Search Results

CEBPA mutation in a case of chronic myeloid leukemia presenting in myeloid blast crisis.

• Authors : Yin, Yafei¹ (AUTHOR); Li, Ji¹ (AUTHOR); Yan, Wenzhe¹ (AUTHOR)

Subjects: *DELETION mutation; *CHRONIC myeloid leukemia; *GENETICS

• Source: Leukemia & Lymphoma. Mar2017, Vol. 58 Issue 3, p708-710. 3p.

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The 9-bp deletion at position 8272 in region V of mitochondrial DNA is associated with renal cell carcinoma outcome.

• Authors : Bai, Yaling¹ (AUTHOR); Guo, Zhanjun² (AUTHOR); Xu, Jinsheng¹ (AUTHOR)

Subjects: *RENAL cell carcinoma; *DELETION mutation; *MITOCHONDRIAL DNA

• Source: Mitochondrial DNA. Part A. May2016, Vol. 27 Issue 3, p1973-1975. 3p. 1 Chart, 1 Graph.

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Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome.

• Authors : Higashimoto, Ken¹; Maeda, Toshiyuki¹; Okada, Junichiro²

Subjects: *DELETION mutation; *EXONS (Genetics); *CHROMOSOME abnormalities

• Source: European Journal of Human Genetics. Nov2013, Vol. 21 Issue 11, p1316-1319. 4p.

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Structural characterization of EGFR exon 19 deletion mutation using molecular dynamics simulation.

• Authors : Tamirat, Mahlet Z.¹; Koivu, Marika^2,3,4; Elenius, Klaus^2,3,5

Subjects: *MOLECULAR dynamics; *DELETION mutation; *EPIDERMAL growth factor receptors

• Source: PLoS ONE. 9/19/2019, Vol. 14 Issue 9, p1-23. 23p.

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Molecular characterization of deletions of the long arm of chromosome 5 (del(5q)) in 94 MDS/AML patients.

• Authors : Douet-Guilbert, N¹; De Braekeleer, E²; Basinko, A¹

Subjects: *CHROMOSOMES; *DELETION mutation; *MYELODYSPLASTIC syndromes

• Source: Leukemia (08876924). Jul2012, Vol. 26 Issue 7, p1695-1697. 3p. 1 Diagram, 1 Graph.

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Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies.

• Authors : Maksić, Jasmina¹; Dobričić, Valerija²; Rasulić, Lukas^3,4

Subjects: *DYSTROPHIN genes; *DELETION mutation; *DUCHENNE muscular dystrophyMONACO

• Source: Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia. Apr2020, Vol. 77 Issue 4, p387-394. 8p.

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Identification of the novel deletion-type PML-RARA mutation associated with the retinoic acid resistance in acute promyelocytic leukemia.

• Authors : Hattori, Hikaru^1,2; Ishikawa, Yuichi¹ ; Kawashima, Naomi¹

Subjects: *ACUTE promyelocytic leukemia; *DELETION mutation; *TRETINOIN

• Source: PLoS ONE. 10/5/2018, Vol. 13 Issue 10, p1-13. 13p.

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Shanghai Jiao Tong University School of Medicine Researchers Report Recent Findings in Dermatology (High-throughput sequencing analysis of deletion mutation of TRAPPC2 in an X-linked spondyloepiphyseal dysplasia tarda pedigree).

Subjects: NUCLEOTIDE sequencing; DELETION mutation; SEQUENCE analysis

• Source: Genomics & Genetics Weekly; 5/17/2024, p1646-1646, 1p

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An adolescent female having hepatocellular carcinoma associated with hepatitis B virus genotype H with a deletion mutation in the pre-S2 region.

• Authors : Oba, Utako¹; Koga, Yuhki¹; Hoshina, Takayuki^1,2

Subjects: *HEPATITIS B virus; *DELETION mutation; *CHILDHOOD cancer

• Source: Journal of Infection & Chemotherapy (Elsevier Inc.). Apr2015, Vol. 21 Issue 4, p302-304. 3p.

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Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?

• Authors : Invernizzi, Federica¹; Zorzi, Giovanna²; Legati, Andrea¹

Subjects: *HUNTINGTON disease; *DELETION mutation; *POINT mutation (Biology)

• Source: European Journal of Medical Genetics. Oct2018, Vol. 61 Issue 10, p581-584. 4p.

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