Channels A tti1 mutation in the Tel2-Tti1-Tti2 complex specifically eliminates the cellular function of Rad3ATR, but not that of other PIKKs in fission yeast
A point mutation in the FAT domain constitutively increases the kinase activity of Rad3ATR and bypasses the requirement for 9-1–1 phosphorylation to activate the DNA replication checkpoint
Effect of Individual Factors Contributing to Entrepreneurship Intention among TTI Trainees in Khuruthang, Punakha
TELO2-interacting protein 1 (TTI1), a novel Wnt/β-catenin target gene, decreases chemo-sensitivity in colorectal cancer by modulating DNA damage responses
Functional identification of a putative stachyose synthase (StaS, Medtr7g106910.1) from Medicago truncatula, by overexpression in the Arabidopsis stachyose deficient double mutant atrs4/atrs5
Cold-responsive interaction between MdRAD23D1 and MdMYB15 confers cold stress tolerance via the CBF pathway in apple (Malus domestica)
MCT8 Deficiency in Two Brothers With a Novel Deletion Mutation in SLC16A2
AFLP and PCR markers for the Ht1, Ht2, Ht3 and Htn1 resistance genes in maize
Hypokalemic Periodic Paralysis Associated With a Rare CACNA1S Variant (p.Leu1243Val): Expanding the Mutational Spectrum
A Rare Case of Concurrent SNRPB Mutation and 22q11.2 Microduplication in a Child With Cerebro-Costo-Mandibular Syndrome
Novel Mutations in the MC2R Gene in a Patient With Familial Glucocorticoid Deficiency (FGD): A Case Report and Functional Study
First Thai Case of Lethal Desbuquois Dysplasia Type I Caused by Novel Compound Heterozygous CANT1 Mutations: Expanding the Molecular Spectrum
Functional profiling of 2,193 ASS1 missense variants: Insights into variant pathogenicity and epistatic interactions in citrullinemia type I
Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature
SV40 exploits the Nesprin-2-SUN1-KPNA4 axis for stepwise targeting and entry into the host nucleus to promote infection
RETRACTION: LncRNA NEAT1/mir‐185‐5p/igf2 Axis Regulates the Invasion and Migration of Colon Cancer
Biomaterial Physical Cues as Gene Regulators for Cellular Agriculture
Sex differences in the regulation and function of cellular immunity in Drosophila
An investigation into the reasons for non-uptake of carrier testing in a family affected by alpha thalassaemia X-linked mental retardation (ATR-X) syndrome
Mutation analysis of the promoter region of CYBRD1, HFE, LTF, HAMP and SLC40A1 in a Tuberculosis cohort
Diaphragmatic Hernia in a Newborn With COL1A1-Associated Classical Ehlers–Danlos Syndrome
Issue Information: (Advanced Genetics 2/07)
Molecular analysis of GJB2 (connexin 26) and GJB6 (connexin 30) gene mutations in non-syndromic hereditary deafness in South Africa
Craniometaphyseal dysplasia with severe maxillary hypoplasia due to gene mutation: A case report
Correlated protein-RNA associations and a requirement for HNRNPU in the long-range recruitment of Polycomb Repressive Complexes by the lncRNAs Airn and Kcnq1ot1
