Výsledky vyhledávání - Futwan Al‐Mohanna

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  1. 1
    A mutation in sigma‐1 receptor causes juvenile amyotrophic lateral sclerosis

    A mutation in sigma‐1 receptor causes juvenile amyotrophic lateral sclerosis Autor Amr Al‐Saif, Futwan Al‐Mohanna, Saeed Bohlega

    Vydáno 2011
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  2. 2
    Native low density lipoprotein-induced calcium transients trigger VCAM-1 and E-selectin expression in cultured human vascular endothelial cells.

    Native low density lipoprotein-induced calcium transients trigger VCAM-1 and E-selectin expression in cultured human vascular endothelial cells. Autor Shelley Allen, Shabeena Khan, Futwan Al‐Mohanna, Puspa Batten, Magdi H. Yacoub

    Vydáno 1998
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  3. 3
    Sugar-sweetened carbonated beverage consumption correlates with BMI, waist circumference, and poor dietary choices in school children

    Sugar-sweetened carbonated beverage consumption correlates with BMI, waist circumference, and poor dietary choices in school children Autor Kate S. Collison, Marya Z. Zaidi, Shazia Subhani, Khalid Al‐Rubeaan, Mohammed Shoukri, Futwan Al‐Mohanna

    Vydáno 2010
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  4. 4
    A C. elegans model to study human metabolic regulation

    A C. elegans model to study human metabolic regulation Autor Sarwar Hashmi, Yi Wang, Ranjit S. Parhar, Kate S. Collison, Walter Conca, Futwan Al‐Mohanna, Randy Gaugler

    Vydáno 2013
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  5. 5
    Gender Dimorphism in Aspartame-Induced Impairment of Spatial Cognition and Insulin Sensitivity

    Gender Dimorphism in Aspartame-Induced Impairment of Spatial Cognition and Insulin Sensitivity Autor Kate S. Collison, Nadine J. Makhoul, Marya Z. Zaidi, Soad Saleh, Bernard L. Andres, Angela Inglis, Rana Al-Rabiah, Futwan Al‐Mohanna

    Vydáno 2012
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  6. 6
    Interactive effects of neonatal exposure to monosodium glutamate and aspartame on glucose homeostasis

    Interactive effects of neonatal exposure to monosodium glutamate and aspartame on glucose homeostasis Autor Kate S. Collison, Nadine J. Makhoul, Marya Z. Zaidi, Rana Al-Rabiah, Angela Inglis, Bernard L. Andres, Rosario Ubungen, Mohammed Shoukri, Futwan Al‐Mohanna

    Vydáno 2012
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  7. 7
    RAGE-mediated neutrophil dysfunction is evoked by advanced glycation end products (AGEs)

    RAGE-mediated neutrophil dysfunction is evoked by advanced glycation end products (AGEs) Autor Kate S. Collison, Ranjit S. Parhar, Soad Saleh, Brian F. Meyer, Aaron Kwaasi, Muhammad M. Hammami, Ann Marie Schmidt, David M. Stern, Futwan Al‐Mohanna

    Vydáno 2002
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  8. 8
    Effect of dietary monosodium glutamate on trans fat-induced nonalcoholic fatty liver disease

    Effect of dietary monosodium glutamate on trans fat-induced nonalcoholic fatty liver disease Autor Kate S. Collison, Zakia Maqbool, Soad Saleh, Angela Inglis, Nadine J. Makhoul, Razan Bakheet, Mohammed A. Al‐Johi, Rana Al-Rabiah, Marya Z. Zaidi, Futwan Al‐Mohanna

    Vydáno 2008
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  9. 9
    A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder

    A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder Autor Hanan E. Shamseldin, Ali Alasmari, Mohammed A. Salih, Manar Samman, Shahzad I. Mian, Tarfa Alshidi, Niema Ibrahim, Mais Hashem, Eissa Faqeih, Futwan Al‐Mohanna, Fowzan S. Alkuraya

    Vydáno 2017
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  10. 10
    Role of ERAB/l-3-Hydroxyacyl-coenzyme A Dehydrogenase Type II Activity in Aβ-induced Cytotoxicity

    Role of ERAB/l-3-Hydroxyacyl-coenzyme A Dehydrogenase Type II Activity in Aβ-induced Cytotoxicity Autor Shi Du Yan, Yigong Shi, Aiping Zhu, Jin Fu, Huaijie Zhu, Yucui Zhu, Lenneen Gibson, Eric Stern, Kate S. Collison, Futwan Al‐Mohanna, Satoshi Ogawa, Alex E. Roher, Steven Clarke, David M. Stern

    Vydáno 1999
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  11. 11
    POC1A Truncation Mutation Causes a Ciliopathy in Humans Characterized by Primordial Dwarfism

    POC1A Truncation Mutation Causes a Ciliopathy in Humans Characterized by Primordial Dwarfism Autor Ranad Shaheen, Eissa Faqeih, Hanan E. Shamseldin, Ramil R. Noche, Asma Sunker, Muneera J. Alshammari, Tarfa Al‐Sheddi, Nouran Adly, Mohammed S. Al-Dosari, Sean G. Megason, Muneera Al-Husain, Futwan Al‐Mohanna, Fowzan S. Alkuraya

