Results 301 to 310 of about 350,738 (380)

Long‐term cardiovascular risk in women with hypertensive disorders of pregnancy: Insights from polygenic risk scores

open access: yesActa Obstetricia et Gynecologica Scandinavica, EarlyView.
FinnGen data of 213 942 women was utilized in order to investigate the risk of cardiovascular disease in women with and without hypertensive disorders of pregnancy and with diverse genetic risks for cardiovascular disease and preeclampsia measured with polygenic risk scores.
Anna Kivioja   +8 more
wiley   +1 more source

Nearly T2T, phased genome assemblies of corals reveal haplotype diversity and the evolutionary process of gene expansion. [PDF]

open access: yesDNA Res
Takeuchi T   +7 more
europepmc   +1 more source

Human amyotrophic lateral sclerosis/motor neuron disease: The disease‐associated microglial pathway is upregulated while APOE genotype governs risk and survival

open access: yesBrain Pathology, EarlyView.
ALS/MND‐related inflammation is investigated in the motor cortex and spinal cord by both transcriptomics and immunohistochemistry. This reveals greater inflammation in the spinal cord and highlights the disease‐associated microglial (DAM) phenotype characterized by ApoE, TREM2, and TYROBP.
Bridget A. Ashford   +10 more
wiley   +1 more source

Novel approaches for the discovery of pharmacogenetic biomarkers of chemotoxicity in patients with colorectal cancer

open access: yesBritish Journal of Pharmacology, EarlyView.
Background and Purpose Chemotherapeutic treatment for colorectal cancer (colorectal cancer) allows for increased patient overall survival. However, current therapeutic regimens are often associated with the development of adverse drug reactions, which represent a morbidity, mortality and economic issue.
Ana Rita Simoes   +20 more
wiley   +1 more source

HLA GENE AND HAPLOTYPE FREQUENCIES IN THE NORTH AMERICAN POPULATION

open access: bronze, 1997
Motomi Mori   +4 more
openalex   +1 more source

The Diverse Genetic Landscape of Hearing Impairment in South African Families

open access: yesClinical Genetics, EarlyView.
South African Families with Nonsyndromic (N = 24) and Syndromic Hearing Impairment (N = 21) with ≥ 2 affected members were analyzed. The underlying etiology was uncovered using exome and Sanger sequencing for 31 of these families. ABSTRACT To elucidate the genetic etiology of hearing impairment (HI) in South Africa, 45 nonsyndromic HI (NSHI) and ...
Thashi Bharadwaj   +10 more
wiley   +1 more source

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