scholarly article | Q13442814 |
P2093 | author name string | James E Trosko | |
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Genomic instability and cancer | Q40435278 | ||
Cancer stem cells persist in many cancer cell lines | Q40581444 | ||
Phase II study of the antiangiogenesis agent thalidomide in recurrent or metastatic squamous cell carcinoma of the head and neck | Q40672192 | ||
Why are human cells resistant to malignant cell transformation in vitro? | Q40798787 | ||
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Neoplastic transformation of human cells in vitro. | Q40902987 | ||
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Growth requirements and neoplastic transformation of two types of normal human breast epithelial cells derived from reduction mammoplasty | Q41117962 | ||
Clonal Origin of Human Tumors | Q41208232 | ||
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Two types of normal human breast epithelial cells derived from reduction mammoplasty: phenotypic characterization and response to SV40 transfection | Q42484134 | ||
Effect of in vivo exposure to the liver tumor promoters phenobarbital or DDT on the gap junctions of rat hepatocytes: a quantitative freeze-fracture analysis | Q42526408 | ||
Novel method for selective killing of transformed rodent cells through intercellular communication, with possible therapeutic applications. | Q42803725 | ||
Direct reprogramming of genetically unmodified fibroblasts into pluripotent stem cells | Q42807434 | ||
Enhanced efficiency of generating induced pluripotent stem (iPS) cells from human somatic cells by a combination of six transcription factors | Q42808820 | ||
Gone with the Wnt/Notch: stem cells in laminopathies, progeria, and aging | Q43105986 | ||
Cancer risk in children with birth defects and in their families: a population based cohort study of 5.2 million children from Norway and Sweden | Q43686732 | ||
Direct generation of ES-like cells from unmodified mouse embryonic fibroblasts by Oct4/Sox2/Myc/Klf4. | Q43815089 | ||
Stem cells: so what's in a niche? | Q43956957 | ||
Redox-mediated enrichment of self-renewing adult human pancreatic cells that possess endocrine differentiation potential | Q44194436 | ||
Connexin26-mediated gap junctional communication reverses the malignant phenotype of MCF-7 breast cancer cells | Q44490298 | ||
Enhancement of experimental photocarcinogenesis by topical retinoic acid | Q44729471 | ||
Reflections on the landmark studies of beta-carotene supplementation | Q45168964 | ||
Accelerated growth and prolonged lifespan of adipose tissue-derived human mesenchymal stem cells in a medium using reduced calcium and antioxidants | Q45278756 | ||
Bowman-Birk inhibitor abates proteasome function and suppresses the proliferation of MCF7 breast cancer cells through accumulation of MAP kinase phosphatase-1. | Q45299364 | ||
Premature aging in persons with Down syndrome: MR findings | Q46074831 | ||
Simpler and safer cell reprogramming | Q46180058 | ||
NPC1 gene deficiency leads to lack of neural stem cell self-renewal and abnormal differentiation through activation of p38 mitogen-activated protein kinase signaling | Q46650127 | ||
Isolation and characterization of stem cell-like precursor cells from primary human anaplastic oligoastrocytoma. | Q48092193 | ||
Switched alternative splicing of oncogene CoAA during embryonal carcinoma stem cell differentiation | Q24682844 | ||
Prospective identification of tumorigenic breast cancer cells | Q24683474 | ||
Induced pluripotent stem cell lines derived from human somatic cells | Q27860597 | ||
Identification and expansion of human colon-cancer-initiating cells | Q27860627 | ||
A human colon cancer cell capable of initiating tumour growth in immunodeficient mice | Q27860831 | ||
Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors | Q27860937 | ||
Induction of pluripotent stem cells from adult human fibroblasts by defined factors | Q27860967 | ||
Generation of germline-competent induced pluripotent stem cells | Q28131699 | ||
THE LIMITED IN VITRO LIFETIME OF HUMAN DIPLOID CELL STRAINS | Q28202269 | ||
Putting tumours in context | Q28207789 | ||
Normal stem cells and cancer stem cells: the niche matters | Q28237647 | ||
Reprogramming of human somatic cells to pluripotency with defined factors | Q28262710 | ||
