Telomerase Activity in Hematopoietic Cells Is Associated with Self-Renewal Potential

The serial cultivation of human diploid cell strains

Hayflick, L., & Moorhead, P. S. (1961) · Experimental Cell Research · doi:10.1016/0014-4827(61)90192-6 · Cited by 8,508

Specific Association of Human Telomerase Activity with Immortal Cells and Cancer

Kim, N. W., Piatyszek, M. A., Prowse, K. R., Harley, C. B., West, M. D., Ho, P. L. C., Coviello, G. M., Wright, W. E., Weinrich, S. L., & Shay, J. W. (1994) · Science · doi:10.1126/science.7605428 · Cited by 7,091

The limited in vitro lifetime of human diploid cell strains

Hayflick, L. (1965) · Experimental Cell Research · doi:10.1016/0014-4827(65)90211-9 · Cited by 5,876

Telomeres shorten during ageing of human fibroblasts

Harley, C. B., Futcher, A. B., & Greider, C. W. (1990) · Nature · doi:10.1038/345458a0 · Cited by 5,750

Identification of a specific telomere terminal transferase activity in tetrahymena extracts

Greider, C. W., & Blackburn, E. H. (1985) · Cell · doi:10.1016/0092-8674(85)90170-9 · Cited by 3,400

Purification and Characterization of Mouse Hematopoietic Stem Cells

Spangrude, G. J., Heimfeld, S., & Weissman, I. L. (1988) · Science · doi:10.1126/science.2898810 · Cited by 2,908

A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes.

Moyzis, R. K., Buckingham, J. M., Cram, L. S., Dani, M. A. C., Deaven, L. L., Jones, M. D., Meyne, J., Ratliff, R. L., & Wu, J. R. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.18.6622 · Cited by 2,326

Telomere length predicts replicative capacity of human fibroblasts.

Allsopp, R. C., Vaziri, H., Patterson, C., Goldstein, S., Younglai, E. V., Futcher, A. B., Greider, C. W., & Harley, C. B. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.21.10114 · Cited by 2,200

Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity.

Counter, C. M., Avilion, A. A., LeFeuvre, C. E., Stewart, N. G., Greider, C. W., Harley, C. B., & Bacchetti, S. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05245.x · Cited by 2,096

Telomere reduction in human colorectal carcinoma and with ageing

Hastie, N. D., Dempster, M., Dunlop, M. G., Thompson, A. M., Green, D. K., & Allshire, R. C. (1990) · Nature · doi:10.1038/346866a0 · Cited by 1,650

Telomerase-targeted therapies in myeloid malignancies

Waksal, J. A., Bruedigam, C., Komrokji, R. S., Jamieson, C. H. M., & Mascarenhas, J. O. (2023) · Blood Advances · doi:10.1182/bloodadvances.2023009903 · Cited by 27

Pharmacologic rationale for early G-CSF prophylaxis in cancer patients and role of pharmacogenetics in treatment optimization

Crea, F., Giovannetti, E., Zinzani, P. L., & Danesi, R. (2008) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2008.10.014 · Cited by 27

Signaling Pathways Regulating Hematopoietic Stem Cell and Progenitor Aging

Singh, A. K., Althoff, M. J., & Cancelas, J. A. (2018) · Current Stem Cell Reports · doi:10.1007/s40778-018-0128-6 · Cited by 27

Telomerase regulation in hematological cancers: A matter of stemness?

Deville, L., Hillion, J., & Ségal-Bendirdjian, E. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2009.01.016 · Cited by 27

CEBP factors regulate telomerase reverse transcriptase promoter activity in whey acidic protein‐T mice during mammary carcinogenesis

Kumar, M., Witt, B., Knippschild, U., Koch, S., Meena, J. K., Heinlein, C., Weise, J. M., Krepulat, F., Kuchenbauer, F. C., Iben, S., et al. (2012) · International Journal of Cancer · doi:10.1002/ijc.27880 · Cited by 26

Stem Cells in Aquatic Invertebrates: Common Premises and Emerging Unique Themes

Rinkevich, Y., Matranga, V., & Rinkevich, B. (2009) · Springer eBooks · doi:10.1007/978-90-481-2767-2_4 · Cited by 26

