Measurement of EPF for detection of cow pregnancy using rosette inhibition test von Ghaffari Laleh, V., Ghaffari Laleh, R., Pirany, N., Moghadaszadeh Ahrabi, M.

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NPM1 and FLT3-(ITD) Gene mutations and laboratory findings in patients with acute myeloid leukemia in Northwest of Iran von Sanaat Z, Shams K, Nejati B, Movasghpour AK, Imani V, Moghadaszadeh M

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Effect of food allergen exculsion on symptoms and quality of life in irritable bowel syndrome von Moghadaszadeh M, Fatahi E, Bonyadi M, Shirzadeh M

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Effect of Nasal Floor Closure on the Size of Alveolar Cleft in Complete Unilateral or Bilateral Primary Cleft Palate von M Moghadaszadeh, E Massah, B Mirzakochaki, SH Abdolahi Fakhim

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Directed evolution of a family of AAV capsid variants enabling potent muscle-directed gene delivery across species von Tabebordbar, Mohammadsharif, Lagerborg, Kim A., Stanton, Alexandra, King, Emily M., Ye, Simon, Tellez, Liana, Krunnfusz, Allison, Tavakoli, Sahar, Widrick, Jeffrey J., Messemer, Kathleen A., Troiano, Emily C., Moghadaszadeh, Behzad, Peacker, Bryan L., Leacock, Krystynne A., Horwitz, Naftali, Beggs, Alan H., Wagers, Amy J., Sabeti, Pardis C.

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Sarcomeres regulate murine cardiomyocyte maturation through MRTF-SRF signaling von Guo, Yuxuan, Cao, Yangpo, Jardin, Blake D., Sethi, Isha, Ma, Qing, Moghadaszadeh, Behzad, Troiano, Emily C., Mazumdar, Neil, Trembley, Michael A., Small, Eric M., Yuan, Guo-Cheng, Beggs, Alan H., Pu, William T.

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The prediction method of tool life on small lot turning process – Development of Digital Twin for production von Bazaz, Sara Moghadaszadeh, Lohtander, Mika, Varis, Juha

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Anemia prevalence in women of reproductive age in low- and middle-income countries between 2000 and 2018 von Kinyoki, Damaris, Osgood-Zimmerman, Aaron E., Bhattacharjee, Natalia V., Kassebaum, Nicholas J., Hay, Simon I.

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Availability of Manufacturing data resources in Digital Twin von Bazaz, Sara Moghadaszadeh, Lohtander, Mika, Varis, Juha

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Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Ea... von Ferreiro, Ana, Quijano-Roy, Susana, Pichereau, Claire, Moghadaszadeh, Behzad, Goemans, Nathalie, Bönnemann, Carsten, Jungbluth, Heinz, Straub, Volker, Villanova, Marcello, Leroy, Jean-Paul, Romero, Norma B., Martin, Jean-Jacques, Muntoni, Francesco, Voit, Thomas, Estournet, Brigitte, Richard, Pascale, Fardeau, Michel, Guicheney, Pascale

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Scolicidal and Apoptotic Activities of 5-hydroxy-1, 4-naphthoquinone as a Potent Agent against Echinococcus granulosus Protoscoleces von Moghadaszadeh, Masoud, Khayyati, Mehdi, Spotin, Adel, Norouzi, Roghayeh, Pagheh, Abdol Sattar, Oliveira, Sonia M. R., Pereira, Maria de Lourdes, Ahmadpour, Ehsan

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Selenoprotein N: an endoplasmic reticulum glycoprotein with an early developmental expression pattern von Petit, Nathalie, Lescure, Alain, Rederstorff, Mathieu, Krol, Alain, Moghadaszadeh, Behzad, Wewer, Ulla M., Guicheney, Pascale

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Selenoproteins and Their Impact on Human Health Through Diverse Physiological Pathways von Moghadaszadeh, Behzad, Beggs, Alan H

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Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome von Merlini, Luciano, Moghadaszadeh, Behzad, Chaigne, Denys, Brockington, Martin, Topaloglu, Haluk, Estournet, Brigitte, Jaillard, Céline, Romero, Norma, Desguerre, Isabelle, Muntoni, Francesco, Roy, Susana Quijano, Guicheney, Pascale, Petit, Nathalie

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Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy von Demir, Ercan, Sabatelli, Patrizia, Allamand, Valérie, Ferreiro, Ana, Moghadaszadeh, Behzad, Makrelouf, Mohamed, Topaloglu, Haluk, Echenne, Bernard, Merlini, Luciano, Guicheney, Pascale

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SMEs’ Support Functionality Analysis Based on Statistical Analysis von Bazaz, Sara Moghadaszadeh, Penttilä, Sakari, Ratava, Juho, Ollikainen, Mikael, Varis, Juha

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ADAM12 induces actin cytoskeleton and extracellular matrix reorganization during early adipocyte differentiation by regulating β1 integrin function von Kawaguchi, Nobuko, Sundberg, Christina, Kveiborg, Marie, Moghadaszadeh, Behzad, Asmar, Meena, Dietrich, Nikolaj, Thodeti, Charles K., Nielsen, Finn C., Möller, Peter, Mercurio, Arthur M., Albrechtsen, Reidar, Wewer, Ulla M.

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Mapping inequalities in exclusive breastfeeding in low- and middle-income countries, 2000–2018 von Bhattacharjee, Natalia V., Schaeffer, Lauren E., Hay, Simon I.

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Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1) von Mercuri, Eugenio, Talim, Beril, Moghadaszadeh, Behzad, Petit, Nathalie, Brockington, Martin, Counsell, Serena, Guicheney, Pascale, Muntoni, Francesco, Merlini, Luciano

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Realizing Waste-Reducing Potential in Small-Lot Production with Digital Twins von Bazaz, Sara Moghadaszadeh, Ratava, Juho, Lohtander, Mika, Reslan, Maya, Alqseer, Naser, Varis, Juha

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