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Molecular differences in the KRAS gene mutation between a primary tumor and related metastatic sites - case report and a literature review.

Author(s): Ewa Anna Kosakowska | Rafał Stec | Radosław Charkiewicz | Marta Skoczek | Lech Chyczewski
The evaluation of human papillomavirus and p53 gene mutation in benign and malignant conjunctiva and eyelid lesions.

Author(s): Reszec Joanna | Zalewska Renata | Pepiński Witold | Skawronska Małgorzata | Piotr Bernaczyk | Lech Chyczewski
MANAGEMENT OF HYPERLIPIDAEMIA (MEDO ROGA) IN AYURVEDA – A REVIEW

Author(s): Ketharaju V.Ramsubba Rao | M.Laxmu Naidu
Translational Medicine and Reliability of Single-Nucleotide Polymorphism Studies: Can We Believe in SNP Reports or Not?

Author(s): Antonis Valachis, Davide Mauri, Christodoulos Neophytou, Nikolaos P. Polyzos, Lampriani Tsali, Antonios Garras, Evangelos G. Papanikolau
Cellular functions of p53 and p53 gene family members p63 and p73

Author(s): Nadir Koçak | İbrahim Halil Yıldırım | Seval Cing Yıldırım
The Frequency of Epidermal Growth Factor Receptor Mutation of Nonsmall Cell Lung Cancer according to the Underlying Pulmonary Diseases

Author(s): Kazuhiro Usui | Tomonori Ushijima | Yoshiaki Tanaka | Chiharu Tanai | Hiromichi Noda | Norifumi Abe | Hajime Horiuchi | Teruo Ishihara
Allografting for Bosutinib, Imatinib, Nilotinib, Dasatinib, and Interferon Resistant Chronic Myeloid Leukemia without ABL Kinase Mutation

Author(s): B. Uz | O. Bektas | E. Eliacık | H. Goker | Y. Erbilgin | M. Sayitoglu | N. Sayinalp | S. Aksu | Y. Buyukasik | O. Ozcebe | I. C. Haznedaroglu
Congenital Central Hypothyroidism due to a Homozygous Mutation in the TSHβ Subunit Gene

Author(s): Sarah Catharina Grünert | Miriam Schmidts | Joachim Pohlenz | Matthias Volkmar Kopp | Markus Uhl | Karl Otfried Schwab
The Novel CFTR Mutation A457P in a Male with a Delayed Diagnosis of Cystic Fibrosis

Author(s): Kate H. Cole | Patrick R. Sosnay | Lonny B. Yarmus | Jonathan B. Zuckerman
Molecular Basis of Medullary Thyroid Carcinoma: The Role of RET Polymorphisms

Author(s): Lucieli Ceolin | Débora R. Siqueira | Mírian Romitti | Carla V. Ferreira | Ana Luiza Maia
No association of GSTM1 null polymorphism with endometriosis in women from central and southern Iran

Author(s): Seyed Morteza Seifati | Kazem Parivar | Abbas Aflatoonian | Razieh Dehghani Firouzabadi | Mohammad Hasan Sheikhha
Evaluation the frequency of factor V Leiden mutation in pregnant women with preeclampsia syndrome in an Iranian population

Author(s): Samieh Karimi | Majid Yavarian | Azadeh Azinfar | Minoo Rajaei | Maryam Azizi Kootenaee
The influence of NMDA receptor 2B subunit (GRIN2B) on cortical electrical oscillation

Author(s): Tien-Wen Lee | Younger W-Y Yu | Chen-Jee Hong | Shih-Jen Tsai | Hung-Chi Wu | Tai-Jui Chen
SWINE FLU - A DESCRIPTIVE REVIEW

Author(s): Nain Parminder | Malik Manisha | Kumar Sunil | Nain Jaspreet
Multiplex-PCR generates false positives in detection of the BRCA1 185delAG recurrent mutation

Author(s): Lucian Negura | Vlad Artenie | Eugen Carasievici | Anca Negura
Neurofibromatosis type 1 molecular testing and clinical presentation of two cases

Author(s): Crsitina Gug | Andrei Anghel | Liviu Tamas | Edward Seclman | Patrick Willems
Evaluation of JAK2V617F mutation prevalence in myeloproliferative neoplasm by AS-RT-PCR

Author(s): Karimzadeh .P | Ghaffari.SH | Chahardouli.B | Zaghal.A | Einollahi.N | Mousavi.SA | Bahar.B | Dargahi.H | Alimoghaddam.K | Ghavamzadeh.A | Togheh.GR | Nadali.F
Mitochondrial DNA Mutation and Oxidative Stress

