Výsledky vyhledávání - "Ghada I. Mossallam"

Akademický článek

Comparing Prothrombin induced by vitamin K absence-II (PIVKA-II) with the oncofetal proteins Glypican-3, Alpha feto protein and Carcinoembryonic antigen in diagnosing hepatocellular carcinoma among Egyptian patients

Autor: Iman A. Abd El Gawad, Ghada I. Mossallam, Noha H. Radwan, Heba M. Elzawahry, Niveen M. Elhifnawy

Publikováno v: Journal of the Egyptian National Cancer Institute, Vol 26, Iss 2, Pp 79-85 (2014)

Background: Hepatocellular carcinoma (HCC) is usually asymptomatic in the early stage and does not show elevated alpha-feto protein (AFP). AFP shows 60–80% sensitivity in diagnosing HCC. Glypican3 (GPC-3) is an oncofetal protein that is only detect

Externí odkaz: https://doaj.org/article/8e06a3ae41fc4c63b3e5e58d446b62d8

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Akademický článek

Lack of association of CTLA-4 +49 A/G polymorphism with predisposition to type 1 diabetes in a cohort of Egyptian families

Autor: Azza M. Kamel, Marwa F. Mira, Ghada I. Mossallam, Gamal T.A. Ebid, Eman R. Radwan, Nelly H. Aly Eldin, Mona Mamdouh, Maha Amin, Nora Badawy, Hafez Bazaraa, Amani Ibrahim, Nermine Salah, John Hansen

Publikováno v: Egyptian Journal of Medical Human Genetics, Vol 15, Iss 1, Pp 25-30 (2014)

Background: Type 1 diabetes is one of the most common chronic childhood illnesses. Interplay between genetic susceptibility and environmental factors is thought to provide the fundamental element for the disease. Apart from the Major Histocompatibili

Externí odkaz: https://doaj.org/article/8eca1d3f359049c88a610141adf094fc

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HLA Haplotypes In 250 Families: The Baylor Laboratory Results And A Perspective On A Core NGS Testing Model For The 17th International HLA And Immunogenetics Workshop

Publikováno v: Human Immunology. 80:897-905

Since their inception, the International HLA & Immunogenetics Workshops (IHIW) served as a collaborative platform for exchange of specimens, reference materials, experiences and best practices. In this report we present a subset of the results of hum

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0ebad06e4472b0c0948e351cfcc12b95
https://doi.org/10.1016/j.humimm.2019.07.298

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Behçet disease, new insights in disease associations and manifestations: a next‐generation sequencing study

Autor: H de Bruin, Mohanad M. Elfishawi, Marcelo Fernandez-Vina, Paul Norman, Gonzalo Montero-Martín, Danillo G. Augusto, Jill A. Hollenbach, Sally Elfishawi, Erik H. Rozemuller, Ghada I. Mossallam, K Zaky, L Van de Pasch, Adriana Abrudescu

Publikováno v: Clin Exp Immunol

Summary Behçet disease is a multi-system disease associated with human leukocyte antigen (HLA) class I polymorphism. High-resolution next-generation sequencing (NGS) with haplotype analysis has not been performed previously for this disease. Sixty E

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccc51e57f94bcf93918ff3fe3e462157
https://europepmc.org/articles/PMC7944360/

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LMP7 polymorphism may modify the presentation and clinical impact of minor histocompatibility antigens in matched related hematopoietic stem cell transplantation

Autor: Manar M. Moneer, Raafat Abdel Fattah, Mahmoud Bokhary, Hossam K. Mahmoud, Ghada I. Mossallam

Publikováno v: Cellular Immunology. 364:104329

Differential expression of minor histocompatibility antigens between the recipient and donor determines their disparity and can be modified by immunoproteasomes that regulate their processing and presentation. We examined the impact of HA-1 and HA-8

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb56ffca88d7c6e560340669947ebf23
https://doi.org/10.1016/j.cellimm.2021.104329

