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Academic Journal

An in-frame deletion mutation in the degron tail of auxin coreceptor IAA2 confers resistance to the herbicide 2,4-D in Sisymbrium orientale .

  • Authors : Figueiredo MRA; Department of Agricultural Biology, Colorado State University, Fort Collins, CO 80523.; Küpper A

Subjects: 2,4-Dichlorophenoxyacetic Acid* ; Insecticides* ; Sequence Deletion*

  • Source: Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2022 Mar 01; Vol. 119 (9).Publisher: National Academy of Sciences Country of Publication: United States NLM ID: 7505876 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Piebaldism resulting from a novel deletion mutation of KIT gene in a five-generation Chinese family.

  • Authors : Chen YJ; Department of Dermatology and Venereology, West China Hospital, Sichuan University, Chengdu, China.; Diao P

Subjects: Sequence Deletion*; Piebaldism/Piebaldism/Piebaldism/*genetics ; Proto-Oncogene Proteins c-kit/Proto-Oncogene Proteins c-kit/Proto-Oncogene Proteins c-kit/*genetics

  • Source: Clinical and experimental dermatology [Clin Exp Dermatol] 2022 Jan; Vol. 47 (1), pp. 232-234. Date of Electronic Publication: 2021 Aug 10.Publisher: Oxford University Press Country of Publication: England NLM ID: 7606847 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene.

  • Authors : Zhou M; Department of Pulmonary and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.; Key Laboratory of Respiratory Diseases, National Ministry of Health of the People's Republic of China and National Clinical Research Center for Respiratory Disease, Wuhan, China.

Subjects: Sequence Deletion*; Alopecia/Alopecia/Alopecia/*genetics ; Arrhythmias, Cardiac/Arrhythmias, Cardiac/Arrhythmias, Cardiac/*genetics Woodhouse Sakati syndrome

  • Source: Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2021 Dec 23; Vol. 12, pp. 770871. Date of Electronic Publication: 2021 Dec 23 (Print Publication: 2021).Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print

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Academic Journal

One-step determination of deletion mutation based on loop-mediated isothermal amplification.

  • Authors : Liu X; College of Life Sciences, Northwest University, Xi'an, Shaanxi, 710069, China.; Zhang C

Subjects: Sequence Deletion*; Carcinoma, Non-Small-Cell Lung/Carcinoma, Non-Small-Cell Lung/Carcinoma, Non-Small-Cell Lung/*genetics ; DNA Mutational Analysis/DNA Mutational Analysis/DNA Mutational Analysis/*methods LAMP assay

  • Source: Analytical biochemistry [Anal Biochem] 2021 Mar 01; Vol. 616, pp. 114087. Date of Electronic Publication: 2020 Dec 19.Publisher: Elsevier Country of Publication: United States NLM ID: 0370535 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

A novel deletion mutation in the LPA gene in a middle-aged woman with ischaemic stroke.

  • Authors : Li Y; Department of Gastroenterology, Hepatology and Nutrition, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, 200062, China.; Wang Y

Subjects: Ischemic Stroke*/Ischemic Stroke*/Ischemic Stroke*/genetics ; Sequence Deletion*; Humans

  • Source: BMC medical genomics [BMC Med Genomics] 2021 May 18; Vol. 14 (1), pp. 132. Date of Electronic Publication: 2021 May 18.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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Academic Journal

Netherton syndrome caused by compound heterozygous mutation, c.80A>G mutation in SPINK5 and large-sized genomic deletion mutation, and successful treatment of intravenous immunoglobulin.

  • Authors : Zhang Z; Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.; Institute of Dermatology, Shanghai Jiaotong University School of Medicine, Shanghai, China.

Subjects: Point Mutation* ; Sequence Deletion*; Netherton Syndrome/Netherton Syndrome/Netherton Syndrome/*genetics

  • Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2021 Mar; Vol. 9 (3), pp. e1600. Date of Electronic Publication: 2021 Jan 16.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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  • 1-10 of  72,993 results for ""DELETION mutation""