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2022

Articles

51 - 

Giant Multinucleated Cells in Aging and Senescence-An Abridgement

Malgorzata Kloc, Ahmed Uosef, Arijita Subuddhi, Jacek Z. Kubiak, Rafal P. Piprek et al.

Biology, 2022, 11 (8), pp.1121.

DOI : https://doi.org/10.3390/biology11081121

Pubmed : 35892977

 

52 - 

Virus interactions with the actin cytoskeleton-what we know and do not know about SARS-CoV-2

Malgorzata Kloc, Ahmed Uosef, Jarek Wosik, Jacek Z. Kubiak, Rafik M. Ghobrial et al.

Archives of Virology, 2022, 167 (3), pp.737-749.

DOI : https://doi.org/10.1007/s00705-022-05366-1

Pubmed : 35102456

 

53 - 

Monocyte-Macrophage Lineage Cell Fusion

Malgorzata Kloc, Arijita Subuddhi, Ahmed Uosef, Jacek Z. Kubiak, Rafik M. Ghobrial et al.

International Journal of Molecular Sciences, 2022, 23 (12), pp.6553.

DOI : https://doi.org/10.3390/ijms23126553

Pubmed : 35742997

 

54 - 

Natural genetic engineering: A programmed chromosome/DNA elimination

Malgorzata Kloc, Jacek Z Kubiak, Rafik M Ghobrial

Developmental Biology, 2022, 486, pp.15-25.

DOI : https://doi.org/10.1016/j.ydbio.2022.03.008

Pubmed : 35321809

 

55 - 

Macrophage-, Dendritic-, Smooth Muscle-, Endothelium-, and Stem Cells-Derived Foam Cells in Atherosclerosis

Malgorzata Kloc, Jacek Z. Kubiak, Rafik M. Ghobrial

International Journal of Molecular Sciences, 2022, 23 (22),

DOI : https://doi.org/10.3390/ijms232214154

Pubmed : 36430636

 

56 - 

Monocyte and Macrophage Function Diversity

Malgorzata Kloc, Jacek Z. Kubiak

International Journal of Molecular Sciences, 2022, 23 (20),

DOI : https://doi.org/10.3390/ijms232012404

Pubmed : 36293261

 

57 - 

Mitochondrial transport, partitioning, and quality control at the heart of cell proliferation and fate acquisition

Rakesh Kumar Sharma, Abderrahman Chafik, Giulia Bertolin

American Journal of Physiology - Cell Physiology, 2022, 322 (2), pp.C311-C325.

DOI : https://doi.org/10.1152/ajpcell.00256.2021

Pubmed : 35044857

 

58 - 

The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder

Smitha Kumble, Amanda Levy, Jaya Punetha, Hua Gao, Nicholas Ah Mew et al.

Human Mutation, 2022, 43 (2), pp.266-282.

DOI : https://doi.org/10.1002/humu.24308

Pubmed : 34859529

 

59 - 

Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder

Sébastien Küry, Frédéric Ebstein, Alice Mollé, Thomas Besnard, Ming-Kang Lee et al.

American Journal of Human Genetics, 2022, 109 (2), pp.361-372.

DOI : https://doi.org/10.1016/j.ajhg.2021.12.011

Pubmed : 35051358

 

60 - 

Rare pathogenic variants in WNK3 cause X-linked intellectual disability

Sébastien Küry, Jinwei Zhang, Thomas Besnard, Alfonso Caro-Llopis, Xue Zeng et al.

Genetics in Medicine, 2022, 24 (9), pp.1941-1951.

DOI : https://doi.org/10.1016/j.gim.2022.05.009

Pubmed : 35678782