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Author(s): Targino, María das Graças
Facilitated Cross-Bridge Interactions with Thin Filaments by Familial Hypertrophic Cardiomyopathy Mutations in α-Tropomyosin

Author(s): Fang Wang | Nicolas M. Brunet | Justin R. Grubich | Ewa A. Bienkiewicz | Thomas M. Asbury | Lisa A. Compton | Goran Mihajlović | Victor F. Miller | P. Bryant Chase
Hepatitis B and Hepatitis C Infection Biomarkers and TP53 Mutations in Hepatocellular Carcinomas from Colombia

Author(s): Maria-Cristina Navas | Iris Suarez | Andrea Carreño | Diego Uribe | Wilson Alfredo Rios | Fabian Cortes-Mancera | Ghyslaine Martel | Beatriz Vieco | Diana Lozano | Carlos Jimenez | Doriane Gouas | German Osorio | Sergio Hoyos | Juan Carlos Restrepo | Gonzalo Correa | Sergio Jaramillo | Rocio Lopez | Luis Eduardo Bravo | Maria Patricia Arbelaez | Jean-Yves Scoazec | Behnoush Abedi-Ardekani | Regina M. Santella | Isabelle Chemin | Pierre Hainaut
Clinical Application of Screening for GJB2 Mutations before Cochlear Implantation in a Heterogeneous Population with High Rate of Autosomal Recessive Nonsyndromic Hearing Loss

Author(s): Masoud Motasaddi Zarandy | Mersedeh Rohanizadegan | Hojjat Salmasian | Nooshin Nikzad | Niloofar Bazazzadegan | Mahdi Malekpour
Novel Heterogenous CHS1 Mutations Identified in Five Japanese Patients with Chediak-Higashi Syndrome

Author(s): Fuminori Tanabe | Hirotake Kasai | Michiko Morimoto | Shigeharu Oh | Hidetoshi Takada | Toshiro Hara | Masahiko Ito
Somatic Mutations During an Immune Response inXenopus Tadpoles

Author(s): Melanie Wilson | Anne Marcuz | Louis Du Pasquier
IPEX as a Result of Mutations in FOXP3

Author(s): Hans J. J. van der Vliet | Edward E. Nieuwenhuis
MÉTHODOLOGIE ACTUELLE DE LA BIOLOGIE MOLÉCULAIRE POUR LA DÉTECTION DES MUTATIONS

Author(s): Lucian Negura | Eugen Carasievici | Anca Mihaela Huma | Vlad Artenie
JOURNALISM AS A RESEARCH FIELD

Author(s): Muniz Sodré
EXPRESSION OF CYCLIN D1 AND KI-67 IN ENDOMETRIAL HYPERPLASIAS AND CARCINOMAS

Author(s): Raluca Balan | Cornelia Amalinei | Eduard Crauciuc | Draga-Irina Caruntu | Vlad Gheorghita | Ovidiu Toma
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
P53 gene snp investigation in squamous cell oesophageal carcinom

Author(s): Catalina Luca | Laura Buburuzan | Dragos Romanescu | Codrut Stanescu | Simona Dima | Irinel Popescu | Vladimir Botnarius | Marieta Costache
Mitochondrial DNA Mutation and Oxidative Stress

Author(s): Taeho Kim | Hans H. Kim | Hyun Joo
A Cohort Study of p53 Mutations and Protein Accumulation in Benign Breast Tissue and Subsequent Breast Cancer Risk

Author(s): Geoffrey C. Kabat | Rita A. Kandel | Andrew G. Glass | Joan G. Jones | Neal Olson | Catherine Duggan | Mindy Ginsberg | Abdissa Negassa | Thomas E. Rohan
Optimization of heteroduplex analysis for the detection of BRCA mutations and SNPs

Author(s): Lucian Negura | Dragos Peptanariu | Anca Negura | Eugen Carasievici | Coneac Andrei | Ungureanu Eugen | Lucian Negura
Unclassified sequence variants (UVS) and genetic predisposition to cancer

Author(s): Lucian Negura | Nancy Uhrhammer | Anca Negura | Eugen Ungureanu | Eugen Carasevici | Yves-Jean Bignon
Optimization of heteroduplex analysis for the detection of BRCA mutations and SNPs

