EDCTP Alumni Network

Fostering excellence and collaboration in the next generation of researchers

Call Career Development Fellowship (CDF)
Programme EDCTP2
Start Date 2020-11-01
End Date 2023-10-31
Project Code TMA2019CDF-2736
Status Active

Title

Targeting fetal-maternal innate response conflict for better placental malaria outcomes (IRMiP)

Host Organisation

Institution Country
Mount Kenya University Trust (MKU) Kenya

Current Organisation

Mount Kenya University

Current Job Title

Research Fellow

Students Supervised

Type Name Title University Start Date End Date
MSc Samuel Chenge JKUAT 2021
Harrison Ngure MKU 2021

Areas Of Specialisation

Malaria

Publications

Authors:
Kobia F , author
Duchi S , author
Deflorian G , author
Vaccari T , author
Date:
2014-03-01
Journal:
Molecular oncology
Content:
Identifiers:
Authors:
Tognon E , author
Kobia F , author
Busi I , author
Fumagalli A , author
De Masi F , author
Vaccari T , author
Date:
2016-01-01
Journal:
Autophagy
Content:
Identifiers:
Authors:
Francis Kobia , author
Jesse Gitaka , author
Francis Makokha , author
Moses Kamita , author
Joshua Kibera , author
Cynthia Mwenda , author
Gladys Mucee , author
Bactrin Kilingo , author
Date:
2019-12-03
Journal:
Content:
Identifiers:
Authors:
Francis Kobia , author
Jesse Gitaka , author
Date:
2020-04-17
Journal:
Content:
Identifiers:
Authors:
Date:
2020-03-06
Journal:
[]
Content:
AbstractCooperative DNA binding is a key feature of transcriptional regulation. Here we examined the role of cooperativity in Notch signaling by CRISPR-mediated engineering of mice in which neither Notch1 nor Notch2 can homo- or heterodimerize, essential for cooperative binding to sequence paired sites (SPS) located near many Notch-regulated genes. While most known Notch-dependent phenotypes were unaffected in Notch1/2 dimer-deficient mice, a subset of tissues proved highly sensitive to loss of cooperativity. These phenotypes include heart development, compromising viability in combination with low gene dose, and the gut, developing ulcerative colitis in response to 1% DSS. The most striking phenotypes – gender imbalance and splenic marginal zone B cell lymphoma – emerged in combination with dose reduction or when challenged by chronic fur mite infestation. This study highlights the role of the environment in malignancy and colitis, and is consistent with Notch-dependent anti-parasite immune responses being compromised in the dimer deficient animals.HighlightsNotch dimerization has an in vivo role in contributing to intestinal homeostasisLoss of cooperativity can manifest as Notch gain or loss of function phenotypesMite infestation exacerbates all phenotypes, triggers MZB hyperproliferation in mutant animalsMite-infested mutant mice develop SMZL with age
Identifiers:
Authors:
Francis M. Kobia , author
Kaushik Maiti , author
Moses M. Obimbo , author
Roger Smith , author
Jesse Gitaka , author
Date:
2022-05-01
Journal:
Trends in Parasitology
Content:
Identifiers:

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