Academic Journals Database
Disseminating quality controlled scientific knowledge

Search Articles for "genetic variant"

ADD TO MY LIST
 
Kappa-Casein Genotypic Frequencies in Holstein-Friesian Dairy Cattle in West Java Province

Author(s): A. Anggraeni | C. Sumantri | A. Farajallah | E. Andreas
Comprehensive genetic assessment of a functional TLR9 promoter polymorphism: no replicable association with asthma or asthma-related phenotypes

Author(s): Lange Nancy | Zhou Xiaobo | Lasky-Su Jessica | Himes Blanca | Lazarus Ross | Soto-Quirós Manuel | Avila Lydiana | Celedón Juan | Hawrylowicz Catherine | Raby Benjamin | Litonjua Augusto
Genetic adult lactase persistence is associated with risk of Crohn's Disease in a New Zealand population

Author(s): Nolan Deborah | Han Dug | Lam Wen | Morgan Angharad | Fraser Alan | Tapsell Linda | Ferguson Lynnette
NOD2, IL23R and ATG16L1 polymorphisms in Lithuanian patients with inflammatory bowel disease

Author(s): Jurgita Sventoraityte, Aida Zvirbliene, Andre Franke, Ruta Kwiatkowski, Gediminas Kiudelis, Limas Kupcinskas, Stefan Schreiber
NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn’s disease

Author(s): Maria Gazouli, Ioanna Pachoula, Ioanna Panayotou, Gerassimos Mantzaris, George Chrousos, Nicholas P Anagnou, Eleftheria Roma-Giannikou
Assessment of MC1R and α-MSH gene sequences in Iranian vitiligo patients

Author(s): Eskandani M | Hasannia S | Vandghanooni S | Pirooznia N | Golchai J
Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study)

Author(s): Hertel Jens | Johansson Stefan | Ræder Helge | Platou Carl | Midthjell Kristian | Hveem Kristian | Molven Anders | Njølstad Pål
Segmental duplication as one of the driving forces underlying the diversity of the human immunoglobulin heavy chain variable gene region

Author(s): Pramanik Sreemanta | Cui Xiangfeng | Wang Hui-Yun | Chimge Nyam-Osor | Hu Guohong | Shen Li | Gao Richeng | Li Honghua
Synopsis and meta-analysis of genetic association studies in osteoporosis for the focal adhesion family genes: the CUMAGAS-OSTEOporosis information system

Author(s): Zintzaras Elias | Doxani Chrysoula | Koufakis Theocharis | Kastanis Alkibiadis | Rodopoulou Paraskevi | Karachalios Theofilos
Genetic variant of V825I in the ATP-binding cassette transporter A1 gene and serum lipid levels in the Guangxi Bai Ku Yao and Han populations

Author(s): Cao Xiao-Li | Yin Rui-Xing | Wu Dong-Feng | Miao Lin | Aung Lynn | Hu Xi-Jiang | Li Qing | Yan Ting-Ting | Lin Wei-Xiong | Pan Shang-Ling
Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics

Author(s): Shen Zhisen | Zheng Jing | Chen Bobei | Peng Guanghua | Zhang Ting | Gong Shasha | Zhu Yi | Zhang Chuqin | Li Ronghua | Yang Li | Zhou Jianjin | Cai Ting | Jin Lihua | Lu Jianxin | Guan Min-Xin
Mitochondrial pathogenic mutations are population-specific

Author(s): Breen Michael | Kondrashov Fyodor
8-oxo-7,8-dihydro-2'-deoxyguanosine as a biomarker of oxidative damage in oesophageal cancer patients: lack of association with antioxidant vitamins and polymorphism of hOGG1 and GST

Author(s): Lagadu Stéphanie | Lechevrel Mathilde | Sichel François | Breton Jean | Pottier Didier | Couderc Rémy | Moussa Fathi | Prevost Virginie
Genetic study of the hepcidin gene (HAMP) promoter and functional analysis of the c.-582A > G variant

Author(s): Parajes Silvia | González-Quintela Arturo | Campos Joaquín | Quinteiro Celsa | Domínguez Fernando | Loidi Lourdes
Combining target enrichment with barcode multiplexing for high throughput SNP discovery

