Search Results - "Sellama Nadifi"

Hypomorphic homozygous mutations in phosphoglucomutase 3 ( PGM3 ) impair immunity and increase serum IgE levels by Sassi, Atfa, PhD, Lazaroski, Sandra, PhD, Wu, Gang, MSc, Haslam, Stuart M., PhD, Fliegauf, Manfred, PhD, Mellouli, Fethi, MD, Patiroglu, Turkan, MD, Unal, Ekrem, MD, Ozdemir, Mehmet Akif, MD, Jouhadi, Zineb, MD, Khadir, Khadija, MD, Ben-Khemis, Leila, MSc, Ben-Ali, Meriem, PhD, Ben-Mustapha, Imen, MD, Borchani, Lamia, PhD, Pfeifer, Dietmar, PhD, Jakob, Thilo, MD, Khemiri, Monia, MD, Asplund, A. Charlotta, BSc, Gustafsson, Manuela O., MSc, Lundin, Karin E., PhD, Falk-Sörqvist, Elin, MSc, Moens, Lotte N., PhD, Gungor, Hatice Eke, MD, Engelhardt, Karin R., PhD, Dziadzio, Magdalena, MD, PhD, Stauss, Hans, MD, PhD, Fleckenstein, Bernhard, MD, Meier, Rebecca, BSc, Prayitno, Khairunnadiya, MSc, Maul-Pavicic, Andrea, PhD, Schaffer, Sandra, Rakhmanov, Mirzokhid, PhD, Henneke, Philipp, MD, Kraus, Helene, MSc, Eibel, Hermann, PhD, Kölsch, Uwe, MD, Nadifi, Sellama, PhD, Nilsson, Mats, PhD, Bejaoui, Mohamed, MD, Schäffer, Alejandro A., PhD, Smith, C.I. Edvard, MD, PhD, Dell, Anne, PhD, Barbouche, Mohamed-Ridha, MD, PhD, Grimbacher, Bodo, MD

“…Background Recurrent bacterial and fungal infections, eczema, and increased serum IgE levels characterize patients with the hyper-IgE syndrome (HIES). Known…”
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p.Arg72Pro polymorphism of P53 and breast cancer risk: a meta-analysis of case-control studies by Diakite, Brehima, Kassogue, Yaya, Dolo, Guimogo, Wang, Jun, Neuschler, Erin, Kassogue, Oumar, Keita, Mamadou L, Traore, Cheick B, Kamate, Bakarou, Dembele, Etienne, Nadifi, Sellama, Murphy, Robert L, Doumbia, Seydou, Hou, Lifang, Maiga, Mamoudou

“…The effect of the p.Arg72Pro variant of the P53 gene on the risk of development ofbreast cancer remains variable in populations. However, the use ofstrategies…”
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The polymorphism G894 T of endothelial nitric oxide synthase (eNOS) gene is associated with susceptibility to essential hypertension (EH) in Morocco by Nassereddine, Sanaa, Hassani Idrissi, Hind, Habbal, Rachida, Abouelfath, Rhizlane, Korch, Farah, Haraka, Majda, Karkar, Adnane, Nadifi, Sellama

“…Hypertension is a multifactorial disease involving both environmental and genetic Factros. G894 T eNOS polymorphism has been suggested to be responsible for…”
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Analysis of the influence of glutathione S-transferase (GSTM1 and GSTT1) genes on the risk of essential hypertension by Nassereddine, Sanaa, Habbal, Rachida, Kassogue, Yaya, Kaltoum, Ait Boujmia Oum, Farah, Korchi, Majda, Haraka, Rhizlane, Abou Elfath, Nadifi, Sellama, Dehbi, Hind

“…Essential hypertension (EH) results from a complex interaction between environmental factors and an individual's genetic background. To assess the relationship…”
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Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population by Marouf, Chaymaa, Göhler, Stella, Filho, Miguel Inacio Da Silva, Hajji, Omar, Hemminki, Kari, Nadifi, Sellama, Försti, Asta

“…Breast cancer (BC) is the most prevalent cancer in women and a major public health problem in Morocco. Several Moroccan studies have focused on studying this…”
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Polymorphisms in oxidative pathway related genes and susceptibility to inflammatory bowel disease by Senhaji, Nezha, Nadifi, Sellama, Zaid, Younes, Serrano, Aurora, Rodriguez, Daniel Arturo Leon, Serbati, Nadia, Karkouri, Mehdi, Badre, Wafaa, Martín, Javier

“…AIM To investigate whether common variants in the oxidative pathway genes influence inflammatory bowel disease（IBD） risk among Moroccan patients. METHODS The…”
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Genetic Polymorphisms of Multidrug Resistance Gene-1 (MDR1/ABCB1) and Glutathione S-Transferase Gene and the Risk of Inflammatory Bowel Disease among Moroccan Patients by Badre, Wafaa, Serbati, Nadia, Fahimi, Mina, Kassogue, Yaya, Senhaji, Nezha, Nadifi, Sellama

“…Inflammatory bowel diseases (IBD) are multifactorial disorders resulting from environmental and genetic factors. Polymorphisms in MDR1 and GSTs genes might…”
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Genetic Polymorphisms of Glutathione S-Transferase and Risk of Acute Myeloid Leukemia: Case-Control Study and Meta-Analysis by Oum Kaltoum Ait Boujmia, Sellama Nadifi, Hind Dehbi, Yaya Kassogue, Mouna Lamchahab, Asma Quessar

