AKPULAT, U. (2023) "Morphological examination is more effective than cell viability assays in the characterization of myotube atrophy", Annals of Medical Research, 30 (11) pp. 1421-1424 [TR Dizin] DOI " data-bs-content-id="YazarBilgi-1159">
AKPULAT, U. (2023) "Morphological examination is more effective than cell viability assays in the characterization of myotube atrophy", Annals of Medical Research, 30 (11) pp. 1421-1424 [TR Dizin] DOI AKPULAT, U. (2023) "Morphological examination is more effective than cell viability assays in the characterization of myotube atrophy", Annals of Medical Research, 30 (11) pp. 1421-1424 [TR Dizin] DOI
GÜLTEN, S., AKPULAT, U., Özcan, S., Özcan, E., Durak, Ö., SOYLU, V.G., Gülhan, M.M., Çalışır, B., Kılınç, Ç., Çöplü, N. (2021) "Biochemical parameters and relation to disease severity in COVID-19 patients", Kastamonu Medical Journal, (0) DOI " data-bs-content-id="YazarBilgi-1160">
GÜLTEN, S., AKPULAT, U., Özcan, S., Özcan, E., Durak, Ö., SOYLU, V.G., Gülhan, M.M., Çalışır, B., Kılınç, Ç., Çöplü, N. (2021) "Biochemical parameters and relation to disease severity in COVID-19 patients", Kastamonu Medical Journal, (0) DOI GÜLTEN, S., AKPULAT, U., Özcan, S., Özcan, E., Durak, Ö., SOYLU, V.G., Gülhan, M.M., Çalışır, B., Kılınç, Ç., Çöplü, N. (2021) "Biochemical parameters and relation to disease severity in COVID-19 patients", Kastamonu Medical Journal, (0) DOI
Sinan, K.I., AKPULAT, U., Aldahish, A.A., ÇELİK-ALTUNOĞLU, Y., BALOĞLU, M.C., Dimitrova, D.Z., Gevrenova, R., Lobine, D., Mahomoodally, M.F., Etienne, O.K., Zengin, G., Mahmud, S., Capasso, R. (2021) "LC-MS/HRMS Analysis, Anti-Cancer, Anti-Enzymatic and Anti-Oxidant Effects of Boerhavia diffusa Extracts: A Potential Raw Material for Functional Applications", ANTIOXIDANTS, 10 (12) [SCI Expanded] DOI " data-bs-content-id="YazarBilgi-1161">
Sinan, K.I., AKPULAT, U., Aldahish, A.A., ÇELİK-ALTUNOĞLU, Y., BALOĞLU, M.C., Dimitrova, D.Z., Gevrenova, R., Lobine, D., Mahomoodally, M.F., Etienne, O.K., Zengin, G., Mahmud, S., Capasso, R. (2021) "LC-MS/HRMS Analysis, Anti-Cancer, Anti-Enzymatic and Anti-Oxidant Effects of Boerhavia diffusa Extracts: A Potential Raw Material for Functional Applications", ANTIOXIDANTS, 10 (12) [SCI Expanded] DOI Sinan, K.I., AKPULAT, U., Aldahish, A.A., ÇELİK-ALTUNOĞLU, Y., BALOĞLU, M.C., Dimitrova, D.Z., Gevrenova, R., Lobine, D., Mahomoodally, M.F., Etienne, O.K., Zengin, G., Mahmud, S., Capasso, R. (2021) "LC-MS/HRMS Analysis, Anti-Cancer, Anti-Enzymatic and Anti-Oxidant Effects of Boerhavia diffusa Extracts: A Potential Raw Material for Functional Applications", ANTIOXIDANTS, 10 (12) [SCI Expanded] DOI
Daimagüler, H.S., AKPULAT, U., Özdemir, Ö., Yiş, U., Güngör, S., Talim, B., Ünlü, A.G.D., Baydan, F., Thiele, H., Altmüller, J., Nürnberg, P., Cirak, S. (2021) "Clinical and genetic characterization of PYROXD1-related myopathy patients from Turkey", AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 185 (6) pp. 1678-1690 [SCI Expanded] DOI " data-bs-content-id="YazarBilgi-1162">
Daimagüler, H.S., AKPULAT, U., Özdemir, Ö., Yiş, U., Güngör, S., Talim, B., Ünlü, A.G.D., Baydan, F., Thiele, H., Altmüller, J., Nürnberg, P., Cirak, S. (2021) "Clinical and genetic characterization of PYROXD1-related myopathy patients from Turkey", AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 185 (6) pp. 1678-1690 [SCI Expanded] DOI Daimagüler, H.S., AKPULAT, U., Özdemir, Ö., Yiş, U., Güngör, S., Talim, B., Ünlü, A.G.D., Baydan, F., Thiele, H., Altmüller, J., Nürnberg, P., Cirak, S. (2021) "Clinical and genetic characterization of PYROXD1-related myopathy patients from Turkey", AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 185 (6) pp. 1678-1690 [SCI Expanded] DOI
