Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Arezou Karamzade"'
Autor:
Narges Bazgir, Azin Tahvildari, Zahra Chavoshzade, Mahnaz Jamee, Zahra Golchehre, Abdollah Karimi, Naghi Dara, Mazdak Fallahi, Mohammad Keramatipour, Arezou Karamzade, Samin Sharafian
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 19, Iss 1, Pp 1-9 (2023)
Abstract Background Caspase-8 is a molecule in the FAS pathway that initiates apoptosis. One of the rarest autoimmune lymphoproliferative syndromes is caspase-8 deficiency. Immunodeficiency, splenomegaly, and lymphadenopathy are the common symptoms o
Externí odkaz:
https://doaj.org/article/b99cfc8fa7444e2abde07c24701f0048
Autor:
Fatemeh Sadat Mahdavi, Mohammad Keramatipour, Sarina Ansari, Samin Sharafian, Arezou Karamzade, Marzieh Tavakol
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 17, Iss 1, Pp 1-9 (2021)
Abstract Background Severe combined immunodeficiency (SCID) is a group of relatively rare primary immunodeficiency disorders (PIDs), characterized by disturbed development of T cells and B cells, caused by several genetic mutations that bring on diff
Externí odkaz:
https://doaj.org/article/16cdeca6770848a0a5a372ec43565760
Autor:
Sarina Ansari, Fatemeh Sadat Mahdavi, Samin Sharafian, Marzieh Tavakol, Arezou Karamzade, Mohammad Keramatipour
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 17, Iss 1, Pp 1-9 (2021)
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
Background Severe combined immunodeficiency (SCID) is a group of relatively rare primary immunodeficiency disorders (PIDs), characterized by disturbed development of T cells and B cells, caused by several genetic mutations that bring on different cli
Autor:
Neda Golchin, Yeganeh Eshaghkhani, Arezou Karamzade, Mohammad Keramatipour, Aysun Khalil Nejad Sani Banaei, Mohammad Reza Saberi, Zahra Golchehre, Meisam Babaei
Publikováno v:
Molecular Biology Reports. 48:5339-5345
Joubert syndrome (JS) is a rare inherited neurodevelopmental condition characterized by hypotonia, ataxia, developmental delay, abnormal eye movements, neonatal respiratory disturbance and unique midbrain-hindbrain malformation, known as the molar to
Publikováno v:
J Pediatr Genet
Introduction Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare disorder caused by perturbation in renal reabsorption of magnesium and calcium. Biallelic pathogenic variants either in gene CLDN16 or CLDN19 are responsi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a641879f8040b0401a84f5e56d7061c0
https://europepmc.org/articles/PMC8416216/
https://europepmc.org/articles/PMC8416216/
Autor:
Mostafa Asadollahi, Yeganeh Eshaghkhani, Arezou Karamzade, Mahdieh Taghizadeh, Parisa Nourmohammadi, Mohammad Keramatipour, Mohammad Reza Saberi, Zahra Golchehre, Arezoo Mohamadifar, Ahmad Amin
Publikováno v:
Rep Biochem Mol Biol
Background Dilated cardiomyopathy (DCM) is a progressive heart condition characterized by left ventricular chamber enlargement associated with systolic heart failure and prolonged action potential duration. Genetic variations in genes that encode cyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dd43ecb6d88fcc30fe3041e225df652
https://europepmc.org/articles/PMC8480302/
https://europepmc.org/articles/PMC8480302/
Autor:
Susan, Akbaroghli, Daniz, Kooshavar, Zahra, Golchehre, Arezou, Karamzade, Mohammad, Saberi, Mohammad Reza, Alaei, Masoud, Abbasi Sadegh, Mostafa, Asadollahi, Mohammad, Keramatipour
Publikováno v:
Iranian journal of child neurology. 16(1)
Bardet-Biedl syndrome (BBS) is an autosomal recessive pleiotropic ciliopathy, which includes multi-organ clinical manifestations. The known genes involved in the development of the disease account for the causality in about 80% of the examined cases.
Autor:
Sylvia E. C. van Beersum, Stephan C.F. Neuhauss, Jeroen van Reeuwijk, Fowzan S. Alkuraya, Mostafa Asadollahi, Julie C. Van De Weghe, Marius Ueffing, Manali Chitre, Dan Doherty, Arezou Karamzade, Caitlin V. Miller, Stef J.F. Letteboer, Tamara D.S. Rusterholz, Michael J. Bamshad, Megan E. Grout, Ruxandra Bachmann-Gagescu, Matthias Gesemann, Heba Morsy, Karsten Boldt, Ronald Roepman, John A. Sayer, Miguel Barroso-Gil, Jennifer C. Dempsey, Ranad Shaheen, Arianna Gomez, Brooke L. Latour, Mohammad Keramatipour, Deborah A. Nickerson
Publikováno v:
Journal of Clinical Investigation, 130, 8, pp. 4423-4439
J Clin Invest
Journal of Clinical Investigation, 130, 4423-4439
J Clin Invest
Journal of Clinical Investigation, 130, 4423-4439
Contains fulltext : 225431.pdf (Publisher’s version ) (Closed access) Joubert syndrome (JBTS) is a recessive neurodevelopmental ciliopathy characterized by a pathognomonic hindbrain malformation. All known JBTS genes encode proteins involved in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa7189d0e48e47effe94af8b9a01c7cf
Autor:
Hamzeh Salmani, Arezou Karamzade, Mohammad Keramatipour, Zahra Golchehre, Seyed Ziaeddin Tabatabaie, Mohammad Reza Saberi
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 113:229-233
Objectives Waardenburg Syndrome (WS) as a congenital auditory-pigmentary syndrome is a clinically and genetically heterogeneous disorder. Based upon clinical manifestations, it can be classified into four types. Loss of function mutations in PAX3 gen
Autor:
Zahra Mohammadi, Arezou Karamzadeh, Mohammad Amin Tabatabaiefar, Hossein Khanahmad, Laleh Shariati
Publikováno v:
Research in Pharmaceutical Sciences, Vol 14, Iss 4, Pp 351-358 (2019)
Green fluorescent protein (GFP) has played an important role in biochemistry and cell biology as a reporter gene. It has been used to assess the potency of promoters for recombinant protein production. This investigation reveals evidences suggesting
Externí odkaz:
https://doaj.org/article/6ffe8e234dab4ae79e16cc72307170e8