Tumorigenic conversion of primary embryo fibroblasts requires at least two cooperating oncogenes | Q28265486 | ||
The clonal evolution of tumor cell populations | Q28271546 | ||
A tumorigenic subpopulation with stem cell properties in melanomas | Q28277490 | ||
Isolation and characterization of tumorigenic, stem-like neural precursors from human glioblastoma | Q28286168 | ||
Aging, tumor suppression and cancer: high wire-act! | Q28299220 | ||
DNA synthesis, apoptosis, and phenotypic expression as determinants of growth of altered foci in rat liver during phenobarbital promotion | Q28335717 | ||
A novel octamer binding transcription factor is differentially expressed in mouse embryonic cells | Q28506765 | ||
Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells | Q28590205 | ||
Intercellular Communication and the Control of Tissue Growth: Lack of Communication between Cancer Cells | Q29027106 | ||
In vitro reprogramming of fibroblasts into a pluripotent ES-cell-like state | Q29614212 | ||
Induction of pluripotent stem cells by defined factors is greatly improved by small-molecule compounds | Q29614344 | ||
Directly reprogrammed fibroblasts show global epigenetic remodeling and widespread tissue contribution | Q29616187 | ||
Stem cell-like glioma cells promote tumor angiogenesis through vascular endothelial growth factor | Q29617062 | ||
Understanding the odd science of aging | Q29617341 | ||
Treatment of sickle cell anemia mouse model with iPS cells generated from autologous skin | Q29619238 | ||
Isolation and in vitro propagation of tumorigenic breast cancer cells with stem/progenitor cell properties | Q29636244 | ||
Nuclear lamins: laminopathies and their role in premature ageing. | Q30355298 | ||
Epigenetic toxicology as toxicant-induced changes in intracellular signalling leading to altered gap junctional intercellular communication | Q33533967 | ||
Gap junctions and the regulation of cellular functions of stem cells during development and differentiation | Q33835826 | ||
Human keratinocytes that express hTERT and also bypass a p16(INK4a)-enforced mechanism that limits life span become immortal yet retain normal growth and differentiation characteristics | Q33962085 | ||
Stem cells find their niche | Q34100153 | ||
A human breast epithelial cell type with stem cell characteristics as target cells for carcinogenesis | Q34106263 | ||
Prepubertal genistein exposure suppresses mammary cancer and enhances gland differentiation in rats. | Q50761648 | ||
Stem cells in differentiation and neoplasia. | Q51252004 | ||
A role for stem cell biology in the physiological and pathological aspects of aging. | Q52040576 | ||
Comparative effects of phenobarbital, DDT, and lindane on mouse hepatocyte gap junctional intercellular communication. | Q52444890 | ||
The connexin gene family in mammals. | Q52841380 | ||
Leukaemia stem cells and the evolution of cancer-stem-cell research. | Q53302987 | ||
Relative difficulties in transforming human and animal cells in vitro. | Q53562122 | ||
Neoplasia: a disease of cell differentiation. | Q53609965 | ||
Elimination of Metabolic Cooperation in Chinese Hamster Cells by a Tumor Promoter | Q54565027 | ||
Thalidomide | Q56091164 | ||
Vitamin A and pattern formation in the regenerating limb | Q59095647 | ||
Oct-3/4 expression reflects tumor progression and regulates motility of bladder cancer cells | Q64376527 | ||
Ultrastructural and biological observations on neoplastic growth control obtained by contact inhibition | Q68743089 | ||
Contact insensitivity of a subpopulation of normal human fetal kidney epithelial cells and of human carcinoma cell lines | Q68985019 | ||
Dietary restriction in mice beginning at 1 year of age: effect on life-span and spontaneous cancer incidence | Q70298117 | ||
Development of multicellular spheroids of HeLa cells cocultured with fibroblasts and their response to X-irradiation | Q71250316 | ||
Concentration-dependent differential effect of retinoic acid on intercellular metabolic cooperation | Q71706563 | ||
Effect of phenobarbital on hepatic gap junctional intercellular communication in rats | Q74455467 | ||
The Bowman-Birk inhibitor from soybeans as an anticarcinogenic agent | Q77665005 | ||
Human stem cells as targets for the aging and diseases of aging processes | Q78968424 | ||
