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
a threadlike strand of DNA in the cell nucleus that carries the genes in a linear order; "humans have 22 chromosome pairs plus two sex chromosomes"

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1. 染色体の転座、欠失、および逆位 chromosomal translocations deletions and inversions
2. 急性骨髄性白血病における細胞遺伝学 cytogenetics in acute myeloid leukemia
3. 血液悪性腫瘍における細胞遺伝子解析の一般的側面 general aspects of cytogenetic analysis in hematologic malignancies
4. 胚、胎児、および幼児における細胞遺伝学的異常 cytogenetic abnormalities in the embryo fetus and infant
5. 男性不妊症の評価 evaluation of male infertility

The 15q13.3 deletion syndrome: Deficient α7-containing nicotinic acetylcholine receptor-mediated neurotransmission in the pathogenesis of neurodevelopmental disorders.

Deutsch SI1, Burket JA2, Benson AD2, Urbano MR2.
Progress in neuro-psychopharmacology & biological psychiatry.Prog Neuropsychopharmacol Biol Psychiatry.2016 Jan 4;64:109-17. doi: 10.1016/j.pnpbp.2015.08.001. Epub 2015 Aug 7.
Array comparative genomic hybridization (array CGH) has led to the identification of microdeletions of the proximal region of chromosome 15q between breakpoints (BP) 3 or BP4 and BP5 encompassing CHRNA7, the gene encoding the α7-nicotinic acetylcholine receptor (α7nAChR) subunit. Phenotypic manife
PMID 26257138

Gene structure variation in segmental duplication block C of human chromosome 7q 11.23 during primate evolution.

Kim YJ1, Ahn K2, Gim JA3, Oh MH4, Han K1, Kim HS5.
Gene.Gene.2015 Dec 1;573(2):285-95. doi: 10.1016/j.gene.2015.07.060. Epub 2015 Jul 18.
Segmental duplication, or low-copy repeat (LCR) event, occurs during primate evolution and is an important source of genomic diversity, including gain or loss of gene function. The human chromosome 7q 11.23 is related to the William-Beuren syndrome and contains large region-specific LCRs composed of
PMID 26196062

The sperm quality and clinical outcomes were not affected by sY152 deletion in Y chromosome for oligozoospermia or azoospermia men after ICSI treatment.

Zhu Y1, Wu T1, Li G1, Yin B1, Liu H1, Wan C1, Zhang H1, Zeng Y2.
Gene.Gene.2015 Dec 1;573(2):233-8. doi: 10.1016/j.gene.2015.07.051. Epub 2015 Jul 16.
Azoospermia factor (AZF) microdeletion plays a key role in the genetic etiology of male infertility. The relationship between sY152 deletion in the AZFc region and clinical outcomes is still unclear. This study was to determine the effects of sY152 deletion on the sperm parameters and clinical outco
PMID 26188156

Telomere-mediated chromosomal truncation in Aspergillus oryzae(GENETICS, MOLECULAR BIOLOGY, AND GENE ENGINEERING)

Tada Sawaki,Ohkuchi Hikaru,Matsushita-Morita Mayumi [他],Furukawa Ikuyo,Hattori Ryota,Suzuki Satoshi,Kashiwagi Yutaka,Kusumoto Ken-Ichi
Journal of bioscience and bioengineering 119(1), 43-46, 2015-01
… We truncated the short arm of chromosome 3 to delete the afiatoxin biosynthesis gene homolog cluster using telomeric repeats in Aspergillus oryzae. … The predicted deletion was confirmed by Southern blot analyses. … This telomeremediated chromosomal truncation method enables the development of an artificial chromosome in A. …
NAID 110009892231

Development of a novel pink-eyed dilution mouse model showing progressive darkening of the eyes and coat hair with aging

ISHIKAWA Akira,SUGIYAMA Makoto,HONDO Eiichi [他],KINOSHITA Keiji,YAMAGISHI Yuki
Experimental Animals 64(2), 207-220, 2015
… pink-eyed dilution castaneus) is a coat color mutant gene on mouse chromosome 7 that arose spontaneously in wild Mus musculus castaneus mice. … Sequence analysis of Oca2p-cas revealed a 4.1-kb deletion involving exons 15 and 16 of its wild-type gene. …
NAID 130005069866

KOMORI Takashi
Neurologia medico-chirurgica 55(1), 28-37, 2015
… Recent genetic studies have revealed that the major categories of gliomas, such as circumscribe astrocytomas, infiltrating astrocytomas/oligodendrogliomas, and glioblastoma, roughly correspond to major genetic alterations, including isocitrate dehydrogenases (IDHs) 1/2 mutations, TP53 mutations, co-deletion of chromosome arms 1p/19q, and BRAF mutation/fusion. …
NAID 130004922265