Citations (36)
Keep up to date with the latest research on this topic with citation updates for this article.
Articles from other publishers (36)
Gyöngyi Farkas, Gábor Székely, Veronika Goda, Krisztián M. Kállay, Zsuzsa S. Kocsis, Katalin Szakszon, Gábor Benyó, Dániel Erdélyi, Zoltán Liptai, Katalin Csordás, Gabriella Kertész, István Szegedi, Gergely Kriván, Zoltán Takácsi‐Nagy, Csaba Polgár & Zsolt Jurányi. (2023) Chromosomal breakage tests in the differential diagnosis of Fanconi anemia and aplastic anemia. European Journal of Haematology 111:2, pages 254-262.
Crossref
Crossref
Haider Nisar, Memoona Khan, Qamar Un Nisa Chaudhry, Raheel Iftikhar & Tariq Ghafoor. (2023) Case report: A novel mutation in RTEL1 gene in dyskeratosis congenita. Frontiers in Oncology 13.
Crossref
Crossref
Alexandre T. Vessoni, Tianpeng Zhang, Annabel Quinet, Ho-Chang Jeong, Michael Munroe, Matthew Wood, Enzo Tedone, Alessandro Vindigni, Jerry W. Shay, Roger A. Greenberg & Luis F.Z. Batista. (2021) Telomere erosion in human pluripotent stem cells leads to ATR-mediated mitotic catastrophe. Journal of Cell Biology 220:6.
Crossref
Crossref
Carsten SpeckmannMDMD, Sushree Sangita Sahoo, Marta RizziMDMD, Shinsuke Hirabayashi, Axel Karow, Nina Kathrin Serwas, Marc HoembergMDMD, Natalja DamatovaPhDPhD, Detlev SchindlerMDMD, Jean-Baptiste VannierPhDPhD, Simon J. BoultonPhDPhD, Ulrich Pannicke, Gudrun Göhring, Kathrin Thomay, J. J. Verdu-Amoros, Holger HauchMDMD, Wilhelm WoessmannMDMD, Gabriele Escherich, Eckart Laack, Liliana Rindle, Maximilian SeidlMDMD, Anne Rensing-Ehl, Ekkehart LauschMDMD, Christine JandrasitsMScMSc, Brigitte StrahmMDMD, Klaus Schwarz, Stephan R. EhlMDMD, Charlotte NiemeyerMDMD, Kaan BoztugMD, PhDMD, PhD & Marcin W. WlodarskiPhDPhD. (2017) Clinical and Molecular Heterogeneity of RTEL1 Deficiency. Frontiers in Immunology 8.
Crossref
Crossref
S. Gupta. 2014. Pathobiology of Human Disease. Pathobiology of Human Disease
1446
1461
.
M Ayas, A Nassar, A A Hamidieh, M Kharfan-Dabaja, T B Othman, A Elhaddad, A Seraihy, F Hussain, K Alimoghaddam, S Ladeb, O Fahmy, A Bazarbachi, S Y Mohamed, M Bakr, E Korthof, M Aljurf & A Ghavamzadeh. (2013) Reduced intensity conditioning is effective for hematopoietic SCT in dyskeratosis congenita-related BM failure. Bone Marrow Transplantation 48:9, pages 1168-1172.
Crossref
Crossref
Chris PepperDuncan M Baird. (2010) Shortened telomeres: a driving force behind leukemia?. Future Oncology 6:11, pages 1681-1686.
Crossref
Crossref
Duncan M. Baird. (2010)
Variation at the
TERT
locus and predisposition for cancer
. Expert Reviews in Molecular Medicine 12.
Crossref
Crossref
Frederick G. Behm. 2010. Molecular Pathology of Hematolymphoid Diseases. Molecular Pathology of Hematolymphoid Diseases
21
64
.
Nicholas D. Allen & Duncan M. Baird. (2009) Telomere length maintenance in stem cell populations. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1792:4, pages 324-328.
Crossref
Crossref
Amanda J. Walne & Inderjeet Dokal. (2008) Dyskeratosis Congenita: A historical perspective. Mechanisms of Ageing and Development 129:1-2, pages 48-59.
Crossref
Crossref
S. Mseddi, N. Ben Aribia, R. Horchani, M. Elloumi, H. Elghezal & T. Souissi. (2006) Discussion nosologique entre dyskératose congénitale et maladie de Fanconi : à propos de 1 cas d'aplasie médullaire constitutionnelle. Archives de Pédiatrie 13:9, pages 1239-1243.
Crossref
Crossref
Christof Dame. 2006. Pädiatrische Hämatologie und Onkologie. Pädiatrische Hämatologie und Onkologie
290
302
.
Audrey Killian, Nathalie Le Meur, Richard Sesboüé, Jeannette Bourguignon, Gaëlle Bougeard, Julien Gautherot, Christian Bastard, Thierry Frébourg & Jean-Michel Flaman. (2004) Inactivation of the RRB1-Pescadillo pathway involved in ribosome biogenesis induces chromosomal instability. Oncogene 23:53, pages 8597-8602.
Crossref
Crossref
Inderjeet Dokal & Tom Vulliamy. (2003) Dyskeratosis congenita: its link to telomerase and aplastic anaemia. Blood Reviews 17:4, pages 217-225.