Author(s): Cummings Nik | King Rob | Rickers Andre | Kaspi Antony | Lunke Sebastian | Haviv Izhak | Jowett Jeremy
Association analysis of PRNP gene region with chronic wasting disease in Rocky Mountain elk

Author(s): White Stephen | Spraker Terry | Reynolds James | O'Rourke Katherine
Polymorphisms in NF-κB, PXR, LXR, PPARγ and risk of inflammatory bowel disease

Author(s): Vibeke Andersen, Jane Christensen, Anja Ernst, Bent A Jacobsen, Anne Tjønneland, Henrik B Krarup, Ulla Vogel
Lymphoid tyrosine phosphatase R620W variant and inflammatory bowel disease in Tunisia

Author(s): Imen Sfar, Walid Ben Aleya, Leila Mouelhi, Houda Aouadi, Thouraya Ben Rhomdhane, Mouna Makhlouf, Salwa Ayed-Jendoubi, Houda Gargaoui, Taoufik Najjar, Taieb Ben Abdallah, Khaled Ayed, Yousr Gorgi
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease

Author(s): Luciana Rigoli, Claudio Romano, Rosario Alberto Caruso, Maria A Lo Presti, Chiara Di Bella, Vincenzo Procopio, Giuseppina Lo Giudice, Maria Amorini, Giuseppe Costantino, Maria D Sergi, Caterina Cuppari, Giovanna Elisa Calabrò, Romina Gallizzi, Carmelo Damiano Salpietro, Walter Fries
Hughes-Stovin Syndrome

Author(s): Khalid Umair | Saleem Taimur
A genetic variant in the APE1/Ref-1 gene promoter -141T/G may modulate risk of glioblastoma in a Chinese Han population

Author(s): Zhou Keke | Hu Dezhi | Lu Juan | Fan Weiwei | Liu Hongliang | Chen Hongyan | Chen Gong | Wei Qingyi | Du Guhong | Mao Ying | Lu Daru | Zhou Liangfu
Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia

Author(s): Al-Khateeb Alyaa | Zahri Mohd | Mohamed Mohd | Sasongko Teguh | Ibrahim Suhairi | Yusof Zurkurnai | Zilfalil Bin
The contribution of a 9p21.3 variant, a KIF6 variant, and C-reactive protein to predicting risk of myocardial infarction in a prospective study

Author(s): Shiffman Dov | O'Meara Ellen | Rowland Charles | Louie Judy | Cushman Mary | Tracy Russell | Devlin James | Psaty Bruce
Hepatitis Associated Aplastic Anemia: A review

Author(s): Rauff Bisma | Idrees Muhammad | Shah Shahida | Butt Sadia | Butt Azeem | Ali Liaqat | Hussain Abrar | Irshad-ur-Rehman | Ali Muhammad
Evaluation and Selection of Mutative Artemisia (Artemisia annua L.) According to the Altitude Variants

Author(s): ENDANG GATI LESTARI | MUHAMAD SYUKUR | RAGAPADMI PURNAMANINGSIH | ROSSA YUNITA | ROHIM FIRDAUS
Lecturer of Ophthalmology, Faculty of Medicine, Zagazig University, Egypt

Author(s): Monika A Pradhan | Dianne M Sharp | Justin S Mora | Mariana Wittmer | Wolfgang Berger | Andrea L Vincent
Polydactyly 24 – a case report

Author(s): Mangalgiri AS | Sherke AR
Molecular biology of heart disease

Author(s): Robert Roberts
Association of Insulin Receptor Substrate-2 Gene Polymorphism with Ovarian Cancer

Author(s): Filiz Çayan | Ramazan Gen | Nurcan Aras Ateş | Lokman Ayaz | Esen Akbay | Saffet Dilek
Molecular biology of heart disease

Author(s): Robert Roberts
Cystathionine β-synthase 844ins68 Genetic Polymorphism in Spontaneous Abortion Susceptibility

Author(s): Radu Anghel POPP | Tania Octavia CRIŞAN | Ioana ROTAR | Marius Florin FARCAŞ | Adrian Pavel TRIFA | Mariela Sanda MILITARU | Ioan Victor POP
Genetic polymorphism of β-lactoglobulin and κ-casein of cattle breeds in Croatia

