Hasil Pencarian - Anna Kiseleva

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  1. 1
    Soil fertility analysis in the Republic of Bashkortostan

    Soil fertility analysis in the Republic of Bashkortostan oleh Ramil Mirsayapov, Ilgiz Asylbaev, Anna Kiseleva, Tatiana Minkina, Nadezhda Kurmasheva

    Diterbitkan 2022-12-01
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  2. 2
    Associations of SNPs of the <i>ADIPOQ</i> Gene with Serum Adiponectin Levels, Unstable Angina, and Coronary Artery Disease

    Associations of SNPs of the <i>ADIPOQ</i> Gene with Serum Adiponectin Levels, Unstable Angina, and Coronary Artery Disease oleh Stepan Smetnev, Marina Klimushina, Vladimir Kutsenko, Anna Kiseleva, Nadezhda Gumanova, Alexander Kots, Olga Skirko, Alexandra Ershova, Elena Yarovaya, Victoria Metelskaya, Alexey Meshkov, Oksana Drapkina

    Diterbitkan 2019-09-01
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  3. 3
    Multiple rare and common variants in APOB gene locus associated with oxidatively modified low-density lipoprotein levels.

    Multiple rare and common variants in APOB gene locus associated with oxidatively modified low-density lipoprotein levels. oleh Eleonora Khlebus, Vladimir Kutsenko, Alexey Meshkov, Alexandra Ershova, Anna Kiseleva, Anton Shevtsov, Natalia Shcherbakova, Anastasiia Zharikova, Vadim Lankin, Alla Tikhaze, Irina Chazova, Elena Yarovaya, Oksana Drapkina, Sergey Boytsov

    Diterbitkan 2019-01-01
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  4. 4
    Murine SEC24D can substitute functionally for SEC24C during embryonic development

    Murine SEC24D can substitute functionally for SEC24C during embryonic development oleh Elizabeth J. Adams, Rami Khoriaty, Anna Kiseleva, Audrey C. A. Cleuren, Kärt Tomberg, Martijn A. van der Ent, Peter Gergics, Vi T. Tang, Guojing Zhu, Mark J. Hoenerhoff, K. Sue O’Shea, Thomas L. Saunders, David Ginsburg

    Diterbitkan 2021-10-01
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  5. 5
    The Double Mutation <i>DSG2</i>-p.S363X and <i>TBX20</i>-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report

    The Double Mutation <i>DSG2</i>-p.S363X and <i>TBX20</i>-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report oleh Roman Myasnikov, Andreas Brodehl, Alexey Meshkov, Olga Kulikova, Anna Kiseleva, Greta Marie Pohl, Evgeniia Sotnikova, Mikhail Divashuk, Marina Klimushina, Anastasia Zharikova, Maria Pokrovskaya, Sergey Koretskiy, Maria Kharlap, Elena Mershina, Valentin Sinitsyn, Elena Basargina, Leila Gandaeva, Vladimir Barskiy, Sergey Boytsov, Hendrik Milting, Oxana Drapkina

    Diterbitkan 2021-06-01
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  6. 6
    Uniparental genetic heritage of belarusians: encounter of rare middle eastern matrilineages with a central European mitochondrial DNA pool.

    Uniparental genetic heritage of belarusians: encounter of rare middle eastern matrilineages with a central European mitochondrial DNA pool. oleh Alena Kushniarevich, Larysa Sivitskaya, Nina Danilenko, Tadeush Novogrodskii, Iosif Tsybovsky, Anna Kiseleva, Svetlana Kotova, Gyaneshwer Chaubey, Ene Metspalu, Hovhannes Sahakyan, Ardeshir Bahmanimehr, Maere Reidla, Siiri Rootsi, Jüri Parik, Tuuli Reisberg, Alessandro Achilli, Baharak Hooshiar Kashani, Francesca Gandini, Anna Olivieri, Doron M Behar, Antonio Torroni, Oleg Davydenko, Richard Villems

    Diterbitkan 2013-01-01
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  7. 7
    A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities

    A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities oleh Anna Bukaeva, Roman Myasnikov, Olga Kulikova, Alexey Meshkov, Anna Kiseleva, Anna Petukhova, Evgenia Zotova, Peter Sparber, Alexandra Ershova, Evgeniia Sotnikova, Maria Kudryavtseva, Anastasia Zharikova, Sergey Koretskiy, Elena Mershina, Vasily Ramensky, Marija Zaicenoka, Yuri Vyatkin, Alisa Muraveva, Alexandra Abisheva, Tatiana Nikityuk, Valentin Sinitsyn, Mikhail Divashuk, Elena Dadali, Maria Pokrovskaya, Oxana Drapkina

    Diterbitkan 2024-07-01
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  8. 8
    Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset

    Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset oleh Andreas Brodehl, Alexey Meshkov, Roman Myasnikov, Anna Kiseleva, Olga Kulikova, Bärbel Klauke, Evgeniia Sotnikova, Caroline Stanasiuk, Mikhail Divashuk, Greta Marie Pohl, Maria Kudryavtseva, Karin Klingel, Brenda Gerull, Anastasia Zharikova, Jan Gummert, Sergey Koretskiy, Stephan Schubert, Elena Mershina, Anna Gärtner, Polina Pilus, Kai Thorsten Laser, Valentin Sinitsyn, Sergey Boytsov, Oxana Drapkina, Hendrik Milting

    Diterbitkan 2021-04-01
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  9. 9
    The genetic regulatory signature of type 2 diabetes in human skeletal muscle

    The genetic regulatory signature of type 2 diabetes in human skeletal muscle oleh Laura J. Scott, Michael R. Erdos, Jeroen R. Huyghe, Ryan P. Welch, Andrew T. Beck, Brooke N. Wolford, Peter S. Chines, John P. Didion, Narisu Narisu, Heather M. Stringham, D. Leland Taylor, Anne U. Jackson, Swarooparani Vadlamudi, Lori L. Bonnycastle, Leena Kinnunen, Jouko Saramies, Jouko Sundvall, Ricardo D'Oliveira Albanus, Anna Kiseleva, John Hensley, Gregory E. Crawford, Hui Jiang, Xiaoquan Wen, Richard M. Watanabe, Timo A. Lakka, Karen L. Mohlke, Markku Laakso, Jaakko Tuomilehto, Heikki A. Koistinen, Michael Boehnke, Francis S. Collins, Stephen C. J. Parker

    Diterbitkan 2016-06-01
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