Author(s): Taeho Kim | Hans H. Kim | Hyun Joo
Accessing and Evaluating AspectJ based Mutation Testing Tools

Author(s): Mayank Singh | Shailendra Mishra | Rajib Mall
Pioneer: A New Tool for Coding of Multi-Level FiniteState Machines Based on Evolution Programming

Author(s): S. Muddappa | R. Z. Makki | Z. Michalewicz | S. Isukapalli
Characterization of porcine β-casein G allele (CSN2G)

Author(s): Mihai Şuteu | Augustin Vlaic | Robert Renaville
Screening of C‐kit gene Mutation in Acute Myeloid Leukaemia in Northern India

Author(s): Hussain SR | Raza ST | Babu SG | Singh P | Naqvi H | Mahdi F
Monodisperse 130 kDa and 260 kDa Recombinant Human Hemoglobin Polymers as Scaffolds for Protein Engineering of Hemoglobin-Based Oxygen Carriers

Author(s): David A. Marquardt | Michael P. Doyle | Jeffrey S. Davidson | Janet K. Epp | Jacqueline F. Aitken | Douglas D. Lemon | Spencer J. Anthony-Cahill
Improvement of Thermal Stability via Outer-Loop Ion Pair Interaction of Mutated T1 Lipase from Geobacillus zalihae Strain T1

Author(s): Rudzanna Ruslan | Raja Noor Zaliha Raja Abd. Rahman | Thean Chor Leow | Mohd Shukuri Mohamad Ali | Mahiran Basri | Abu Bakar Salleh
Mitochondrial DNA mutations in gynecological cancers

Author(s): Kinga Księżakowska | Anna Nowińska-Serwach | Jacek R. Wilczyński
Novel SCN5A mutation associated with idiopathic ventricular fibrillation due to subclinical Brugada syndrome

Author(s): Juan Jiménez-Jáimez | Miguel Álvarez-López | Luis Tercedor-Sánchez | Pablo Santiago | Maria Algarra | Rocio Peñas | Francisca Valverde | Rafael Melgares-Moreno
Community Detection via Improved Genetic Algorithm in Complex Network

Author(s): Shangguang Wang | Hua Zou | Qibo Sun | Xilu Zhu | Fangchun Yang
Impact of HIV subtype on response and resistance in antiretroviral-naïve adults comparing treatment with once daily versus twice daily ritonavir boosted fosamprenavir in combination with Abacavir/Lamivudine

Author(s): Lisa L. Ross | Marjorie D. Robinson | Giampiero Carosi | Adriano Lazzarin | Hans-Juergen Stellbrink | Graeme Moyle | Naomi Givens | William G. Nichols
Prevalence of Dihydrofolate reductase gene mutations in Plasmodium falciparum isolate from pregnant women in Nigeria

Author(s): Olusola Ojurongbe | Bukola D. Tijani | Adegboyega A. Fawole | Oluwaseyi A. Adeyeba | Juergen F. Kun
A rare case of coinheritance of Hemoglobin H disease and sickle cell trait combined with severe iron deficiency

Author(s): Michael Medinger | Elisabeth Saller | Cornelis L. Harteveld | Thomas Lehmann | Lukas Graf | Alicia Rovo | Andreas Buser | Jakob Passweg | André Tichelli
Polyploid induction of Allium ascalonicum L. by colchicine

Author(s): SUMINAH | SUTARNO | AHMAD DWI SETYAWAN
A rare case of an aldosterone secreting metastatic adrenocortical carcinoma and papillary thyroid carcinoma in a 31-year-old male

Author(s): Stephen M. Wanta | Marina Basina | Steven D. Chang | Daniel T. Chang | James M. Ford | Ralph Greco | Kerry Kingham | Robert E. Merritt | Pamela L. Kunz
JAK2-V617F Mutation Combined with Philadelphia Chromosome-Positive Chronic Myeloid Leukaemia: a Case Report

Author(s): Mehrdad Payande | Mohammad Erfan Zare | Saber Ghanbari Haji Shure | Farhad Shaveisi Zadeh
Evaluation of Common Genetic Disorders in Myeloproliferative Neoplasms

Author(s): Mehrdad Payandeh | Farhad Shaveisi Zadeh | Mohammad Erfan Zare | Kamran Mansouri | Reza Khodarahmi | Saeed Alimoradi | Hoshang Yousefi | Fatemeh Darabi
CFTR F508del mutation and 5T allele in patients with chronic pancreatitis and pancreatic adenocarcinoma