    Vydáno 2012
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  12. 12
    TSH overcomes BrafV600E-induced senescence to promote tumor progression via downregulation of p53 expression in papillary thyroid cancer

    TSH overcomes BrafV600E-induced senescence to promote tumor progression via downregulation of p53 expression in papillary thyroid cancer Autor Minjing Zou, Essa Y. Baitei, Roua A. Al‐Rijjal, Ranjit S. Parhar, Futwan Al‐Mohanna, Shioko Kimura, Catrin Pritchard, Huda A. BinEssa, Ali S. Alzahrani, Huda H. Al‐Khalaf, Abbas Hawwari, M Akhtar, Abdullah M. Assiri, Brian F. Meyer, Yufei Shi

    Vydáno 2015
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  13. 13
    Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome

    Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome Autor Anas M. Alazami, Amr Al‐Saif, Abdulaziz Alsemari, Saeed Bohlega, Soumaya Zlitni, Fatema Alzahrani, Prashant Bavi, Namik Kaya, Dilek Çolak, Hanif Khalak, Andy Baltus, Borut Peterlin, Sumita Danda, Kailash P. Bhatia, Susanne A. Schneider, Nadia Sakati, Christopher A. Walsh, Futwan Al‐Mohanna, Brian F. Meyer, Fowzan S. Alkuraya

    Vydáno 2008
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  14. 14
    Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking

    Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking Autor Leslie E. Sanderson, Kristina Lanko, Maysoon Alsagob, Rawan Almass, Nada Al-Ahmadi, Maryam Najafi, Mohammad A. Al–Muhaizea, Hamad Alzaidan, Hesham Aldhalaan, Elena Perenthaler, Herma C. van der Linde, Anita Nikoncuk, Nikolas A. Kühn, Dinu Antony, Tarek Mustafa Owaidah, Salmo Raskin, Luana Gabriela Dalla Rosa Vieira, Romulo Mombach, Najmeh Ahangari, Tainá Regina Damaceno Silveira, Najim Ameziane, Arndt Rolfs, Aljohara Alharbi, Raghda M Sabbagh, Khalid AlAhmadi, Bashayer S. Alawam, Hazem Ghebeh, Aljouhra AlHargan, Anoud Albader, Faisal S. BinHumaid, Ewa Goljan, Dorota Monies, Osama M Mustafa, Mazhor Aldosary, Albandary AlBakheet, Banan Al‐Younes, Faten Almutairi, Ali Al‐Odaib, Dürdane Aksoy, A. Nazlı Başak, Robin Palvadeau, Daniah Trabzuni, Jill A. Rosenfeld, Ehsan Ghayoor Karimiani, Brian F. Meyer, Bedri Karakas, Futwan Al‐Mohanna, Stefan T. Arold, Dilek Çolak, Reza Maroofian, Henry Houlden, Aida M. Bertoli‐Avella, Miriam Schmidts, Tahsin Stefan Barakat, Tjakko J. van Ham, Namik Kaya

    Vydáno 2021
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  15. 15
    Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases

    Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases Autor Elena Perenthaler, Anita Nikoncuk, Soheil Yousefi, Woutje M. Berdowski, Maysoon Alsagob, Ivan Čapo, Herma C. van der Linde, Paul van den Berg, Edwin H. Jacobs, Darija Putar, Mehrnaz Ghazvini, Eleonora Aronica, Wilfred F. J. van IJcken, Walter G. de Valk, Evita Medici-van den Herik, Marjon van Slegtenhorst, Lauren Brick, Mariya Kozenko, Jennefer N. Kohler, Jonathan A. Bernstein, Kristin G. Monaghan, Amber Begtrup, Rebecca I. Torene, Amna Al‐Futaisi, Fathiya Al Murshedi, Renjith Mani, Faisal Al Azri, Erik-Jan Kamsteeg, Majid Mojarrad, Atieh Eslahi, Zaynab Khazaei, Fateme Massinaei Darmiyan, Mohammad Doosti, Ehsan Ghayoor Karimiani, Jana Vandrovcová, Faisal Zafar, Nuzhat Rana, Krishna Kumar Kandaswamy, Jozef Hertecant, Peter Bauer, Mohammed A. AlMuhaizea, Mustafa A. Salih, Mazhor Aldosary, Rawan Almass, Laila AlQuait, Wafa Qubbaj, Serdar Coşkun, Khaled O. Alahmadi, Muddathir H. Hamad, Salem Alwadaee, Khalid Awartani, Anas Dababo, Futwan Al‐Mohanna, Dilek Çolak, Mohammadreza Dehghani, Mohammad Yahya Vahidi Mehrjardi, Murat Günel, A. Gulhan Ercan‐Sencicek, Gouri Rao Passi, Huma Arshad Cheema, Stéphanie Efthymiou, Henry Houlden, Aida M. Bertoli‐Avella, Alice S. Brooks, Kyle Retterer, Reza Maroofian, Namik Kaya, Tjakko J. van Ham, Tahsin Stefan Barakat

    Vydáno 2019
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