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Nuclear factor-κB1 and MicroRNA-146a polymorphisms and risk of acute graft versus host disease post allogeneic stem cell transplantation

Autor: Raafat Abdel Fattah, Ghada I. Mossallam, Hossam K. Mahmoud

Publikováno v: Immunobiology. 225:151876

Acute graft-versus-host disease (aGVHD) is a severe inflammatory complication of haematopoeitic stem cell transplantation. The nuclear factor- Kappa Beta (NF-κB) signaling pathway regulates T cell activation. The NF-κB controls the expression of mi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aa01d91342d93c7e5c4aa9a5448d2b4
https://doi.org/10.1016/j.imbio.2019.11.011

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HLA Class I in Egyptian patients with Behçet's disease: new association with susceptibility, protection, presentation and severity of manifestations

Autor: Ghada I. Mossallam, AbdAllah Gad, Mostafa Alfishawy, Mohanad M. Elfishawi, Sally Elfishawi, Imman Mokhtar, Fatema T. Elgengehy

Publikováno v: Immunological investigations. 48(2)

Behçet's disease is an autoimmune disease with diverse clinical manifestations with vasculitis being the hallmark of the disease. The aim of this work is to study the genetic association between human leukocyte antigen (HLA) class-I molecules of Egy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da731edbce65d537fff61f6575feb84
https://pubmed.ncbi.nlm.nih.gov/30260727

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Report from the Killer-cell Immunoglobulin-like Receptors (KIR) component of the 17th International HLA and Immunogenetics Workshop

Autor: Marcelo Fernandez-Vina, Rafael González-Fernández, Jill A. Hollenbach, Betsy A. González-Quezada, Jan A. Hofmann, Sally Elfishawi, Ravi Dandekar, Jose L. Vicario, Alexander J. Mentzer, Maria J. Herrero-Mata, Carlos Vilches, Annettee Nakimuli, Francesco Colucci, Derek Middleton, G Martín, Dolores Planelles, Merhan A. Fouda, Danillo G. Augusto, Wesley M. Marin, Cynthia Vierra-Green, Sam Q. Hollenbach, Paul Norman, José Luis Caro-Oleas, Elisa Cisneros, Jorge R. Oksenberg, Peter Parham, Florentino Sánchez-García, Jürgen Sauter, F. Sánchez-Gordo, Steven G.E. Marsh, John Trowsdale, M. L. Petzl-Erler, Alexander H. Schmidt, Kirsten M. Anderson, WP Bultitude, James A. Traherne, Clara Gorodezky, Arend Große, Miguel A. Moreno‐Hidalgo, Stephen Oppenheimer, Neda Nemat-Gorgani, Maneesh K. Misra, Ghada I. Mossallam, Luciana de Brito Vargas, Ashley Moffett, Antonio Balas

Publikováno v: Human Immunology
HUMAN IMMUNOLOGY
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Human immunology, vol 79, iss 12

The goals of the KIR component of the 17th International HLA and Immunogenetics Workshop (IHIW) were to encourage and educate researchers to begin analyzing KIR at allelic resolution, and to survey the nature and extent of KIR allelic diversity acros

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b01e7e3079ff6080b046f12026b34b0f

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Impact of CYP1A1, GSTP1 and XRCC1 genes polymorphisms on toxicity and response to chemotherapy in childhood acute lymphoblastic leukemia

Autor: Ghada I. Mossallam, Asmaa Abo-bakr, Ragia H. Badawy, Hanafy Hafez, Nevin El Azhary

Publikováno v: Journal of the Egyptian National Cancer Institute, Vol 29, Iss 3, Pp 127-133 (2017)

Background Acute lymphoblastic leukemia (ALL) is the most common childhood malignancy. The interindividual genetic variations in drug metabolizing enzymes and DNA repair genes influence the efficacy and toxicity of numerous chemotherapeutic drugs aff

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f230e07cfbda80b9dbc7ee489ed7499
https://pubmed.ncbi.nlm.nih.gov/28844589

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