Author(s): Lucian Negura | Dragos Peptanariu | Anca Negura | Eugen Carasievici | Coneac Andrei | Ungureanu Eugen | Lucian Negura
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
Massive Proteinuria and Autosomal Dominant Polycystic Kidney Disease: a Rare Coincidence

Author(s): Shokoufeh Savaj | Mahmoud Parvin | Javad Savoj
Mitochondrial DNA mutations in gynecological cancers

Author(s): Kinga Księżakowska | Anna Nowińska-Serwach | Jacek R. Wilczyński
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
Carbonic Anhydrase IX as a target for renal cell carcinoma therapy

Author(s): Cameron Collier | Snezana Petrovic
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
Disruption of Axonal Transport in Motor Neuron Diseases

Author(s): Kensuke Ikenaka | Masahisa Katsuno | Kaori Kawai | Shinsuke Ishigaki | Fumiaki Tanaka | Gen Sobue
Assessment of Tumor Prevention in Type 1 Neurofibromatosis using a Nitroxide Compound

Author(s): Jad El-Hoss | Aaron S. Micallef | Kathryn E. Fairfull-Smith | Steven E. Bottle | David G. Little | Aaron Schindeler
The Roles of Guanine Nucleotide Binding Proteins in Health and Disease

Author(s): A.O. Ibegbu | I. Mullaney | L. Fyfe | D. MacBean
Role of ATG16L, NOD2 and IL23R in Crohn’s disease pathogenesis

Author(s): Saleh A Naser | Melissa Arce | Anam Khaja | Marlene Fernandez | Najih Naser | Sammer Elwasila | Saisathya Thanigachalam
Molecular Diagnostic and Pathogenesis of Hereditary Hemochromatosis

Author(s): Paulo C. J. L. Santos | Jose E. Krieger | Alexandre C. Pereira
Back to BAC: The Use of Infectious Clone Technologies for Viral Mutagenesis

Author(s): Robyn N. Hall | Joanne Meers | Elizabeth Fowler | Timothy Mahony
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
A Case of Megalencephalic Leukoencephalopathy with Subcortical Cysts in an Iranian Consanguineous Family

Author(s): Mahmoud-Reza Ashrafi | Ariana Kariminejad | Houman Alizadeh | Bita Bozorgmehr | Sepideh Amoeian | Mohammad-Hasan Kariminejad
Premature Loss of Permanent Teeth in Allgrove (4A) Syndrome in Two Related Families

Author(s): Zahra Razavi | Mohammad-Mehdi Taghdiri | Fatemeh Eghbalian | Nooshin Bazzazi
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
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
Molecular Pathogenesis of Desmoid Tumors

Author(s): S Amini Nik | K Van Dam | A Jadidizadeh | S Tejpa | JJ Cassiman
Induced mutations by gamma ray irradiation to Argomulyo soybean (Glycine max) variety

Author(s): DIANA SOFIA HANAFIAH | TRIKOESOEMANINGTYAS | SUDIRMAN YAHYA | DESTA WIRNAS
Genetic Diversity and Drug Resistance Mutations in HIV-1 from Untreated Patients in Niamey, Niger

Author(s): Saïdou Mamadou | Yahayé Hanki | Amadou Roufaï Ali Maazou | Balki Aoula | Sanata Diallo
Mutations in Lettuce Improvement

Author(s): Beiquan Mou
Henipavirus Mediated Membrane Fusion, Virus Entry and Targeted Therapeutics

Author(s): Deborah L. Steffen | Kai Xu | Dimitar B. Nikolov | Christopher C. Broder
Genetic Basis for Diagnosis of Novel Mutation of LDL Receptor Gene

Author(s): Samia Perwaiz Khan | Rubina Ghani | Khwaja Zafar Ahmed | Zia Yaqub
ACVR1, a Therapeutic Target of Fibrodysplasia Ossificans Progressiva, Is Negatively Regulated by miR-148a

Author(s): Hao Song | Qi Wang | Junge Wen | Shunai Liu | Xuesong Gao | Jun Cheng | Deli Zhang
A new clonal chromosomal aberration (47, XY, +21) in atrial myxoma from an elderly male patient

