Search Results - "phenotyping"

The Effect of Antioxidant and Anti-Inflammatory Capacity of Diet on Psoriasis and Psoriatic Arthritis Phenotype: Nutrition as Therapeutic Tool? by Pelagia Katsimbri, Emmanouil Korakas, Aikaterini Kountouri, Ignatios Ikonomidis, Elias Tsougos, Dionysios Vlachos, Evangelia Papadavid, Athanasios Raptis, Vaia Lambadiari

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Case report: Expansion of phenotypic and genotypic data in TENM3-related syndrome: Report of two cases by Fen Lu, Xin Xu, Bixia Zheng, Chunli Wang, Wei Zhou, Jian Tang, Xiaoke Zhao

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Novel TTC37 Mutations in a Patient with Immunodeficiency without Diarrhea: Extending the Phenotype of Trichohepatoenteric Syndrome. by Nicholas L Rider, Nicholas L Rider, Bertrand eBoisson, Soma eJyonouchi, Eric eHanson, Sergio eRosenzweig, Jean-Laurent eCasanova, Jean-Laurent eCasanova, Jordan eOrange, Jordan eOrange

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Phenotypic and Genotypic Analysis of Bacterial Pathogens Recovered from Patients Diagnosed with Fever of Unknown Origin in Egypt by Shimaa H. Mostafa, Sarra E. Saleh, Eman F. Khaleel, Rehab Mustafa Badi, Khaled M. Aboshanab, Samira M. Hamed

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Target Identification of Mycobacterium tuberculosis Phenotypic Hits Using a Concerted Chemogenomic, Biophysical, and Structural Approach by Grace Mugumbate, Grace Mugumbate, Vitor Mendes, Michal Blaszczyk, Mohamad Sabbah, George Papadatos, Joel Lelievre, Lluis Ballell, David Barros, Chris Abell, Tom L. Blundell, John P. Overington, John P. Overington

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Higher serum concentrations of vimentin and DAKP1 are associated with aggressive breast tumour phenotypes in Ghanaian women by Benjamin Arko-Boham, Justice Tanihu Lomotey, Emmanuel Nomo Tetteh, Emmanuel Ayitey Tagoe, Nii Ayite Aryee, Ewurama Ampadu Owusu, Isaac Okai, Richard Michael Blay, Joe-Nat

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A novel c.-22T>C mutation in <it>GALK1 </it>promoter is associated with elevated galactokinase phenotype by Kim Jin Q, Park Kyoung, Kim Yoon-Kyoung, Park Hyung-Doo, Song Young-Han, Song Junghan

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DYRK1a Inhibitor Mediated Rescue of Drosophila Models of Alzheimer's Disease-Down Syndrome Phenotypes by Bangfu Zhu, Tom Parsons, Wenche Stensen, Wenche Stensen, John S. Mjøen Svendsen, John S. Mjøen Svendsen, Anders Fugelli, James J. L. Hodge

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The Effect of CYP2D6 Phenotypes on the Pharmacokinetics of Propafenone: A Systematic Review and Meta-Analysis by Quyen Thi Tran, In-hwan Baek, Na-young Han, Hwi-yeol Yun, Jung-woo Chae

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Vitamin B12 Ameliorates the Pathological Phenotypes of Multiple Parkinson's Disease Models by Alleviating Oxidative Stress by Yue Wu, Zhongting Zhao, Naidi Yang, Chenqi Xin, Zheng Li, Jiajia Xu, Bo Ma, Kah-Leong Lim, Lin Li, Qiong Wu, Changmin Yu, Chengwu Zhang

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Heterogeneous Phenotypic Responses of Antibiotic-Resistant <i>Salmonella Typhimurium</i> to Food Preservative-Related Stresses by Jiseok Yi, Juhee Ahn

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Identification of a novel FGF3 variant and a new phenotype in three LAMM syndrome families by Qiang Du, Yike Zhang, Rujian Hong, Nuermaimaiti Tulamaiti, Maiheba Abulaiti, Nueraili Awuti, Wulamu Wusiman, Xirinayi Alimu, Ayinuer Wusiman, Nueraihaimaiti Kadier, Huilin Li, Zhifei Zhang, Huan Qi, Zhipeng Xia, Ayituersun Abudukeyoumu, Huawei Li, Luo Guo

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Prenatal ultrasound diagnostics of atrioventricular communication in combination with the tetralogy of Fallot in a fetus with Down's syndrome phenotype by M.P. Veropotvelian, A.O. Bondarenko, О.V. Shashko, T.V. Usenko, D.I. Lailo

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Digital photometric analysis as a non-invasive method to determine gingival phenotype: A comparative study by Seham Altaweel, Maha Sehli, Mirna Khogeer, Rahmah Ayyash, Saleh Al Zahrani, Thamer Al-Ghalib, Mohamed Abdelrasoul

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GENOTYPE-PHENOTYPE CORRELATIONS OF THE COURSE OF CYSTIC FIBROSIS IN RUSSIAN CHILDREN. THE FIRST DESCRIPTION OF ELEVEN NEW MUTATIONS by Yulia V. Gorinova, Kirill V. Savostyanov, Alexandr A. Pushkov, Alexey G. Nikitin, Evgeniy L. Pen'kov, Stanislav A. Krasovskiy, Olga I. Simonova, L. S. Namazova-Baranova

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A Greek multicenter study comparing the clinical and immunologic phenotypes between adult and juvenile- onset lupus by Papachristou F, Farmaki E, Pratsidou-Gerts P, Galanopoulou V, Trachana M, Siamopoulou A, Stefanidou S, Alfantaki S, Nalbanti P, Garyphallos A, Kanakoudi-Tsakalidou F

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Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review by Mohammad-Reza Ghasemi, Sahand Tehrani Fateh, Aysan Moeinafshar, Hossein Sadeghi, Parvaneh Karimzadeh, Reza Mirfakhraie, Mitra Rezaei, Farzad Hashemi-Gorji, Morteza Rezvani Kashani, Fatemehsadat Fazeli Bavandpour, Saman Bagheri, Parinaz Moghimi, Masoumeh Rostami, Rasoul Madannejad, Hassan Roudgari, Mohammad Miryounesi

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Phenotypic and molecular spectra of patients with switch/sucrose nonfermenting complex-related intellectual disability disorders in Korea by Yena Lee, Yunha Choi, Go Hun Seo, Gu-Hwan Kim, Changwon Keum, Yoo-Mi Kim, Hyo-Sang Do, Jeongmin Choi, In Hee Choi, Han-Wook Yoo, Beom Hee Lee

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Association of hypertriglyceridemic‐waist phenotype with liver enzymes and cardiometabolic risk factors in adolescents: the CASPIAN‐III study by Roya Kelishadi, Fahimeh Jamshidi, Mostafa Qorbani, Mohammad Esmaeil Motlagh, Ramin Heshmat, Gelayol Ardalan, Silva Hovsepian

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Noncompact Myocardium with Dilated Phenotype: Manifestations, Treatment and Outcomes in Comparison with Other Forms of Dilated Cardiomyopathy Syndrome by O. V. Blagova, E. V. Pavlenko, N. V. Varionchik, V. P. Sedov, N. V. Gagarina, E. A. Mershina, M. E. Polyak, E. V. Zaklyazminskaya, A. V. Nedostup

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