Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Mehdi Yeganeh"'
Autor:
Mehdi Yeganeh, Christiane Auray‐Blais, Bruno Maranda, Amanda Sabovic, Robert J. DeVita, Michael B. Lazarus, Sander M. Houten
Publikováno v:
JIMD Reports, Vol 64, Iss 6, Pp 440-445 (2023)
Abstract Hyperlysinemia is a rare autosomal recessive deficiency of 2‐aminoadipic semialdehyde synthase (AASS) affecting the initial step in lysine degradation. It is thought to be a benign biochemical abnormality, but reports on cases remain scarc
Externí odkaz:
https://doaj.org/article/103b38baeae4401682c5bdb0acf2a50e
Autor:
Rajani Kandhi, Mehdi Yeganeh, Akihiko Yoshimura, Alfredo Menendez, Sheela Ramanathan, Subburaj Ilangumaran
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionHepatic stellate cells (HSC) become activated, differentiate to myofibroblasts and produce extracellular fibrillar matrix during liver fibrosis. The hepatic fibrogenic response is orchestrated by reciprocal interactions between HSCs and m
Externí odkaz:
https://doaj.org/article/82662f90734940d6bf41d4964b94a60f
Autor:
Mehdi Yeganeh, Kaitlin March, Catherine Jones, Gloria Ho, Kathryn A. Selby, Jean-Pierre Chanoine, Sylvia Stockler, Ramona Salvarinova, Gabriella Horvath, Catherine Brunel-Guitton
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 35, Iss , Pp 100961- (2023)
Introduction: LPIN1 deficiency is an autosomal recessive form of early childhood recurrent severe rhabdomyolysis. Although not completely lucid yet, LPIN1 has been shown to modulate endosomal-related pro-inflammatory responses via peroxisome prolifer
Externí odkaz:
https://doaj.org/article/4bbe55608bd74b03b3b3a13e4421fb26
Autor:
Parviz Tabatabaie, Asghar Aghamohammadi, Setareh Mamishi, Anna Isaeian, Golnaz Heidari, Sina Abdollahzade, Pirouz Pirouzi, Nima Rezaei, Hassan Heidarnazhad, Bahram MirSaeid Ghazi, Mehdi Yeganeh, Taher Cheraghi, Hasan Abolhasani, Shiva Saghafi, Houman Alizadeh, Mohammad Reza Anaraki
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 7, Iss 2 (2008)
Bronchiectasis is a chronic debilitating condition characterized by abnormal dilated thick-walled bronchi. To investigate humoral immune function in bronchiectatic patients, this study was performed. Forty patients with established diagnosis of bronc
Externí odkaz:
https://doaj.org/article/05f15c3b403e496885eb4b239e5fcd51
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 4, Iss 4 (2005)
Autoimmune lymphoproliferative syndrome (ALPS) is a prototypic disorder of abnormal lymphocyte homeostasis. In the September 2005 issue of The Iranian Journal of Allergy, Asthma and Immunology, a patient with clinical features consistent with ALPS wa
Externí odkaz:
https://doaj.org/article/7589857c4889465c9645d549e477a3aa
Autor:
Duncan Lejtenyi, Reza Alizadehfar, David S. Rosenblatt, Bruce Mazer, Lina Sobhi Abdrabo, Sophie Ran Wang, Joël Lafond-Lapalme, Mehdi Yeganeh, Christine McCusker, Jean-Baptiste Rivière, Tallal Basha
Publikováno v:
LymphoSign Journal. 7:25-36
Background: Patients with chromosome 18 abnormalities can present with an immune phenotype that resembles common variable immunodeficiency. Knowledge of the genes underlying the immune defects related to chromosome 18 aberrations could improve our un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c84672cb32d80265ff14a590c52e161
https://doi.org/10.14785/lymphosign-2019-0013
https://doi.org/10.14785/lymphosign-2019-0013
Autor:
Md Gulam Musawwir Khan, Nadia Boufaied, Mehdi Yeganeh, Rajani Kandhi, Stephanie Petkiewicz, Ankur Sharma, Akihiko Yoshimura, Gerardo Ferbeyre, David P. Labbé, Sheela Ramanathan, Subburaj Ilangumaran
Publikováno v:
Cancers
Volume 15
Issue 3
Pages: 905
Volume 15
Issue 3
Pages: 905
SOCS1 deficiency, which increases susceptibility to hepatocellular carcinoma (HCC), promotes CDKN1A expression in the liver. High CDKN1A expression correlates with disease severity in many cancers. Here, we demonstrate a crucial pathogenic role of CD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de867edafa320975817dd4a451428cf1
https://doi.org/10.3390/cancers15030905
https://doi.org/10.3390/cancers15030905
Autor:
Gulam Musawwir Khan, Nadia Boufaied, Mehdi Yeganeh, David P. Labbé, Stephanie Petkiewicz, Ankur Sharma, Amit Ghosh, Rezvan Bagheri, Subburaj Ilangumaran, Rajani Kandhi, Sheela Ramanathan, Akihiko Yoshimura, Gerardo Ferbeyre
SOCS1 and SOCS3 genes, frequently repressed in hepatocellular carcinoma (HCC), function as tumor suppressors in hepatocytes. However, TCGA transcriptomic data revealed that SOCS1-low/SOCS3-high specimens displayed more aggressive HCC than SOCS1-low/S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8f7f43d63c9db3b15f5f892623f97c6
https://doi.org/10.1101/2021.10.21.465149
https://doi.org/10.1101/2021.10.21.465149
Publikováno v:
Seizure. 74:31-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a50cce1c8009bce9bcc0eb1c5f98c28b
https://doi.org/10.1016/j.seizure.2019.11.008
https://doi.org/10.1016/j.seizure.2019.11.008
Autor:
Daniela Buhas, Garey Noritz, Marvin R. Natowicz, Mehdi Yeganeh, Heng Wang, John Barnard, Joseph R Abraham
Publikováno v:
Biochemical and biophysical research communications. 512(2)
HERC2 is a giant protein with E3 ubiquitin ligase activity and other known and suspected functions. Mutations of HERC2 are implicated in the pathogenesis of various cancers and result in severe neurological conditions in Herc2-mutant mice. Recently,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb4b28c91ef84f90ad27c96708d0f9a4
https://pubmed.ncbi.nlm.nih.gov/30902390
https://pubmed.ncbi.nlm.nih.gov/30902390