Search results for mutations
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Journal of Neurology and Neuroscience
Molecular Analysis of PANK2 Gene in Two Thai Classic Pantothenate Kinase- Associated Neurodegeneration (PKAN) Patients
Author(s): Piradee Suwanpakdee, Napakjira Likasitthananon, Charcrin Nabangchang, Yutthana Pansuwan, Siriporn Pattharathitikul and Boonchai Boonyawat
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Journal of Neurology and Neuroscience
Progressive Cavitating Leukoencephalopathy in an Infant Baby: A Case Report
Author(s): Rayya A. Almarwani*, Fahad A. Alsayed, Ehab S. Showki, Khalid O Alahmadi, Hesham Aldhalaan
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Journal of Molecular Genetics and Medicine
Critical Analysis of the Patients with Congenital Prekallikrein Deficiency and a "Purported " Bleeding Tendency
Author(s): Girolami Antonio, Cosi Elisabetta, Ferrari Silvia, Santarossa Claudia
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Journal of Biology and Medical Research
Properties and Prevention: A Review of Pseudomonas aeruginosa
Author(s): Matthew Jenny and Jeffrey Kingsbury
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Journal of Biology and Medical Research
Investigating Mutations in Member 6 (ABCC6) gene, of Sub-family C (CFTR/MRP) of the ATP-binding Cassette Causing Pseudoxanthoma Elasticum
Author(s): Sharika Akhter, Thomas Georgas, Georgios Giannoukos
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Journal of Translational Neurosciences
Translational Research on Amyotrophic Lateral Sclerosis (ALS): The Preclinical SOD1 Mouse Model
Author(s): Maria Mina, Eleni Konsolaki and Laskaro Zagoraiou*
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Genetics and Molecular Biology Research
Involvement of a Specific Ubiquitin Ligase in Assembly of the Cytoplasmic Dynein Motor in Neurospora crassa
Author(s): Elsenpeter R, Schnittker R and Plamann M
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Journal of Medical Oncology
Is the Target therapy have a role in the treatment of Metastatic lung cancer in patients who is not fit for chemotherapy? Case Report
Author(s): Ayman Rasmy, Mohamed Mashiaki and Amal Ameen
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Biochemistry & Molecular Biology Journal
A C. briggsae Genetic Suppressor Screen to Identify Dosage Compensation Pathway Components
Author(s): Jacqueline C Alexander, Jihye Lee, August P Miguez, Jason E Webb and Te-Wen Lo
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Journal of Genomics & Gene Study
Frequency of Factor V Leiden, Prothrombin G20210A and MTHFR C667T Mutations in Beta-Thalassemia Patients Compare with Normal Individuals from North of Iran
Author(s): Seyed Mohammad Bagher, Hashemi-Soteh1, Aily Aliasgharian, Alireza Tafazoli, Hossein Karami, Mehrnosh Kowsaryan