Results 121 to 130 of about 863,797 (309)
INTRODUCTION: Although the prevalence of hepatitis virus infections in Pakistan is still unknown, limited data indicate that the exposure rate to HBV is 35-38% with 4% being carriers and 32% having anti-HBV surface antibodies through natural conversion ...
Kazmi SU, Hakim ST, Bagasra O
doaj
imputed-seq-genotypes-Chr29.9110000-10110000.vcf
Imputed genotypes for variants within 1Mbp of the Chr29:9.61 LC QTL, for 357 ...
Thomas Lopdell (511314) +10 more
core +1 more source
The PAM pathway and its impact on cellular metabolism. Color‐coded key symbols represent Rapamycin (R, orange, targeting mTOR) and Dactolisib (D, green, targeting PI3K/mTOR), indicating their sites of action. Created with BioRenders.com. Glioblastoma resists therapy through interconnected survival programs.
Kai Zhao +23 more
wiley +1 more source
imputed-seq-genotypes-Chr17.55970000-56970000.vcf
Imputed genotypes for variants within 1Mbp of the Chr17:56.47 LC QTL, for 357 ...
Thomas Lopdell (511314) +10 more
core +1 more source
Chronobiology of Cancer: How Aging Fuels Oncogenesis at the Molecular Level
This graphical abstract illustrates the key biological pathways linking aging with cancer development and progression. In the upper left, cumulative exposure to ultraviolet radiation, toxins, and reactive oxygen species (ROS) causes DNA damage and genomic instability, whereas age‐related decline in repair mechanisms, such as ATM/ATR, BER, and NER ...
Anu Singh, Aroonima Misra, Sufian Zaheer
wiley +1 more source
VCF file containing genotypes of the Parus major individuals. Individual names can be matched with the names found in the individuals.txt file in order to extract site of origin, coordinates, and urbanization ...
Arnaud Gregoire (3267345) +5 more
core +1 more source
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source
Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach +23 more
wiley +1 more source
imputed-seq-genotypes-Chr6.37260000-38260000.vcf
Imputed genotypes for variants within 1Mbp of the Chr6:37.76 LC QTL, for 357 ...
Thomas Lopdell (511314) +21 more
core +1 more source

