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Differential Gene Expression in Peripheral White Blood Cells with Permissive Underfeeding and Standard Feeding in Critically Ill Patients: A Descriptive Sub-study of the PermiT Randomized Controlled Trial
Arabi, Yaseen M., Al-Balwi, Mohammed, Hajeer, Ali H., Jawdat, Dunia, Sadat, Musharaf, Al-Dorzi, Hasan M., Tamim, Hani, Afesh, Lara, Almashaqbeh, Walid, Alkadi, Haitham, Alwadaani, Deemah, UdayaRaja, G. K., Abdulkareem, Ibrahim B. Al, Al-Dawood, Abdulaziz
Published in Scientific reports (20.12.2018)
Published in Scientific reports (20.12.2018)
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Genome-wide association study of chronic hepatitis B virus infection reveals a novel candidate risk allele on 11q22.3
Al-Qahtani, Ahmed, Khalak, Hanif G, Alkuraya, Fowzan S, Al-hamoudy, Waleed, Alswat, Khalid, Al Balwi, Mohammed A, Al AbdulKareem, Ibrahim, Sanai, Faisal M, Abdo, Ayman A
Published in Journal of medical genetics (01.11.2013)
Published in Journal of medical genetics (01.11.2013)
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Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia
Tesson, Christelle, Nawara, Magdalena, Salih, Mustafa A.M., Rossignol, Rodrigue, Zaki, Maha S., Al Balwi, Mohammed, Schule, Rebecca, Mignot, Cyril, Obre, Emilie, Bouhouche, Ahmed, Santorelli, Filippo M., Durand, Christelle M., Oteyza, Andrés Caballero, El-Hachimi, Khalid H., Al Drees, Abdulmajeed, Bouslam, Naima, Lamari, Foudil, Elmalik, Salah A., Kabiraj, Mohammad M., Seidahmed, Mohammed Z., Esteves, Typhaine, Gaussen, Marion, Monin, Marie-Lorraine, Gyapay, Gabor, Lechner, Doris, Gonzalez, Michael, Depienne, Christel, Mochel, Fanny, Lavie, Julie, Schols, Ludger, Lacombe, Didier, Yahyaoui, Mohamed, Al Abdulkareem, Ibrahim, Zuchner, Stephan, Yamashita, Atsushi, Benomar, Ali, Goizet, Cyril, Durr, Alexandra, Gleeson, Joseph G., Darios, Frederic, Brice, Alexis, Stevanin, Giovanni
Published in American journal of human genetics (07.12.2012)
Published in American journal of human genetics (07.12.2012)
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A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra‐amelia in two Saudi families
Eyaid, Wafaa, Al‐Qattan, Mohammad M., Al Abdulkareem, Ibrahim, Fetaini, Nouf, Al Balwi, Mohammed
Published in American journal of medical genetics. Part A (01.03.2011)
Published in American journal of medical genetics. Part A (01.03.2011)
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Monomeric C-reactive protein and Notch-3 co-operatively increase angiogenesis through PI3K signalling pathway
Boras, Emhamed, Slevin, Mark, Alexander, M. Yvonne, Aljohi, Ali, Gilmore, William, Ashworth, Jason, Krupinski, Jerzy, Potempa, Lawrence A., Al Abdulkareem, Ibrahim, Elobeid, Adila, Matou-Nasri, Sabine
Published in Cytokine (Philadelphia, Pa.) (01.10.2014)
Published in Cytokine (Philadelphia, Pa.) (01.10.2014)
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A novel mutation in the SHH long‐range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency
Al‐Qattan, Mohammad M., Al Abdulkareem, Ibrahim, Al Haidan, Yazied, Al Balwi, Mohammed
Published in American journal of medical genetics. Part A (01.10.2012)
Published in American journal of medical genetics. Part A (01.10.2012)
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Clinical characteristics and genetic subtypes of Fanconi anemia in Saudi patients
Ghazwani, Yahya, AlBalwi, Mohammed, Al-Abdulkareem, Ibrahim, Al-Dress, Mohammed, Alharbi, Talal, Alsudairy, Reem, Alomari, Ali, Aljamaan, Khalid, Essa, Mohammed, Al-Zahrani, Mohsen, Alsultan, Abdulrahman
Published in Cancer genetics (01.04.2016)
Published in Cancer genetics (01.04.2016)
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Novel human pathological mutations. Gene symbol: EDAR. Disease: Ectodermal dysplasia, hypohidrotic
Al Balwi, Mohammed, Ibrahim, Al Abdulkareem, Abdulrahman, Al Swaid
Published in Human genetics (01.01.2010)
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Published in Human genetics (01.01.2010)
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Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report
Al Balwi, Mohammed, Al Ajaji, Sulaiman, Al Abdulkareem, Ibrahim, Hajeer, Ali
Published in Cases journal (30.07.2009)
Published in Cases journal (30.07.2009)
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Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report
Al Balwi, Mohammed, Al Ajaji, Sulaiman, Al Abdulkareem, Ibrahim, Hajeer, Ali
Published in Cases journal (30.07.2009)
Published in Cases journal (30.07.2009)
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A novel mutation in the SHH long-range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency
Al-Qattan, Mohammad M., Al Abdulkareem, Ibrahim, Al Haidan, Yazied, Al Balwi, Mohammed
Published in American Journal of Medical Genetics Part A (01.10.2012)
Published in American Journal of Medical Genetics Part A (01.10.2012)
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A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra-amelia in two Saudi families
Eyaid, Wafaa, Al-Qattan, Mohammad M., Al Abdulkareem, Ibrahim, Fetaini, Nouf, Al Balwi, Mohammed
Published in American Journal of Medical Genetics Part A (01.03.2011)
Published in American Journal of Medical Genetics Part A (01.03.2011)
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