Crossref
Crossref
Y Dror, M H Freedman, M Leaker, J Verbeek, C A Armstrong, F E Saunders & J J Doyle. (2003) Low-intensity hematopoietic stem-cell transplantation across human leucocyte antigen barriers in dyskeratosis congenita. Bone Marrow Transplantation 31:10, pages 847-850.
Crossref
Crossref
George Martin, Fuki Hisama & Sherman WeissmanAnnemarie Poustka & Nina Heiss. 2003. Chromosomal Instability and Aging. Chromosomal Instability and Aging.
Martin Digweed & Karl Sperling. 2003. Molekularmedizinische Grundlagen von hämatologischen Neoplasien. Molekularmedizinische Grundlagen von hämatologischen Neoplasien
3
38
.
Blanche P Alter. (2002) Bone marrow failure syndromes in children. Pediatric Clinics of North America 49:5, pages 973-988.
Crossref
Crossref
N.S. Heiss & A. Poustka. 2002. Wiley Encyclopedia of Molecular Medicine. Wiley Encyclopedia of Molecular Medicine.
M Priolo, M Silengo, M Lerone & R Ravazzolo. (2008) Ectodermal dysplasias: not only ‘skin’ deep. Clinical Genetics 58:6, pages 415-430.
Crossref
Crossref
Inderjeet Dokal. (2001) Dyskeratosis congenita in all its forms. British Journal of Haematology 110:4, pages 768-779.
Crossref
Crossref
Nina S. Heiss, Dietmar Bächner, Rüdiger Salowsky, Anja Kolb, Petra Kioschis & Annemarie Poustka. (2000) Gene Structure and Expression of the Mouse Dyskeratosis Congenita Gene, Dkc1. Genomics 67:2, pages 153-163.
Crossref
Crossref
N. S. Heiss, A. Girod, R. Salowsky, S. Wiemann, R. Pepperkok & A. Poustka. (1999) Dyskerin Localizes to the Nucleolus and Its Mislocalization Is Unlikely to Play a Role in the Pathogenesis of Dyskeratosis Congenita. Human Molecular Genetics 8:13, pages 2515-2524.
Crossref
Crossref
Hagop Youssoufian, Vazganoush Gharibyan & Mohammed Qatanani. (1999) Analysis of Epitope-Tagged Forms of the Dyskeratosis Congenita Protein (Dyskerin): Identification of a Nuclear Localization Signal. Blood Cells, Molecules, and Diseases 25:5, pages 305-309.
Crossref
Crossref
&NA;. (1999) Guest Commentaries. Journal of Pediatric Hematology/Oncology 21:5, pages 344-349.
Crossref
Crossref
S.W. Knight, N.S. Heiss, T.J. Vulliamy, S. Greschner, G. Stavrides, G.S. Pai, G. Lestringant, N. Varma, P.J. Mason, I. Dokal & A. Poustka. (1999) X-Linked Dyskeratosis Congenita Is Predominantly Caused by Missense Mutations in the DKC1 Gene. The American Journal of Human Genetics 65:1, pages 50-58.
Crossref
Crossref
Blanche P. Alter. (1999) Bone Marrow Failure Syndromes. Clinics in Laboratory Medicine 19:1, pages 113-134.
Crossref
Crossref
Stuart Knight, Tom Vulliamy, Adrian Copplestone, Eliane Gluckman, Philip Mason & Inderjeet Dokal. (2002) Dyskeratosis Congenita (DC) Registry: identification of new features of DC. British Journal of Haematology 103:4, pages 990-996.
Crossref
Crossref
Vanderson Rocha, Gnès Devergie, Gerard SociÉ, Patricia Ribaud, Hélène EspÉrou, Nathalie Parquet & Eliane Gluckman. (2002) Unusual complications after bone marrow transplantation for dyskeratosis congenita. British Journal of Haematology 103:1, pages 243-248.
Crossref
Crossref
Brigitte Solder, Michael Weiss, Andrea Jager & Bernd H. Belohradsky. (2016) Dyskeratosis Congenita: Multisystemic Disorder with Special Consideration of Immunologic Aspects. Clinical Pediatrics 37:9, pages 521-530.
Crossref
Crossref
Amyna Merchant, Tong-Zheng Zhao & C.Stephen Foster. (1998) Chronic keratoconjunctivitis associated with congenital dyskeratosis and erythrokeratodermia variablis. Ophthalmology 105:7, pages 1286-1291.
Crossref
Crossref
Nina S. Heiss, Stuart W. Knight, Tom J. Vulliamy, Sabine M. Klauck, Stefan Wiemann, Philip J. Mason, Annemarie Poustka & Inderjeet Dokal. (1998) X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions. Nature Genetics 19:1, pages 32-38.
Crossref
Crossref
Eulalia Baselga, Beth A. Drolet, Peter van Tuinen, Nancy B. Esterly & Rudolf Happle. (1998) Dyskeratosis congenita with linear areas of severe cutaneous involvement. American Journal of Medical Genetics 75:5, pages 492-496.
Crossref
Crossref
Blanche P. Alter. (1996) Aplastic Anemia, Pediatric Aspects. The Oncologist 1:6, pages 361-366.
Crossref
Crossref
S W Knight, T Vulliamy, G L Forni, D Oscier, P J Mason & I Dokal. (1996) Fine mapping of the dyskeratosis congenita locus in Xq28.. Journal of Medical Genetics 33:12, pages 993-995.
Crossref
Crossref