Results 1 to 10 of about 137,611 (281)

Temporal hampering of thyroid hormone synthesis just before hatching impeded the filial imprinting in domestic chicks

open access: yesFrontiers in Physiology, 2023
Thyroid hormones play a critical role in the initiation of the sensitive period of filial imprinting. The amount of thyroid hormones in the brains of chicks increases intrinsically during the late embryonic stages and peaks immediately before hatching ...
Shouta Serizawa   +6 more
doaj   +1 more source

Dental pulp stem cells as a promising model to study imprinting diseases

open access: yesInternational Journal of Oral Science, 2022
Parental imprinting is an epigenetic process leading to monoallelic expression of certain genes depending on their parental origin. Imprinting diseases are characterized by growth and metabolic issues starting from birth to adulthood. They are mainly due
Eloïse Giabicani   +9 more
doaj   +1 more source

The Impact of Socialist Imprinting and Search for Knowledge on Resource Change: An Empirical Study of Firms in Lithuania [PDF]

open access: yes, 2002
In this paper we examine how firms change their resources in response to exogenous shocks in their business environment. Building on core ideas from the literatures on organizational imprinting and firm resources, we suggest that founding conditions ...
Kale, Prashant, Kriauciunas, Aldas
core   +3 more sources

A Facile Surface-Imprinting Strategy for Trypsin-Imprinted Polymeric Chemosensors Using Two-Step Spin-Coating

open access: yesChemosensors, 2023
Surface imprinting used for protein recognition in functional cavities is highly effective in imprinting biomacromolecules to avoid template encapsulation during the formation of a molecularly imprinted polymer (MIP) matrix. Herein, we introduce a facile
Je Wook Byeon   +5 more
doaj   +1 more source

Imprinting Mechanisms [PDF]

open access: yesGenome Research, 1998
A number of recent studies have provided new insights into mechanisms that regulate genomic imprinting in the mammalian genome. Regions of allele-specific differential methylation (DMRs) are present in all imprinted genes examined. Differential methylation is erased in germ cells at an early stage of their development, and germ-line-specific ...
Constância, Miguel   +3 more
openaire   +3 more sources

Combinations of maternal-specific repressive epigenetic marks in the endosperm control seed dormancy

open access: yeseLife, 2021
Polycomb Repressive Complex 2 (PRC2)-mediated trimethylation of histone H3 on lysine 27 (H3K27me3) and methylation of histone 3 on lysine 9 (H3K9me) are two repressive epigenetic modifications that are typically localized in distinct regions of the ...
Hikaru Sato   +2 more
doaj   +1 more source

AIJ: joint test for simultaneous detection of imprinting and non-imprinting allelic expression imbalance

open access: yesMathematical Biosciences and Engineering, 2020
Epigenetics is the study of heritable changes in gene expression or cellular phenotype caused by mechanisms other than changes in the underlying DNA sequence.
Dao-Peng Chen   +2 more
doaj   +1 more source

Video Imprint [PDF]

open access: yesIEEE Transactions on Pattern Analysis and Machine Intelligence, 2019
A new unified video analytics framework (ER3) is proposed for complex event retrieval, recognition and recounting, based on the proposed video imprint representation, which exploits temporal correlations among image features across video frames. With the video imprint representation, it is convenient to reverse map back to both temporal and spatial ...
Zhanning Gao   +5 more
openaire   +3 more sources

Stability of Imprinting and Differentiation Capacity in Naïve Human Cells Induced by Chemical Inhibition of CDK8 and CDK19

open access: yesCells, 2021
Pluripotent stem cells can be stabilized in vitro at different developmental states by the use of specific chemicals and soluble factors. The naïve and primed states are the best characterized pluripotency states.
Raquel Bernad   +5 more
doaj   +1 more source

Epigenetics in Prader-Willi Syndrome

open access: yesFrontiers in Genetics, 2021
Prader-Willi Syndrome (PWS) is a rare neurodevelopmental disorder that affects approximately 1 in 20,000 individuals worldwide. Symptom progression in PWS is classically characterized by two nutritional stages.
Aron Judd P. Mendiola, Janine M. LaSalle
doaj   +1 more source

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