Author(s): Ante Ivanković | Jelena Ramljak | Admir Dokso | Nikolina Kelava | Miljenko Konjačić | Saša Paprika
Gilbert Omenn and his syndrome

Author(s): Ahmad Al Aboud | Khalid Al Aboud
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
Relationship between genotype – technological environment and productive performances in Japanese quail (Coturnix coturnix)

Author(s): Vasile Cighi | Teofil Oroian | Simona Paşcalău | Dorel Dronca | Bogdan Georgescu
BREAKING A FEISTEL-TYPE BLOCK CIPHER BY BACTERIA ENGINEERING

Author(s): Arash Karimi | Hadi Shahriar Shahhoseini
Variant within CELSR2/PSRC1/SORT1, but not within CILP2/PBX4, PCSK9 and APOB genes, has a potential to influence statin treatment efficacy

Author(s): Jaroslav Alois Hubacek | Vera Adamková | Vera Lanska | Dana Dlouha | Jitka Rynekrova | Lukas Zlatohlavek | Martina Prusikova | Richard Ceska | Michal Vrablik
Role of Genetic Changes in the Progression of Cardiovascular Diseases

Author(s): S. A. Sheweita | H. Baghdadi | A. R. Allam
The C677T Variant in the Methylenetetrahydrofolate Reductase Gene and Idiopathic Spontaneous Abortion in a Romanian Population Group

Author(s): Radu A. POPP | Tania O. CRISAN | Adrian P. TRIFA | Mariela S. MILITARU | Ioana C. ROTAR | Marius F. FARCAS | Ioan V. POP
New Pineapple Somaclonal Variants: P3R5 and Dwarf

Author(s): Carlos Aragón | Lourdes Yabor | Justo González | José Carlos Lorenzo | Miriam Isidrón | Ermis Yanez | Guillermo Pérez | Andrew Mbogholi | Fernando Sagarra | Bárbara Valle
Association of Genetic Variation in the Promoter Region of OXTR with Differences in Social Affective Neural Processing

Author(s): Christian Montag | Jeremy Hall | Martin Reuter | Andrew C. Stanfield | Garret O’Connell | Heather C. Whalley | Prerona Mukherjee
Association of Genetic Variation in the Promoter Region of OXTR with Differences in Social Affective Neural Processing

Author(s): Christian Montag | Jeremy Hall | Martin Reuter | Andrew C. Stanfield | Garret O’Connell | Heather C. Whalley | Prerona Mukherjee
Sequence Variants and Haplotype Analysis of Cat ERBB2 Gene: A Survey on Spontaneous Cat Mammary Neoplastic and Non-Neoplastic Lesions

Author(s): Sara Santos | Estela Bastos | Cláudia S. Baptista | Daniela Sá | Christophe Caloustian | Henrique Guedes-Pinto | Fátima Gärtner | Ivo G. Gut | Raquel Chaves
LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype

Author(s): Jianding Cheng | David W. Van Norstrand | Argelia Medeiros-Domingo | David J. Tester | Carmen R. Valdivia | Bi-Hua Tan | Matteo Vatta | Jonathan C. Makielski | Michael J. Ackerman
Immunohistochemical Assessment of Expression of Centromere Protein—A (CENPA) in Human Invasive Breast Cancer

Author(s): Ashish B. Rajput | Nianping Hu | Sonal Varma | Chien-Hung Chen | Keyue Ding | Paul C. Park | Judy-Anne W. Chapman | Sandip K. SenGupta | Yolanda Madarnas | Bruce E. Elliott | Harriet E. Feilotter
LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype

Author(s): Jianding Cheng | David W. Van Norstrand | Argelia Medeiros-Domingo | David J. Tester | Carmen R. Valdivia | Bi-Hua Tan | Matteo Vatta | Jonathan C. Makielski | Michael J. Ackerman
Pancreatic cancer risk variant ABO rs505922 in patients with cholangiocarcinoma