Telomere Biology of Human Hematopoietic Stem Cells

Elwood, N. J. (2004) · Cancer Control · doi:10.1177/107327480401100214 · Cited by 26

Many Functions of Telomerase Components: Certainties, Doubts, and Inconsistencies

Udroiu, I., Marinaccio, J., & Sgura, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315189 · Cited by 25

The molecular basis of ageing in stem cells

Tam, W. L., Ang, Y.-S., & Lim, B. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.11.020 · Cited by 25

Muti-target rationale design of novel substituted N-phenyl-2-((6-phenylpyridazin-3-yl)thio)acetamide candidates as telomerase/JAK1/STAT3/TLR4 inhibitors: In vitro and in vivo investigations

Shaldam, M. A., Mousa, M. H. A., Tawfik, H. O., El‐Dessouki, A. M., Sharaky, M. M., Saleh, M. M., Alzahrani, A. Y. A., Moussa, S. B., & Al-Karmalawy, A. A. (2024) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2024.107843 · Cited by 24

TGF-β induces telomerase-dependent pancreatic tumor cell cycle arrest

Cassar, L., Li, H., Jiang, F., & Liu, J. (2010) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.02.002 · Cited by 26

Stem Cells: An Overview

Denham, M., Conley, B. J., Olsson, F., Cole, T. J., & Mollard, R. (2005) · Current Protocols in Cell Biology · doi:10.1002/0471143030.cb2301s28 · Cited by 30

The elements of stem cell self-renewal: a genetic perspective

Pazianos, G., Uqoezwa, M., & Reya, T. (2003) · BioTechniques · doi:10.2144/03356ss03 · Cited by 26

Aspects of lymphocyte developmental biology

von Bochmer, H. (1997) · Immunology Today · doi:10.1016/s0167-5699(97)80018-7 · Cited by 24

Molecular mechanism of extrinsic factors affecting anti-aging of stem cells

Wong, T. (2015) · World Journal of Stem Cells · doi:10.4252/wjsc.v7.i2.512 · Cited by 24

The Telomerase Complex Directly Controls Hematopoietic Stem Cell Differentiation and Senescence in an Induced Pluripotent Stem Cell Model of Telomeropathy

Jose, S. S., Tidu, F., Búřilová, P., Kepák, T., Bendíčková, K., & Frič, J. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00345 · Cited by 24

Human short-term repopulating cells have enhanced telomerase reverse transcriptase expression

Järås, M., Edqvist, A., Rebetz, J., Salford, L. G., Widegren, B., & Fan, X. (2006) · Blood · doi:10.1182/blood-2005-09-008904 · Cited by 23

Children are not little adults: just ask their hematopoietic stem cells

Williams, D., Xu, H., & Cancelas, J. A. (2006) · Journal of Clinical Investigation · doi:10.1172/jci30083 · Cited by 23

UNRELATED CORD BLOOD TRANSPLANT EXPERIENCE BY THE PEDIATRIC BLOOD AND MARROW TRANSPLANT CONSORTIUM

Yu, L. C., Wall, D. A., Sandler, E. S., Chan, K. A., Grayson, G. H., & Kletzel, M. (2001) · Pediatric Hematology and Oncology · doi:10.1080/088800101750238531 · Cited by 22

Telomerase activity in ecological studies: What are its consequences for individual physiology and is there evidence for effects and trade‐offs in wild populations

Smith, S., Hoelzl, F., Zahn, S., & Criscuolo, F. (2021) · Molecular Ecology · doi:10.1111/mec.16233 · Cited by 22

Critical Roles of Reactive Oxygen Species in Age‐Related Impairment in Ischemia‐Induced Neovascularization by Regulating Stem and Progenitor Cell Function

Lam, Y. T. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/7095901 · Cited by 22

Erythroid expansion and survival in response to acute anemia stress: The role of EPO receptor, GATA‐1, Bcl‐xL and caspase‐3

Aispuru, G. R., Aguirre, M. V., Aquino‐Esperanza, J., Lettieri, C. N., Juaristi, J. A., & Brandan, N. C. (2008) · Cell Biology International · doi:10.1016/j.cellbi.2008.04.014 · Cited by 21

Recent progress in identifying genes regulating hematopoietic stem cell function and fate

Jordan, C. T., & Zant, G. E. V. (1998) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(98)80112-9 · Cited by 21

The Therapeutic Potential of Fetal and Neonatal Hematopoietic Stem Cells

Gluckman, É. (1996) · New England Journal of Medicine · doi:10.1056/nejm199612123352411 · Cited by 21

Bcl-2 expression and apoptosis in the regulation of hematopoietic stem cells

Orelio, C. C., & Dzierzak, E. A. (2007) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428190601032529 · Cited by 20

Stem cell ageing: does it happen and can we intervene?