AKPULAT, U., Wang, H., Becker, K., Contreras, A., Partridge, T., Novak, J., Cirak, S. (2018) "Shorter Phosphorodiamidate Morpholino Splice-Switching Oligonucleotides May Increase Exon-Skipping Efficacy in DMD", Molecular Therapy-Nucleic Acids, 13 (1) pp. 534-542 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-1163">
AKPULAT, U., Wang, H., Becker, K., Contreras, A., Partridge, T., Novak, J., Cirak, S. (2018) "Shorter Phosphorodiamidate Morpholino Splice-Switching Oligonucleotides May Increase Exon-Skipping Efficacy in DMD", Molecular Therapy-Nucleic Acids, 13 (1) pp. 534-542 [SCI Expanded] Link DOI AKPULAT, U., Wang, H., Becker, K., Contreras, A., Partridge, T., Novak, J., Cirak, S. (2018) "Shorter Phosphorodiamidate Morpholino Splice-Switching Oligonucleotides May Increase Exon-Skipping Efficacy in DMD", Molecular Therapy-Nucleic Acids, 13 (1) pp. 534-542 [SCI Expanded] Link DOI
Ghosh, S.G., Becker, K., Huang, H., Dixon-Salazar, T., Chai, G., Salpietro, V., Al-Gazali, L., Waisfisz, Q., Wang, H., Vaux, K.K., Stanley, V., Manole, A., AKPULAT, U., Weiss, M.M., Efthymiou, S., Hanna, M.G., Minetti, C., Striano, P., Pisciotta, L., De, G.E., Altmüller, J., Nürnberg, P., Thiele, H., Yiş, U., Okur, T.D., Polat, A.I., Amiri, N., Doosti, M., Karimani, E.G., Toosi, M.B., Haddad, G., Karakaya, M., Wirth, B., Van, H.J., Wolf, N.I., Maroofian, R., Houlden, H., Cirak, S., Gleeson, J.G. (2018) "Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome", AMERICAN JOURNAL OF HUMAN GENETICS, 103 (3) pp. 431-439 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-1164">
Ghosh, S.G., Becker, K., Huang, H., Dixon-Salazar, T., Chai, G., Salpietro, V., Al-Gazali, L., Waisfisz, Q., Wang, H., Vaux, K.K., Stanley, V., Manole, A., AKPULAT, U., Weiss, M.M., Efthymiou, S., Hanna, M.G., Minetti, C., Striano, P., Pisciotta, L., De, G.E., Altmüller, J., Nürnberg, P., Thiele, H., Yiş, U., Okur, T.D., Polat, A.I., Amiri, N., Doosti, M., Karimani, E.G., Toosi, M.B., Haddad, G., Karakaya, M., Wirth, B., Van, H.J., Wolf, N.I., Maroofian, R., Houlden, H., Cirak, S., Gleeson, J.G. (2018) "Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome", AMERICAN JOURNAL OF HUMAN GENETICS, 103 (3) pp. 431-439 [SCI Expanded] Link DOI Ghosh, S.G., Becker, K., Huang, H., Dixon-Salazar, T., Chai, G., Salpietro, V., Al-Gazali, L., Waisfisz, Q., Wang, H., Vaux, K.K., Stanley, V., Manole, A., AKPULAT, U., Weiss, M.M., Efthymiou, S., Hanna, M.G., Minetti, C., Striano, P., Pisciotta, L., De, G.E., Altmüller, J., Nürnberg, P., Thiele, H., Yiş, U., Okur, T.D., Polat, A.I., Amiri, N., Doosti, M., Karimani, E.G., Toosi, M.B., Haddad, G., Karakaya, M., Wirth, B., Van, H.J., Wolf, N.I., Maroofian, R., Houlden, H., Cirak, S., Gleeson, J.G. (2018) "Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome", AMERICAN JOURNAL OF HUMAN GENETICS, 103 (3) pp. 431-439 [SCI Expanded] Link DOI