Author(s): Ewa Stępień | Grzegorz Grudzień | Marek Andres | Małgorzata Jakóbczyk | Dorota Czapczak | Przemysław Kapusta | Wiesław Frasik | Tomasz Myrdko | Jerzy Sadowski
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
CAUSES OF ADULT SPLANCHNIC VEIN THROMBOSIS IN THE MEDITERRANEAN AREA

Author(s): Valerio De Stefano | Tommaso Za | Angela Ciminello | Laura Betti | Elena Rossi
IVS8 Polyt and M470V Polymorphisms in Healthy Individuals and Cystic fibrosis Patients in Mazandaran Province, Iran

Author(s): Kholghi Oskooei V | Esmaeeli Douki MR | Tabaripour R | Tavakkoly Bazzaz J | Larijani B | Akhavan-Niaki H
Segmental Duplications: A Possible Mechanism of Hominid Uplift through MicroRNA Diversification

Author(s): Marla A. Endriga | Aldrich Ivan Lois D. Burog | Denise Lauren V. Dalmacion | Custer C. Deocaris
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
Regulation of melanogenesis: the role of cAMP and MITF

Author(s): Michał Otręba | Jakub Rok | Ewa Buszman | Dorota Wrześniok
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
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
Dilated cardiomyopathy (DCM) and myocarditis: Classification, clinical and autoimmune features

Author(s): Alida L. P. Caforio | Stefania Bottaro | Sabino Iliceto
Mutations modulate soluble carbohydrates composition in seeds of Lathyrus sativus L.

Author(s): Agnieszka I. Piotrowicz-Cieślak | Wojciech Rybiński | Dariusz J. Michalczyk
Role of Genetic Changes in the Progression of Cardiovascular Diseases

Author(s): S. A. Sheweita | H. Baghdadi | A. R. Allam
Gene Polymorphism of Complement Factor H in a Turkish Patient With Membranoproliferative Glomerulonephritis Type II

Author(s): Betul Sozeri | Sevgi Mir | Afig Berdeli | Nida Dincel | Banu Sarsik
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
SPT5 affects the rate of mRNA degradation and physically interacts with CCR4 but does not control mRNA deadenylation*

Author(s): Darren J. Lee | Clyde L. Denis | Palaniswamy Viswanathan | Yajun Cui | Yueh-Chin Chiang
In Vitro Investigation of DNA Damage Induced by the DNA Cross-Linking Agents Oxaliplatin and Satraplatin in Lymphocytes of Colorectal Cancer Patients

Author(s): Eduardo Cemeli | Diana Anderson | Mojgan Najafzadeh | Amal Alotaibi | Adolf Baumgartner
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
In Vitro Investigation of DNA Damage Induced by the DNA Cross-Linking Agents Oxaliplatin and Satraplatin in Lymphocytes of Colorectal Cancer Patients

Author(s): Eduardo Cemeli | Diana Anderson | Mojgan Najafzadeh | Amal Alotaibi | Adolf Baumgartner
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
Mining the Protein Data Bank to Differentiate Error from Structural Variation in Clustered Static Structures: An Examination of HIV Protease

Author(s): Balasubramanian Venkatakrishnan | Miorel-Lucian Palii | Mavis Agbandje-McKenna | Robert McKenna
A noninvasive multi-analyte diagnostic assay: combining protein and DNA markers to stratify bladder cancer patients

Author(s): Fernandez CA | Millholl | JM | Zwarthoff EC | Feldman AS | Karnes RJ | Shuber AP
Study for identification FecXI and FecXH mutations in Tunisian Barbarine sheep

Author(s): Jemmali Borni, | Bedhiaf Sonia | Djemali M. Naouer
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
Tyrosine kinase domain gene polymorphism of epidermal growth factor receptor in gastric cancer in northern Iran

Author(s): Jeivad F | Abediankenari S | Shokrzadeh M | Ghasemi M | Taghvaei T | Ansari Z | Najafi Fard M | Hassannia H | Sayiari Mazandarani M | Biranvand E
JOURNALISM AS A RESEARCH FIELD

Author(s): Muniz Sodré
Caracterización de una delta endotoxina mutante de Bacillus thuringiensis con estabilidad y toxicidad aumentadas

Author(s): Syed Rehan A. Hussain | Flórez Álvaro M. | Osorio Cristina | Dean Donald H. | Alzate Óscar
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