Expression of the embryonic transcription factor Oct4 in canine neoplasms: a potential marker for stem cell subpopulations in neoplasia | Q80039753 | ||
Development. Is therapeutic cloning dead? | Q80241359 | ||
Impaired functions of neural stem cells by abnormal nitric oxide-mediated signaling in an in vitro model of Niemann-Pick type C disease | Q81026512 | ||
Isolation of cancer stem cells from adult glioblastoma multiforme | Q81042698 | ||
Commentary: "re-programming or selecting adult stem cells?" | Q81122100 | ||
A combined chemical and genetic approach for the generation of induced pluripotent stem cells | Q81393717 | ||
Structural and functional diversity of connexin genes in the mouse and human genome | Q34137753 | ||
Characterization of gap junctional intercellular communication in immortalized human pancreatic ductal epithelial cells with stem cell characteristics | Q34166895 | ||
Three down and counting: the transformation of human mammary cells from normal to malignant in three steps | Q34207903 | ||
Commentary: is the concept of "tumor promotion" a useful paradigm? | Q34218256 | ||
Permeability of membrane junctions | Q34229781 | ||
Stem cells and aging: expanding the possibilities | Q34232196 | ||
Connexins and cell signaling in development and disease | Q34357394 | ||
Oct4 expression in adult human stem cells: evidence in support of the stem cell theory of carcinogenesis | Q34363073 | ||
Radiation and the microenvironment - tumorigenesis and therapy | Q34472892 | ||
Maternal genistein alters coat color and protects Avy mouse offspring from obesity by modifying the fetal epigenome | Q34508191 | ||
Persistence of a small subpopulation of cancer stem-like cells in the C6 glioma cell line | Q34544440 | ||
Imprinting of genes and the Barker hypothesis | Q34546506 | ||
OCT-4, an embryonic stem cell marker, is highly expressed in bladder cancer | Q34598234 | ||
Similar MLL-associated leukemias arising from self-renewing stem cells and short-lived myeloid progenitors | Q34641731 | ||
How stem cells age and why this makes us grow old. | Q34667132 | ||
Caloric restriction, the traditional Okinawan diet, and healthy aging: the diet of the world's longest-lived people and its potential impact on morbidity and life span. | Q34711105 | ||
Cancer incidence in atomic bomb survivors. Part II: Solid tumors, 1958-1987. | Q34727354 | ||
Development of human cloned blastocysts following somatic cell nuclear transfer with adult fibroblasts | Q34737309 | ||
Generation of pluripotent stem cells from adult mouse liver and stomach cells | Q34750323 | ||
Genetic insights into familial cancers-- update and recent discoveries | Q34783505 | ||
Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging. | Q34790173 | ||
Pluripotent stem cells induced from adult neural stem cells by reprogramming with two factors | Q34791180 | ||
Evidence that transgenes encoding components of the Wnt signaling pathway preferentially induce mammary cancers from progenitor cells | Q34792452 | ||
Gap junctions as targets for cancer chemoprevention and chemotherapy | Q35007606 | ||
The role of stem cells and gap junctional intercellular communication in carcinogenesis | Q35051102 | ||
Human acute myeloid leukemia stem cells | Q35633955 | ||
Evaluation of the differentiation potential of WB-F344 rat liver epithelial stem-like cells in vivo. Differentiation to hepatocytes after transplantation into dipeptidylpeptidase-IV-deficient rat liver | Q35763863 | ||
Neoplasms, differentiations and mutations | Q35875063 | ||
The Beta-Carotene and Retinol Efficacy Trial: incidence of lung cancer and cardiovascular disease mortality during 6-year follow-up after stopping beta-carotene and retinol supplements | Q35968226 | ||
The emperor wears no clothes in the field of carcinogen risk assessment: ignored concepts in cancer risk assessment | Q36077542 | ||
Toward a unified theory of caloric restriction and longevity regulation | Q36127231 | ||
Oxygen in the cultivation of stem cells | Q36167426 | ||
Stem cells in the etiology and treatment of cancer | Q36353139 | ||
The difference in contact inhibition of cell replication between normal cells and cells transformed by different carcinogens | Q36385486 | ||
Adult stem cell theory of the multi-stage, multi-mechanism theory of carcinogenesis: role of inflammation on the promotion of initiated stem cells | Q36455092 | ||
