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Helicobacter pylori eradication rates with concomitant and tailored therapy based on 23S rRNA point mutation: A multicenter randomized controlled trial
Ong, Sungmoon, Kim, Sung Eun, Kim, Ji Hyun, Yi, Nam Hee, Kim, Tae Young, Jung, Kyoungwon, Park, Moo In, Jung, Hwoon‐Yong
Published in Helicobacter (Cambridge, Mass.) (01.10.2019)
Published in Helicobacter (Cambridge, Mass.) (01.10.2019)
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A double point mutation of SOD1 targeting net charge promotes aggregation under destabilizing conditions: Correlation of charge distribution and ALS-provoking mutation
Mavadat, Elaheh, Seyedalipour, Bagher, Hosseinkhani, Saman
Published in Biochimica et biophysica acta. General subjects (01.05.2023)
Published in Biochimica et biophysica acta. General subjects (01.05.2023)
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Case Report: A Novel Point Mutation of SOX3 in a Subject With Growth Hormone Deficiency, Hypogonadotrophic Hypogonadism, and Borderline Intellectual Disability
Li, Jing, Zhong, Yuxia, Guo, Tao, Yu, Yerong, Li, Jianwei
Published in Frontiers in endocrinology (Lausanne) (28.02.2022)
Published in Frontiers in endocrinology (Lausanne) (28.02.2022)
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A point mutation in LTT1 enhances cold tolerance at the booting stage in rice
Xu, Yufang, Wang, Ruci, Wang, Yueming, Zhang, Li, Yao, Shanguo
Published in Plant, cell and environment (01.04.2020)
Published in Plant, cell and environment (01.04.2020)
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RID is required for both repeat-induced point mutation and nucleation of a novel transitional heterochromatic state for euchromatic repeats
He, Zhen, Wu, Nannan, Yao, Ruonan, Tan, Huawei, Sun, Yingying, Chen, Jingxuan, Xue, Lan, Chen, Xiaonan, Yang, Sihai, Hurst, Laurence D, Wang, Long, Huang, Ju
Published in Nucleic acids research (20.03.2025)
Published in Nucleic acids research (20.03.2025)
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Aphid Thermal Tolerance Is Governed by a Point Mutation in Bacterial Symbionts
Dunbar, Helen E, Wilson, Alex C. C, Ferguson, Nicole R, Moran, Nancy A
Published in PLoS biology (01.05.2007)
Published in PLoS biology (01.05.2007)
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Specificity Assessment of CRISPR Genome Editing of Oncogenic EGFR Point Mutation with Single-Base Differences
Bae, Taegeun, Kim, Hanseop, Kim, Jeong Hee, Kim, Yong Jun, Lee, Seung Hwan, Ham, Byung-Joo, Hur, Junho K.
Published in Molecules (Basel, Switzerland) (22.12.2019)
Published in Molecules (Basel, Switzerland) (22.12.2019)
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Human Telomeric RNA G‑Quadruplex Response to Point Mutation in the G‑Quartets
Agarwala, Prachi, Kumar, Santosh, Pandey, Satyaprakash, Maiti, Souvik
Published in The journal of physical chemistry. B (02.04.2015)
Published in The journal of physical chemistry. B (02.04.2015)
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A Novel Point Mutation of the Human Glucocorticoid Receptor Gene Causes Primary Generalized Glucocorticoid Resistance Through Impaired Interaction With the LXXLL Motif of the p160 Coactivators: Dissociation of the Transactivating and Transreppressive Activities
Nicolaides, Nicolas C., Roberts, Michael L., Kino, Tomoshige, Braatvedt, Geoffrey, Hurt, Darrell E., Katsantoni, Eleni, Sertedaki, Amalia, Chrousos, George P., Charmandari, Evangelia
Published in The journal of clinical endocrinology and metabolism (01.05.2014)
Published in The journal of clinical endocrinology and metabolism (01.05.2014)
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Ca2+ signaling in human induced pluripotent stem cell-derived cardiomyocytes (iPS-CM) from normal and catecholaminergic polymorphic ventricular tachycardia (CPVT)-afflicted subjects
Zhang, X.-H., Haviland, S., Wei, H., Šarić, T., Fatima, A., Hescheler, J., Cleemann, L., Morad, M.
Published in Cell calcium (Edinburgh) (01.08.2013)
Published in Cell calcium (Edinburgh) (01.08.2013)
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Automated DNA extraction using cellulose magnetic beads can improve EGFR point mutation detection with liquid biopsy by efficiently recovering short and long DNA fragments
Nakashima, Chiho, Sato, Akemi, Abe, Tomonori, Kato, Junichi, Hirai, Mitsuharu, Nakamura, Tomomi, Komiya, Kazutoshi, Sueoka, Eisaburo, Kimura, Shinya, Sueoka-Aragane, Naoko
Published in Oncotarget (18.05.2018)
Published in Oncotarget (18.05.2018)
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Novel integrin-dependent platelet malfunction in siblings with leukocyte adhesion deficiency-III (LAD-III) caused by a point mutation in FERMT3
Jurk, Kerstin, Schulz, Ansgar S, Kehrel, Beate E, Räpple, Daniel, Schulze, Harald, Möbest, Dieter, Friedrich, Wilhelm W, Omran, Heymut, Deak, Erika, Henschler, Reinhard, Scheele, Jürgen S, Zieger, Barbara
Published in Thrombosis and haemostasis (01.05.2010)
Published in Thrombosis and haemostasis (01.05.2010)
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HNF-1 binding point mutation of the AFP gene promotes cirrhosis in post-menopausal women
Wang, Jing-wen, Chen, Yong, Liu, Qi-cai, Liu, Guo-zhong, Zhang, Shu-yu, Guo, Yu-jia, Li, Dong-hong, Chen, Xing-ting, Lin, Chen, Gao, Feng
Published in The International journal of biological markers (01.03.2020)
Published in The International journal of biological markers (01.03.2020)
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Genotype-Specific Cortisol Reserve in a Cohort of Subjects With Nonclassic Congenital Adrenal Hyperplasia (NCCAH)
Koren, Ilana, Weintrob, Naomi, Kebesch, Rebekka, Majdoub, Hussein, Stein, Nili, Naor, Shulamit, Segev-Becker, Anat
Published in The journal of clinical endocrinology and metabolism (01.03.2024)
Published in The journal of clinical endocrinology and metabolism (01.03.2024)
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