Bellantuono, I., & Keith, W. N. (2007) · Expert Reviews in Molecular Medicine · doi:10.1017/s146239940700049x · Cited by 21

Stem cells on the way to restorative medicine

Keller, R. (2002) · Immunology Letters · doi:10.1016/s0165-2478(02)00065-2 · Cited by 20

Telomere Biology in Stem Cells and Reprogramming

Batista, L. F. Z. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-397898-1.00003-7 · Cited by 22

Stem cell function and maintenance – ends that matter: Role of telomeres and telomerase

Saeed, H., & Iqtedar, M. (2013) · Journal of Biosciences · doi:10.1007/s12038-013-9346-3 · Cited by 19

Role for Telomerase in Listeria monocytogenes Infection

Samba‐Louaka, A., Stavru, F., & Cossart, P. (2012) · Infection and Immunity · doi:10.1128/iai.00614-12 · Cited by 22

Side population of a murine mantle cell lymphoma model contains tumour‐initiating cells responsible for lymphoma maintenance and dissemination

Vega, F., Davuluri, Y., Cho‐Vega, J. H., Singh, R. R., Ma, S., Wang, R., Multani, A. S., Drakos, E., Pham, L. V., Lin-Lee, Y.-C., et al. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00865.x · Cited by 19

Regeneration and Repair

Friedman, R. S., & Krause, D. S. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04411.x · Cited by 18

Stability and plasticity of wild‐type and Pax5‐deficient precursor B cells

Rolink, A. G., Schaniel, C., & Melchers, F. (2002) · Immunological Reviews · doi:10.1034/j.1600-065x.2002.18708.x · Cited by 18

Inherited Predispositions to Myeloid Neoplasms: Pathogenesis and Clinical Implications

Liu, Y., Eldomery, M. K., Maciaszek, J. L., & Klco, J. M. (2024) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-111523-023420 · Cited by 17

Alternative Splicing of Human Telomerase Reverse Transcriptase May Not Be Involved in Telomerase Regulation During all-trans-Retinoic Acid-Induced HL-60 Cell Differentiation

Liu, W., Zhang, Y., Zhang, Z.-X., & Ding, J. (2004) · Journal of Pharmacological Sciences · doi:10.1254/jphs.fp0030600 · Cited by 17

Genetic and epigenetic trends in telomere research: a novel way in immunoepigenetics

Melicher, D., Buzás, E. I., & Falus, A. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1991-2 · Cited by 17

Murine Yolk Sac and Bone Marrow Hematopoietic Cells with High Proliferative Potential Display Different Capacities for Producing Colony-Forming Cells Ex Vivo

Yöder, M. C., & Hiatt, K. K. (1999) · Stem Cells and Development · doi:10.1089/152581699320180 · Cited by 17

Regulation of Cellular Immortalization and Steady-State Levels of the Telomerase Reverse Transcriptase through Its Carboxy-Terminal Domain

Middleman, E. J., Choi, J., Venteicher, A. S., Cheung, P., & Artandi, S. E. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.6.2146-2159.2006 · Cited by 17

Suppression of telomerase activity and cytokine messenger RNA levels in acute myelogenous leukemia cells in vivo in patients by amifostine and interleukin 4.