Correlation of umbilical cord blood haematopoietic stem and progenitor cell levels with birth weight: implications for a prenatal influence on cancer risk | Q36459783 | ||
The common biology of cancer and ageing | Q36911187 | ||
Gap junctional intercellular communication as a biological "Rosetta stone" in understanding, in a systems biological manner, stem cell behavior, mechanisms of epigenetic toxicology, chemoprevention and chemotherapy | Q36981221 | ||
Adventures in hepatocarcinogenesis | Q37014680 | ||
The magic continues for the iPS strategy | Q37075850 | ||
A drug-inducible transgenic system for direct reprogramming of multiple somatic cell types | Q37124767 | ||
iPS cells: a more critical review | Q37143483 | ||
Metastatic cancer DNA phenotype identified in normal tissues surrounding metastasizing prostate carcinomas | Q37388848 | ||
A contact-insensitive subpopulation in Syrian hamster cell cultures with a greater susceptibility to chemically induced neoplastic transformation | Q37525160 | ||
Reversible transdifferentiation of secretory epithelial cells into adipocytes in the mammary gland | Q37695777 | ||
Two-event model for carcinogenesis: biological, mathematical, and statistical considerations | Q37940155 | ||
Phenotypic diversity in experimental hepatomas: the concept of partially blocked ontogeny. The 10th Walter Hubert Lecture | Q38593507 | ||
Beta-sitosterol from psyllium seed husk (Plantago ovata Forsk) restores gap junctional intercellular communication in Ha-ras transfected rat liver cells | Q39292228 | ||
Down's syndrome and Alzheimer's disease: a review | Q39479045 | ||
Prooxidant states and tumor promotion | Q39492603 | ||
Differentiation-linked leukemogenesis in lymphocytes | Q39746908 | ||
Positive correlations of Oct-4 and Nanog in oral cancer stem-like cells and high-grade oral squamous cell carcinoma | Q39966384 | ||
Isolation and characterization of human gastric cell lines with stem cell phenotypes | Q40103732 | ||
Tumor subpopulation interactions in neoplasms | Q40165571 | ||
Multistage carcinogenesis involves multiple genes and multiple mechanisms | Q40182710 | ||
Mouse skin: a useful model system for studying the mechanism of chemical carcinogenesis | Q40263944 | ||
Human embryonic stem cell genes OCT4, NANOG, STELLAR, and GDF3 are expressed in both seminoma and breast carcinoma | Q40361266 | ||
Retention of intrinsic stem cell hierarchies in carcinoma-derived cell lines. | Q40365745 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial 3.0 Unported | Q18810331 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 1 | |
P921 | main subject | carcinogenesis | Q1637543 |
neoplastic stem cells | Q1638475 | ||
P304 | page(s) | 8-26 | |
P577 | publication date | 2008-11-01 | |
P1433 | published in | International journal of stem cells | Q26842430 |
P1476 | title | Human adult stem cells as the target cells for the initiation of carcinogenesis and for the generation of "cancer stem cells" | |
P478 | volume | 1 |
Q61817973 | Cancer Prevention and Therapy of Two Types of Gap Junctional Intercellular Communication⁻Deficient "Cancer Stem Cell" |
Q90746119 | Evidence for immortality and autonomy in animal cancer models is often not provided, which causes confusion on key issues of cancer biology |
Q37344013 | Evolution of energy metabolism, stem cells and cancer stem cells: how the warburg and barker hypotheses might be linked. |
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Q37690877 | Localisation Microscopy of Breast Epithelial ErbB-2 Receptors and Gap Junctions: Trafficking after γ-Irradiation, Neuregulin-1β, and Trastuzumab Application. |
Q37971244 | Oxidative stress-induced biomarkers for stem cell-based chemical screening |
Q41205103 | Stem cell manipulation, gene therapy and the risk of cancer stem cell emergence |
Q34678350 | The gap junction as a "Biological Rosetta Stone": implications of evolution, stem cells to homeostatic regulation of health and disease in the Barker hypothesis |
Q90354560 | What Can Chemical Carcinogenesis Shed Light on the LNT Hypothesis in Radiation Carcinogenesis? |
Q42314685 | What roles do colon stem cells and gap junctions play in the left and right location of origin of colorectal cancers? |
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