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  1. 101
    A sequencing-based method for quantifying gene-deletion mutants of bacteria in the intracellular environment

    A sequencing-based method for quantifying gene-deletion mutants of bacteria in the intracellular environment by Xiao Fei, Xiao Fei, Zengzhi Yuan, Zengzhi Yuan, Sandra Marina Wellner, Yibing Ma, John Elmerdahl Olsen

    Published 2025-01-01
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  2. 102
    Survivability-Aware Topology Evolution Model with Link and Node Deletion in Wireless Sensor Networks

    Survivability-Aware Topology Evolution Model with Link and Node Deletion in Wireless Sensor Networks by Yanliang Jin, Xuqin Zhou, Zhishu Bai, Wei Ma, Lina Xu, Zhuo Wu, Su Ki Ooi, Yue Liu

    Published 2014-04-01
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  3. 103
    Angiotensin-Converting Enzyme Insertion/Deletion Gene Polymorphism in Chronic Rhinosinusitis with Nasal Polyps

    Angiotensin-Converting Enzyme Insertion/Deletion Gene Polymorphism in Chronic Rhinosinusitis with Nasal Polyps by Mehmet Emre Sivrice, Vural Akın, Hasan Yasan, Kuyaş Hekimler Öztürk, Yusuf Çağdaş Kumbul

    Published 2024-09-01
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  4. 104
    Genetic Deletion of Soluble Epoxide Hydrolase Attenuates Inflammation and Fibrosis in Experimental Obstructive Nephropathy

    Genetic Deletion of Soluble Epoxide Hydrolase Attenuates Inflammation and Fibrosis in Experimental Obstructive Nephropathy by Chin-Wei Chiang, Hsueh-Te Lee, Der-Cherng Tarng, Ko-Lin Kuo, Li-Ching Cheng, Tzong-Shyuan Lee

    Published 2015-01-01
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  5. 105
    Acquired Elliptocytosis as a Manifestation of Myelodysplastic Syndrome Associated with Deletion of Chromosome 20q

    Acquired Elliptocytosis as a Manifestation of Myelodysplastic Syndrome Associated with Deletion of Chromosome 20q by Sukesh Manthri, Naresh K. Vasireddy, Sindhura Bandaru, Swati Pathak

    Published 2018-01-01
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  6. 106
    Deletion of Ovarian Hormones Induces a Sickness Behavior in Rats Comparable to the Effect of Lipopolysaccharide

    Deletion of Ovarian Hormones Induces a Sickness Behavior in Rats Comparable to the Effect of Lipopolysaccharide by Hamid Azizi-Malekabadi, Mahmoud Hosseini, Masoume Pourganji, Hoda Zabihi, Mohsen Saeedjalali, Akbar Anaeigoudari

    Published 2015-01-01
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  7. 107
    Asistentes digitales en la experiencia del patrimonio cultural: Beacons en el Museo Naval de Madrid

    Asistentes digitales en la experiencia del patrimonio cultural: Beacons en el Museo Naval de Madrid by María Jesús Rosado García, Ramón Argüelles Bustillo

    Published 2024-03-01
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  8. 108
    ¿Tabletas o móviles? Uso de dispositivos para un aplicativo de lectura durante la pandemia

    ¿Tabletas o móviles? Uso de dispositivos para un aplicativo de lectura durante la pandemia by Dalia Marilyn Leonor Rojas Saldaña, María Elisa López Estrada, Santiago Cueto Caballero, Juan León Jara-Almonte

    Published 2025-01-01
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  9. 109
    Telefony i komputery w codziennym życiu uczniów w młodszym wieku szkolnym

    Telefony i komputery w codziennym życiu uczniów w młodszym wieku szkolnym by Agnieszka Lewicka-Zelent, Agnieszka Pytka

    Published 2018-06-01
    Subjects: “…telefon…”
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  10. 110
    Analysis of unmapped regions associated with long deletions in Korean whole genome sequences based on short read data

    Analysis of unmapped regions associated with long deletions in Korean whole genome sequences based on short read data by Yuna Lee, Kiejung Park, Insong Koh

