Results 181 to 190 of about 218,683 (273)
Compensatory evolution facilitates loss of prfB autoregulation in Pseudomonas fluorescens SBW25. [PDF]
Lim S +3 more
europepmc +1 more source
(主査) 教授 横山 敦郎, 教授 鄭 漢忠, 准教授 石川 誠 歯学研究科(口腔医学専攻)
openaire
ABSTRACT Background and Objectives Multiple sclerosis (MS) exhibits racially disparate rates of disease progression. Black people with MS (B‐PwMS) experience a more severe disease course than non‐Hispanic White people with MS (NHW‐PwMS). Here we investigated structural and functional connectivity as well as structure–function decoupling in the ...
Emilio Cipriano +11 more
wiley +1 more source
Structure-informed mutagenesis identifies combinatorial contributions to mouse insulin receptor IRES function. [PDF]
Dahl WB, Lan TCT, Rouskin S, Marr MT.
europepmc +1 more source
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
Native Mass Spectrometry Reveals Binding Modes of the Tumor Suppressor Protein p53 to Different DNA Response Elements. [PDF]
Siefke E, Arlt C, Sinz A.
europepmc +1 more source
ABSTRACT Objective Stereoelectroencephalography‐guided radiofrequency thermocoagulation (SEEG‐RFTC) has emerged as a safe and effective minimally invasive treatment for children with drug‐resistant focal epilepsy. Although evidence from real‐world studies remains limited, numerous pediatric cases have demonstrated promising outcomes. This retrospective
Weitao Chen +7 more
wiley +1 more source
Circular MIMO antenna with ML-based bandwidth and isolation prediction for 6G communications. [PDF]
Alam MM +7 more
europepmc +1 more source
Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone +8 more
wiley +1 more source
Integrated conjugative elements drive the formation of pandemic clones of Escherichia coli with hybrid chromosomes. [PDF]
Berruga-Fernández T +7 more
europepmc +1 more source

