Works by Baradaran-Heravi, Alireza

Results: 18

Small molecule Y-320 stimulates ribosome biogenesis, protein synthesis, and aminoglycoside-induced premature termination codon readthrough.

Published in:

PLoS Biology, 2021, v. 19, n. 5, p. 1, doi. 10.1371/journal.pbio.3001221

By:

Hosseini-Farahabadi, Sara;
Baradaran-Heravi, Alireza;
Zimmerman, Carla;
Choi, Kunho;
Flibotte, Stephane;
Roberge, Michel

Publication type:

Article

Novel Mutation in the SLC19A2 Gene in an Iranian Family with Thiamine-Responsive Megaloblastic Anemia: A Series of Three Cases.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2013, v. 5, n. 3, p. 199, doi. 10.4274/Jcrpe.969

By:

Ghaemi, Nosrat;
Ghahraman, Martha;
Abbaszadegan, Mohammad Reza;
Baradaran-Heravi, Alireza;
Vakili, Rahim

Publication type:

Article

The antimalarial drug mefloquine enhances TP53 premature termination codon readthrough by aminoglycoside G418.

Published in:

PLoS ONE, 2019, v. 14, n. 5, p. 1, doi. 10.1371/journal.pone.0216423

By:

Ferguson, Michael W.;
Gerak, Chloe A. N.;
Chow, Christalle C. T.;
Rastelli, Ettore J.;
Elmore, Kyle E.;
Stahl, Florian;
Hosseini-Farahabadi, Sara;
Baradaran-Heravi, Alireza;
Coltart, Don M.;
Roberge, Michel

Publication type:

Article

Three novel CYP21A2 mutations and their protein modelling in patients with classical 21-hydroxylase deficiency from northeastern Iran.

Published in:

Clinical Endocrinology, 2007, v. 67, n. 3, p. 335, doi. 10.1111/j.1365-2265.2007.02886.x

By:

Baradaran-Heravi, Alireza;
Vakili, Rahim;
Robins, Tiina;
Carlsson, Jonas;
Ghaemi, Nosrat;
A'rabi, Azadeh;
Abbaszadegan, Mohammad Reza

Publication type:

Article

Evaluation of Novel Enhancer Compounds in Gentamicin-Mediated Readthrough of Nonsense Mutations in Rett Syndrome.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 14, p. 11665, doi. 10.3390/ijms241411665

By:

Wong, Keit Men;
Wegener, Eike;
Baradaran-Heravi, Alireza;
Huppke, Brenda;
Gärtner, Jutta;
Huppke, Peter

Publication type:

Article

Effect of small molecule eRF3 degraders on premature termination codon readthrough.

Published in:

Nucleic Acids Research, 2021, v. 49, n. 7, p. 3692, doi. 10.1093/nar/gkab194

By:

Baradaran-Heravi, Alireza;
Balgi, Aruna D;
Hosseini-Farahabadi, Sara;
Choi, Kunho;
Has, Cristina;
Roberge, Michel

Publication type:

Article

Novel small molecules potentiate premature termination codon readthrough by aminoglycosides.

Published in:

Nucleic Acids Research, 2016, v. 44, n. 14, p. 6583, doi. 10.1093/nar/gkw638

By:

Baradaran-Heravi, Alireza;
Balgi, Aruna D.;
Zimmerman, Carla;
Kunho Choi;
Shidmoossavee, Fahimeh S.;
Tan, Jason S.;
Bergeaud, Célia;
Krause, Alexandra;
Flibotte, Stéphane;
Yoko Shimizu;
Anderson, Hilary J.;
Mouly, Vincent;
Jan, Eric;
Pfeifer, Tom;
Jaquith, James B.;
Roberge, Michel

Publication type:

Article

Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression.

Published in:

Human Molecular Genetics, 2012, v. 21, n. 11, p. 2572, doi. 10.1093/hmg/dds083

By:

Baradaran-Heravi, Alireza;
Cho, Kyoung Sang;
Tolhuis, Bas;
Sanyal, Mrinmoy;
Morozova, Olena;
Morimoto, Marie;
Elizondo, Leah I.;
Bridgewater, Darren;
Lubieniecka, Joanna;
Beirnes, Kimberly;
Myung, Clara;
Leung, Danny;
Fam, Hok Khim;
Choi, Kunho;
Huang, Yan;
Dionis, Kira Y.;
Zonana, Jonathan;
Keller, Kory;
Stenzel, Peter;
Mayfield, Christy

Publication type:

Article

PIK3CA, a hotspot for postzygotic mutations in nonhereditary overgrowth syndromes.

Published in:

Clinical Genetics, 2012, v. 82, n. 6, p. 523, doi. 10.1111/cge.12001

By:

Baradaran-Heravi, Alireza

Publication type:

Article

FMRP-dependent production of large dosage-sensitive proteins is highly conserved.

Published in:

Genetics, 2022, v. 221, n. 4, p. 1, doi. 10.1093/genetics/iyac094

By:

Flanagan, Keegan;
Baradaran-Heravi, Alireza;
Qi Yin;
Dao Duc, Khanh;
Spradling, Allan C.;
Greenblatt, Ethan J.

