Results 61 to 70 of about 3,275,705 (300)
Genetic heterogeneity of murine coronaviruses [PDF]
Several mouse hepatitis viruses (MHV) with different pathogenicity were studied by oligonucleotide fingerprinting. Two strains, MHV-K and MHV-D, which were isolated in Japan and, which cause anaplasia and necrosis of bone marrow and diarrhea, respectively, were found to be closely related to MHV-A59, the prototype MHV.
Lai, M. M. C. +3 more
openaire +2 more sources
ABSTRACT Pediatric intramedullary low‐grade gliomas (PIMLGGs) are rare neoplasms that present unique clinical and management challenges. Although surgery remains the primary tool for tissue diagnosis and decompression, complete gross‐total resection is frequently unfeasible due to the infiltrative nature of these lesions.
Olga M. Sergeenko +5 more
wiley +1 more source
Estimation of genetic variation in residual variance in female and male broiler chickens [PDF]
In breeding programs, robustness of animals and uniformity of end product can be improved by exploiting genetic variation in residual variance. Residual variance can be defined as environmental variance after accounting for all identifiable effects.
Mulder, H. A. +6 more
core +1 more source
Genetic conflicts and intercellular heterogeneity [PDF]
Adaptation is what elevates biology above mere chemistry and physics, and the salient feature of adaptation is that it is generally associated with individual organisms. The edge of an organism is a crucial boundary, within which we generally find adaptive cooperation and outside of which we find competition and conflict.
J E, Strassmann, D C, Queller
openaire +2 more sources
ABSTRACT Background Adult survivors of childhood acute lymphoblastic leukemia (ALL) are at risk of reduced exercise capacity, decreased physical activity levels, persistent fatigue, and neurocognitive deficits. The aim was to investigate exercise capacity and physical activity levels of adult survivors of childhood ALL and their associations with ...
Laura Jess +5 more
wiley +1 more source
Dementia-related genetic variants in an Italian population of early-onset Alzheimer’s disease
Early-onset Alzheimer’s disease (EOAD) is the most common form of early-onset dementia. Although three major genes have been identified as causative, the genetic contribution to the disease remains unsolved in many patients.
Anna Bartoletti-Stella +20 more
doaj +1 more source
Identifying Patterns of Hospitalizations Among Childhood Cancer Survivors: A Population‐Based Study
ABSTRACT Background Childhood cancer survivors (CCSs) experience more hospitalizations than the general population. We aimed to identify distinct hospitalization patterns among Queensland CCSs and the associated characteristics. Methods Cases (aged ≤14 years) diagnosed between 1995 and 2019 while residents of Queensland were identified through the ...
Hai Pham +7 more
wiley +1 more source
Early-Onset Epileptic Encephalopathy with Phospholipase C Beta 1 Deficiency
The clinical presentation and evolution of epileptic encephalopathy associated with a loss-of-function mutation in the phospholipase C-b 1 gene are reported in a male infant with infantile spasms treated at the University of Birmingham School of Medicine,
J Gordon Millichap
doaj +1 more source
Genetic Heterogencity of Collagens.
The term collagen has recently been expanded to include at least 7 genetically distinct structural elements of mammalian connective tissues. It is assumed that differences in the primary structure specify the interactions of these different collagens with one another and with noncollagen connective tissue elements. The specific biomechanical properties
openaire +2 more sources
ABSTRACT Febrile neutropenia (FN) is a frequent and serious complication in children receiving cancer therapy. Standardizing FN management across Asia is challenging due to variable healthcare infrastructure, diagnostic capacity, and infection patterns; however, it could improve resource use and patient outcomes.
Joliza Patricia Cañeba +29 more
wiley +1 more source

