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1. 臍帯卵膜付着と前置血管 velamentous umbilical cord insertion and vasa previa
2. 鎌状赤血球症の腎症状 renal manifestations of sickle cell disease
3. 妊婦における腟出血の病因および評価の概要 overview of the etiology and evaluation of vaginal bleeding in pregnant women
4. 前置胎盤の臨床的特徴、診断、および経過 clinical features diagnosis and course of placenta previa
5. 胎盤の肉眼的評価 gross examination of the placenta

English Journal

Confocal microscopy reveals uniform male reproductive anatomy in eriophyoid mites (Acariformes, Eriophyoidea) including spermatophore pump and paired vasa deferentia.

Chetverikov PE1.
Experimental & applied acarology.Exp Appl Acarol.2015 Aug;66(4):555-74. doi: 10.1007/s10493-015-9924-1. Epub 2015 Jun 5.
Male internal genitalia of eriophyoid mites comprise cuticle lined (anterior genital apodeme, genital chamber and ductus ejculatorius) and soft (paired vasa deferentia and single testis) organs. Three-dimensional reconstructions based on autofluorescence show that a thin-walled genital chamber is us
PMID 26043829

Molecular cloning and characterization of oocyte-specific Pat1a in Rana rugosa frogs.

Nakamura Y1,2, Iwasaki T2, Umei Y2, Saotome K2, Nakajima Y2, Kitahara S2, Uno Y3, Matsuda Y3, Oike A2, Kodama M2, Nakamura M2.
Journal of experimental zoology. Part A, Ecological genetics and physiology.J Exp Zool A Ecol Genet Physiol.2015 Jul 2. doi: 10.1002/jez.1938. [Epub ahead of print]
The Pat1 gene is expressed in the immature oocytes of Xenopus, and is reportedly involved in regulating the translation of maternal mRNAs required for oocyte-maturation. However, it is still unknown when Pat1a first appears in the differentiating ovary of amphibians. To address this issue, we isolat
PMID 26136381

Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment.

Trampush JW1,2,3, Lencz T1,2,3, Knowles E4, Davies G5,6, Guha S1, Pe'er I7,8, Liewald DC5, Starr JM5,9, Djurovic S10,11, Melle I10,11,12, Sundet K10,12, Christoforou A13,14, Reinvang I15, Mukherjee S1,2, DeRosse P1,2, Lundervold A16,17,18, Steen VM13,14, John M1,2, Espeseth T15,19, Räikkönen K20, Widen E21, Palotie A21,22,23, Eriksson JG24,25,26,27,28, Giegling I29, Konte B29, Ikeda M30, Roussos P31, Giakoumaki S32, Burdick KE31, Payton A33, Ollier W33, Horan M34, Scult M35, Dickinson D36, Straub RE36,37, Donohoe G38, Morris D38, Corvin A38, Gill M38, Hariri A35, Weinberger DR36,37, Pendleton N39, Iwata N30, Darvasi A40, Bitsios P41, Rujescu D29, Lahti J20,42, Le Hellard S13,14, Keller MC43, Andreassen OA10,11,12, Deary IJ5,6, Glahn DC4, Malhotra AK1,2,3.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.Am J Med Genet B Neuropsychiatr Genet.2015 Jul;168(5):363-73. doi: 10.1002/ajmg.b.32319. Epub 2015 May 7.
Cognitive deficits and reduced educational achievement are common in psychiatric illness; understanding the genetic basis of cognitive and educational deficits may be informative about the etiology of psychiatric disorders. A recent, large genome-wide association study (GWAS) reported a genome-wide
PMID 25951819