المؤلفون: Issa, Mahmoud

المصدر: A New Critical Approach to the History of Palestine. (2019) 125-140

مصطلحات موضوعية: Oral history, Palestinian Arabs -- Historiography

الوصول الحر: https://uli.nli.org.il/discovery/search?query=isbn,exact,9780367146375&tab=LibraryCatalog&search_scope=MyInstitution&vid=972NNL_ULI_C:MAINTest

المؤلفون: Hashem, Tareq N.^{1, 2, 1}, Issa, Mahmoud S.^{1, 2}, Iapadre, Giulia^{1, 2}, Hamdan, Farah I.^{1, 2}

المصدر: International Journal of Medical Research & Health Sciences 7(7):151-161. 2018

المؤلفون: Accogli, Andrea, Zaki, Maha S, Al-Owain, Mohammed, Otaif, Mansour Y, Jackson, Adam, Argilli, Emanuela, Chandler, Kate E, De Goede, Christian GEL, Cora, Tülün, Alvi, Javeria Raza, Eslahi, Atieh, Asl Mohajeri, Mahsa Sadat, Ashtiani, Setareh, Au, PY Billie, Scocchia, Alicia, Alakurtti, Kirsi, Pagnamenta, Alistair T, Toosi, Mehran Beiraghi, Ghayoor Karimiani, Ehsan, Mojarrad, Majid, Arab, Fatemeh, Duymuş, Fahrettin, Scantlebury, Morris H, Yeşil, Gözde, Rosenfeld, Jill Anne, Türkyılmaz, Ayberk, Sağer, Safiye Güneş, Sultan, Tipu, Ashrafzadeh, Farah, Zahra, Tatheer, Rahman, Fatima, Maqbool, Shazia, Abdel-Hamid, Mohamed S, Issa, Mahmoud, Efthymiou, Stephanie, Bauer, Peter, Zifarelli, Giovanni, Salpietro, Vincenzo, Al-Hassnan, Zuhair, Banka, Siddharth, Sherr, Elliot H, Gleeson, Joseph G, Striano, Pasquale, Houlden, Henry, Severino, Mariasavina, Maroofian, Reza

مصطلحات موضوعية: Pediatric, Neurosciences, Genetics, Neurodegenerative, Clinical Research, Congenital Structural Anomalies, Brain Disorders, Rare Diseases, Human Genome, Epilepsy, 2.1 Biological and endogenous factors, Aetiology, Mental health, Neurological, Clinical sciences, Biological psychology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/77b7h8njTest

المؤلفون: Zaki, Maha S, Sharaf‐Eldin, Wessam E, Rafat, Karima, Elbendary, Hasnaa M, Kamel, Mona, Elkhateeb, Nour, Noureldeen, Mahmoud M, Abdeltawab, Mohamed A, Sadek, Abdelrahim A, Essawi, Mona L, Lau, Tracy, Murphy, David, Abdel‐Hamid, Mohamed S, Holuden, Henry, Issa, Mahmoud Y, Gleeson, Joseph G

المصدر: Clinical Genetics. 104(2)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Neurodegenerative, Clinical Research, Neurosciences, Brain Disorders, Rare Diseases, Aetiology, 2.1 Biological and endogenous factors, Neurological, Humans, Egypt, Guanine Nucleotide Exchange Factors, DNA Mutational Analysis, Mutation, ALS2, IAHSP, JPLS, UMNL, Clinical Sciences, Genetics & Heredity, Clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/2tn8t7jdTest

المؤلفون: Wang, Lu, Heffner, Caleb, Vong, Keng loi, Barrows, Chelsea, Ha, Yoo-Jin, Lee, Sangmoon, Lara-Gonzalez, Pablo, Jhamb, Ishani, Van Der Meer, Dennis, Loughnan, Robert, Parker, Nadine, Sievert, David, Mittal, Swapnil, Issa, Mahmoud Y, Andreassen, Ole A, Dale, Anders, Dobyns, William B, Zaki, Maha S, Murray, Stephen A, Gleeson, Joseph G

المصدر: Proceedings of the National Academy of Sciences of the United States of America. 120(4)

