development: the ectodermal story |
Q26800258 | The role of perlecan and endorepellin in the control of tumor angiogenesis and endothelial cell autophagy |
Q90283959 | Type XVIII Collagen Modulates Keratohyalin Granule Formation and Keratinization in Oral Mucosa |
Q39436960 | Ultraviolet-B irradiation induces epidermal up-regulation of heparanase expression and activity |
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