Author(s): Marcin Krawczyk | Florentina Mihalache | Aksana Höblinger | Monica Acalovschi | Frank Lammert | Vincent Zimmer
Dziedziczne podłoże czerniaka – wyniki badań własnych na tle piśmiennictwa

Author(s): Tadeusz Dębniak | Romuald Maleszka | Jan Lubiński
Pancreatic cancer risk variant ABO rs505922 in patients with cholangiocarcinoma

Author(s): Marcin Krawczyk | Florentina Mihalache | Aksana Höblinger | Monica Acalovschi | Frank Lammert | Vincent Zimmer
Genetic variants of Anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases

Author(s): Silaghi Cornelia | Liebisch Gabriele | Pfister Kurt
Engineering of an E. coli outer membrane protein FhuA with increased channel diameter

Author(s): Krewinkel Manuel | Dworeck Tamara | Fioroni Marco
Casein SNP in Norwegian goats: additive and dominance effects on milk composition and quality

Author(s): Dagnachew Binyam | Thaller Georg | Lien Sigbjørn | Ådnøy Tormod
Case-control study for colorectal cancer genetic susceptibility in EPICOLON: previously identified variants and mucins

Author(s): Abulí Anna | Fernández-Rozadilla Ceres | Alonso-Espinaco Virginia | Muñoz Jenifer | Gonzalo Victoria | Bessa Xavier | González Dolors | Clofent Joan | Cubiella Joaquin | Morillas Juan | Rigau Joaquim | Latorre Mercedes | Fernández-Bañares Fernando | Peña Elena | Riestra Sabino | Payá Artemio | Jover Rodrigo | Xicola Rosa | Llor Xavier | Carvajal-Carmona Luis | Villanueva Cristina | Moreno Victor | Piqué Josep | Carracedo Angel | Castells Antoni | Andreu Montserrat | Ruiz-Ponte Clara | Castellví-Bel Sergi
The public goods hypothesis for the evolution of life on Earth

Author(s): McInerney James | Pisani Davide | Bapteste Eric | O'Connell Mary
Degeneration of penicillin production in ethanol-limited chemostat cultivations of Penicillium chrysogenum: A systems biology approach

Author(s): Douma Rutger | Batista Joana | Touw Kai | Kiel Jan | Krikken Arjen | Zhao Zheng | Veiga Tânia | Klaassen Paul | Bovenberg Roel | Daran Jean-Marc | Heijnen Joseph | van Gulik Walter
Vertical decomposition with Genetic Algorithm for Multiple Sequence Alignment

Author(s): Naznin Farhana | Sarker Ruhul | Essam Daryl
LIN28B, LIN28A, KISS1, and KISS1R in idiopathic central precocious puberty

Author(s): Tommiska Johanna | Sørensen Kaspar | Aksglaede Lise | Koivu Rosanna | Puhakka Lea | Juul Anders | Raivio Taneli
Genetic mutations in non-syndromic deafness patients of uyghur and han chinese ethnicities in xinjiang, China: a comparative study

Author(s): Chen Yu | Tudi Mayila | Sun Jie | He Chao | Lu Hong-li | Shang Qing | Jiang Di | Kuyaxi Pilidong | Hu Bin | Zhang Hua
Antiretroviral treatment-induced dyslipidemia in HIV-infected patients is influenced by the APOC3-related rs10892151 polymorphism

Author(s): Aragonès Gerard | Alonso-Villaverde Carlos | Pardo-Reche Pedro | Rull Anna | Beltrán-Debón Raúl | Rodríguez-Gallego Esther | Fernández-Sender Laura | Camps Jordi | Joven Jorge
The landscape of inherited and de novo copy number variants in a plasmodium falciparum genetic cross

Author(s): Samarakoon Upeka | Gonzales Joseph | Patel Jigar | Tan Asako | Checkley Lisa | Ferdig Michael
Alzheimer-specific variants in the 3'UTR of Amyloid precursor protein affect microRNA function

Author(s): Delay Charlotte | Calon Frédéric | Mathews Paul | Hébert Sébastien
Association of ADIPOR2 gene variants with cardiovascular disease and type 2 diabetes risk in individuals with impaired glucose tolerance: the Finnish Diabetes Prevention Study