“…Background: Acute myeloid leukemia (AML) is a complex disease that is linked to genetic and environmental factors. The gluthatione S-transferase (GST) is a…”
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Association of PIN3 16-bp duplication polymorphism of TP53 with breast cancer risk in Mali and a meta-analysis by Diakite, Brehima, Kassogue, Yaya, Dolo, Guimogo, Kassogue, Oumar, Keita, Mamadou Lassine, Joyce, Brian, Neuschler, Erin, Wang, Jun, Musa, Jonah, Traore, Cheick Bougari, Kamate, Bakarou, Dembele, Etienne, Nadifi, Sellama, Isichei, Mercy, Holl, Jane L, Murphy, Robert, Doumbia, Seydou, Hou, Lifang, Maiga, Mamoudou

“…Breast cancer, the most common tumor in women in Mali and worldwide has been linked to several risk factors, including genetic factors, such as the PIN3 16-bp…”
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A synergic effect between CYP2C192, CYP2C193 loss-of-function and CYP2C1917 gain-of-function alleles is associated with Clopidogrel resistance among Moroccan Acute Coronary Syndromes patients by Hassani Idrissi, Hind, Hmimech, Wiam, Khorb, Nada El, Akoudad, Hafid, Habbal, Rachida, Nadifi, Sellama

“…The main objective of our study was to investigate the association of CYP2C19*2 and CYP2C19*3 loss-of-function and CYP2C19*17 gain-of-function variants of…”
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Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile by Kindil, Zineb, Senhaji, Mohamed Amine, Bakhchane, Amina, Charoute, Hicham, Chihab, Soumia, Nadifi, Sellama, Barakat, Abdelhamid

“…Xeroderma pigmentosum (XP) is a genetically and clinically heterogeneous disease, associated with an inherited defect in one of eight different genes (XPA to…”
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The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease by Zaid, Younes, Senhaji, Nezha, Bakhtaoui, Fatima Zahra, Serrano, Aurora, Serbati, Nadia, Karkouri, Mehdi, Badre, Wafaa, Oudghiri, Mounia, Martin, Javier, Nadifi, Sellama

“…In view of the discrepant data regarding the association between the protein tyrosine phosphatase non-receptor 22 (PTPN22) rs2476601 (R620W, 1858C→T)…”
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Relationships of plasma total homocysteine (HCY), folates and vitamin B12 levels to vertebral fracture and bone mineral density in Moroccan healthy postmenopausal women by El Maataoui, Aissam, Ennefah, Lamiae, Mounach, Aziza, Toufik, Hamza, Nadifi, Sellama, El Maghraoui, Abdellah, Ouzzif, Zahra

“…INTRODUCTION: A potential role of Homocysteine (HCY) in bone metabolism has been considered from the observation of high prevalence of osteoporosis in subjects…”
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A Proteomic Approach for the Involvement of the GAPDH in Alzheimer Disease in the Blood of Moroccan FAD Cases by El Kadmiri, Nadia, Cuardos, Raquel, El Moutawakil, Bouchra, Slassi, Ilham, Avila, Jesus, Nadifi, Sellama, Hachem, Ahmed, Soukri, Abdelaziz

“…Several articles have highlighted the potential involvement of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in neurodegeneration by showing a…”
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Synergistic effect of MTHFR C677T and F2 G20210A polymorphisms on ischemic stroke by They-They, Thierry Paluku, Battas, Omar, Nadifi, Sellama

“…The predisposition to stroke might involve interactive effects among variants in several genes.We tested this hypothesis by examining the influence of…”
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Impact of I/D polymorphism of angiotensin-converting enzyme (ACE) gene on myocardial infarction susceptibility among young Moroccan patients by Hmimech, Wiam, Idrissi, Hind Hassani, Diakite, Brehima, Korchi, Farah, Baghdadi, Dalila, Tahri Joutey Hassani Idrissi, Hind, Haboub, Meriem, Habbal, Rachida, Nadifi, Sellama

“…Our case-control study aimed to access the potential association of insertion/deletion (I/D) ACE (angiotensin converting enzyme) gene polymorphism with…”
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Dilated cardiomyopathy: A rare and late complication of the hemolytic-uremic syndrome by Naour, Oumaima, Drighil, Abdenasser, Idouz, Kaoutar, Nadifi, Sellama, Rochdi, Fatima Ezzahra, Bouayed, Kenza, Mikou, Nabiha

“…Hemolytic uremic syndrome (HUS) is a non-exceptional, progressive complication of acute gastroenteritis in children, especially secondary to Escherichia coli…”
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Food hygiene assessment in catering establishments in Hay Hassani district-Casablanca by El Kadmiri, Nadia, Bakouri, Halima, Bassir, Fatima, Barmaki, Saadia, Rachad, Laila, Nadifi, Sellama, Kadmiri, Omar El, Amina, Bouleghmane

“…Contaminated food is responsible for a significant amount of illnesses. In Morocco, it has become a worrying concern. Numerous awareness campaigns are…”
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Association of Glutathione S-transferase Genes (M1 and T1) with the Risk of Acute Myeloid Leukemia in a Moroccan Population by Ait Boujmia Oum Kaltoum, Nadifi Sellama, Dehbi Hind, Kassogue Yaya, Lamchahab Mouna, Quessar Asma

“…Background: Acute myeloid leukemia, as most cancers, results from exposure to carcinogens and an impaired inherited individual capacity to eliminate…”
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Association du polymorphisme de la méthylènetétrahydrofolate réductase C677T avec le risque de cancer colorectal sporadique by Baghad, Imane, Erreguibi, Driss, Boufettal, Rachid, Eljai, Saad Rifki, Chihab, Farid, Nadifi, Sellama

“…Le cancer colorectal (CCR) est un problème majeur de santé publique dans le monde. Le métabolisme des folates est impliqué dans la synthèse, la réparation et…”
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