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Akademický článek

Structure of the HLA-DR-DQ-genotype in children with coeliac disease

Autor: Yu. A. Dmitrieva, E. A. Roslavtseva, V. A. Kuryaninova, I. N. Zakharova, T. E. Borovik, E. N. Kasatkina, L. Ya. Klimov, A. V. Ivanova, E. R. Radchenko, O. V. Shuleshko

Publikováno v: Медицинский совет, Vol 0, Iss 10, Pp 74-80 (2020)

Introduction. Coeliac disease is a genetically determined disease associated with the HLA-DQ2 and DQ8 genes. According to European data, these alleles are detected in more than 95% of patients. The results of earlier studies in various regions of the

Externí odkaz: https://doaj.org/article/9dd4ad1bac834a328a99c3108cc2c94b

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Structure of the HLA-DR-DQ-genotype in children with coeliac disease

Autor: A.V. Ivanova, T. E. Borovik, O. V. Shuleshko, V. A. Kuryaninova, E. N. Kasatkina, Irina Zakharova, L. Ya. Klimov, Yu. A. Dmitrieva, E. R. Radchenko, E. A. Roslavtseva

Publikováno v: Медицинский совет, Vol 0, Iss 10, Pp 74-80 (2020)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13b62c758ea9391b4877bf1ea6408215
https://www.med-sovet.pro/jour/article/view/5723

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Akademický článek

Distribution of the human leukocyte antigen class II alleles in Brazilian patients with chronic hepatitis C virus infection

Autor: D.B. Corghi, N.S.L. Gonçales, S.B.D. Marques, F.L. Gonçales Jr.

Publikováno v: Brazilian Journal of Medical and Biological Research, Vol 41, Iss 10, Pp 884-889 (2008)

Hepatitis C virus (HCV) infection is a global medical problem. The current standard of treatment consists of the combination of peginterferon plus ribavirin. This regimen eradicates HCV in 55% of cases. The immune response to HCV is an important dete

Externí odkaz: https://doaj.org/article/3745a094648241a89e60ba5cb943e65a

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Akademický článek

Selection of Unrelated Donors for Bone Marrow Transplantation is Improved by HLA Class II Genotyping with Oligonucleotide Hybridization

Autor: Morel, C., Freidel, A. C., Zwahlen, F., Gebuhrer, L., Betuel, H., Jeannet, M., Mach, B.

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America, 1991 Aug . 88(16), 7121-7125.

Externí odkaz: https://www.jstor.org/stable/2357633

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First-appearing islet autoantibodies for type 1 diabetes in young children: Maternal life events during pregnancy and the child’s genetic risk

Autor: Hemang Parikh, Marian Rewers, Åke Lernmark, Markus Lundgren, Roswith Roth, Beena Akolkar, Jorma Toppari, William Hagopian, Suzanne Bennett Johnson, Jeffrey P. Krischer, Jin-Xiong She, Kristian Lynch, Anette-G. Ziegler

Publikováno v: Diabetologia 64, 591-602 (2021)
Diabetologia

Aims/hypothesis: Psychological stress has long been considered a possible trigger of type 1 diabetes, although prospective studies examining the link between psychological stress or life events during pregnancy and the child’s type 1 diabetes risk

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3e77d3f707d333499e8af5a0565654c
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=60926

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Association of HLA‐DR‐DQ alleles, haplotypes, and diplotypes with type 1 diabetes in Saudis

Autor: Jorma Ilonen, Inas ElGhazali, Waleed H Omer, Nezar Eltayeb-Elsheikh, Mohammed A. Alghofely, Geyhad ElGhazali, Suphia M. Sherbeeni, Abdullah Aljurayyan, Eltahir A G Khalil, Hanan Alharthi, Mohamed Mubasher

Publikováno v: Diabetes/Metabolism Research and Reviews. 36

AIMS Type 1 diabetes (T1D) is an autoimmune disease that affects many children worldwide. Genetic factors and environmental triggers play crucial interacting roles in the aetiology. This study aimed to assess the contribution of HLA-DRB1-DQA1-DQB1 al

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dce222c1b308095bbb85893795bb214b
https://doi.org/10.1002/dmrr.3345

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Author response for 'HLA‐DR‐DQ haplotypes and specificity of the initial autoantibody in islet specific autoimmunity'

Autor: null Mari‐Liis Mikk, null Sophie Pfeiffer, null Minna Kiviniemi, null Antti‐Pekka Laine, null Johanna Lempainen, null Taina Härkönen, null Jorma Toppari, null Riitta Veijola, null Mikael Knip, null Jorma Ilonen, null Per‐Henrik Groop, null Timo Otonkoski, null Alar Abram, null Henrikka Aito, null Ivan Arkhipov, null Elina Blanco‐Sequeiros, null Jonas Bondestam, null Markus Granholm, null Maarit Haapalehto‐Ikonen, null Torsten Horn, null Hanna Huopio, null Joakim Janer, null Christian Johansson, null Liisa Kalliokoski, null Päivi Keskinen, null Anne Kinnala, null Maarit Korteniemi, null Hanne Laakkonen, null Jyrki Lähde, null Päivi Miettinen, null Päivi Nykänen, null Erik Popov, null Mari Pulkkinen, null Maria Salonen, null Pia Salonen, null Juhani Sankala, null Virpi Sidoroff, null Anne‐Maarit Suomi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::41bb33feafc91d2cd50c34cf946c9a4b
https://doi.org/10.1111/pedi.13073/v2/response1

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Eplet-Based HLA Class II Matching for Transplantation: Design of a Repertoire of Interlocus Eplets Shared between HLA-DR, -DQ and -DP Alleles

Autor: Marilyn Marrari, Rene J. Duquesnoy

Publikováno v: OBM Transplantation. 4

Many studies have demonstrated that HLA-DR, HLA-DQ and HLA-DP matching at the eplet level reduces allograft rejection and improves transplant outcome. Such studies have examined the eplet effect for the individual class II loci, but until now little

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bb5749a010e1cfadc2deff7112536c4e
https://doi.org/10.21926/obm.transplant.2001099

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Akademický článek

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Correction: Reinauer et al., The Clinical Course of Patients with Preschool Manifestation of Type 1 Diabetes Is Independent of the HLA DR-DQ Genotype. Genes 2017, 8, 146

Autor: Christina Reinauer, Beate Karges, Reinhard W. Holl, Elisa De Franco, Sian Ellard, Michael Roden, Joachim Rosenbauer, Christian Herder, Jürgen Enczmann, Christina Bächle, Thomas Meissner

Publikováno v: Genes 9(2), 13 (2018). doi:10.3390/genes9010013 special issue: "Special Issue "Genetics and Functional Genomics of Diabetes Mellitus" / Guest Editor: Prof. Dr. Bernhard O. Boehm, M.D., FRCP, Professor of Metabolic Disease, LKC School of Medicine, A Joined Medical School by Imperial College London and Nanyang Technological University, Singapore; Genome Institute of Singapore, A*STAR, Singapore; Guest Editor: Dr. Rajkumar Dorajoo, Genome Institute of Singapore, A*STAR, Singapore"
Genes

The article entitled “The Clinical Course of Patients with Preschool Manifestation of Type 1 Diabetes is Independent of the HLA DR-DQ Genotype” contained a calculation error in Table 2 and the statistical methods used were not completely describe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c92cf5c7314e200d2eeb9ceac9f6bef

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