Diagnostic and prognostic assessments of adrenocortical carcinomas by pathological features, immunohistochemical markers and reticular histochemistry staining by Wenting Gan, Xue Han, Yuxi Gong, Yefan Yang, Cong Wang, Zhihong Zhang

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Genetic variants in CYP11B1 influence the susceptibility to coronary heart disease by Xiaoli Huang, Yimin Cheng, Na Wang

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New Insights in the Functional Zonation of the Canine Adrenal Cortex by K. Sanders, J.A. Mol, H.S. Kooistra, A. Slob, S. Galac

Subjects: “…CYP11B1…”
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CYP11B1 gene polymorphisms and susceptibility to ischemic stroke in a Chinese Han population by Gaowen Liu, Ying Duan

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Combined Pharmacophore Modeling, 3D-QSAR, Homology Modeling and Docking Studies on CYP11B1 Inhibitors by Rui Yu, Juan Wang, Rui Wang, Yong Lin, Yong Hu, Yuanqiang Wang, Mao Shu, Zhihua Lin

Subjects: “…CYP11B1 inhibitors…”
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Immunohistochemical Analysis of CYP11B2, CYP11B1 and β-catenin Helps Subtyping and Relates With Clinical Characteristics of Unilateral Primary Aldosteronism by Luyan Sun, Yiran Jiang, Jing Xie, Hongyuan Zhu, Luming Wu, Xu Zhong, Weiwei Zhou, Tingwei Su, Weiqing Wang, Weiqing Wang

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Targeted long-read sequencing identifies missing pathogenic variant in unsolved 11β-hydroxylase deficiency by Jidong Liu, Huihui Tian, Xinchen Jin, Yanxiang Wang, Zhenhong Zhang, Mengxue Li, Lulu Dai, Xiaoli Zhang, Ling Jiang

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A Chinese patient with 11β-hydroxylase deficiency due to novel compound heterozygous mutation in CYP11B1 gene: a case report by Xianxian Yuan, Lin Lu, Shi Chen, Jun Jiang, Xiangqing Wang, Zhihui Liu, Huijuan Zhu, Hui Pan, Zhaolin Lu

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Clinical Presentation and Genetic Analysis of Neonatal 11β-Hydroxylase Deficiency Induced by a Chimeric CYP11B2/CYP11B1 Gene by Wenjuan Cai, Dan Yu, Jian Gao, Qian Deng, Huihui Lin, Yuqing Chen

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Clinical and Molecular Analysis of Four Patients With 11β-Hydroxylase Deficiency by Qiaoli Zhou, Dandan Wang, Chunli Wang, Bixia Zheng, Qianqi Liu, Ziyang Zhu, Zhanjun Jia, Wei Gu

Subjects: “…CYP11B1 gene…”
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Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: clinical, biochemical and molecular characteristics and long-term outcomes by Elida Mercado Santis, Ariadna Campos, Paula Fernández, Josep Oriola, Diego Yeste, Víctor Pérez, María Clemente

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Cell foundry with high product specificity and catalytic activity for 21-deoxycortisol biotransformation by Shuting Xiong, Ying Wang, Mingdong Yao, Hong Liu, Xiao Zhou, Wenhai Xiao, Yingjin Yuan

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Exploration of KCNJ5 Somatic Mutation and CYP11B1/CYP11B2 Staining in Multiple Nodules in Primary Aldosteronism by Jing Xie, Jing Xie, Cui Zhang, Xuefeng Wang, Yiran Jiang, Luming Wu, Lei Ye, Xuan Wang, Wen Xie, Haimin Xu, Weiqing Wang

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Rapid Action of Retinoic Acid on the Hypothalamic Pituitary Adrenal Axis by Peter I. Imoesi, Ellen E. Bowman, Patrick N. Stoney, Sylwia Matz, Peter McCaffery

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Corrigendum: Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country by Agustini Utari, Agustini Utari, Sultana M. H. Faradz, Annastasia Ediati, Annastasia Ediati, Tuula Rinne, Mahayu Dewi Ariani, Achmad Zulfa Juniarto, Stenvert L. S. Drop, Antonius E. van Herwaarden, Hedi L. Claahsen-van der Grinten

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Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country by Agustini Utari, Agustini Utari, Sultana M. H. Faradz, Annastasia Ediati, Annastasia Ediati, Tuula Rinne, Mahayu Dewi Ariani, Achmad Zulfa Juniarto, Stenvert L. S. Drop, Antonius E. van Herwaarden, Hedi L. Claahsen-van der Grinten

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The association of five polymorphisms with milk production traits in Czech Fleckvieh cattle by J. Boleckova, J. Matejickova, M. Stipkova, J. Kyselova, L. Barton

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11β-hydroxylase deficiency caused by a novel CYP11B1 variant: A case report by Hossam A Aldosari, Rawand N Alharbi

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Different cell compositions and a novel somatic KCNJ5 variant found in a patient with bilateral adrenocortical adenomas secreting aldosterone and cortisol by Liling Zhao, Jinjing Wan, Yujun Wang, Wenjun Yang, Qi Liang, Jinrong Wang, Ping Jin

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Case Report: A combination of chimeric CYP11B2/CYP11B1 and a novel p.Val68Gly CYP11B1 variant causing 11β-Hydroxylase deficiency in a Chinese patient by Jialin Li, Fenglan Zhang, Miao Xu, Hao Qiu, Cheng Zhou, Li Li, Lan Qin

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