Author(s): Siitonen Niina | Pulkkinen Leena | Lindström Jaana | Kolehmainen Marjukka | Schwab Ursula | Eriksson Johan | Ilanne-Parikka Pirjo | Keinänen-Kiukaanniemi Sirkka | Tuomilehto Jaakko | Uusitupa Matti
Evolution and diversity of community-associated methicillin-resistant Staphylococcus aureus in a geographical region

Author(s): Coombs Geoffrey | Monecke Stefan | Pearson Julie | Tan Hui-leen | Chew Yi-Kong | Wilson Lynne | Ehricht Ralf | O'Brien Frances | Christiansen Keryn
Activating mutation in MET oncogene in familial colorectal cancer

Author(s): Neklason Deborah | Done Michelle | Sargent Nykole | Schwartz Ann | Anton-Culver Hoda | Griffin Constance | Ahnen Dennis | Schildkraut Joellen | Tomlinson Gail | Strong Louise | Miller Alexander | Stopfer Jill | Burt Randall
Whole-exome sequencing of DNA from peripheral blood mononuclear cells (PBMC) and EBV-transformed lymphocytes from the same donor

Author(s): Londin Eric | Keller Margaret | D'Andrea Michael | Delgrosso Kathleen | Ertel Adam | Surrey Saul | Fortina Paolo
Amplified fragment length polymorphism of clinical and environmental Vibrio cholerae from a freshwater environment in a cholera-endemic area, India

Author(s): Mishra Arti | Taneja Neelam | Sharma Ram | Kumar Rahul | Sharma Naresh | Sharma Meera
Serotonin receptor 3A polymorphism c.-42C > T is associated with severe dyspepsia

Author(s): Mujakovic Suhreta | ter Linde José | de Wit Niek | van Marrewijk Corine | Fransen Gerdine | Onland-Moret N Charlotte | Laheij Robert | Muris Jean | Grobbee Diederick | Samsom Melvin | Jansen Jan | Knottnerus André | Numans Mattijs
Characteristics of epstein barr virus variants associated with gastric carcinoma in Southern Tunisia

Author(s): BenAyed-Guerfali Dorra | Ayadi Wajdi | Miladi-Abdennadher Imen | Khabir Abdelmajid | Sellami-Boudawara Tahia | Gargouri Ali | Mokdad-Gargouri Raja
LQTS-Associated Mutation A257G in Alpha1-Syntrophin Interacts with the Intragenic Variant P74L to Modify its Biophysical Phenotype

Author(s): Jianding Cheng | David W. Van Norstrand | Argelia Medeiros-Domingo | David J. Tester | Carmen R. Valdivia | Bi-Hua Tan | Matteo Vatta | Jonathan C. Makielski | Michael J. Ackerman
Association of Tumor Necrosis Factor-Alpha Gene Polymorphisms With Juvenile Systemic Lupus Erythematosus Nephritis in a Cohort of Egyptian Patients

Author(s): Tarek M Farid | Abeer Mohamed Nour Eldin Abd El Baky | Eman S Khalefa | Ahmed A Talaat | Amal A Mohamed | Tamer A Gheita | Randa F Abdel-Salam
Predisposition for borderline personality disorder with comorbid major depression is associated with that for polycystic ovary syndrome in female Japanese population

Author(s): Kawamura S, Maesawa C, Nakamura K, Nakayama K, Morita M, Hiruma Y, Yoshida T, Sakai A, Masuda T
"Deafness –Associated Connexin 26 Gene (GJB2) Mutations in Iranian Population"

Author(s): M Hashemzadeh Chaleshtori | DD Farhud | R Taylor | V Hadavi | MA Patton | AR Afzal
"Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations"

Author(s): "M Hashemzadeh Chaleshtori | M Dowlati | DD Farhud | L Hoghooghi Rad | R Sasanfar A Hoseinipour | M Montazer Zohour | A Tolooi | M Ghadami | HR Pourjafari | MA Oshaghi | MA Patton "
Autosomal Recessive and Sporadic Non Syndromic Hearing Loss and the Incidence of Cx26 Mutations in a Province of Iran