Author(s): Nikolić Aleksandra | Dinić Jelena | Radojković Dragica | Lukić Snežana | Popović Dragan | Uglješić Milenko | Knežević Srboljub
The expression of p53, Rb, and c-myc protein in cervical cancer by immunohistochemistry stain

Author(s): ADI PRAYITNO | RUBEN DARMAWAN | ISTAR YULIADI | AMBAR MUDIGDO
Molecular Diagnostic and Pathogenesis of Hereditary Hemochromatosis

Author(s): Paulo C. J. L. Santos | Jose E. Krieger | Alexandre C. Pereira
"Osteogenesis Imperfecta: Report of a new pedigree in Iran "

Author(s): "Farhoud D | Mohammadi Asl J | Derakhshandeh P "
Detection of RET Proto-oncogene Cys634Arg Mutation, the Cause of Medullary Thyroid Carcinoma, in an Iranian Child

Author(s): Ehsan Alvandi |  Mehrdad Pedram | Ahmad-Reza Soroush |  Babak Noori Naier |  Seyed Mohammad Akrami
Cardiac and Renal Malformations in a Patient with Sepsis and Severe Congenital Neutropenia

Author(s): Aziz Eghbali | Peyman Eshghi | Fatemeh Malek | Nima Rezaei
Ehlers-Danlos Syndrome Type VI in a 17-Year-Old Iranian Boy with Severe Muscular Weakness – A Diagnostic Challenge?

Author(s): Ariana Kariminejad | Bita Bozorgmehr | Ali-Reza Khatami | Mohamad-Hasan Kariminejad | Cecilia Giunta | Beat Steinmann
Detecting Common CFTR Mutations by Reverse Dot Blot Hybridization Method in Cystic Fibrosis; First Report from Northern Iran

Author(s): Mohammad-Reza Dooki Esmaeili | Haleh Akhavan-Niaki | Ali Juibary Ghabeli
A Case of Henoch-Schönlein Purpura with P369S Mutation in MEFV Gene

Author(s): Pelin Ertan | Gökhan Tekin | Gülseren Evirgen Şahin | Fatma Taneli | Ali-Riza Kandioğlu | Betül Sözeri
Studies on potential mutagenic and genotoxic activity of Setarud

Author(s): HR Khorram Khorshid | Y.A Novitsky | M Abdollahi | M.H Shahhosseiny | B Sadeghi | H Madani | R Rahimi | B Farzamfar
Evaluation of human leukocyte antigens in Papillon Lefevre Syndrome

Author(s): Lotf Azar M. | Gharesi Fard B. | Fargadian Sh.
Papillon Lefevre Syndrome

Author(s): Lotfazar M.
The Spectrum of β -thalassemia Mutations in Isfahan Province of Iran

Author(s): P Derakhshandeh-Peykar | H Hourfar | M Heidari | M Kheirollahi | M Miryounesi
Microglia in Gemistocytic Astrocytomas

Author(s): F Geranmayeh | BW Scheithauer | MB Graeber
Stat1 Expression is an Independent Indicator of Prognosis in Lymph node Positive Breast Carcinomas

Author(s): Z Madjd | A Al -Atta | NFS Watson | I Spendlove | I Ellis | LG Durrant
Molecular Biology of Hepatitis C Virus: Interactions with the IFN-Betta Signalling Pathway

Author(s): M Sabourighannad | C McCormick | A MacDonald | D Rowlands | M Harris
Non-cell autonomous influence of the astrocyte system xc− on hypoglycaemic neuronal cell death

Author(s): Nicole A Jackman | Shannon E Melchior | James A Hewett | Sandra J Hewett
Induced mutations by gamma ray irradiation to Argomulyo soybean (Glycine max) variety

Author(s): DIANA SOFIA HANAFIAH | TRIKOESOEMANINGTYAS | SUDIRMAN YAHYA | DESTA WIRNAS
MULTICLASS CLASSIFIER DESIGNED USING STEPWISE CROSSOVER AND SPECIAL MUTATION TECHNIQUE

Author(s): Pankaj Patidar | Bhupendra Verma | Arpit Bhardwaj
The mTOR Signalling Pathway in Human Cancer

Author(s): Helena Pópulo | José Manuel Lopes | Paula Soares
Comparison of Hubs in Effective Normal and Tumor Protein Interaction Networks

Author(s): Mitra Mirzarezaee | Babak N. Araabi | Mehdi Sadeghi
Optimal Control of Gene Mutation in DNA Replication

