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Department Of Human Genetics Yokohama City University Graduate School Of Medicine | 論文
- Microarray comparative genomic hybridization analysis of 59 patients with schizophrenia
- A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano
- Recent progress in genetics of Marfan syndrome and Marfan-associated disorders
- Complete hydatidiform mole and normal live birth following intracytoplasmic sperm injection
- Laparoscopy for the treatment of unexplained infertility
- IS-42 Gene expression of cyclic nucleotide phosphodiesterase (PDE) subtypes in rat hypothalamus and their effect on GnRH secretion from GnRH neuron
- Hypoadiponectinemia in Lean Lactating Women : Prolactin Inhibits Adiponectin Secretion from Human Adipocytes
- P-IS-56 Prolactin inhibits apoptosis of choriocarcinoma cells; possible role of decidual Prolactin on trophoblasts at early pregnancy(Reproduction 1,Group 102,International Session)
- A case of Baraitser-Winter syndrome with unusual brain MRI findings : Pachygyria, subcortical-band heterotopia, and periventricular heterotopia
- Retrospective analysis of laparoscopic salpingostomy and conservative expectant management of tubal ectopic pregnancy
- P-IS-57 The role of calcium sensing receptor on GnRH secretion from immortalized GnRH neuronal cell line(Reproduction 2,Group 103,International Session)
- Multiplicity of signaling pathway on the mediation of dopamine : induced GnRH release in GT1 cells(Reproduction 6)
- Effects of Saireito on the ovarian function of patients with polycystic ovary syndrome
- Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features
- Chronic noninfectious uveitis associated with Vogt-Koyanagi-Harada disease treated with low-dose weekly systemic methotrexate
- De novo 19q13.42 duplications involving NLRP gene cluster in a patient with systemic-onset juvenile idiopathic arthritis
- Breakpoint determination of X;autosome balanced translocations in four patients with premature ovarian failure
- Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features
- A family of oculofaciocardiodental syndrome (OFCD) with a novel BCOR mutation and genomic rearrangements involving NHS
- Physicians' opinion for 'new' genetic testing in Japan