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The Journal of Infectious Diseases|July 12, 2011
Genetic and functional evidence implicating DLL1 as the gene that influences susceptibility to visceral leishmaniasis at chromosome 6q27Michaela Fakiola, E Nancy Miller, Manal Fadl, et al.
Nature Cancer|December 15, 2022
Targeting the bicarbonate transporter SLC4A4 overcomes immunosuppression and immunotherapy resistance in pancreatic cancerFederica Cappellesso, Marie-Pauline Orban, Niranjan Shirgaonkar, et al.
Cancers|June 10, 2023
Follicular Helper and Regulatory T Cells Drive the Development of Spontaneous Epstein-Barr Virus Lymphoproliferative DisorderElshafa Hassan Ahmed, Mark Lustberg, Claire Hale, et al.
Nature Metabolism|November 24, 2020
KRAS-regulated glutamine metabolism requires UCP2-mediated aspartate transport to support pancreatic cancer growthSusanna Raho, Loredana Capobianco, Rocco Malivindi, et al.
Frontiers in Neurology|September 7, 2021
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic ParaplegiaAshraf Yahia, Liena E O Elsayed, Remi Valter, et al.
European Journal of Human Genetics : EJHG|February 5, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile EpilepsyMahmoud Koko, Maha A Elseed, Inaam N Mohammed, et al.
Acta Physiologica (Oxford, England)|February 27, 2026
pH-Dependent Microenvironmental Ionic Signaling in Pancreatic Ductal AdenocarcinomaAlbrecht Schwab, Micol Rugi, Pawel Swietach, et al.
European Journal of Human Genetics : EJHG|September 8, 2016
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in SudanLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
European Journal of Human Genetics : EJHG|April 3, 2023
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerationsAshraf Yahia, Ahlam A A Hamed, Inaam N Mohamed, et al.
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