Search Results - "intron"

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  1. 301
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    Evaluating the association of common <it>PBX1 </it>variants with type 2 diabetes by Hercberg Serge, Tichet Jean, Marre Michel, Charpentier Guillaume, Duesing Konsta, Balkau Beverley, Froguel Philippe, Gibson Fernando

    Published 2008
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  2. 302
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    Population genetics of PDE4B (phosphodiesterase‐4B) in neglected Native Americans: Implications for cancer pharmacogenetics by Rennan Garcias Moreira, Julia Maria Saraiva‐Duarte, Alexandre Costa Pereira, Martha Sosa‐Macias, Carlos Galaviz‐Hernandez, Meddly Lesley Santolalla, Wagner C. S. Magalhães, Camila Zolini, Thiago Peixoto Leal, Zsolt Balázs, Adrián Llerena, Robert H. Gilman, José Geraldo Mill, Victor Borda, Heinner Guio, Timothy D. O'Connor, Eduardo Tarazona‐Santos, Fernanda Rodrigues‐Soares

    Published 2022
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  3. 303
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    MRX87 family with <it>Aristaless X </it>dup24bp mutation and implication for polyAlanine expansions by D'Urso Michele, Neri Giovanni, Ventruto Valerio, D'Eustacchio Angela, Maiorino Antonio, Monfregola Jlenia, D'Adamo Pio, Spizzichino Letizia, Laperuta Carmela, Chiurazzi Pietro, Ursini Matilde, Miano Maria

    Published 2007
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  4. 304
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    Analysis of MEFV exon methylation and expression patterns in familial Mediterranean fever by Ozdogan Huri, Hatemi Gulen, Celikyapi Erdem Gokce, Arisoy Nil, Kasapcopur Ozgur, Kirectepe Asli K, Tahir Turanli Eda

    Published 2011
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  5. 305
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    THE ASSOCIATION OF GENE POLYMORPHISMS WITH ATHLETE STATUS IN UKRAINIANS by Svitlana B. Drozdovska, Victor E. Dosenko, Ildus I. Ahmetov, Vladimir N. Ilyin

    Published 2013
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  6. 306
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    Co-upregulation of miR-31 and its host gene lncRNA MIR31HG in oral squamous cell carcinoma by Hsi-Feng Tu, Chung-Ji Liu, Wan-Wen Hung, Tzong-Ming Shieh

    Published 2022
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  7. 307
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    Genome-Wide Identification of Superoxide Dismutase and Expression in Response to Fruit Development and Biological Stress in <i>Akebia trifoliata</i>: A Bioinformatics Study by Huai Yang, Qiuyi Zhang, Shengfu Zhong, Hao Yang, Tianheng Ren, Chen Chen, Feiquan Tan, Guoxing Cao, Jun Liu, Peigao Luo

    Published 2023
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  8. 308
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    Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center by Yangho Yoo, Mi Sun Chang, Jieun Lee, Sung Yoon Cho, Sung Won Park, Dong-Kyu Jin, Hyung-Doo Park

    Published 2013
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  9. 309
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    Differentially expressed alternatively spliced genes in skeletal muscle from cancer patients with cachexia by Ashok Narasimhan, Russell Greiner, Oliver F. Bathe, Vickie Baracos, Sambasivarao Damaraju

    Published 2018
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  10. 310
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    A novel PAX5 rearrangement in TCF3-PBX1 acute lymphoblastic leukemia: a case report by Thayana Conceição Barbosa, Bruno Almeida Lopes, Caroline Barbieri Blunck, Marcela Braga Mansur, Adriana Vanessa Santini Deyl, Mariana Emerenciano, Maria S. Pombo-

    Published 2018
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  11. 311
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    Novel bone morphogenetic protein 15 (BMP15) gene variants implicated in premature ovarian insufficiency by Fatemeh Afkhami, Shirin Shahbazi, Laya Farzadi, Shahla Danaei

    Published 2022
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  12. 312
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    Updated DPYD HapB3 haplotype structure and implications for pharmacogenomic testing by Amy J. Turner, Cyrine E. Haidar, Wenjian Yang, Erin C. Boone, Steven M. Offer, Philip E. Empey, Andrew Haddad, Saba Tahir, Gunter Scharer, Ulrich Broeckel, Andrea Gaedigk

    Published 2024
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  13. 313
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    Mary Richards Is Pale by Marshall Anderson

    Published 2008
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  14. 314
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    Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene by Carlo Fusco, Carlotta Spagnoli, Grazia Gabriella Salerno, Elena Pavlidis, Daniele Frattini, Francesco Pisani

    Published 2017
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  15. 315
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    Targeting RNA-Mediated Toxicity in C9orf72 ALS and/or FTD by RNAi-Based Gene Therapy by Raygene Martier, Jolanda M. Liefhebber, Ana García-Osta, Jana Miniarikova, Mar Cuadrado-Tejedor, Maria Espelosin, Susana Ursua, Harald Petry, Sander J. van Deventer, Melvin M. Evers, Pavlina Konstantinova

    Published 2019
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  16. 316
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    A RARE CASE OF HUNTER SYNDROME - CASE REPORT by Lorena Elena Melit, Oana Marginean, Carmen Duicu, Cristina Campean, Maria Oana Marginean

    Published 2015
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  17. 317
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    Association study analysis of CD9 as candidate gene for Duroc pig sperm motility and kinematic characteristics by Yong-dae Jeong, Jin-Young Jeong, Ki-Hyun Kim, Eun-Seok Cho, Dong-Jo Yu, Jung-Woo Choi, Hyun-Jun Jang, Sungk-won Park, Soo-Jin Sa, Jae-Seok Woo

    Published 2016
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  18. 318
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    <it>PLAUR </it>polymorphisms and lung function in UK smokers by Connolly Martin J, Wardlaw Andrew J, Moffat Miriam F, Parker Stuart G, Hall Ian P, Stewart Ceri E, Ruse Charlotte, Sayers Ian

    Published 2009
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  19. 319
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    Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malfor... by Chih-Ping Chen, Tung-Yao Chang, Wan-Yuo Guo, Yi-Ning Su, Yi-Yung Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2013
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  20. 320
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    Association of kinase insert domain-containing receptor (KDR) gene polymorphism/ haplotypes with recurrent spontaneous abortion and genetic structure by Shiva Shahsavari, Zahra Noormohammadi, Shohreh Zare Karizi

    Published 2015
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