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2022

International refereed journal articles

51 - 

Monocyte-Macrophage Lineage Cell Fusion

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

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

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

Pubmed : 35742997

 

52 - 

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

 

53 - 

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

 

54 - 

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

 

55 - 

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

 

56 - 

The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder

Smitha Kumble, Amanda Levy, Jaya Punetha, Hua Gao, Nicholas Ah Mew, Kwame Anyane-Yeboa, Paul Benke, Sara Berger, Lise Bjerglund, Belinda Campos-Xavier, Michael Ciliberto, Julie Cohen, Anne Comi, Cynthia Curry, Lena Damaj et al.

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

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

Pubmed : 34859529

 

57 - 

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, Virginie Vignard, Tiphaine Hery, Mathilde Nizon, Grazia M.S. Mancini, Jacques Giltay, Benjamin Cogné, Kirsty Mcwalter, Wallid Deb, Hagar Mor-Shaked, Hong Li 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

 

58 - 

Rare pathogenic variants in WNK3 cause X-linked intellectual disability

Sébastien Küry, Jinwei Zhang, Thomas Besnard, Alfonso Caro-Llopis, Xue Zeng, Stephanie Robert, Sunday Josiah, Emre Kiziltug, Anne-Sophie Denommé-Pichon, Benjamin Cogné, Adam Kundishora, Le Hao, Hong Li, Roger Stevenson, Raymond Louie et al.

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

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

Pubmed : 35678782

 

59 - 

LncRNAs in domesticated animals: from dog to livestock species

Sandrine Lagarrigue, Matthias Lorthiois, Fabien Degalez, David Gilot, Thomas Derrien

Mammalian Genome, 2022, 33 (2), pp.248-270.

DOI : https://doi.org/10.1007/s00335-021-09928-7

Pubmed : 34773482

 

60 - 

Impact of Chromosomal Context on Origin Selection and the Replication Program

Lilian Lanteri, Anthony Perrot, Diane Schausi-Tiffoche, Pei-Yun Jenny Wu

Genes, 2022, 13 (7), pp.1244.

DOI : https://doi.org/10.3390/genes13071244

Pubmed : 35886027