Author(s): Juanyi Yu | Jr-Shin Li | Tzyh-Jong Tarn
Genetic Basis for Diagnosis of Novel Mutation of LDL Receptor Gene

Author(s): Samia Perwaiz Khan | Rubina Ghani | Khwaja Zafar Ahmed | Zia Yaqub
Improved Citric Acid Production by Radiation Mutant Aspergillus niger Using Sugarcane Bagasse Extract

Author(s): Abdullah-Al-Mahin | A.B.M. Sharifuzzaman | M.O. Faruk | M.A. Kader | J. Alam | R. Begum | Harun-Or-Rashid
DISTRIBUTION OF PFCRT HAPLOTYPES AND IN-VIVO EFFICACY OF CHLOROQUINE IN TREATMENT OF UNCOMPLICATED P. FALCIPARUM MALARIA BEFORE DEPLOYMENT OF ARTEMISININ COMBINATION THERAPIES IN URBAN POPULATION OF KOLKATA, INDIA

Author(s): PABITRA SAHA, SHRABANEE MULLICK, SUBHASISH K. GUHA, SONALI DAS, SWAGATA GANGULY, MITALI CHATTERJEE, ASIT BISWAS, DILIP K. BERA, ABHIRAM CHAKRAVORTY, BASUDEB MUKHERJEE, MADHUSUDAN DAS , PRATIP K. KUNDU, KRISHNANGSHU RAY ARDHENDU K. MAJI
Efficacy of imatinib dose escalation in Chinese gastrointestinal stromal tumor patients

Author(s): Jian Li | Ji-Fang Gong | Jie Li | Jing Gao | Nai-Ping Sun | Lin Shen
PROGNOSTIC SIGNIFICANCE OF NRAS GENE MUTATIONS IN CHILDREN WITH ACUTE MYELOGENOUS LEUKEMIA

Author(s): Rabab Aly | Mohamed R. El-sharnoby | Adel A. Hagag
ACUTE PROMYELOCYTIC LEUKEMIA: AN EXPERIENCE ON 95 GREEK PATIENTS TREATED IN THE ALL-TRANS-RETINOIC ACID ERA

Author(s): Maria Pagoni | Maria Garofalaki | Fotios Panitsas | Kalliopi Manola | Katerina Psarra | Panagiotis Economopoulos
Using PCR-SSCP for detecting polymorphism 1843 in the ryanodine receptor gene

Author(s): Susan L. Castro-Molina | Manuel F. Ariza-Botero | Marcela Ríos-Rodriguez | Diana J. Moreno | Germán H. Guerrero-Castillo
Germline mutation analysis of MLH1 and MSH2 in Malaysian Lynch syndrome patients

Author(s): Mohd Nizam Zahary | Gurjeet Kaur | Muhammad Radzi Abu Hassan | Harjinder Singh | Venkatesh R Naik | Ravindran Ankathil
A case of Cowden syndrome diagnosed from multiple gastric polyposis

Author(s): Minsu Ha | Jun Won Chung | Ki Baik Hahm | Yoon Jae Kim | Woochang Lee | Jungsuk An | Dong Kyu Kim | Myeong Gun Kim
Description and interpretation of various SNPs identified by BRCA2 gene sequencing

Author(s): Anca Negura | Nancy Uhrhammer | Yves-Jean Bignon | Lucian Negura
Comparative Studies of the (Anti) Mutagenicity of Baccharis dracunculifolia and Artepillin C by the Bacterial Reverse Mutation Test

Author(s): Flávia Aparecida Resende | Carla Carolina Munari | Moacir de Azevedo Bentes Monteiro Neto | Denise Crispim Tavares | Jairo Kenupp Bastos | Ademar Alves da Silva Filho | Eliana Aparecida Varanda
Searching for Tourette’s syndrome gene. Part 2. Patient’s genome variability

Author(s): Anna Kowalska | Alina T. Midro | Piotr Janik | Anna Gogol | Wojciech Służewski | Andrzej Rajewski
Relationship Between Fluoroquinolone Resistance and gyrA, parC Gene in Streptococcus suis Type 2 Isolates in Hebei Province China

Author(s): Ping Rui | Zengjun Ma | QiuYue Wang | Hai Fang | JianHua Wu | ZhiXin Fu | Qing Hui Jia | Xuexia Wen
Cloning and Sequence Analysis of Donkey Growth Hormone Gene

Author(s): Wenjin Zhu | Yongmei Su | Jianhua Wu
Detection of the Major Macrolide Resistance Genes in Streptococcus suis Serotype 2 Isolates in Hebei Province China