Preisler, H. D., Li, Y., Yang, B., Huang, R. W., Devemy, E., Venugopal, P., Tao, M., Chopra, H., Gregory, S. A., Adler, S., et al. (2000) · PubMed · Cited by 17

LINEAGE BIOLOGY AND LIVER

Xu, A. S. L., Luntz, T. L., Macdonald, J. M., Kubota, H., Hsu, E. W., London, R. E., & Reid, L. M. (2000) · Elsevier eBooks · doi:10.1016/b978-012436630-5/50045-3 · Cited by 17

Germline-somatic JAK2 interactions are associated with clonal expansion in myelofibrosis

Brown, D. W., Zhou, W., Wang, Y., Jones, K. M., Luo, W., Dagnall, C. L., Teshome, K., Klein, A., Zhang, T., Lin, S., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32986-7 · Cited by 16

Embryonic Stem Cell-Derived Haematopoiesis

Hole, N. (1999) · Cells Tissues Organs · doi:10.1159/000016698 · Cited by 16

Telomerase activity in human hematopoietic progenitor cells.

Hohaus, S., Voso, M. T., Barbera, E., Cavallo, S., Bellacosa, A., Rutella, S., Rumi, C., Genuardi, M., Neri, G., & Leone, G. G. M. (1997) · PubMed · Cited by 15

Telomere dysfunction and cell cycle checkpoints in hematopoietic stem cell aging

Ju, Z., Zhang, J., Gao, Y., & Cheng, T. (2011) · International Journal of Hematology · doi:10.1007/s12185-011-0882-z · Cited by 14

BIX-01294 promotes the differentiation of adipose mesenchymal stem cells into adipocytes and neural cells in Arbas Cashmere goats

Wang, Q., Wang, X., Lai, D., Deng, J., Hou, Z., Liang, H., & Liu, D. (2018) · Research in Veterinary Science · doi:10.1016/j.rvsc.2018.05.009 · Cited by 14

IL-6 precludes the differentiation induced by IL-3 on expansion of CD34+ cells from cord blood.

Encabo, A., Mateu, E., Carbonell‐Uberos, F., & Miñana, M. D. (2003) · PubMed · Cited by 14

Identification of a coronary stem cell in the human heart

Leri, A., Hosoda, T., Kajstura, J., Anversa, P., & Rota, M. (2011) · Journal of Molecular Medicine · doi:10.1007/s00109-011-0769-8 · Cited by 14

Senescence of Hematopoietic Stem Cells and Bone Marrow Failure

Chen, J. (2005) · International Journal of Hematology · doi:10.1532/ijh97.05094 · Cited by 13

Our Perception of Developmental Plasticity Esse Est Percipi (to be is to be Perceived)?

Askenasy, N., Yaniv, I., Stein, J., & Sharkis, S. J. (2006) · Current Stem Cell Research & Therapy · doi:10.2174/157488806775269089 · Cited by 13

Telomerase dynamics in stem cells: Unraveling the molecular nexus of cellular aging and regeneration

Jiang, Y., Zhou, Y., Wang, Y., Li, Z., Ashraf, G. M., & Guo, L. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102853 · Cited by 12

Telomere length and age-dependent telomere attrition: the blood-and-muscle model

Chahine, M. N., Toupance, S., El-Hakim, S., Labat, C., Gautier, S., Moussallem, T., Yared, P., Asmar, R. G., & Bénétos, A. (2019) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2018-0582 · Cited by 12

Stem-like T cells and niches: Implications in human health and disease

Yi, L., & Li, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.907172 · Cited by 15

Telomerase regulation and progressive telomere shortening of rat hepatic stem-like epithelial cells during in vitro aging

Oh, B.-K., Lee, C.-H., Park, C., & Park, Y. N. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2004.04.032 · Cited by 12

Stem Cells and Genetics in the Study of Development, Aging, and Longevity

Zant, G. E. V. (2000) · Results and problems in cell differentiation · doi:10.1007/978-3-540-48003-7_11 · Cited by 12

Interleukin 6 receptor expression by human cord blood‐ or peripheral blood‐derived primitive haematopoietic progenitors implies acquisition of different functional properties

Minamiguchi, H., Yahata, N., Kimura, T., Fujiki, H., Harada, S., Wang, J., Okuda, K., Kaneko, H., Hodohara, K., Banba, T., et al. (2000) · British Journal of Haematology · doi:10.1046/j.1365-2141.2000.02148.x · Cited by 12

