Results 1 to 10 of about 43,290 (163)

Human Mind and its Psychological Disposition: A Comparative Analysis of Ghazalian Nafs-e -Lawwamma and Freudian Superego

الإيضاح, 2021
The current paper aims to provide the venue to the spiritual insights of Ghazalian thought to be integrated into the study of Freudian psychoanalysis. The study has adopted descriptive and analytical approach to make a comparative analysis of Ghazalian ...
Sabeen Akber, Shumaila Mazhar
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The Establishment of a Moderate & Peaceful State, A Journey from Fantasy to Reality “Problems & their Solution”

الإيضاح, 2021
Unfortunately the objective of Pakistan is still to be materialized. Many factors led to the disordered and immoderate state: lack of proper education and inappropriate grooming of young generation in line with the Islamic teachings and abuse of rights ...
Oumar Saleem, Sadna Zeb
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4E-BP1 counteracts human mesenchymal stem cell senescence via maintaining mitochondrial homeostasis

Protein & 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, Qianzhao Ji, Zeming Wu, Yusheng Cai, Jian Yin, Yiyuan Zhang, Sheng Zhang, Xiaoqian Liu, Weiqi Zhang, Guang-Hui Liu, Si Wang, Moshi Song, J. Qu   +12 more
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The expression and significance of p4E‐BP1/4E‐BP1 in prostate cancer

Journal of clinical laboratory analysis (Print), 2022
Although the phosphorylation of 4E‐BP1 that has been detected in high‐grade prostate cancer has been reported in previous studies, overexpression of p4E‐BP1 and 4EBP1 and their clinical significance in prostate cancer still remain unknown.
Kai-Yun Wang, Ke-jie Wang, Qi Ma
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Fusarium BP1 is a reader of H3K27 methylation

Nucleic 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, Jianlong Yuan, Jing Wang, Yi-Zhe Zhang, Sijie Xie, Hongkai Wang, Zeng Tao, Huiquan Liu, H. Kistler, Youfu Zhao, Cheng-Guo Duan, Wende Liu, Zhonghua Ma, Yun Chen   +13 more
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BAP1 promotes viability and migration of ECA109 cells through KLF5/CyclinD1/FGF‐BP1

FEBS 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, Ming Luo, Honglan Qu, Yufeng Cheng   +3 more
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Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families

International Journal of Molecular Sciences, 2021
The 15q11.2 BP1-BP2 deletion (Burnside-Butler) syndrome is emerging as the most common cytogenetic finding in patients with neurodevelopmental or autism spectrum disorders (ASD) presenting for microarray genetic testing.
Isaac Baldwin, Robin L. Shafer, Waheeda A. Hossain, S. Gunewardena, O. Veatch, Matthew W. Mosconi, M. Butler   +6 more
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Recognition of narrators in Sahih Al-Bukhari, views of Hafiz Ibn Hajar and Imam Al-Kermani (A Critical comparative study)

الإيضاح, 2021
Sahih al-Bukhari by Imam Abu Abdullah Mohammad al-Bukhari stands next to the Holy Quran as a primary authentic source of Islam. “Al Kawakib ad Durari” by Imam al-kirmani is an important explanation of Sahih Bukhari. In “Fath al Bari” Al Hafiz Ibn e Hajar
Mati ur Rehman, Fateh Rahman Gorashi
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Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.

JAMA 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, I. Sønderby, T. Kaufmann, G. Walters, A. Abdellaoui, D. Ames, K. Amunts, M. Andersson, N. Armstrong, M. Bernard, Nicholas B. Blackburn, J. Blangero, D. Boomsma, H. Brodaty, R. Brouwer, R. Bülow, W. Cahn, V. Calhoun, S. Caspers, G. Cavalleri, C. Ching, S. Cichon, S. Ciufolini, A. Corvin, B. Crespo-Facorro, J. Curran, S. Dalvie, P. Dazzan, E. D. de Geus, G. D. de Zubicaray, S. D. de Zwarte, N. Delanty, Anouk den Braber, S. Desrivières, M. di Forti, J. Doherty, G. Donohoe, S. Ehrlich, E. Eising, T. Espeseth, S. Fisher, T. Fladby, O. Frei, V. Frouin, M. Fukunaga, Thomas Gareau, D. Glahn, H. Grabe, N. Groenewold, Ó. Gústafsson, J. Haavik, A. Håberg, R. Hashimoto, J. Hehir-Kwa, D. Hibar, M. Hillegers, P. Hoffmann, L. Holleran, J. Hottenga, H. H. Hulshoff Pol, M. Ikeda, S. Jacquemont, N. Jahanshad, C. Jockwitz, S. Johansson, E. Jönsson, M. Kikuchi, E. Knowles, J. Kwok, S. Le Hellard, D. Linden, Jingyu Liu, A. Lundervold, A. Lundervold, N. Martin, K. Mather, S. Mathias, K. Mcmahon, A. McRae, S. Medland, T. Moberget, C. Moreau, D. Morris, Thomas W. Mühleisen, R. Murray, J. Nordvik, L. Nyberg, Loes M. Olde Loohuis, R. Ophoff, M. Owen, T. Paus, Z. Pausova, J. Peralta, B. Pike, Carlos Prieto, E. Quinlan, C. Reinbold, T. Reis Marques, J. Rucker, P. Sachdev, S. Sando, P. Schofield, A. Schork, G. Schumann, Jean Shin, E. Shumskaya, Ana I. Silva, S. Sisodiya, V. Steen, Dan J Stein, Lachlan T. Strike, C. K. Tamnes, A. Teumer, A. Thalamuthu, D. Tordesillas-Gutiérrez, A. Uhlmann, M. Ulfarsson, D. van ‘t Ent, M. V. D. van den Bree, E. Vassos, W. Wen, K. Wittfeld, M. Wright, T. Zayats, A. Dale, S. Djurovic, I. Agartz, L. Westlye, H. Stefánsson, K. Stefánsson, P. Thompson, O. Andreassen   +131 more
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The 15q11.2 BP1-BP2 Microdeletion (Burnside–Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Disorders

International Journal of Molecular Sciences, 2020
The 15q11.2 BP1-BP2 microdeletion (Burnside–Butler) syndrome is emerging as the most frequent pathogenic copy number variation (CNV) in humans associated with neurodevelopmental disorders with changes in brain morphology, behavior, and cognition. In this
Syed K. Rafi, M. Butler
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