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
of or relating to interstices

PrepTutorEJDIC

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 急性骨髄性白血病における細胞遺伝学 cytogenetics in acute myeloid leukemia
2. 特発性間質性肺炎：臨床症状および病理 idiopathic interstitial pneumonias clinical manifestations and pathology
3. 骨髄異形成症候群における細胞遺伝学および分子遺伝学 cytogenetics and molecular genetics of myelodysplastic syndromes
4. 幼児および小児における間質性肺疾患分類 classification of interstitial lung disease in infants and children
5. 染色体の転座、欠失、および逆位 chromosomal translocations deletions and inversions

An interstitial de-novo microdeletion of 3q26.33q27.3 causing severe intrauterine growth retardation.

Bouman A1, Weiss M, Jansen S, Hankel M, Nieuwint A, Adriaanse B, van de Kamp J, Tan-Sindhunata G.
Clinical dysmorphology.Clin Dysmorphol.2015 Apr;24(2):68-74. doi: 10.1097/MCD.0000000000000075.
Chromosomal abnormalities involving an interstitial or a terminal deletion of 3q26.33 and/or 3q27 have rarely been described. Here we report on a fetus of 22+1 weeks' gestational age with severe intrauterine growth restriction and multiple abnormalities detected by ultrasound examination. Post-morte
PMID 25714561

Calsequestrin 2 deletion causes sinoatrial node dysfunction and atrial arrhythmias associated with altered sarcoplasmic reticulum calcium cycling and degenerative fibrosis within the mouse atrial pacemaker complex1.

Glukhov AV1, Kalyanasundaram A1, Lou Q1, Hage LT1, Hansen BJ1, Belevych AE1, Mohler PJ1, Knollmann BC2, Periasamy M1, Györke S1, Fedorov VV3.
European heart journal.Eur Heart J.2015 Mar 14;36(11):686-97. doi: 10.1093/eurheartj/eht452. Epub 2013 Nov 11.
AIMS: Loss-of-function mutations in Calsequestrin 2 (CASQ2) are associated with catecholaminergic polymorphic ventricular tachycardia (CPVT). CPVT patients also exhibit bradycardia and atrial arrhythmias for which the underlying mechanism remains unknown. We aimed to study the sinoatrial node (SAN)
PMID 24216388

The relationship of TP53 R72P polymorphism to disease outcome and TP53 mutation in myelodysplastic syndromes.

McGraw KL1, Zhang LM2, Rollison DE3, Basiorka AA4, Fulp W5, Rawal B6, Jerez A7, Billingsley DL8, Lin HY5, Kurtin SE9, Yoder S2, Zhang Y5, Guinta K7, Mallo M10, Solé F10, Calasanz MJ11, Cervera J11, Such E11, González T12, Nevill TJ13, Haferlach T14, Smith AE15, Kulasekararaj A15, Mufti G15, Karsan A13, Maciejewski JP7, Sokol L1, Epling-Burnette PK16, Wei S16, List AF1.
Blood cancer journal.Blood Cancer J.2015 Mar 13;5:e291. doi: 10.1038/bcj.2015.11.
Nonsynonymous TP53 exon 4 single-nucleotide polymorphism (SNP), R72P, is linked to cancer and mutagen susceptibility. R72P associations with specific cancer risk, particularly hematological malignancies, have been conflicting. Myelodysplastic syndrome (MDS) with chromosome 5q deletion is characteriz
PMID 25768405

Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion

OKAMOTO Nana,HAYASHI Shin,MASUI Ayako,KOSAKI Rika,OGURI Izumi,HASEGAWA Tomoko,IMOTO Issei,MAKITA Yoshio,HATA Akira,MORIYAMA Keiji,INAZAWA Johji
Journal of human genetics 57(3), 191-196, 2012-03-01
NAID 10030712085

Dissection and cytological mapping of barley chromosome 2H in the genetic background of common wheat

JOSHI Giri Prasad,NASUDA Shuhei,ENDO Takashi R.
Genes & genetic systems 86(4), 231-248, 2011-08-25
… The aberrant 2H chromosomes were of either deletion or translocation or complicated structural change. … We also recognized an EST-marker or gene-rich region in the 2HL interstitial region slightly to the telomere. …
NAID 10030209558