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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/01/14 18:42:48」(JST)

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Medically unexplained somatic symptoms and bipolar spectrum disorders: A systematic review and meta-analysis.

Edgcomb JB1, Tseng CH2, Kerner B3.
Journal of affective disorders.J Affect Disord.2016 Nov 1;204:205-13. doi: 10.1016/j.jad.2016.06.029. Epub 2016 Jun 14.
BACKGROUND: Patients with bipolar spectrum disorders (BSD) frequently report medically unexplained somatic symptoms. However, the prevalence and the consequences for treatment and outcome are currently unknown.METHODS: To estimate the prevalence of somatic symptoms in BSD, we conducted a systematic
PMID 27371906

Effect of genotype and previous growth hormone treatment on adiposity in adults with Prader-Willi syndrome.

Coupaye M1, Tauber M2,3, Cuisset L4, Laurier V5, Bieth E6, Lacorte JM7, Oppert JM1,8, Clément K1,8, Poitou C1,8.
The Journal of clinical endocrinology and metabolism.J Clin Endocrinol Metab.2016 Sep 23:jc20162163. [Epub ahead of print]
CONTEXT: Adults with Prader-Willi Syndrome (PWS) have an increased proportion of subcutaneous fat mass compared to BMI-matched controls, but whether the genotype influences body composition and metabolic profile remains controversial.OBJECTIVE: To assess body composition and metabolic features in ad
PMID 27662437

Obesity and developmental delay in a patient with uniparental disomy of chromosome 2.

Yu T1,2, Li J3, Li N1,2, Liu R4, Ding Y3, Chang G3, Chen Y3, Shen Y1,5, Wang X1,3, Wang J1,2.
International journal of obesity (2005).Int J Obes (Lond).2016 Sep 22. doi: 10.1038/ijo.2016.160. [Epub ahead of print]
BACKGROUND: Uniparental disomy (UPD) is an unusual situation wherein two homologous chromosomes are inherited from the same parent. UPDs can cause clinical abnormalities due to the aberrant dosage of genes regulated by epigenetic imprinting or homozygosity of variants for recessive phenotypes.AIMS:
PMID 27654142

Copy Number Alteration and Uniparental Disomy Analysis Categorizes Japanese Papillary Thyroid Carcinomas into Distinct Groups

Matsuse Michiko,Sasaki Kensaku,Nishihara Eijun,Minami Shigeki,Hayashida Chisa,Kondo Hisayoshi,Suzuki Keiji,Saenko Vladimir,Yoshiura Koh-ichiro,Mitsutake Norisato,Yamashita Shunichi
PLoS ONE 7(4), e36063, 2012-04-30
… Twenty-five PTCs (11 with BRAF V600E, 4 with RET/PTC1, and 10 without mutation in HRAS, KRAS, NRAS, BRAF, RET/PTC1, or RET/PTC3) were analyzed using Genome-Wide Human SNP Array 6.0 which allows us to detect copy number alteration (CNA) and uniparental disomy (UPD), also referred to as copy neutral loss of heterozygosity, in a single experiment. … Seven cases (28%) showed CNA(s), and 6 (24%) showed UPD(s). … Interestingly, CNA and UPD were rarely overlapped in the same tumor; …
NAID 120004205048