Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Elham Jaberi"'
Publikováno v:
Healthcare, Vol 12, Iss 2, p 208 (2024)
Background: Unlicensed and off-label (UL/OL) prescriptions have been associated with an increased risk of drug-related problems. Data of their prevalence at hospital discharge remain insufficient. We aimed to describe the prevalence of UL/OL drugs in
Externí odkaz:
https://doaj.org/article/0417af7b50124bdcb84e5ea47c3dfd91
Autor:
Elham Jaberi, Emilie Tresse, Kirsten Grønbæk, Joachim Weischenfeldt, Shohreh Issazadeh-Navikas
Publikováno v:
EBioMedicine, Vol 57, Iss , Pp 102868- (2020)
Background: Point mutations and structural variations (SVs) in mitochondrial DNA (mtDNA) contribute to many neurodegenerative diseases. Technical limitations and heteroplasmy, however, have impeded their identification, preventing these changes from
Externí odkaz:
https://doaj.org/article/bd07e6c2fdc94842820b8d8aa555511f
Autor:
Zargham Sepehrizadeh, Mohammad Mohammadi, Amirhossein Emami, Mojtaba Tabatabaei Yazdi, Saeed Hashemi Bozchlou, Mohammad Reza Khorramizadeh, Mina Bahrololoumi Shapourabadi, Elham Jaberi, Naghmeh Rajaei, Neda Setayesh
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 2, Pp 149-154 (2014)
OBJECTIVE: One of the major goals of cancer treatment is the monitoring of chemotherapeutic protocols. Quantitative and comparative cytokine expression profiling could be reliable to be used for biomarkers in deadly and fast-growing cancers such as a
Externí odkaz:
https://doaj.org/article/8d541630b69a454cb7e99b9cd5ff279a
Publikováno v:
Biological Research, Vol 42, Iss 2, Pp 137-146 (2009)
The present work aims to study a new NADH-cytochrome b5 reductase (cb5r) from Mucor racemosus PTCC 5305. A cDNA coding for cb s r was isolated from a Mucor racemosus PTCC 5305 cDNA library. The nucleotide sequence of the cDNA including coding and seq
Externí odkaz:
https://doaj.org/article/474521bfd0d64ec1b53fee8bde96fa03
Publikováno v:
Therapies.
Drug-related problems (DRPs) are one of the leading causes of hospital readmissions. Children with chronic diseases are more likely to experience DRPs than adults. The burden and characteristics of drug-related readmissions at and after hospital disc
Autor:
Nídia Fernandez Ros, Elham Jaberi, Brice Ozenne, Kristian Linnet, Shohreh Issazadeh-Navikas, Hanne D. Hansen, Lene Lundgaard Donovan, Sys Stybe Johansen, Gitte M. Knudsen, Jens Vilstrup Johansen
Publikováno v:
European Neuropsychopharmacology. 42:1-11
Psilocybin has in some studies shown promise as treatment of major depressive disorder and psilocybin therapy was in 2019 twice designated as breakthrough therapy by the U.S. Food and Drug Administration (FDA). A very particular feature is that inges
Autor:
Elham Jaberi, Lluís Riera-Ponsati, Wei Qi Guinevere Sew, Shohreh Issazadeh-Navikas, Karsten Ruscher, Emilie Tresse
Publikováno v:
EMBO J
Mitochondrial homeostasis is essential for providing cellular energy, particularly in resource‐demanding neurons, defects in which cause neurodegeneration, but the function of interferons (IFNs) in regulating neuronal mitochondrial homeostasis is u
Autor:
Nathalie Paret, Yanis Mimouni, Behrouz Kassai, Elham Jaberi, Nadine Bossard, Inesse Boussaha, Laurent Roche, Corinne Alberti, K.A. Nguyen, Laurent Remontet, Laure Guittard, Evelyne Jacqz-Aigrain, Thierry Vial
Publikováno v:
Therapie. 76(6)
Summary Introduction To date, few studies have shown a significant association between off-label drug use and adverse drug reactions (ADRs). The main aims of this study is to evaluate the relationship between adverse drug reactions and unlicensed or
Autor:
Emilie Tresse, Joachim Weischenfeldt, Kirsten Grønbæk, Shohreh Issazadeh-Navikas, Elham Jaberi
Publikováno v:
Jaberi, E, Tresse, E, Grønbæk, K, Weischenfeldt, J & Issazadeh-Navikas, S 2020, ' Identification of unique and shared mitochondrial DNA mutations in neurodegeneration and cancer by single-cell mitochondrial DNA structural variation sequencing (MitoSV-seq) ', EBioMedicine, vol. 57, 102868, pp. 1-17 . https://doi.org/10.1016/j.ebiom.2020.102868
EBioMedicine, Vol 57, Iss, Pp 102868-(2020)
EBioMedicine
EBioMedicine, Vol 57, Iss, Pp 102868-(2020)
EBioMedicine
Background: Point mutations and structural variations (SVs) in mitochondrial DNA (mtDNA) contribute to many neurodegenerative diseases. Technical limitations and heteroplasmy, however, have impeded their identification, preventing these changes from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dcdfb3950b32ff6118ffa396c794707
https://curis.ku.dk/ws/files/246674452/1_s2.0_S2352396420302437_main.pdf
https://curis.ku.dk/ws/files/246674452/1_s2.0_S2352396420302437_main.pdf
Autor:
Elham Jaberi, Casey Turk, Frank J. Steemers, Abolfazl Moghadam, Jian-Bing Fan, Masoud Soleimani, Gholam Ali Shahidi, Farid Keramatian, Elahe Elahi, Ehsan Arefian, Brandy Klotzle, Shahriar Nafissi, Mohsen Karimi Arzenani, Mohammad Rohani
Publikováno v:
Movement Disorders. 31:1004-1011
Background We aimed to identify the genetic cause of neurological disease in an Iranian family whose manifestations include symptoms of parkinsonism and cognitive dysfunction. Methods Clinical data on the patients were gathered by interviews with par