Results 1 to 10 of about 49,552 (162)

Prader–Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review

open access: yesInternational Journal of Molecular Sciences, 2023
Prader–Willi syndrome (PWS) is a complex genetic disorder with three PWS molecular genetic classes and presents as severe hypotonia, failure to thrive, hypogonadism/hypogenitalism and developmental delay during infancy. Hyperphagia, obesity, learning and
M. Butler
semanticscholar   +1 more source

SGCE promotes breast cancer stemness by promoting the transcription of FGF-BP1 by Sp1

open access: yesJournal of Biological Chemistry, 2023
Breast cancer stem cells are mainly responsible for poor prognosis, especially in triple-negative breast cancer (TNBC). In a previous study, we demonstrated that ε-Sarcoglycan (SGCE), a type Ⅰ single-transmembrane protein, is a potential oncogene that ...
Ting Qiu   +9 more
semanticscholar   +1 more source

The dynamic mechanism of 4E-BP1 recognition and phosphorylation by mTORC1.

open access: yesMolecules and Cells, 2021
The activation of cap-dependent translation in eukaryotes requires multisite, hierarchical phosphorylation of 4E-BP by the 1 MDa kinase mammalian target of rapamycin complex 1 (mTORC1). To resolve the mechanism of this hierarchical phosphorylation at the
R. Böhm   +5 more
semanticscholar   +1 more source

4E-BP1 counteracts human mesenchymal stem cell senescence via maintaining mitochondrial homeostasis

open access: yesProtein & Cell, 2022
Although the mTOR-4E-BP1 signaling pathway is implicated in aging and aging-related disorders, the role of 4E-BP1 in regulating human stem cell homeostasis remains largely unknown.
Yifang He   +12 more
semanticscholar   +1 more source

Fusarium BP1 is a reader of H3K27 methylation

open access: yesNucleic Acids Research, 2021
Histone H3 lysine 27 methylation catalyzed by polycomb repressive complex 2 (PRC2) is conserved from fungi to humans and represses gene transcription. However, the mechanism for recognition of methylated H3K27 remains unclear, especially in fungi.
G. Tang   +13 more
semanticscholar   +1 more source

BAP1 promotes viability and migration of ECA109 cells through KLF5/CyclinD1/FGF‐BP1

open access: yesFEBS Open Bio, 2021
More than 40 000 patients worldwide die from esophageal cancer annually. The 5‐year survival rate of patients is only ~ 15–20%, and thus, there is an ongoing need to improve diagnosis and treatment of esophageal cancer.
Fengyun Wang   +3 more
semanticscholar   +1 more source

BAD regulates mammary gland morphogenesis by 4E-BP1-mediated control of localized translation in mouse and human models

open access: yesNature Communications, 2021
Elucidation of non-canonical protein functions can identify novel tissue homeostasis pathways. Herein, we describe a role for the Bcl-2 family member BAD in postnatal mammary gland morphogenesis.
J. M. Githaka   +12 more
semanticscholar   +1 more source

TELAAH PEMIKIRAN HADIS MAHMUD ABU RAYYAH DALAM BUKU “AḌWA’ ‘ALA AL-SUNNAH AL-MUHAMMADIYAH”

open access: yesHunafa: Jurnal Studia Islamika, 2012
: In the development of contemporary hadith studies, especially after the time of Muhammad Abduh, a number of figures who appear to have a critical view of the classical era of hadith studies. Some people rate them as al-Sunnah inkār modern.
Sochimin Sochimin
doaj   +3 more sources

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.

open access: yesJAMA psychiatry, 2020
Importance Recurrent microdeletions and duplications in the genomic region 15q11.2 between breakpoints 1 (BP1) and 2 (BP2) are associated with neurodevelopmental disorders.
D. van der Meer   +131 more
semanticscholar   +1 more source

MENGEMBANGKAN PERILAKU SEHAT MELALUI PENDEKATAN SOCIAL LEARNING THEORY

open access: yesHunafa: Jurnal Studia Islamika, 2007
Prior to 1990s, the major cause of death is a cute disorder such as tuberculosis, small fox, leprosy and various infections convinced to be brought about by viruses and bacteria.
Fatimah Saguni
doaj   +1 more source

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