Wang, H., Salter, C.G., Refai, O., Hardy, H., Barwick, K.E.S., AKPULAT, U., Kvarnung, M., Chioza, B.A., Harlalka, G., Taylan, F., Sejersen, T., Wright, J., Zimmerman, H.H., Karakaya, M., Stueve, B., Weis, J., Schara, U., Russell, M.A., Abdul-Rahman, O.A., Chilton, J., Blakely, R.D., Baple, E.L., Cirak, S., Crosby, A.H. (2017) "Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization", BRAIN, 140 (11) pp. 2838-2850 [SCI] DOI " data-bs-content-id="YazarBilgi-1166">
Wang, H., Salter, C.G., Refai, O., Hardy, H., Barwick, K.E.S., AKPULAT, U., Kvarnung, M., Chioza, B.A., Harlalka, G., Taylan, F., Sejersen, T., Wright, J., Zimmerman, H.H., Karakaya, M., Stueve, B., Weis, J., Schara, U., Russell, M.A., Abdul-Rahman, O.A., Chilton, J., Blakely, R.D., Baple, E.L., Cirak, S., Crosby, A.H. (2017) "Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization", BRAIN, 140 (11) pp. 2838-2850 [SCI] DOI Wang, H., Salter, C.G., Refai, O., Hardy, H., Barwick, K.E.S., AKPULAT, U., Kvarnung, M., Chioza, B.A., Harlalka, G., Taylan, F., Sejersen, T., Wright, J., Zimmerman, H.H., Karakaya, M., Stueve, B., Weis, J., Schara, U., Russell, M.A., Abdul-Rahman, O.A., Chilton, J., Blakely, R.D., Baple, E.L., Cirak, S., Crosby, A.H. (2017) "Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization", BRAIN, 140 (11) pp. 2838-2850 [SCI] DOI
AKPULAT, U., Onbaşılar, İ., Kocaefe, Y.Ç. (2016) "Tenotomy immobilization as a model to investigate skeletal muscle fibrosis with emphasis on Secreted frizzled related protein 2", Physiological Genomics, 48 (6) pp. 397-408 [SCI] Link DOI " data-bs-content-id="YazarBilgi-1167">
AKPULAT, U., Onbaşılar, İ., Kocaefe, Y.Ç. (2016) "Tenotomy immobilization as a model to investigate skeletal muscle fibrosis with emphasis on Secreted frizzled related protein 2", Physiological Genomics, 48 (6) pp. 397-408 [SCI] Link DOI AKPULAT, U., Onbaşılar, İ., Kocaefe, Y.Ç. (2016) "Tenotomy immobilization as a model to investigate skeletal muscle fibrosis with emphasis on Secreted frizzled related protein 2", Physiological Genomics, 48 (6) pp. 397-408 [SCI] Link DOI
AKPULAT, U., Yıldız, Y., Özdemir, C., Akçay, D., Kocaefe, Y.Ç. (2016) "A role for Klf5 in myoblasts as a differentiation switch fromproliferation to fusion", Journal of Muscle Research and Cell Motility, (0) [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-1168">
AKPULAT, U., Yıldız, Y., Özdemir, C., Akçay, D., Kocaefe, Y.Ç. (2016) "A role for Klf5 in myoblasts as a differentiation switch fromproliferation to fusion", Journal of Muscle Research and Cell Motility, (0) [SCI Expanded] Link DOI AKPULAT, U., Yıldız, Y., Özdemir, C., Akçay, D., Kocaefe, Y.Ç. (2016) "A role for Klf5 in myoblasts as a differentiation switch fromproliferation to fusion", Journal of Muscle Research and Cell Motility, (0) [SCI Expanded] Link DOI
Arık, Z., Kılıçkap, S., AKPULAT, U., Şendur, M.A.N., Kocaefe, Y.Ç., Erman, M. (2016) "Effect of Zoledronic Acid on Rats Tissue SDF 1 Expression", Uluslararası Hematoloji-Onkoloji Dergisi, 26 (4) pp. 215-219 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-1169">
Arık, Z., Kılıçkap, S., AKPULAT, U., Şendur, M.A.N., Kocaefe, Y.Ç., Erman, M. (2016) "Effect of Zoledronic Acid on Rats Tissue SDF 1 Expression", Uluslararası Hematoloji-Onkoloji Dergisi, 26 (4) pp. 215-219 [SCI Expanded] Link DOI Arık, Z., Kılıçkap, S., AKPULAT, U., Şendur, M.A.N., Kocaefe, Y.Ç., Erman, M. (2016) "Effect of Zoledronic Acid on Rats Tissue SDF 1 Expression", Uluslararası Hematoloji-Onkoloji Dergisi, 26 (4) pp. 215-219 [SCI Expanded] Link DOI
