Search results for mutation

Page 11 of 62

• Advanced Techniques in Clinical Microbiology

  Based on Clinical Trials: Evolution of Plasmid Mediated Antibiotic Resistance

  Author(s): Manmath Kumar Rout*

  Abstract | Full-Text |   PDF

• Journal of Genomics & Gene Study

  Deficiency in ORC1 Affects Heterochromatin Organization, Sister Chromatid Cohesion and the Response to DNA Damage in Meier-Gorlin Syndrome

  Author(s): Meryem Alagoz

  Abstract | Full-Text |   PDF

• Journal of Biomedical Sciences

  Is Heterogeneity in the Nature of the Mutation?

  Author(s): Michailovna Bilal *

  Abstract | Full-Text |   PDF

• Journal of Healthcare Communications

  Sensing the Smell of Beginning of Cytokine Storm: A Report on Study of Early Markers of the Complications

  Author(s): Niyati Bakhtar, Nikhil Bakhtar, Kirit Pandey and Neha Bakhtar (Pandey)

  Abstract | Full-Text |   PDF

• Journal of Genomics & Gene Study

  Molecular Characterization of Families Affected With Autosomal Recessive Primary Microcephaly.

  Author(s): Sarah Sabir

  Abstract |   PDF

• Journal of Genomics & Gene Study

  Genetic Markers Associated With Inflammatory Bowel Disease - Detection of NODI, 2 Mutations In Inflammatory Bowel Disease Among Sudanese Patients

  Author(s): Asmaa Al-Fadil Hassan Khalifa

  Abstract |   PDF

• Journal of Rare Disorders: Diagnosis & Therapy

  Pulmonary Manifestations and the Effectiveness of Enzyme replacement in Fabry Disease with the p.R227X Mutation

  Author(s): Päivi Pietilä-Effati^1*,  Johan Söderström² , Jukka T. Saarinen³, Eliisa Löyttyniemi⁴, Ilkka Kantola⁵

  Abstract | Full-Text |   PDF

• Journal of Stem Cell Biology and Transplantation

  Evaluation of anti-aging effects of vitamins in Drosophila

  Author(s): Kirtypal Singh

  Abstract |   PDF

• Journal of Pharmacy and Pharmaceutical Research

  The Association of Endoplasmic Reticulum Stress Response and Clearance Pathways with Trafficking Deficiency of HERG Mutation and Pharmacological Rescue

  Author(s): Lian JF

  Abstract |   PDF

• Journal of Neurology and Neuroscience

  A new rare homozygous mutation in the POLR3A gene causes ataxo-spasmodic leukodystrophy

  Author(s): Ouardia Belarbi 1, Hakim Si Ahmed 1, Smail Daoudi 1, Pierre Labauge 2, Carra Dallier Clarisse 2,
  Schmitt Perrine 2, Sanchez Pauline 2, Séverine Drunate 3, Hélène Cavé3

  Abstract | Full-Text |   PDF

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