truncated ABL protooncogene 1 nonreceptor tyrosine kinase, partial [Ho - Protein

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Human ABL1 deficiency syndrome (HADS) is a recognizable syndrome distinct from ABL1-related congenital heart defects and skeletal malformations syndrome. [Hum Genet. 2024]
Human ABL1 deficiency syndrome (HADS) is a recognizable syndrome distinct from ABL1-related congenital heart defects and skeletal malformations syndrome.
AlAbdi L, Neuhann T, Prott EC, Schön U, Abdulwahab F, Faqeih E, Alkuraya FS. Hum Genet. 2024 Jun; 143(6):739-745. Epub 2024 May 14.
Zinc as a potential regulator of the BCR-ABL oncogene in chronic myelocytic leukemia cells. [J Trace Elem Med Biol. 2024]
Zinc as a potential regulator of the BCR-ABL oncogene in chronic myelocytic leukemia cells.
Zhu B, Sun L, Li Z, Shang P, Yang C, Li K, Li J, Zhi Q, Hua Z. J Trace Elem Med Biol. 2024 May; 83:127407. Epub 2024 Feb 2.
A case report of a truncated ABL1 mutation in 2 cases with Philadelphia chromosome-positive B cell precursor acute lymphoblastic leukemia. [Int J Hematol. 2024]
A case report of a truncated ABL1 mutation in 2 cases with Philadelphia chromosome-positive B cell precursor acute lymphoblastic leukemia.
Kato K, Takagi S, Takano H, Tsunoda S, Watanabe O, Yamaguchi K, Kageyama K, Kaji D, Taya Y, Nishida A, et al. Int J Hematol. 2024 Feb; 119(2):205-209. Epub 2024 Jan 18.