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Mutation

UGT1A1 variants in Chinese Uighur and Han newborns and its correlation with neonatal hyperbilirubinemia

Hui Yang, Huijun Li, [ ... ], Liye Yang

The Drosophila melanogaster attP40 docking site and derivatives are insertion mutations of msp-300

Kevin van der Graaf, Saurabh Srivastav, [ ... ], Michael Stern

Structural basis for matriglycan synthesis by the LARGE1 dual glycosyltransferase

Michael Katz, Ron Diskin

Genomic landscape of alpha-variant of SARS-CoV-2 circulated in Pakistan

Nazia Fiaz, Imran Zahoor, Saima Saima, Atia Basheer

Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia

Vu Viet Ha Vuong, Thinh Huy Tran, [ ... ], Van-Khanh Tran

Transcriptome analysis and development of EST-SSR markers in Anoectochilus emeiensis (Orchidaceae)

Song Lu

Kidney tumors associated with germline mutations of FH and SDHB show a CpG island methylator phenotype (CIMP)

Christopher J. Ricketts, J. Keith Killian, [ ... ], W. Marston Linehan

The deletion of HK-1 gene affects the bacterial virulence of Pseudomonas stutzeri LH-42

Si Shan, Tingting Hu, Yu Yang

High prevalence of low-allele-fraction somatic mutations in STAT3 in peripheral blood CD8+ cells in multiple sclerosis patients and controls

Miko Valori, Joonas Lehikoinen, [ ... ], Pentti Tienari

A genetic approach to identify amino acids in Gcn1 required for Gcn2 activation

Susanne Gottfried, Siaosi M. B. M. J. Koloamatangi, [ ... ], Evelyn Sattlegger

Mutation analysis of the GSDME gene in a Chinese family with non-syndromic hearing loss

Peiliang Lei, Qingwen Zhu, [ ... ], Yuan Jiang

Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophy

Kristy Iskandar, Agung Triono, [ ... ], Gunadi

Remdesivir does not affect mitochondrial DNA copy number or deletion mutation frequency in aged male rats: A short report

Allen Herbst, Solbie Choi, [ ... ], Jonathan Wanagat

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