Imran Ullah

Mutational analysis in different genes underlying severe combined immunodeficiency in seven consanguineous Pakistani families.

Fayyaz H, Zaman A, Shabbir S, Khan ZK, Haider N, Saleem AF, Ahamad W, Ullah I.

Mol Biol Rep. 2024 Feb 14. 51(1):302. PMID: 38355773

Utilizing the drug repurposing strategy on current drugs: new leads for peptic ulcers via biochemical and biomolecular dynamics studies.

Khan M, Nizamani A, Shah L, Ullah I, Waqas M, Halim SA, Ataya FS, Elgazzar AM, Batiha GE, Khan A, Al-Harrasi A.

J Biomol Struct Dyn. 2024 Jan 15. 1-14. PMID: 38225797

Artemisinin resistance mutations in Pfcoronin impede hemoglobin uptake.

Ullah I, Farringer MA, Burkhard AY, Hathaway E, Willett BC, Khushu M, Shin SH, Sharma AI, Shao KL, Martin MC, Dvorin JD, Hartl DL, Volkman SK, Bopp S, Absalon S, Wirth DF.

bioRxiv. 2023 Dec 22. PMID: 38187525

Sequence variants in different genes underlying Bardet-Biedl syndrome in four consanguineous families.

Ali A, Bilal M, Mis EK, Lakhani SA, Ahmad W, Ullah I.

Mol Biol Rep. 2023 Dec. 50(12):9963-9970. PMID: 37897612

Sequence variants in DLX5, HOXD13 and 445?kb-microduplication surrounding BTRC cause split-hand/foot malformation in three different families.

Hussain S, Ji W, Khan H, Mis EK, Mushtaq R, Chodhary M, Raza MH, Jan A, Ullah I, Khokha MK, Lakhani SA, Ahmad W.

Clin Genet. 2024 01. 105(1):109-111. PMID: 37776184

A variant in sperm-specific glycolytic enzyme enolase 4 (ENO4) causes human male infertility.

Nawaz S, Hussain S, Bilal M, Syed N, Liaqat K, Ullah I, Akil AA, Fakhro KA, Ahmad W.

J Gene Med. 2024 Jan. 26(1):e3583. PMID: 37640479

A variant in the LDL receptor-related protein encoding gene LRP4 underlying polydactyly and phalangeal synostosis in a family of Pakistani origin.

Khan H, Ullah K, Jan A, Ali H, Ullah I, Ahmad W.

Congenit Anom (Kyoto). 2023 Nov. 63(6):190-194. PMID: 37563890

Src- and Abl-family kinases activate spleen tyrosine kinase to maximize phagocytosis and Leishmania infection.

Ullah I, Barrie U, Kernen RM, Mamula ET, Khuong FTH, Booshehri LM, Rhodes EL, Bradford JM, Datta A, Wetzel DM.

J Cell Sci. 2023 07 15. 136(14). PMID: 37357611

A novel homozygous splice site variant in CERS3 causes autosomal recessive congenital ichthyosis.

Jan H, Wasif N, Naqvi SK, Ullah I, Ahmad W.

Congenit Anom (Kyoto). 2023 07. 63(4):127-128. PMID: 37128664

Author Correction: Partial differential equations modeling of thermal transportation in Casson nanofluid flow with arrhenius activation energy and irreversibility processes.

Al Oweidi KF, Jamshed W, Goud BS, Ullah I, Mohamed Isa SSP, El Din SM, Guedri K, Jaleel RA.

Sci Rep. 2023 Jan 31. 13(1):1754. PMID: 36720992