Author(s): M Hashemzadeh Chaleshtori | M Montazer Zohour | L Hoghooghi Rad | H Pour-Jafari | DD Farhud | M Dolati | K Safa Chaleshtori | R Sasanfar | A Hosseinipour | L Andonian | A Tolouei | M Ghadami | MA Patton
Glucose-6-phosphate dehydrogenase (G6PD) Deficiency

Author(s): DD Farhud | L Yazdanpanah
Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases

Author(s): M Hashemzadeh Chaleshtori | DD Farhud | AH Crosby | E Farrokhi | H Pour Jafari | K Ghatreh Samani | K Safa Chaleshtori | M Kasiri | M Shahrani | GR Mobini | M Mansouri | D Modarresinia | M Jafari
Prevalence and Molecular Identification of Mediterranean Glucose-6-Phosphate Dehydrogenase Deficiency in Khuzestan Province, Iran

Author(s): SR Kazemi Nezhad | A Mashayekhi | SR Khatami | S Daneshmand | F Fahmi | M Ghaderigandmani | MA Jalali-Far
Studying the 3'UTR (1484insG) polymorphism of PTP1B gene in insulin-resistant and type 2 diabetic subjects

Author(s): A Mosapour | M Taghikhani | R Meshkani | SH Khatami | S Bakhtiari | K Haghani
Evaluation of Sugarcane (Saccharum officinarum L.) Somaclonals Tolerance to Salinity Via In Vitro and In Vivo

Author(s): MAHMOUD SHOMEILI | MAJID NABIPOUR | MOSA MESKARBASHEE | HAMID RAJABI MEMARI
Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant

Author(s): Quinn S. Wells | Natalie L. Ausborn | Birgit H. Funke | Jean P. Pfotenhauer | Joseph L. Fredi | Samantha Baxter | Thomas G. DiSalvo | Charles C. Hong
Tafazzin gene mutations are uncommon causes of dilated cardiomyopathy in adults

Author(s): Matthew Taylor | Dobromir Slavov | Ernesto Salcedo | Xiao Zhu | Deborah Ferguson | Jean Jirikowic | Andrea Di Lenarda | Gianfranco Sinagra | Luisa Mestroni
The interpretation of genetic tests in inherited cardiovascular diseases

Author(s): Lorenzo Monserrat | Andrea Mazzanti | Martin Ortiz-Genga | Roberto Barriales-Villa | Diego Garcia-Giustiniani | Juan Ramon Gimeno-Blanes
Guest Editorial

Author(s): Deng-Yiv Chiu | Chen-Shu Wang | Wen-Chih Chang
A selective sweep of >8 Mb on chromosome 26 in the Boxer genome

Author(s): Quilez Javier | Short Andrea | Martínez Verónica | Kennedy Lorna | Ollier William | Sanchez Armand | Altet Laura | Francino Olga
Studies of a genetic variant in HK1 in relation to quantitative metabolic traits and to the prevalence of type 2 diabetes

Author(s): Gjesing Anette | Nielsen Aneta | Brandslund Ivan | Christensen Cramer | Sandbæk Anneli | Jørgensen Torben | Witte Daniel | Bonnefond Amélie | Froguel Phillippe | Hansen Torben | Pedersen Oluf
NMD and microRNA expression profiling of the HPCX1 locus reveal MAGEC1 as a candidate prostate cancer predisposition gene

Author(s): Mattila Henna | Schindler Martin | Isotalo Jarkko | Ikonen Tarja | Vihinen Mauno | Oja Hannu | Tammela Teuvo | Wahlfors Tiina | Schleutker Johanna
Cloning and expression profiling of the VLDLR gene associated with egg performance in duck (Anas platyrhynchos)

Author(s): Wang Cui | Li Shi-jun | Yu Wen-hua | Xin Qing-wu | Li Chuang | Feng Yan-ping | Peng Xiu-li | Gong Yan-zhang
Genetic polymorphisms in glutathione S-transferase (GST) superfamily and risk of arsenic-induced urothelial carcinoma in residents of southwestern Taiwan

