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Department Of Obstetrics And Gynecology Asahikawa Medical College | 論文
- The IHPK1 gene is disrupted at the 3p21. 31 breakpoint of t(3 ; 9) in a family with type 2 diabetes mellitus
- A catalog of 106 single-nucleotide polymorphisms (SNPs) and 11 other types of variations in genes for transforming growth factor-β1 (TGF-β1) and its signaling pathway
- LRP5, low-density-lipoprotein-receptor-related protein 5, is a determinant for bone mineral density
- 出生時の臍帯血および羊水エリスロポエチン値と胎児心拍異常との関連
- Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest
- Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid
- Isolation and localization of an IDDMK1,2-22-related human endogenous retroviral gene, and identification of a CA repeat marker at its locus
- POLYMORPHIC AND TISSUE-SPECIFIC IMPRINTING OF THE HUMAN WILMS TUMOR GENE, WT1
- IS-29 Relaxation of IGF-II Gene Imprinting and Immunohistochemical Analysis in Human Gynecologic Tumors
- IS-19 Telomerase mRNA and telomerase activity in human gynecologic tumors
- 大型ウサギの血管系インターベンショナルラジオロジーに対する有用性の検討
- Core fucosylation of E-cadherin enhances cell-cell adhesion in human colon carcinoma WiDr cells
- Functional roles of N-glycans in cell signaling and cell adhesion in cancer
- The Role of Superoxide Dismutase in the Human Ovary and Fallopian Tube
- PHYSICAL MAP OF A YAC CONTIG CONTAINING THE REGION OF THE HUMAN GENE (HYRC) COMPLEMENTING HYPER-RADIOSENSITIVITY OF THE SCID MOUSE MUTATION
- Does increased nuchal translucency indicate a fetal abnormality? A retrospective study to clarify the clinical significance of nuchal translucency in Japan
- Congenital diaphragmatic hernia : an evaluation of the prognostic value of the lung-to-head ratio
- Prenatal Vitamin E Treatment Improves Lung Growth in Fetal Rats with Congenital Diaphragmatic Hernia
- Histological and Immunohistochemical Analysis of Fetal Hypoplastic Lungs: Preliminary Study
- Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta