Correction to: Assessment of the contribution of VDR and VDBP/GC genes in the pathogenesis of celiac disease [0.03%]
Correction to: 维生素D受体和VDBP/GC基因在乳糜泻发病机制中的作用评估
Pratibha Banerjee,Harinder Singh,Priyanka Tiwari et al.
Pratibha Banerjee et al.
THPO promoter mutation: a familial study on congenital amegakaryocytic thrombocytopenia [0.03%]
THPO启动子突变：先天性特发性血小板减少性巨核细胞缺乏症的家族研究
Reyhaneh Dehghanzad,Roghayeh Rahbar Parvaneh,Maryam Jamshidifar et al.
Reyhaneh Dehghanzad et al.
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare inherited bone marrow failure syndrome, which is characterized by a severe thrombocytopenia at birth without predictive stigmata and by a risk for progression into aplastic anaemi...
Case Reports
Journal of genetics. 2025:104:12. DOI: 2025
Analysis of whole-exome data of nonobese NAFLD patients from India reveals association with new markers on functionally relevant genes and pathways [0.03%]
对印度非肥胖NAFLD患者外显子组数据的分析揭示了与功能相关基因和途径的新标志物之间的关联
Arnab Ghosh,Anamita Barik,Rajesh K Rai et al.
Arnab Ghosh et al.
Nonalcoholic fatty liver disease (NAFLD) occurs in a significant number of nonobese individuals, especially in Asian populations. Many genetic loci are associated with NAFLD. However, no exome-wide analysis of polymorphism data to identify ...
Wenlan Li,Xinwei Hou,Zhaodong Meng et al.
Wenlan Li et al.
The nonexpressor of pathogenesis-related 1 (NPR1) is the salicylic acid (SA) receptor, which plays an important regulatory role in plant immunity. However, the NPR1-like gene family in maize has not been comprehensively identified and analy...
Generation of albino C57BL/6J mice by CRISPR embryo editing of the mouse tyrosinase locus [0.03%]
利用CRISPR胚胎编辑技术在小鼠TYR基因座生成白化C57BL/6J品系
M Kasim Diril,Kerem Esmen,Tugba Sehitogullari et al.
M Kasim Diril et al.
After the arrival of the CRISPR/Cas9 genome editing technology, genetic engineering of model organisms has become much faster and more efficient. The development of genetically modified mouse models is also facilitated by the application of...
Gonadal mosaicism and paradoxical phenotype in NEXMIF encephalopathy: a case report of two siblings [0.03%]
NEXMIF脑病的性腺嵌合体和矛盾表型的病例报告：两兄弟姐妹的病例报告
Naik Adarsha,Haseena Sait
Naik Adarsha
The neurite extension and migration factor (NEXMIF) encephalopathy is an X-linked disorder that is characterized by intellectual disability, behavioural abnormalities and seizures. The majority of pathogenic variants are de novo. Here, we r...
Case Reports
Journal of genetics. 2025:104:6. DOI: 2025
Maternal effect on the inheritance of pericarp colour and grain dimension in rice (Oryza sativa L.) [0.03%]
稻谷皮层颜色和谷粒大小母体效应的研究(Oryza sativa L.)
Sakthi Anand Muthazhagu Kuppuraj,Yoglakshmi Chokkalingam,Karthick Jothiganapathy et al.
Sakthi Anand Muthazhagu Kuppuraj et al.
This study aimed to understand the maternal influence on the inheritance of pericarp colour and grain dimensions in rice, serving as a model for maternal effects in plants. Four crosses, namely Kalarata (red pericarp) x DRR Dhan 58 (white p...
The sev-Gal4 driver in Drosophila melanogaster does not express in the eight pairs of dorsomedial and some other neurons in larval ventral ganglia: a correction [0.03%]
在黑腹果蝇中，sev-Gal4启动子并不在幼虫腹神经索的八对背内侧及其他一些神经元中表达：勘误
Vanshika Kaushik,Subhash C Lakhotia
Vanshika Kaushik
The sev-Gal4 driver is widely used in Drosophila to express the target gene in specific subsets of cells in ommatidial units of the developing eye. A 2015 report (Ray and Lakhotia, J. Genet. 94, 407-416) from our laboratory claimed that bes...
YY1 as a mediator to enhance the resistance of KRAS mutant colorectal cancer cells to cetuximab [0.03%]
YY1作为介导因子增强KRAS突变型结肠癌细胞对西妥昔单抗的耐药性
Yi Ma,Yi Lin,Congying Wang et al.
Yi Ma et al.
Cetuximab has been indicated as the mainstay of metastatic colorectal cancer (CRC) therapy, of which application was impeded by chemoresistance that was casually attributed to KRAS mutation. This study sought to determine whether YY1 mediat...
JAG1 overexpression partially rescues muscle function in a zebrafish model of duchenne muscular dystrophy [0.03%]
JAG1过表达部分挽救了杜氏肌营养不良斑马鱼模型的肌肉功能
Vishakha Nesari,Suresh Balakrishnan,Upendra Nongthomba
Vishakha Nesari
Duchenne muscular dystrophy (DMD) is a severe genetic disorder characterized by progressive muscle degeneration and loss of function due to the absence of dystrophin. In this study, we utilized a zebrafish model with a dmd gene knockout to ...