Results 11 to 20 of about 3,917,874 (426)

Genetics of Somatic Mammalian Cells: Demonstration of a Human Esterase Activator Gene Linked to the AdeB Gene [PDF]

open access: greenProceedings of the National Academy of Sciences of the United States of America, 1972
Prototrophic hybrids formed from an adenine-requiring Chinese hamster cell and human fibroblasts uniformly display new esterase activity that differs from that of either parental cell in electrophoretic mobility and substrate specificity.
Fa‐Ten Kao, Theodore T. Puck
openalex   +2 more sources

Genetics of Plasminogen Activator Inhibitor-1 (PAI-1) in a Ghanaian Population. [PDF]

open access: goldPLoS ONE, 2015
Plasminogen activator inhibitor 1 (PAI-1), a major modulator of the fibrinolytic system, is an important factor in cardiovascular disease (CVD) susceptibility and severity.
Marquitta J White   +7 more
doaj   +3 more sources

Mouse genetics: Catalogue and scissors [PDF]

open access: yesBMB Reports, 2012
Phenotypic analysis of gene-specific knockout (KO) mice hasrevolutionized our understanding of in vivo gene functions. Asthe use of mouse embryonic stem (ES) cells is inevitable forconventional gene targeting, the generation of knockout miceremains a ...
Han-Woong Lee
doaj   +2 more sources

MPF Regulates Oocyte and Embryo Development During Parthenogenesis Induction in Silkworm, <i>Bombyx mori</i>. [PDF]

open access: yesInsects
In most species, oocytes are arrested at the prophase or metaphase of meiosis I and require sperm-derived or external stimuli to resume meiosis. Maturation-promoting factor (MPF) is an oocyte maturation factor composing the catalytic subunit Cdc2 and the
Ma C   +11 more
europepmc   +2 more sources

Unraveling the impact of blood RANKL and OPG levels on Alzheimer's disease: Independent of bone mineral density and inflammation. [PDF]

open access: yesAlzheimers Dement (N Y)
INTRODUCTION Observational studies have revealed a close relationship between reduced bone mineral density (BMD) and Alzheimer's disease (AD) risk. The receptor activator of nuclear factor kappa‐B ligand (RANKL) and osteoprotegerin (OPG) system, pivotal ...
Guo X, Shi W, Lu J, Tang P, Li R.
europepmc   +2 more sources

CRISPR-Cas9 Technology for the Creation of Biological Avatars Capable of Modeling and Treating Pathologies: From Discovery to the Latest Improvements

open access: yesCells, 2022
This is a spectacular moment for genetics to evolve in genome editing, which encompasses the precise alteration of the cellular DNA sequences within various species. One of the most fascinating genome-editing technologies currently available is Clustered
Ali Nasrallah   +4 more
doaj   +1 more source

Active information requirements for fixation on the Wright-Fisher model of population genetics [PDF]

open access: yesBIO-Complexity 2020(4):1-6, 2021
In the context of population genetics, active information can be extended to measure the change of information of a given event (e.g., fixation of an allele) from a neutral model in which only genetic drift is taken into account to a non-neutral model that includes other sources of frequency variation (e.g., selection and mutation).
arxiv   +1 more source

Targeted mutagenesis in the malaria mosquito using TALE nucleases. [PDF]

open access: yesPLoS ONE, 2013
Anopheles gambiae, the main mosquito vector of human malaria, is a challenging organism to manipulate genetically. As a consequence, reverse genetics studies in this disease vector have been largely limited to RNA interference experiments.
Andrea L Smidler   +4 more
doaj   +1 more source

Recent advances in genetically modified large-animal models of human diseases

open access: yesBIO Integration, 2022
Large-animal models show greater advantages than rodents in recapitulating human genetic diseases, primarily because of their higher similarity to humans in terms of anatomy, physiology and genetics.
Jing Zhang, Xiaoyue Sun, Chunwei Cao
doaj   +1 more source

KATP channel mutations in congenital hyperinsulinism: Progress and challenges towards mechanism-based therapies

open access: yesFrontiers in Endocrinology, 2023
Congenital hyperinsulinism (CHI) is the most common cause of persistent hypoglycemia in infancy/childhood and is a serious condition associated with severe recurrent attacks of hypoglycemia due to dysregulated insulin secretion.
Assmaa ElSheikh   +2 more
doaj   +1 more source

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