Epidemics In The 21st Century: A Multifaceted Challenge by Shawana Sharif

Subjects: “…genetic mutations…”
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Novel compound heterozygous OBSCN variants in Chinese children with congenital pulmonary airway malformation by Jiali Xu, Siyu Ma, Zhaocong Yang, Yang Xu, Jirong Qi, Min Da, Xuming Mo

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Hypertrophic Cardiomyopathy: Genes and Mechanisms by Jinli Chen, Yang Xing, Jie Sun, Yongming Liu, Zekun Lang, Lei Zhang, Jinggang Yang

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HYPERTROPHIC CARDIOMYOPATHY: GENETIC ALTERATIONS, PATHOGENESIS AND PATHOPHYSIOLOGY by N. T. Vatutin, G. G. Taradin, M. S. Maron

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Study of a panel of genetic mutations in fibrocalcific pancreatic diabetes (FCPD): SPINK1 (N34S) mutation unlikely to be relevant by Vijay Budhwar, Susmita Dutta, Kaushik Pandit, Pradip Mukhopadhyay, Nitai P. Bhattacharyya, Sujoy Ghosh

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Two patients with type A insulin resistance syndrome carried mutation with insulin receptor gene c.3449T＞C by WANG Huiping, REN Weidong, REN Yanlin, SHI Li

Subjects: “…type a insulin resistance syndrome|genetic mutations…”
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Primary Cutaneous Rhabdomyosarcomatous Melanomas—A Report of Two Cases and Literature Review by Andreea Iliesiu, Victor Nimigean, Dana Antonia Tapoi, Mariana Costache

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HEREDITY, MUTABILITY AND PATHOLOGY by P. F. Litvitskii

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Obstructive hypertrophic cardiomyopathy: from genetic insights to a multimodal therapeutic approach with mavacamten, aficamten, and beyond by Khadija Sarwer, Saeeda Lashari, Nida Rafaqat, Maher, Abdul Raheem, Muneeb Ur Rehman, Syed Muhammad Iraj Abbas

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Spuriously low thyroid-stimulating hormone? A laboratory phenomenon by S Danalakshmi, Mamta Soni

Subjects: “…genetic mutations…”
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Tectorial membrane: structure, function, and its implications for hearing loss by Panpan Bian, Jiong Dang, Bai-cheng Xu

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A brief review of Lynch syndrome: understanding the dual cancer risk between endometrial and colorectal cancer by Sneha Pallatt, Sibin Nambidi, Subhamay Adhikary, Antara Banerjee, Surajit Pathak, Asim K. Duttaroy

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Unraveling the molecular landscape of congenital pseudoarthrosis of the tibia: insights from a comprehensive analysis of 159 probands by Rui Wang, Yu Zheng, Ge Yang, Zhenchao Xu, Yaoxi Liu, Weihua Zhao, Hua Wang, Haibo Mei, Guanghui Zhu

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Leber Hereditary Optic Neuropathy: Still a Dilemma? by Nishi Meghna Satish, Soveeta Rath, Kritika Chopra, Rolli Khurana, Neha Chawla, B.P. Guliani

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Drug resistance of <i>M. tuberculosis</i> (historical aspects, current level of knowledge) by I. A. Burmistrova, A. G. Samoylova, T. E. Tyulkova, E. V. Vaniev, G. S. Balasanyants, I. A. Vasilyeva

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Global research trends and emerging hotspots of RNF213 in Moyamoya disease: A bibliometric analysis (2011–2024) by Xiaozan Chang, Lei Wang

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A systematic review of candidate genes and their relevant pathways for metastasis among adults diagnosed with breast cancer by Gina M. Gehling, Miad Alfaqih, Lisiane Pruinelli, Angela Starkweather, Jennifer R. Dungan

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Advances in Mouse Models of Amyotrophic Lateral Sclerosis by LUO Lianlian, YUAN Yanchun, WANG Junling, SHI Guangsen

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Case Report: Exploring the spectrum of A20 haploinsufficiency in children by Sahana Jayaraman, Nayimisha Balmuri

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In Silico Design of Quantitative Polymerase Chain Reaction (qPCR) Assay Probes for Prostate Cancer Diagnosis, Prognosis, and Personalised Treatment by Trevor Kenneth Wilson, Oliver Tendayi Zishiri

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