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| - vědecký článek publikovaný v roce 1995 (cs)
- artículu científicu espublizáu en 1995 (ast)
- наукова стаття, опублікована в грудні 1995 (uk)
- 1995 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած (hyw)
- 1995 թվականի դեկտեմբերին հրատարակված գիտական հոդված (hy)
- مقالة علمية (نشرت في ديسمبر 1995) (ar)
- vedecký článok (publikovaný 1995/12/01) (sk)
- wetenschappelijk artikel (gepubliceerd op 1995/12/01) (nl)
- article publié dans la revue scientifique Journal of Biological Chemistry (fr)
- im Dezember 1995 veröffentlichter wissenschaftlicher Artikel (de)
- scientific journal article (en)
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| author name string
| - A. A. Welcher
- U. Suter
- V. Taylor
- A. E. Program
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| rdfs:label
| - Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family (en)
- Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family (nl)
- Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family (ast)
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| skos:prefLabel
| - Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family (en)
- Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family (nl)
- Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family (ast)
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| name
| - Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family (en)
- Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family (nl)
- Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family (ast)
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| title
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| title
| - Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family (en)
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| - release_yk3v7te4wre5xcxxvuvytage5e
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| is cites work
of | - Wnt signaling protects 3T3-L1 preadipocytes from apoptosis through induction of insulin-like growth factors
- Transgenic mouse models of CMT1A and HNPP.
- Characterization of a tumor-associated gene, a member of a novel family of genes encoding membrane glycoproteins
- SpL201: a conditionally immortalized Schwann cell precursor line that generates myelin
- HNMP-1: a novel hematopoietic and neural membrane protein differentially regulated in neural development and injury.
- Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage
- Epithelial membrane protein-2 is expressed in discrete anatomical regions of the eye
- EMP1 regulates caspase-9 and VEGFC expression and suppresses prostate cancer cell proliferation and invasion
- The tetraspan protein EMP2 increases surface expression of class I major histocompatibility complex proteins and susceptibility to CTL-mediated cell death
- EMP1, a member of a new family of antiproliferative genes in breast carcinoma
- EMP1 inhibits nasopharyngeal cancer cell growth and metastasis through induction apoptosis and angiogenesis
- EMP-1 promotes tumorigenesis of NSCLC through PI3K/AKT pathway
- Peripheral myelin protein 22 is in complex with alpha6beta4 integrin, and its absence alters the Schwann cell basal lamina.
- A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish family
- The four-transmembrane protein IP39 of Euglena forms strands by a trimeric unit repeat.
- Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocation.
- Peripheral myelin protein 22 is a constituent of intercellular junctions in epithelia
- The PMP22 gene and its related diseases
- SEMP1, a senescence-associated cDNA isolated from human mammary epithelial cells, is a member of an epithelial membrane protein superfamily
- Clonal multipotency of skeletal muscle-derived stem cells between mesodermal and ectodermal lineage.
- The tmp gene, encoding a membrane protein, is a c-Myc target with a tumorigenic activity
- The cell junction protein VAB-9 regulates adhesion and epidermal morphology in C. elegans
- Tetraspan vesicle membrane proteins: synthesis, subcellular localization, and functional properties.
- Heterozygous peripheral myelin protein 22-deficient mice are affected by a progressive demyelinating tomaculous neuropathy
- Transcriptional changes in organoculture of full-thickness human skin following topical application of all-trans retinoic acid
- Genetic dissection of dome formation in a mammary cell line: identification of two genes with opposing action
- Analysis of gene expression profile induced by EMP-1 in esophageal cancer cells using cDNA Microarray
- Peripheral myelin protein-22 (PMP22) modulates alpha 6 integrin expression in the human endometrium
- Expression analysis of PMP22/Gas3 in premalignant and malignant pancreatic lesions
- The roles of claudin superfamily proteins in paracellular transport
- Claudins--key pieces in the tight junction puzzle
- Many facets of the peripheral myelin protein PMP22 in myelination and disease.
- Modulation of epithelial morphology, monolayer permeability, and cell migration by growth arrest specific 3/peripheral myelin protein 22
- The peripheral myelin protein 22 and epithelial membrane protein family
- Epithelial membrane protein 1 negatively regulates cell growth and metastasis in colorectal carcinoma
- A mammalian lysosomal membrane protein confers multidrug resistance upon expression in Saccharomyces cerevisiae.
- Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22.
- Promoter hypermethylation of the EMP3 gene in a series of 229 human gliomas
- The epithelial membrane protein 1 is a novel tight junction protein of the blood-brain barrier
- Abnormal Schwann cell/axon interactions in the Trembler-J mouse
- Development of early postnatal peripheral nerve abnormalities in Trembler-J and PMP22 transgenic mice.
- Close relationship between motor impairments and loss of functional motoneurons in a Charcot-Marie-Tooth type 1A model
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