Biological basis of extensive pleiotropy between blood traits and cancer risk

Pardo-Cea, M. Á., Farré, X., Esteve, A., Palade, J., Espín, R., Mateo, F., Alsop, E. B., Alorda, M., Blay, N., Baiges, A., et al. (2024) · Genome Medicine · doi:10.1186/s13073-024-01294-8 · Cited by 12

Oxidized low‐density lipoprotein induces hematopoietic stem cell senescence

Zhang, X., Zhang, G., Wang, Y., Liu, J., 魏强, Xu, C., Wang, J., & Wang, Y. (2013) · Cell Biology International · doi:10.1002/cbin.10121 · Cited by 11

The effects of proliferation and DNA damage on hematopoietic stem cell function determine aging

Khurana, S. (2016) · Developmental Dynamics · doi:10.1002/dvdy.24388 · Cited by 11

Early B Cell Development to a Mature, Antigen-Sensitive Cell

Melchers, F., & Kincade, P. W. (2004) · Elsevier eBooks · doi:10.1016/b978-012053641-2/50008-3 · Cited by 11

Biology of Hematopoietic Stem and Progenitor Cells

Manz, M. G., Akashi, K., & Weissman, I. L. (2003) · Wiley eBooks · doi:10.1002/9780470987070.ch8 · Cited by 11

Short-term treatment with imetelstat sensitizes hematopoietic malignant cells to a genotoxic agent via suppression of the telomerase-mediated DNA repair process

Hidaka, D., Onozawa, M., Miyashita, N., Yokoyama, S., Nakagawa, M., Hashimoto, D., & Teshima, T. (2020) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428194.2020.1779256 · Cited by 10

TRAPping telomerase within the intestinal stem cell niche

Pech, M. F., & Artandi, S. E. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.51 · Cited by 10

Growing and aging of hematopoietic stem cells

Udroiu, I., & Sgura, A. (2021) · World Journal of Stem Cells · doi:10.4252/wjsc.v13.i6.594 · Cited by 10

Expandable Lung Epithelium Differentiated from Human Embryonic Stem Cells

Kotasová, H., Capandová, M., Pelková, V., Dumková, J., Koledova, Z. S., Remšík, J., Souček, K., Garlíková, Z., Sedláková, V., Rabata, A., et al. (2022) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-022-00458-0 · Cited by 10

Telomerase: from Aging to Human Cancers

Parsa, N. (2012) · Springer eBooks · doi:10.1007/978-94-007-4632-9_1 · Cited by 15

Re: Yves Allorya, Willemien Beukers, Ana Sagrera, et al. Telomerase Reverse Transcriptase Promoter Mutations in Bladder Cancer: High Frequency Across Stages, Detection in Urine, and Lack of Association with Outcome. Eur Urol 2014;65:360–6

Rane, J. K., Simms, M. S., & Maitland, N. J. (2014) · European Urology · doi:10.1016/j.eururo.2014.02.030 · Cited by 10

Treatment of Myelodysplastic Syndromes

Komrokji, R. S. (2023) · Wiley eBooks · doi:10.1002/9781119823193.ch13 · Cited by 10

Cord Blood Banking and Transplant in Europe

Gluckman, É., Rocha, V., & Chastang, C. (1998) · Springer eBooks · doi:10.1007/978-1-4615-5619-0_18 · Cited by 10

Evolution of normal and neoplastic tissue stem cells: progress after Robert Hooke

Weissman, I. L. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2014.0364 · Cited by 9

Immunosenescence in Childhood Cancer Survivors and in Elderly: A Comparison and Implication for Risk Stratification

Lázničková, P., Bendíčková, K., Kepák, T., & Frič, J. (2021) · Frontiers in Aging · doi:10.3389/fragi.2021.708788 · Cited by 10

The dual distinct role of telomerase in repression of senescence and myofibroblast differentiation

Harada, M., Hu, B., Lu, J., Wang, J., Rinke, A. E., Wu, Z. B., Liu, T., & Phan, S. H. (2021) · Aging · doi:10.18632/aging.203246 · Cited by 9

Stem Cells, Cell Differentiation, and Cancer

Dalerba, P. D., Diehn, M., Weissman, I. L., & Clarke, M. F. (2020) · Elsevier eBooks · doi:10.1016/b978-0-323-47674-4.00007-4 · Cited by 9