Author(s): Ping Rui | PeiGuo Li | Zengjun Ma | QinYe Song | CaiRan Yang | Ping Shen | SuMin Pan | Yufang Guo
Ruxolitinib for the treatment of myelofibrosis: its clinical potential

Author(s): Ostojic A | Vrhovac R | Verstovsek S
Clinical significance of factor V G1691A- and prothrombin G20210A-mutations in cerebral infarction and patent foramen ovale

Author(s): Bernhard Stephan | Joachim-Friedrich Schenk | Aida Beye | Gerhard Pindur
Role of Genetic Changes in the Progression of Cardiovascular Diseases

Author(s): S. A. Sheweita | H. Baghdadi | A. R. Allam
Interaction of haptoglobin with hemoglobin octamers based on the mutation αAsn78Cys or βGly83Cys

Author(s): Corinne Vasseur | Shoucheng Du | Elisa Domingues-Hamdi | Véronique Baudin-Creuza | Chien Ho | Regina Kettering | Michael C. Marden | Thomas Brillet | Joanne I. Yeh | Nancy T. Ho | Tong-Jian Shen
Novel variants in the hepatocyte nuclear factor-1-alpha gene in MODY and early onset NIDDM: Evidence for a mutational hotspot in exon 5

Author(s): Suman Kalyan Paine | Surajita Banerjee | Basudev Bhattacharya | Subhankar Chowdhury | Aditi Sen | Chaitry Ghosal | Kaushik Pandit | Shuvodip Chowdhury
Effects of Serum from a Fibrodysplasia Ossificans Progressiva Patient on Osteoblastic Cells

Author(s): Toshitsugu Sugimoto | Hiroshi Kaji | Takenobu Katagiri | Itoko Hisa | Akira Kawara
A New Method for Fastening the Convergence of Immune Algorithms Using an Adaptive Mutation Approach

Author(s): Nabil Sabor | Ahmad F. Al-Ajlouni | Mohammed Abo-Zahhad | Sabah M. Ahmed
Novel variants in the hepatocyte nuclear factor-1-alpha gene in MODY and early onset NIDDM: Evidence for a mutational hotspot in exon 5

Author(s): Suman Kalyan Paine | Surajita Banerjee | Basudev Bhattacharya | Subhankar Chowdhury | Aditi Sen | Chaitry Ghosal | Kaushik Pandit | Shuvodip Chowdhury
Effects of Serum from a Fibrodysplasia Ossificans Progressiva Patient on Osteoblastic Cells

Author(s): Toshitsugu Sugimoto | Hiroshi Kaji | Takenobu Katagiri | Itoko Hisa | Akira Kawara
A New Method for Fastening the Convergence of Immune Algorithms Using an Adaptive Mutation Approach

Author(s): Nabil Sabor | Ahmad F. Al-Ajlouni | Mohammed Abo-Zahhad | Sabah M. Ahmed
In vitro anti-mycobacterial activity of (E)-N´-(monosubstituted-benzylidene) isonicotinohydrazide derivatives against isoniazid-resistant strains

Author(s): Tatiane S. Coelho | Jessica B. Cantos | Marcelle L.F. Bispo | Raoni S.B. Gonçalves | Camilo H.S. Lima | Pedro E.A. da Silva | Marcus De Souza
Identification of c.483C>T polymorphism in the caprine tyrosinase-related protein 1 (TYRP1) gene

Author(s): Bouabid Badaoui | Arianna Manunza | Mariasilvia D'Andrea | Fabio Pilla | Juan Capote | Jordi Jordana | Ainhoa Ferrando | Amparo Martínez | Juan V. Delgado | Vincenzo Landi | Mariano Gómez | Agueda L. Pons Barro | Mabrouk El Ouni | Oriol Vidal | Marcel Amills
Study for identification FecXI and FecXH mutations in Tunisian Barbarine sheep

Author(s): Jemmali Borni, | Bedhiaf Sonia | Djemali M. Naouer
Effect Of Polygamy With Selection In Genetic Algorithms

Author(s): Rakesh Kumar | Jyotishree
PTEN - Somatic mutations causing cancer: Cancer Genome Sequence Analysis

Author(s): Rashmi K. Ambasta*,$, Ira Dave* and Pravir Kumar*,#
The occurrence and contribution of germline BRCA1/2 sequence alterations in Iranian patients with breast cancer

Author(s): Keshavarzi F | Nafissi N | Sirati F | Fallah MS | Salehi R | Harriry Z | Shahab Movahead Z | Vahidi M | Sharifi Z | Sharafi Farzad M | Zeinali S
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