Author(s): Hsu Ling-I | Chen Wu-Ping | Yang Tse-Yen | Chen Yu-Hsin | Lo Wann-Cheng | Wang Yuan-Hung | Liao Ya-Tang | Hsueh Yu-Mei | Chiou Hung-Yi | Wu Meei-Maan | Chen Chien-Jen
Variable Frequencies of Apolipoprotein E Genotypes and Its Effect on Serum Lipids in the Guangxi Zhuang and Han Children

Author(s): Peng Hu | Yuan Han Qin | Feng Ying Lei | Juan Pei | Bo Hu | Ling Lu
Antimicrobial Pattern and Clonal Dissemination of Extended-Spectrum Beta-Lactamase Producing Klebsiella Spp Isolates

Author(s): Sobhan Ghafourian | Nourkhoda Sadeghifard | Zamberi bin Sekawi | Vasantha K. Neela | Mariana N. Shamsudin | Reza Mohebi | Mohammad Rahbar | Mohammad Raftari
Full sequence analysis and characterization of the South Korean Norovirus GII-4 variant CUK-3

Author(s): Park Jeong-Woong | Lee Sung-Geun | Lee Young-Min | Jheong Weon-Hwa | Ryu Sangryeol | Paik Soon-Young
ENGINES: exploring single nucleotide variation in entire human genomes

Author(s): Amigo Jorge | Salas Antonio | Phillips Christopher
MCP1 haplotypes associated with protection from pulmonary tuberculosis

Author(s): Intemann Christopher | Thye Thorsten | Förster Birgit | Owusu-Dabo Ellis | Gyapong John | Horstmann Rolf | Meyer Christian
Detecting differential allelic expression using high-resolution melting curve analysis: application to the breast cancer susceptibility gene CHEK2

Author(s): Nguyen-Dumont Tú | Jordheim Lars | Michelon Jocelyne | Forey Nathalie | McKay-Chopin Sandrine | Sinilnikova Olga | Le Calvez-Kelm Florence | Southey Melissa | Tavtigian Sean | Lesueur Fabienne
Evidence of association with type 1 diabetes in the SLC11A1 gene region

Author(s): Yang Jennie | Downes Kate | Howson Joanna | Nutland Sarah | Stevens Helen | Walker Neil | Todd John
Different models of genetic variation and their effect on genomic evaluation

Author(s): Clark Samuel | Hickey John | van der Werf Julius
MDM2 SNP309, gene-gene interaction, and tumor susceptibility: an updated meta-analysis

Author(s): Wan Yan | Wu Wei | Yin Zhihua | Guan Peng | Zhou Baosen
Genetic variation in DNA-repair pathways and response to radiochemotherapy in esophageal adenocarcinoma: a retrospective cohort study of the Eastern Cooperative Oncology Group

Author(s): Yoon Harry | Catalano Paul | Murphy Kathleen | Skaar Todd | Philips Santosh | Powell Mark | Montgomery Elizabeth | Hafez Michael | Offer Steven | Liu Geoffrey | Meltzer Stephen | Wu Xifeng | Forastiere Arlene | Benson Al | Kleinberg Lawrence | Gibson Michael
A formalized description of the standard human variant nomenclature in Extended Backus-Naur Form

Author(s): Laros Jeroen | Blavier André | den Dunnen Johan | Taschner Peter
ANGPTL4 variants E40K and T266M are associated with lower fasting triglyceride levels in Non-Hispanic White Americans from the Look AHEAD Clinical Trial

Author(s): Smart-Halajko Melissa | Kelley-Hedgepeth Alyson | Montefusco Maria | Cooper Jackie | Kopin Alan | McCaffery Jeanne | Balasubramanyam Ashok | Pownall Henry | Nathan David | Peter Inga | Talmud Philippa | Huggins Gordon
A More Common Mucocutaneous Lesion : Pemphigus

Author(s): S.K. Padmakumar | S.Sunil
An Efficient Grouping Genetic Algorithm

Author(s): R. Sivaraj | T. Ravichandran
Unclassified sequence variants (UVS) and genetic predisposition to cancer

Author(s): Lucian Negura | Nancy Uhrhammer | Anca Negura | Eugen Ungureanu | Eugen Carasevici | Yves-Jean Bignon
Why do you need a reservation system?      Save time & money - Smart Internet Solutions