    Published 2019-12-01
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  11. 111
    A Novel Approach for Model Interpretability and Domain Aware Fine-Tuning in AdaBoost

    A Novel Approach for Model Interpretability and Domain Aware Fine-Tuning in AdaBoost by Raj Joseph Kiran, J. Sanil, S. Asharaf

    Published 2024-09-01
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  12. 112
    Tolerance in TCR/Cognate Antigen Double-TransgenicMice Mediated by Incomplete Thymic Deletion andPeripheral Receptor Downregulation

    Tolerance in TCR/Cognate Antigen Double-TransgenicMice Mediated by Incomplete Thymic Deletion andPeripheral Receptor Downregulation by Clio Mamalaki, Marianna Murdjeva, Mauro Tolaini, Trisha Norton, Phillip Chandler, Alain Townsend, Elizabeth Simpson, Dimitris Kioussis

    Published 1995-01-01
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  13. 113
    The Phonetic Description of Eshtehrdi Dialect

    The Phonetic Description of Eshtehrdi Dialect by محمّد پارسانسب

    Published 2011-12-01
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  14. 114
    Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome

    Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome by Masatake Toshimitsu, Shinichi Nagaoka, Shuusaku Kobori, Maki Ogawa, Fumihiko Suzuki, Takema Kato, Shunsuke Miyai, Rie Kawamura, Hidehito Inagaki, Hiroki Kurahashi, Jun Murotsuki

    Published 2019-01-01
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  15. 115
    Novel Copy Number Deletion Involving NUS1 Associated With Epilepsy, Tremor, and Intellectual Disability

    Novel Copy Number Deletion Involving NUS1 Associated With Epilepsy, Tremor, and Intellectual Disability by Jing Y. Hsu, Daniah H. Ibrahim, Riza Ali, Elaine Marchi, Maureen Gavin, Karen Amble, Gholson J. Lyon

    Published 2025-01-01
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  16. 116
    Squamous Cell Carcinoma of the Lung with Metastasis to the GI Tract Associated with EGFR Exon 19 Deletion

    Squamous Cell Carcinoma of the Lung with Metastasis to the GI Tract Associated with EGFR Exon 19 Deletion by Glen J. Weiss, Agnes K. Liman, Jeffrey Allen, Philip Y. Cheung, Rajesh N. Kukunoor

    Published 2013-01-01
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  17. 117
    An Efficient Method for Immortalizing Mouse Embryonic Fibroblasts by CRISPR-mediated Deletion of the Tp53 Gene

    An Efficient Method for Immortalizing Mouse Embryonic Fibroblasts by CRISPR-mediated Deletion of the Tp53 Gene by Srisathya Srinivasan, Hsin-Yi Ho

    Published 2025-01-01
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  18. 118
    Prenatal ultrasound phenotype of fetuses with recurrent 1q21.1 deletion and duplication syndrome

    Prenatal ultrasound phenotype of fetuses with recurrent 1q21.1 deletion and duplication syndrome by Fengyang Wang, Huijuan Peng, Guiyu Lou, Yanxin Ren, Shixiu Liao

    Published 2025-01-01
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  19. 119
    Mitochondrial trifunctional protein deficiency caused by a deep intronic deletion leading to aberrant splicing

    Mitochondrial trifunctional protein deficiency caused by a deep intronic deletion leading to aberrant splicing by Thomas Cassini, Sarah Silverstein, Molly Behan, Cynthia J. Tifft, May Christine Malicdan, David R. Adams, Undiagnosed Diseases Network, Sun‐Young Ahn, Debra S. Regier

    Published 2025-01-01
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  20. 120
    A deletion variant in LMX1B causing nail–patella syndrome in Japanese twins

    A deletion variant in LMX1B causing nail–patella syndrome in Japanese twins by Nozomu Kishio, Kazuhiro Iwama, Sayuri Nakanishi, Ryosuke Shindo, Masaki Yasui, Naoki Nicho, Atsushi Takahashi, Mana Kohara, Michisato Hirata, Takahiro Kemmotsu, Miki Tanoshima, Shuichi Ito

    Published 2024-02-01
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