Özdemir, C., AKPULAT, U., Akçay, D., Onbaşılar, İ., Kocaefe, Y.Ç. (2016) "AEBP1 ACLP is upregulated in differentiation injury repair andfibrotic degeneration of skeletal muscle", Journal of Muscle Research and Cell Motility, (0) [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-1170">
Özdemir, C., AKPULAT, U., Akçay, D., Onbaşılar, İ., Kocaefe, Y.Ç. (2016) "AEBP1 ACLP is upregulated in differentiation injury repair andfibrotic degeneration of skeletal muscle", Journal of Muscle Research and Cell Motility, (0) [SCI Expanded] Link DOI Özdemir, C., AKPULAT, U., Akçay, D., Onbaşılar, İ., Kocaefe, Y.Ç. (2016) "AEBP1 ACLP is upregulated in differentiation injury repair andfibrotic degeneration of skeletal muscle", Journal of Muscle Research and Cell Motility, (0) [SCI Expanded] Link DOI
Akçay, D., AKPULAT, U., Kocaefe, Y.Ç. (2016) "Generation of targeted insertion in the Klf5 gene of mousemyoblasts C2C12 cells using CRISPR Cas9 system", Journal of Muscle Research and Cell Motility, (0) [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-1171">
Akçay, D., AKPULAT, U., Kocaefe, Y.Ç. (2016) "Generation of targeted insertion in the Klf5 gene of mousemyoblasts C2C12 cells using CRISPR Cas9 system", Journal of Muscle Research and Cell Motility, (0) [SCI Expanded] Link DOI Akçay, D., AKPULAT, U., Kocaefe, Y.Ç. (2016) "Generation of targeted insertion in the Klf5 gene of mousemyoblasts C2C12 cells using CRISPR Cas9 system", Journal of Muscle Research and Cell Motility, (0) [SCI Expanded] Link DOI
AKPULAT, U., Cirak, S. (2022) "DMD hastalarında kendiliğinden distrofin ifade etme yeteneği kazanan revertant kas liflerinin yeni tedavilerin geliştitilmesinde potansiyel katkıları", GENÇ MERAKLILAR İÇİN NÖROGENETİK SEMİNERİ , İstanbul, Türkiye, (Haziran 2022)
AKPULAT, U. (2021) "Fare Miyoblast Hücre Hattında Klf5 Geninin Farklılaşma Sürecine Etkileri", 8. Uluslararası Tıp ve Sağlık Bilimleri Araştırmaları Kongresi , Ankara, Türkiye, (Aralık 2021)
AKPULAT, U., Cirak, S. (2021) "DMD hastalarının yeniden distrofin ifade etme yeteneği kazanan kas liflerinin yeni yaklaşımlar ile analizi", Uluslararası Katılımlı 21. Biyoteknoloji Kongresi , Kastamonu, Türkiye, (Aralık 2021)
Saka, C.Ö., AKPULAT, U., Onbaşılar, İ., Kocaefe, Y.Ç. (2016) "AEBP1/ACLP is upregulated in differentiation, injury repair and fibrotic degeneration of skeletal muscle", FEBS JOURNAL , (pp. 287), Kusadasi, (Eylül 2016)
AKPULAT, U., Yıldız, Y., Saka, C.Ö., Akçay, D., Kocaefe, Y.Ç. (2016) "Klf5 acts as a differentiation switch from proliferation to fusion in myoblasts", FEBS JOURNAL , (pp. 114), Kusadasi, (Eylül 2016)
AKPULAT, U., Wang, H., Becker, K., Novak, J., Partridge, T., Cirak, S. (2018) "Efficient short splice-switching morpholino antisense oligonucleotides for the treatment of Duchene Muscular Dystrophy", 6th International BAU-Drug Design Congress , Türkiye, (Aralık 2018)
AKPULAT, U. (2019) "Duchenne kas distrofisi’nin ekson-skipping temelli tedavietkinliğinin artırılması", 16. Tıbbi Biyoloji ve Genetik Kongresi , Muğla, Türkiye, (Ekim 2019)
AKPULAT, U., Novak, J., Becker, K., Partridge, T., Cirak, S. (2017) "Antisense morpholino oligonucleotides enter dystrophic muscle fibres via myoblast cell fusion in-vivo and provide a rational approach for efficient dystrophin restoration in Duchene Muscular Dystrophy", 33rd Ernst Klenk Symposium in Molecular Medicine , Köln, Almanya, (Ekim 2017)