مصطلحات موضوعية: Biochemistry and Cell Biology, Biomedical and Clinical Sciences, Biological Sciences, Genetics, Clinical Research, Intellectual and Developmental Disabilities (IDD), Brain Disorders, Neurological, Animals, Humans, Mice, Ependymoglial Cells, Mice, Knockout, Neocortex, TMEM161B, gyrification, CDC42, knock-in crispant mice, patient-derived brain organoids

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5d58c7krTest

المؤلفون: Salpietro, Vincenzo, Maroofian, Reza, Zaki, Maha S., Wangen, Jamie, Ciolfi, Andrea, Barresi, Sabina, Efthymiou, Stephanie, Lamaze, Angelique, Aughey, Gabriel N., Al Mutairi, Fuad, Rad, Aboulfazl, Rocca, Clarissa, Calì, Elisa, Accogli, Andrea, Zara, Federico, Striano, Pasquale, Mojarrad, Majid, Tariq, Huma, Giacopuzzi, Edoardo, Taylor, Jenny C., Oprea, Gabriela, Skrahina, Volha, Rehman, Khalil Ur, Abd Elmaksoud, Marwa, Bassiony, Mahmoud, El Said, Huda G., Abdel-Hamid, Mohamed S., Al Shalan, Maha, Seo, Gohun, Kim, Sohyun, Lee, Hane, Khang, Rin, Issa, Mahmoud Y., Elbendary, Hasnaa M., Rafat, Karima, Marinakis, Nikolaos M., Traeger-Synodinos, Joanne, Ververi, Athina, Sourmpi, Mara, Eslahi, Atieh, Khadivi Zand, Farhad, Beiraghi Toosi, Mehran, Babaei, Meisam, Jackson, Adam, Bertoli-Avella, Aida, Pagnamenta, Alistair T., Niceta, Marcello, Battini, Roberta, Corsello, Antonio, Leoni, Chiara

المصدر: The American Journal of Human Genetics ; volume 111, issue 1, page 200-210 ; ISSN 0002-9297

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1016/j.ajhg.2023.11.012Test
https://api.elsevier.com/content/article/PII:S0002929723004305?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0002929723004305?httpAccept=text/plainTest

المؤلفون: Ghosh, Shereen G, Scala, Marcello, Beetz, Christian, Helman, Guy, Stanley, Valentina, Yang, Xiaoxu, Breuss, Martin W, Mazaheri, Neda, Selim, Laila, Hadipour, Fatemeh, Pais, Lynn, Stutterd, Chloe A, Karageorgou, Vasiliki, Begtrup, Amber, Crunk, Amy, Juusola, Jane, Willaert, Rebecca, Flore, Leigh A, Kennelly, Kelly, Spencer, Christopher, Brown, Martha, Trapane, Pamela, Hurst, Anna CE, Lane Rutledge, S, Goodloe, Dana H, McDonald, Marie T, Shashi, Vandana, Schoch, Kelly, Tomoum, Hoda, Zaitoun, Raghda, Hadipour, Zahra, Galehdari, Hamid, Pagnamenta, Alistair T, Mojarrad, Majid, Sedaghat, Alireza, Dias, Patrícia, Quintas, Sofia, Eslahi, Atiyeh, Shariati, Gholamreza, Bauer, Peter, Simons, Cas, Houlden, Henry, Issa, Mahmoud Y, Zaki, Maha S, Maroofian, Reza, Gleeson, Joseph G

المصدر: European Journal of Human Genetics. 29(2)

مصطلحات موضوعية: Biological Sciences, Genetics, Brain Disorders, Rare Diseases, Clinical Research, Neurosciences, Human Genome, Pediatric, Neurodegenerative, Intellectual and Developmental Disabilities (IDD), 2.1 Biological and endogenous factors, Aetiology, Child, Child, Preschool, Codon, Nonsense, Exome, Exons, Female, Homozygote, Humans, Male, Microcephaly, Nerve Tissue Proteins, Neurodevelopmental Disorders, Pedigree, RNA Splice Sites, RNA Splicing, Syndrome, Vesicular Transport Proteins, Undiagnosed Diseases Network, Clinical Sciences, Genetics & Heredity, Clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8rz7m8qmTest

