KRAS Mutation - Articles - Scientific Research Publishing

Mutation pattern in human adrenoleukodystrophy protein in terms of amino-acid pair predictability (Articles)

Shao-Min Yan, Guang Wu

Journal of Biomedical Science and Engineering Vol.3 No.3，April 8, 2010

DOI: 10.4236/jbise.2010.33035 5,465 Downloads 8,980 Views Citations
Fungicide tolerance of Trichoderma asperelloides and T. harzianum strains (Articles)

Adriana Paola Chaparro, Lilliana Hoyos Carvajal, Sergio Orduz

Agricultural Sciences Vol.2 No.3，August 8, 2011

DOI: 10.4236/as.2011.23040 8,462 Downloads 16,255 Views Citations
Build mutant and build homology protein structure predictions for indonesian avian influenza neuraminidase (Articles)

Sigit Jaya Herlambang, Rosari Saleh

Journal of Biophysical Chemistry Vol.3 No.2，May 29, 2012

DOI: 10.4236/jbpc.2012.32020 5,421 Downloads 9,646 Views Citations
JAK2 Mutations in Chronic Myeloproliferative Neoplasm; Towards the Application of Personalized Treatments for Saudi Patients (Articles)

Mamdooh Gari, Fatin Al-Sayes, Farid Ahmed, Abdul Ali Peerzada, Adel Abuzenadah, Lubna S. Mira, Mohammed Al-Qahtani, Ashraf Dallol, Adeel Chaudhary, Mohammed Mahnashi, Ghazi Damanhouri

Open Journal of Blood Diseases Vol.2 No.2，June 25, 2012

DOI: 10.4236/ojbd.2012.22004 6,283 Downloads 12,260 Views Citations
Interaction of nonsense suppressor tRNAs and codon nonsense mutations or termination codons (Articles)

Zixian Lu

Advances in Biological Chemistry Vol.2 No.3，August 23, 2012

DOI: 10.4236/abc.2012.23038 10,132 Downloads 15,554 Views Citations
Mutation Status of KRAS, BRAF, PIK3CA and Expression Level of AREG and EREG Identify Responders to Cetuximab in a Large Panel of Patient Derived Colorectal Carcinoma Xenografts of All Four UICC Stages (Articles)

Paulina Pechańska, M. Becker, T. Mayr, B. Hinzmann, H.-P. Adams, I. Klaman, K.-H. Kretschmar, K. Kretschmar, K. Stecker, R. Mantke, R. Pauli, J. Pertschy, K. Hertel, K. Ridwelski, K. Hellwig, M. Pross, C. Radke, I. Fichtner, J. Hoffmann, A. Rosenthal

Journal of Cancer Therapy Vol.4 No.2，April 26, 2013

DOI: 10.4236/jct.2013.42083 5,031 Downloads 7,633 Views Citations
The Relationship between Mouth Squamous Cell Carcinoma (MSCC) with HPV Infection and the Presence of p53 & c-myc Mutation (Articles)

Adi Prayitno, Elyana Asnar, Suhartono Taat Putra

Journal of Cancer Therapy Vol.4 No.5，June 28, 2013

DOI: 10.4236/jct.2013.45105 3,632 Downloads 5,779 Views Citations
Better Selection Model for EML4-ALK Fusion Gene Test in Patients with Non-Small-Cell Lung Cancer (Articles)

Dekel Shlomi, Amir Onn, Maya Gottfried, Jair Bar, Haim Biran, Maya Ilouze, Addie Dvir, Hovav Nechushtan, Lior Soussan-Gutman, Nir Peled

Journal of Cancer Therapy Vol.4 No.8A，September 3, 2013

DOI: 10.4236/jct.2013.48A009 3,900 Downloads 6,082 Views Citations
This article belongs to the Special Issue on Advances in lung Cancer and Treatment Research
Cleidocranial dysplasia with a rare mutation: Study of a family with review of literature (Articles)

Ahmet Ercan Sekerci, Burhan Balta, Oğuzhan Bahadir, Yildiray Sisman, Munis Dundar, Turgut Tursem Tokmak, Stefan Mundlos

Open Journal of Stomatology Vol.3 No.8，November 15, 2013

DOI: 10.4236/ojst.2013.38068 3,867 Downloads 5,602 Views Citations
Clinical Pathological Correlation Quiz: A 7-Month-Old Girl with Congenital Neutropenia and Increased Bone Morrow “Blasts” (Articles)

