Search results for mutation

Page 41 of 62

• Journal of Clinical & Experimental Nephrology

  Hereditary Angioedema Type 1 and Serious Vascular Lesions Associated with Segmental and Focal Hyalinosis: Is there a Causal Connection?

  Author(s): Gueye Serigne, Kane Yaya, Dahri Souad, Kounde Clement, Soumeila Illiassou, Dridat Meryem, Ged Etienne, Asma Allal, Delas Audrey, Sidi Aly (Ould Mohamed) A and Rostaing Lionel

  Abstract | Full-Text |   PDF

• Journal of Dental and Craniofacial Research

  Association of TGFβ3 variants with Nonsyndromic Cleft Lip and Palate in Guatemalan Population.

  Author(s): Alia Said Aljabeiti, Reem Salahuddin, Miroslav Tolar, Marie M Tolarova

  Abstract | Full-Text |   PDF

• Journal of Autoimmune Disorders

  Pathogenic Participation of MuSK-Biglycan Linkage Contributive to Synaptic Stability and Signalings in Myasthenia Gravis

  Author(s): Masaharu Takamori*

  Abstract | Full-Text |   PDF

• Journal of Genetic Disorders

  Editor's Note (J Genet Disord)

  Author(s): Zina MA Alshami

  Abstract | Full-Text |   PDF

• Journal of Neurology and Neuroscience

  Pathogenic Mechanisms of the Prion Protein Gene Mutations: A Review and Speculative Hypotheses for Pathogenic Potential of the Pro39Leu Mutation in the Associated FTD-Like Phenotype

  Author(s): Livia Bernardi, Chiara Cupidi and Amalia C Bruni

  Abstract | Full-Text |   PDF

• Journal of Neoplasm

  The Role of BRCA1 and BRCA2 Genes in the Appearance of Pediatric and Adolescent Disorders

  Author(s): Ioannis Drikos, Alexandros Sachinidis, Ioanna Vassi4, Effrossyni Boutou

  Abstract | Full-Text |   PDF

• Journal of Clinical Epigenetics

  The “Master Code of DNA”: Towards the Discovery of the SNPs Function (Single-Nucleotide Polymorphism)

  Author(s): Jean-Claude Perez

  Abstract | Full-Text |   PDF

• European Journal of Experimental Biology

  Single Nucleotide Polymorphism (SNPs) in the Genes Associated with Tooth Agenesis

  Author(s): Mohammad Shahid, Joshi S, Nasser R Alqhtani, Mohammed AlSaidan, Khaled Aldossari, Abdulwahab Ali Abuderman, Mannaa Aldowsar, Sameer Al-Ghamdi, Hanan A Balto, Nouf Al-Hammad, Sandeep Agrawal, Altaf H Shah, Arif Ahmed, Varinderpal S. Dhillon

  Abstract | Full-Text |   PDF

• Journal of Molecular Biology and Biotechnology

  Mutations of a Single Glycine in Vc-NhaP2, a Cation-Proton Antiporter in Vibrio cholerae, Confer the Ability to Exchange Li+ for H+

  Author(s): Carla B Schubiger, Muntahi Mourin, Craig T Resch, Pavel Dibrov and Claudia C Häse

  Abstract | Full-Text |   PDF

• Cellular & Molecular Medicine: Open access

  Identification of Genetic Diseases Using Breast Milk Cell Analysis: The Case of Transient Neonatal Zinc Deficiency (TNZD)

  Author(s): Yarden Golan, Baruch Yerushalmi, Edna Efrati, Yehuda G Assaraf

  Abstract | Full-Text |   PDF

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