المؤلفون: Chai, Guoliang, Webb, Alice, Li, Chen, Antaki, Danny, Lee, Sangmoon, Breuss, Martin W, Lang, Nhi, Stanley, Valentina, Anzenberg, Paula, Yang, Xiaoxu, Marshall, Trevor, Gaffney, Patrick, Wierenga, Klaas J, Chung, Brian Hon-Yin, Tsang, Mandy Ho-Yin, Pais, Lynn S, Lovgren, Alysia Kern, VanNoy, Grace E, Rehm, Heidi L, Mirzaa, Ghayda, Leon, Eyby, Diaz, Jullianne, Neumann, Alexander, Kalverda, Arnout P, Manfield, Iain W, Parry, David A, Logan, Clare V, Johnson, Colin A, Bonthron, David T, Valleley, Elizabeth MA, Issa, Mahmoud Y, Abdel-Ghafar, Sherif F, Abdel-Hamid, Mohamed S, Jennings, Patricia, Zaki, Maha S, Sheridan, Eamonn, Gleeson, Joseph G

المصدر: Neuron. 109(2)

مصطلحات موضوعية: Biological Psychology, Biomedical and Clinical Sciences, Neurosciences, Psychology, Rare Diseases, Genetics, Neurodegenerative, Brain Disorders, Orphan Drug, Human Genome, Aetiology, 2.1 Biological and endogenous factors, Neurological, Amino Acid Sequence, Animals, Cell Cycle Proteins, Cerebellar Diseases, Cohort Studies, Female, Gene Knockout Techniques, HEK293 Cells, Heredodegenerative Disorders, Nervous System, Humans, Male, Mice, Mice, Inbred C57BL, Mice, Transgenic, Microcephaly, Mutation, Pedigree, Peptidylprolyl Isomerase, Protein Structure, Secondary, Protein Structure, Tertiary, RNA Splicing Factors, Spliceosomes, NMR, PCHM, PPIL1, PRP17, alternative splicing, brain development, cyclophilin, microcephaly, neurodegeneration, pontocerebellar hypoplasia, proline isomerase, recessive disease, spliceosome, Cognitive Sciences, Neurology & Neurosurgery, Biological psychology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/6w53352fTest

المؤلفون: Issa, Mahmoud Y, Chechlacz, Zinayida, Stanley, Valentina, George, Renee D, McEvoy-Venneri, Jennifer, Belandres, Denice, Elbendary, Hasnaa M, Gaber, Khaled R, Nabil, Ahmed, Abdel-Hamid, Mohamed S, Zaki, Maha S, Gleeson, Joseph G

المصدر: BMC Medical Genomics. 13(1)

مصطلحات موضوعية: Reproductive Medicine, Biomedical and Clinical Sciences, Genetics, Biological Sciences, Prevention, Pediatric, Clinical Research, Reproductive health and childbirth, Good Health and Well Being, Child, Preschool, Female, Genes, Recessive, Genetic Markers, Genetic Predisposition to Disease, Genetic Testing, Genotype, High-Throughput Nucleotide Sequencing, Humans, Infant, Infant, Newborn, Male, Mutation, Nervous System Diseases, Pedigree, Pregnancy, Prenatal Diagnosis, Recurrence, Retrospective Studies, Medical Biochemistry and Metabolomics, Oncology and Carcinogenesis, Genetics & Heredity, Medical biochemistry and metabolomics

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/6jq364tfTest

المؤلفون: Motasem Issa Mahmoud Abu Zer, Kader Reyhan

المصدر: Iconarp International Journal of Architecture and Planning, Vol 11, Iss 1 (2023)

مصطلحات موضوعية: Architectural reproduction, cultural heritage, globalization, muqarnas, simulation strategy, Architecture, NA1-9428, City planning, HT165.5-169.9

وصف الملف: electronic resource

العلاقة: https://iconarp.ktun.edu.tr/index.php/iconarp/article/view/961Test; https://doaj.org/toc/2147-9380Test

الوصول الحر: https://doaj.org/article/e5ef93b8d3cd49e5831c335b1d09ceb9Test