Ruchika Sharma, Jessica A. Hemminger, Samir B. Kahwash

Open Journal of Pathology Vol.4 No.1，January 7, 2014

DOI: 10.4236/ojpathology.2014.41001 4,337 Downloads 7,134 Views Citations
A Research of Pachyonychia Congenita Type 1 and Literature Analysis (Articles)

Kun Guo, Shengxiang Xiao, Songmei Geng

Open Journal of Genetics Vol.4 No.1，March 5, 2014

DOI: 10.4236/ojgen.2014.41003 3,149 Downloads 4,399 Views Citations
Kilin-Klyosov TMRCA Calculator for Time Spans up to Millions of Years (Articles)

Anatole A. Klyosov, Vladimir V. Kilin

Advances in Anthropology Vol.6 No.3，August 24, 2016

DOI: 10.4236/aa.2016.63007 3,475 Downloads 6,758 Views Citations
Study of Hepatitis B Virus Genotypes and Mutation in 1762 & 1764 Nucleotides of X Gene in Chronic HBV Patients from Golestan Province—Iran (Articles)

Sareh Zhand, Ghassem Rostamian, Alijan Tabarraei, Abdolvahab Moradi

Health Vol.8 No.13，October 21, 2016

DOI: 10.4236/health.2016.813140 3,487 Downloads 4,467 Views Citations
This article belongs to the Special Issue on Exercise and Fitness
Comparison of Two Possible Evolutionary Mechanisms of the 62 tRNA Codon Sequences (Articles)

Fangping Wei, Zhenxiong Lan, Luming Shen, Bourong Liu, Yu Xue

Journal of Biomedical Science and Engineering Vol.10 No.4，April 30, 2017

DOI: 10.4236/jbise.2017.104014 1,146 Downloads 1,826 Views Citations
Exploration of Mutation and DNA Methylation of Polo-Like Kinase 1 (PLK1) in Colorectal Cancer (Articles)

Wayne Ng, Joo-Shik Shin, Bin Wang, Cheok Soon Lee

Open Journal of Pathology Vol.7 No.3，July 19, 2017

DOI: 10.4236/ojpathology.2017.73005 1,187 Downloads 2,473 Views Citations
Common Prothrombotic Gene Mutations in Cerebral Venous Sinus Thrombosis in North-West of Iran (Articles)

Elyar Sadeghi-Hokmabadi, Ebrahim Sakhinia, Mehdi Farhoudi, Somayyeh Hasaneh, Morteza Ghojazadeh, Mohammad Amin Farzi, Sasan Andalib, Masoumeh Nemati, Omid Abbaszadeh, Reza Rikhtegar, Reshad Mirnour

Neuroscience and Medicine Vol.8 No.4，December 4, 2017

DOI: 10.4236/nm.2017.84009 1,099 Downloads 2,533 Views Citations
Conditional Mutations in Drosophila: Concept of Genes That Control Individual Development (Articles)

Boris F. Chadov, Eugenia V. Chadova, Nina B. Fedorova

Advances in Bioscience and Biotechnology Vol.9 No.6，June 19, 2018

DOI: 10.4236/abb.2018.96017 1,134 Downloads 3,722 Views Citations
Study of Radio-Sensitivity of Strawberry Runners cv. Fortuna under Moroccan Conditions (Articles)

Aicha El Oualkadi, Mohammed Mouhib, Badr Hajjaj

American Journal of Plant Sciences Vol.10 No.10，October 31, 2019

DOI: 10.4236/ajps.2019.1010135 747 Downloads 1,589 Views Citations
Prediction of Mutations in H7 Hemagglutinins from Influenza A Virus (Articles)

Shaomin Yan, Guang Wu

Journal of Biomedical Science and Engineering Vol.13 No.8，August 13, 2020

DOI: 10.4236/jbise.2020.138017 577 Downloads 1,456 Views Citations
Severe Wolfram Syndrome Caused by a Novel Frameshift Mutation in WFS1 Gene: Effect on the WFS1/CaM Interaction and Phenotype-Genotype Correlation (Articles)

Mouna Tabebi, Rahma Felhi, Houcem Elomma Mrabet, Wajdi Safi, Baha Zantour, Mohamed Habib Sfar, Mohammed Abid, Mouna Mnif Feki, Faiza Fakhfakh

Open Journal of Genetics Vol.11 No.4，November 25, 2021

DOI: 10.4236/ojgen.2021.114008 278 Downloads 1,680 Views Citations

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