Isolation and therapeutic potential of human haemopoietic stem cells

Clark, A. D., Jørgensen, H. G., Mountford, J. C., & Holyoake, T. L. (2003) · Cytotechnology · doi:10.1023/a:1024822722285 · Cited by 9

Tight co-twin similarity of monozygotic twins for hTERT protein level of T cell subsets, for telomere length and mitochondrial DNA copy number, but not for telomerase activity

Melicher, D., Illés, A., Pállinger, É., Kovács, Á. F., Littvay, L., Tárnoki, Á. D., Tárnoki, D. L., Bikov, A., Molnár, M. J., Buzás, E. I., et al. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2738-z · Cited by 8

Aging and Carcinogenesis – Insufficient Metabolic Cell Repair as the Common Link

Baramiya, M. G. (2000) · Gerontology · doi:10.1159/000022186 · Cited by 8

Cibler les télomères pour forcer les cellules cancéreuses à rentrer en sénescence

Londoño‐Vallejo, A., Lenain, C., & Gilson, É. (2008) · médecine/sciences · doi:10.1051/medsci/2008244383 · Cited by 13

Poor prognosis acute myelogenous leukemia: 1 – response to treatment with high dose cytarabine/mitoxantrone/ethyol @ (Amifostine)

Preisler, H. D., Venugopal, P., Gregory, S. A., Hsu, W.-T., Loew, J. M., Adler, S., Gezer, S., Creech, S., Galvez, A. G., Slivnick, D. J., et al. (2000) · Leukemia Research · doi:10.1016/s0145-2126(00)00037-0 · Cited by 8

Management of high-risk myelodysplastic syndromes

Pisani, F., & Rainaldi, A. (2001) · Critical Reviews in Oncology/Hematology · doi:10.1016/s1040-8428(01)00093-2 · Cited by 8

Telomeres and haemopoiesis

Wynn, R. F., Cross, M. A., & Testa, N. G. (1998) · British Journal of Haematology · doi:10.1046/j.1365-2141.1998.01092.x · Cited by 8

Adaptive and Maladaptive Clonal Hematopoiesis in Telomere Biology Disorders

Lasho, T. L., & Patnaik, M. M. (2023) · Current Hematologic Malignancy Reports · doi:10.1007/s11899-023-00719-2 · Cited by 8

Sensitive bioanalytical methods for telomerase activity detection: a cancer biomarker

Afshari, N., Al-Gazally, M. E., Rasulova, I., Jalil, A. T., Matinfar, S., & Momeninejad, M. (2022) · Analytical Methods · doi:10.1039/d2ay01315k · Cited by 7

Food Supplement 20070721-GX May Increase CD34+Stem Cells and Telomerase Activity

Lin, P., Chiou, T., Liu, P.-Y., Chen, S., Wang, H.-I., Huang, P.-C., Lin, S., & Harn, H. (2012) · BioMed Research International · doi:10.1155/2012/498051 · Cited by 7

Induction of telomerase activity during an early burst of proliferation in pancreatic regeneration

Oh, B.-K., Seong, J. K., Lee, J. E., Chae, K. J., Roh, K. J., Park, C., & Park, Y. N. (2002) · Cancer Letters · doi:10.1016/s0304-3835(02)00320-8 · Cited by 7

Stem cells: a primer.

Lin, T. C. Y., & Lee, O. K. S. (2008) · PubMed · Cited by 7

Gene Regulation in T-Cell Lineage Commitment

Rothenberg, E. V. (1998) · Humana Press eBooks · doi:10.1007/978-1-4757-2778-4_18 · Cited by 7

Telomeres as hallmarks of iPSC aging: A review on telomere dynamics during stemness and cellular reprogramming

Tavares-Marcos, C., Correia, M., & de Jesus, B. B. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102773 · Cited by 6

Induction of telomerase activity in stimulated human lymphocytes precedes expression of topoisomerase II α

Feist, H., Zeidler, R., Skrebsky, T., Schmatloch, S., & Kreipe, H. H. (1998) · Annals of Hematology · doi:10.1007/s002770050374 · Cited by 6

Poor prognosis acute myelogenous leukemia 2 — biological and molecular biological characteristics and treatment outcome