Publication type:

Article

Phenotypic Evolution of UNC80 Loss of Function.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170, n. 12, p. 3106, doi. 10.1002/ajmg.a.37929

By:

Valkanas, Elise;
Schaffer, Katherine;
Dunham, Christopher;
Maduro, Valerie;
du Souich, Christèle;
Rupps, Rosemarie;
Adams, David R.;
Baradaran‐Heravi, Alireza;
Flynn, Elise;
Malicdan, May C.;
Gahl, William A.;
Toro, Camilo;
Boerkoel, Cornelius F.

Publication type:

Article

Bone marrow transplantation in Schimke immuno-osseous dysplasia.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 10, p. 2609, doi. 10.1002/ajmg.a.36111

By:

Baradaran‐Heravi, Alireza;
Lange, Jonas;
Asakura, Yumi;
Cochat, Pierre;
Massella, Laura;
Boerkoel, Cornelius F.

Publication type:

Article

SMARCAL1 deficiency predisposes to non-Hodgkin lymphoma and hypersensitivity to genotoxic agents in vivo.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 9, p. 2204, doi. 10.1002/ajmg.a.35532

By:

Baradaran-Heravi, Alireza;
Raams, Anja;
Lubieniecka, Joanna;
Cho, Kyoung Sang;
DeHaai, Kristi A.;
Basiratnia, Mitra;
Mari, Pierre-Olivier;
Xue, Yutong;
Rauth, Michael;
Olney, Ann Haskins;
Shago, Mary;
Choi, Kunho;
Weksberg, Rosanna A.;
Nowaczyk, Malgorzata J.M.;
Wang, Weidong;
Jaspers, Nicolaas G.J.;
Boerkoel, Cornelius F.

Publication type:

Article

Premature termination codon readthrough upregulates progranulin expression and improves lysosomal function in preclinical models of GRN deficiency.

Published in:

Molecular Neurodegeneration, 2020, v. 15, n. 1, p. 1, doi. 10.1186/s13024-020-00369-5

By:

Frew, Jonathan;
Baradaran-Heravi, Alireza;
Balgi, Aruna D.;
Wu, Xiujuan;
Yan, Tyler D.;
Arns, Steve;
Shidmoossavee, Fahimeh S.;
Tan, Jason;
Jaquith, James B.;
Jansen-West, Karen R.;
Lynn, Francis C.;
Gao, Fen-Biao;
Petrucelli, Leonard;
Feldman, Howard H.;
Mackenzie, Ian R.;
Roberge, Michel;
Nygaard, Haakon B.

Publication type:

Article

Schimke immunoosseous dysplasia associated with undifferentiated carcinoma and a novel SMARCAL1 mutation in a child.

Published in:

Pediatric Blood & Cancer, 2013, v. 60, n. 9, p. E88, doi. 10.1002/pbc.24542

By:

Carroll, Clinton;
Badu‐Nkansah, Akosua;
Hunley, Tracy;
Baradaran‐Heravi, Alireza;
Cortez, David;
Frangoul, Haydar

Publication type:

Article

Improved outcome with immunosuppressive monotherapy after renal transplantation in Schimke-immuno-osseous dysplasia.

Published in:

Pediatric Transplantation, 2009, v. 13, n. 4, p. 482, doi. 10.1111/j.1399-3046.2008.01013.x

By:

Lücke, Thomas;
Kanzelmeyer, Nele;
Baradaran-Heravi, Alireza;
Boerkoel, Cornelius F.;
Burg, Michael;
Ehrich, Jochen H. H.;
Pape, Lars

Publication type:

Article

Two novel mutations in CYP11B1 and modeling the consequent alterations of the translated protein in classic congenital adrenal hyperplasia patients.

Published in:

Endocrine (1355008X), 2013, v. 44, n. 1, p. 212, doi. 10.1007/s12020-012-9861-2

By:

Abbaszadegan, Mohammad;
Hassani, Soolmaz;
Vakili, Rahim;
Saberi, Mohammad;
Baradaran-Heravi, Alireza;
A'rabi, Azadeh;
Hashemipour, Mahin;
Razzaghi-Azar, Maryam;
Moaven, Omeed;
Baratian, Ali;
Ahadian, Mitra;
Keify, Fatemeh;
Meurice, Nathalie

Publication type:

Article

Erratum to: Two novel mutations in CYP11B1 and modeling the consequent alterations of the translated protein in classic congenital adrenal hyperplasia patients.

Published in:

2013

By:

Abbaszadegan, Mohammad;
Hassani, Soolmaz;
Vakili, Rahim;
Saberi, Mohammad;
Baradaran-Heravi, Alireza;
A'rabi, Azadeh;
Hashemipour, Mahin;
Razzaghi-Azar, Maryam;
Moaven, Omeed;
Baratian, Ali;
Ahadian, Mitra;
Keify, Fatemeh;
Meurice, Nathalie

Publication type:

Correction Notice