WordNet

the act of deleting something written or printed
the omission that is made when an editorial change shortens a written passage; "an editors deletions frequently upset young authors"; "both parties agreed on the excision of the proposed clause" (同)excision, cut
(genetics) the loss or absence of one or more nucleotides from a chromosome
having identical alleles at corresponding chromosomal loci; "these two fruit flies are homozygous for red eye color"

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削除;〈C〉削除箇所

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1. 遺伝性ヘモクロマトーシスの遺伝学genetics of hereditary hemochromatosis [show details]
…comorbid feature (eg, excess alcohol consumption, steatosis, diabetes) was also present . Homozygous deletion of the HFE-containing region of chromosome 6p has been described in a number of cases of phenotypic …
2. ディジョージ症候群（22q11.2欠失）：疫学および病因digeorge 22q11 2 deletion syndrome epidemiology and pathogenesis [show details]
…by heterozygous deletions in this region, although several cases of a DGS-like phenotype have been reported in association with duplications of the 22q11.2 region . Homozygous deletions in chromosome 22q11 …
3. 健常者および患者における胎児性ヘモグロビン（ヘモグロビンF）fetal hemoglobin hemoglobin f in health and disease [show details]
… concentration was 12 to 13 g/dL, and their HbF was 98 percent. Both were homozygous for rs7482144, homozygous for the 3-bp deletion HBS1L-MYB intergenic polymorphism at rs66650371, and heterozygous for the …
4. 皮膚剥脱症候群peeling skin syndrome [show details]
…Genomic deletion at the PSORS1 locus removing the entire CDSN gene and a large homozygous deletion of six genes including CDSN have also been reported as the cause of type B PSS . This genomic deletion resulting …
5. ヘモグロビン分析法およびヘモグロビン異常症を特定するための検査法methods for hemoglobin analysis and hemoglobinopathy testing [show details]
…alpha gene deletion from the other parent, these large deletions result in Hb H disease (3 total gene deletions, -α/--). Hemoglobin H is a tetramer composed of four beta globin chains. Homozygous inheritance …

English Journal

Novel mutations of the SERPINF1 and FKBP10 genes in Chinese families with autosomal recessive osteogenesis imperfecta.

Zhang H1, Xu Y1, Yue H1, Wang C1, Gu J1, He J1, Fu W1, Hu W1, Zhang Z1.
International journal of molecular medicine.Int J Mol Med.2018 Jun;41(6):3662-3670. doi: 10.3892/ijmm.2018.3542. Epub 2018 Mar 7.
PMID 29512769

Two consecutive successful live birth in woman with 17α hydroxylase deficiency by frozen-thaw embryo transfer under hormone replacement endometrium preparation.

Kitajima M1, Miura K1, Inoue T1, Murakami Y1, Kitajima Y1, Murakami N1, Taniguchi K1, Yoshiura KI2, Masuzaki H1.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.Gynecol Endocrinol.2018 May;34(5):381-384. doi: 10.1080/09513590.2017.1393512. Epub 2017 Oct 25.
PMID 29068264

Characterization of the impact of glutaredoxin-2 (GRX2) deficiency on superoxide/hydrogen peroxide release from cardiac and liver mitochondria.

Chalker J1, Gardiner D1, Kuksal N1, Mailloux RJ2.
Redox biology.Redox Biol.2018 May;15:216-227. doi: 10.1016/j.redox.2017.12.006. Epub 2017 Dec 14.
PMID 29274570