Li, Y., Yang, J. W., Tao, M., Nayini, J., Horvath, E. Z., Chopra, H., Meyer, P., Venugopal, P., & Preisler, H. D. (2000) · Leukemia Research · doi:10.1016/s0145-2126(00)00035-7 · Cited by 6

The correlation of telomerase and IL-10 with leukemia transformation in a mouse model of chronic lymphocytic leukemia (CLL)

Peng, B., Zhang, M., Sun, R. K. P., Lin, Y.-C., Chong, S. Y., Lai, H., Stein, D., & Raveche, E. S. (1998) · Leukemia Research · doi:10.1016/s0145-2126(98)00021-6 · Cited by 6

Leukemia and Leukemic Stem Cells

Jamieson, C. H. M., Passegue, E. A., & Weissman, I. L. (2004) · Research and perspectives in neurosciences · doi:10.1007/978-3-642-18883-1_12 · Cited by 6

In vitro detection of marine invertebrate stem cells: utilizing molecular and cellular biology techniques and exploring markers

Mohajer, F., Khoradmehr, A., Riazalhosseini, B., Zendehboudi, T., Nabipour, I., & Baghban, N. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1440091 · Cited by 5

Stem Cells in Cardiovascular Disease: Methods and Protocols

Penn, M. S., & Mal, N. (2006) · Humana Press eBooks · doi:10.1385/1-59745-213-0:329 · Cited by 5

Telomere maintenance in soft tissue sarcomas

Eastley, N. C., Ottolini, B., Garrido, C., Shaw, J., McCulloch, T. A., Ashford, R. U., & Royle, N. J. (2017) · Journal of Clinical Pathology · doi:10.1136/jclinpath-2016-204151 · Cited by 7

Telomeres: an organized string linking plants and mammals

Pietro, E. D., Burla, R., Torre, M. L., González‐García, M. P., Ioio, R. D., & Saggio, I. (2024) · Biology Direct · doi:10.1186/s13062-024-00558-y · Cited by 5

Telomere and Telomerase for the Regulation of Stem Cells

Hiyama, E., & Hiyama, K. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-227-8_11 · Cited by 4

Aging of Human Haematopoietic Stem Cells

Garrick, D., Djeghloul, D., Kuranda, K., & Goodhardt, M. (2015) · Springer eBooks · doi:10.1007/978-3-7091-1232-8_7 · Cited by 4

Inhibition of TERC inhibits neural apoptosis and inflammation in spinal cord injury through Akt activation and p-38 inhibition via the miR-34a-5p/XBP-1 axis

Ding, W., Xu, W., Lu, D., Sheng, H.-F., Xu, X., Xu, B., & Zheng, A. (2023) · Open Medicine · doi:10.1515/med-2022-0619 · Cited by 4

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Sonoda, S., & Yamaza, T. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1151429 · Cited by 4

Genesis of clone size heterogeneity in megakaryocytic and other hemopoietic colonies

Paulus, J., Levin, J., Debili, N., Albert, A., & Vainchenker, W. (2001) · Experimental Hematology · doi:10.1016/s0301-472x(01)00728-7 · Cited by 4

Cancer origin in committed versus stem cells: Hypothetical antineoplastic mechanism/s associated with stem cells

Torres-Montaner, A. (2011) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2011.01.003 · Cited by 4

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Chiu, C., Dragowska, W., Kim, N. W., Vaziri, H., Yui, J., Thomas, T. E., Harley, C. B., & Lansdorp, P. M. (1996) · STEM CELLS · doi:10.1002/stem.140239 · Cited by 388

Telomerase Promotes the Self-Renewal of Human Hematopoietic Progenitor Cells but Does Not Maintain Telomere Length.

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Telomerase activity in human hematopoietic progenitor cells.

Hohaus, S., Voso, M. T., Barbera, E., Cavallo, S., Bellacosa, A., Rutella, S., Rumi, C., Genuardi, M., Neri, G., & Leone, G. G. M. (1997) · PubMed · Cited by 15

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Yui, J., Chiu, C.-P., & Lansdorp, P. M. (1998) · Blood · doi:10.1182/blood.v91.9.3255 · Cited by 216