Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Erdyni N Tsitsikov"'
Autor:
Erdyni N Tsitsikov, Khanh P Phan, Yufeng Liu, Alla V Tsytsykova, Rosalia Paterno, David M Sherry, Anthony C Johnson, Ian F Dunn
Publikováno v:
PLoS ONE, Vol 19, Iss 12, p e0290487 (2024)
Here, we describe a spontaneous mouse mutant with a deletion in a predicted gene 2310061I04Rik (Rik) of unknown function located on chromosome 17. A 59 base pair long deletion occurred in the first intron of the Rik gene and disrupted its expression.
Externí odkaz:
https://doaj.org/article/1877d9130b76445ebfc9cb37a8e35338
Autor:
Erdyni N. Tsitsikov, Khanh P. Phan, Yufeng Liu, Alla V. Tsytsykova, Mike Kinter, Lauren Selland, Lori Garman, Courtney Griffin, Ian F. Dunn
Publikováno v:
iScience, Vol 26, Iss 8, Pp 107474- (2023)
Summary: Targeted deletion of TRAF7 revealed that it is a crucial part of shear stress-responsive MEKK3-MEK5-ERK5 signaling pathway induced in endothelial cells by blood flow. Similar to Mekk3-, Mek5- or Erk5-deficient mice, Traf7-deficient embryos d
Externí odkaz:
https://doaj.org/article/38b835baed654e939447be815a05ea30
Autor:
Erdyni N. Tsitsikov, Sanaa Hameed, Sherwin A. Tavakol, Tressie M. Stephens, Alla V. Tsytsykova, Lori Garman, Wenya Linda Bi, Ian F. Dunn
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
IntroductionMeningiomas are the most common primary central nervous system (CNS) tumors in adults, representing approximately one-third of all primary adult CNS tumors. Although several recent publications have proposed alternative grading systems of
Externí odkaz:
https://doaj.org/article/35e8dab11b6b4aee83e6e5851b493547
Autor:
Khanh P. Phan, Panayiotis Pelargos, Alla V. Tsytsykova, Erdyni N. Tsitsikov, Graham Wiley, Chuang Li, Melissa Bebak, Ian F. Dunn
Publikováno v:
Journal of Developmental Biology, Vol 11, Iss 1, p 13 (2023)
The COMMD (copper metabolism MURR1 domain containing) family includes ten structurally conserved proteins (COMMD1 to COMMD10) in eukaryotic multicellular organisms that are involved in a diverse array of cellular and physiological processes, includin
Externí odkaz:
https://doaj.org/article/36dc1a838a5a4c8f88e9ec04e6148565
Autor:
Erdyni N. Tsitsikov, Khanh P. Phan, Yufeng Liu, Alla V. Tsytsykova, Mike Kinter, Lauren Selland, Lori Garman, Courtney Griffin, Ian F. Dunn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::231be9ae1b74a964dffa784fe9e1a1f9
https://doi.org/10.2139/ssrn.4397183
https://doi.org/10.2139/ssrn.4397183
Autor:
Amanda Reiter, Janet Chou, Erdyni N. Tsitsikov, Kanyun Xue, Raif S. Geha, Fatima Zaman, Megan Day-Lewis, Christina S.K. Yee, Abduarahman Almutairi
Publikováno v:
The Journal of Allergy and Clinical Immunology: In Practice. 8:3543-3548
Background Chronic granulomatous disease is a primary immunodeficiency characterized by recurrent bacterial and fungal infections, granuloma formation, and inflammatory disease. Impaired neutrophil oxidative function is an essential diagnostic criter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0404a2fa3df0163b5d8d045be05fd67
https://doi.org/10.1016/j.jaip.2020.07.012
https://doi.org/10.1016/j.jaip.2020.07.012
Autor:
Alla V, Tsytsykova, Graham, Wiley, Chuang, Li, Richard C, Pelikan, Lori, Garman, Francis A, Acquah, Blaine H M, Mooers, Erdyni N, Tsitsikov, Ian F, Dunn
Publikováno v:
iScience. 25(8)
Krüppel-like factor 4 (KLF4) is a transcription factor that has been proven necessary for both induction and maintenance of pluripotency and self-renewal. Whole-genome sequencing defined a unique mutation in KLF4 (KLF4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f7c2754c3981c8a34d309dacfa5484dc
https://pubmed.ncbi.nlm.nih.gov/35996584
https://pubmed.ncbi.nlm.nih.gov/35996584
Autor:
Janet Chou, Luigi D. Notarangelo, Maxim I. Lutskiy, Erdyni N. Tsitsikov, Anahita F. Dioun, Raif S. Geha
Publikováno v:
Journal of Allergy and Clinical Immunology. 134:223-226
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84012397675f4a856611d46b8cc5c660
https://doi.org/10.1016/j.jaci.2014.01.041
https://doi.org/10.1016/j.jaci.2014.01.041
Publikováno v:
Handbook of Tuberculosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2287852526a24e1996313ec7dd8778f
https://doi.org/10.1002/9783527611614.ch30
https://doi.org/10.1002/9783527611614.ch30
Publikováno v:
Blood. 110:743-751
The NF-κB2 gene is recurrently mutated in human lymphoid malignancies. However, a causal relationship between NF-κB2 mutation and lymphomagenesis has not been established. It is also unclear how the mutation may lead to lymphoid malignancies. We re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26628e28dc2c8e48584fa24997264a2a
https://doi.org/10.1182/blood-2006-11-058446
https://doi.org/10.1182/blood-2006-11-058446