A Homolog of Structural Maintenance of Chromosome 1 Is a Persistent Centromeric Protein Which Associates With Nuclear Pore Components in Toxoplasma gondii

Autor: Maria E. Francia, Sheila Bhavsar, Li-Min Ting, Matthew M. Croken, Kami Kim, Jean-Francois Dubremetz, Boris Striepen

Publikováno v: Frontiers in Cellular and Infection Microbiology, Vol 10 (2020)

Apicomplexa are obligate intracellular parasites which cause various animal and human diseases including malaria, toxoplasmosis, and cryptosporidiosis. They proliferate by a unique mechanism that combines physically separated semi-closed mitosis of t

Externí odkaz: https://doaj.org/article/8c4e0c090ba84f2bb3d303373c853bb9

Intragenomic Redistribution of Host Transcription Factor Binding With Toxoplasma Gondii Infection

Autor: Shahina Maqbool, Claudia A. Simões-Pires, Amit Verma, Sanchari Bhattacharyya, Yu Kong, Andrew D. Johnston, N. Ari Wijetunga, Matthew M. Croken, Zofia Wicik, Netha Ulahannan, Masako Suzuki, John M. Greally

The intracellular pathogenToxoplasma gondiimodifies a number of host cell processes. The mechanisms by whichT. gondiialters host gene expression are incompletely understood. This study focuses on how the regulators of gene expression in human host ce

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5957632eb25409b959f92fa933292da1

The Toxoplasma nuclear factor TgAP2XI-4 controls bradyzoite gene expression and cyst formation

Autor: Robert, Walker, Mathieu, Gissot, Matthew M, Croken, Ludovic, Huot, David, Hot, Kami, Kim, Stanislas, Tomavo

Publikováno v: Molecular microbiology. 87(3)

Toxoplasma gondii undergoes many phenotypic changes during its life cycle. The recent identification of AP2 transcription factors in T. gondii has provided a platform for studying the mechanisms controlling gene expression. In the present study, we r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e0a178d4ea3c7246f9fabd6c009a0a14
https://pubmed.ncbi.nlm.nih.gov/23240624

Dual Diagnosis of Ellis-van Creveld Syndrome and Hearing Loss in a Consanguineous Family.

Autor: Vona B; Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany., Maroofian R; Medical Research, RILD Wellcome Wolfson Centre, University of Exeter Medical School, Royal Devon & Exeter NHS Foundation Trust, Exeter, UK., Mendiratta G; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA., Croken M; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA., Peng S; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA., Ye X; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Department of Dentistry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; College of Dentistry, University of Illinois at Chicago, Chicago, Illinois, USA., Rezazadeh J; Genetic Counselling and Rehabilitation Unit, Welfare Organization, South Khorasan, Iran., Bahena P; Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany., Lekszas C; Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany., Haaf T; Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany., Edelmann L; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA., Shi L; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Publikováno v: Molecular syndromology [Mol Syndromol] 2017 Dec; Vol. 9 (1), pp. 5-14. Date of Electronic Publication: 2017 Sep 22.