Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence

スポンサーリンク

概要

• 論文の詳細を見る
• Springer-Verlag Tokyoの論文
• 2000-05-01

著者

• NAKAMURA Yusuke

  Division of Clinical Genetics, Department of Medical Genetics, Biomedical Research Center

• Nakamura Y

  Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science The University Of

• KURAHASHI Hiroki

  Division of Clinical Genetics, Department of Medical Genetics, Biomedical Research Center, Faculty o

• Okada Shintaro

  The Research Foundation For Microbial Diseases Of Osaka University

• Okada Shintaro

  Department Of Pediatrics D-5 Developmental Medicine Osaka University Graduate School Of Medical Scie

• Nakamura Y

  Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science University Of Toky

• Nakamura Yusuke

  Division Of Clinical Genetics Biomedical Research Center

• Ono Jiro

  Department Of Developmental Medicine (pediatrics) Osaka University Graduate School Of Medicine

• Ono Jiro

  Division Of Pediatrics Toyonaka Municipal Hospital

• SAKAMOTO Michiko

  Division of Clinical Genetics, Department of Medical Genetics, B9, Biomedical Research Center Osaka

• OKADA Shintaro

  Division of Pediatrics, D5, Osaka University Medical School

• Kurahashi H

  Division Of Functional Genomics Department Of Post-genomics And Diseases Osaka University Graduate S

• Kurahashi Hiroki

  Division Of Clinical Genetics Department Of Medical Genetics Biomedical Research Center Faculty Of M

• Okada Shintaro

  Department Of Developmental Medicine (pediatrics) Osaka University Graduate School Of Medical Scienc

• Okada Shintaro

  Division Of Pediatrics D5 Osaka University Medical School

• Sakamoto Michiko

  Division Of Clinical Genetics Department Of Medical Genetics B9 Biomedical Research Center Osaka Uni

• Nakamura Yusuke

  Laboratory Of Genome Technology Human Genome Center Institute Of Medical Science The University Of T

関連論文

• EphA4 receptor, overexpressed in pancreatic ductal adenocarcinoma, promotes cancer cell growth
• Novel tumor marker REG4 detected in serum of patients with resectable pancreatic cancer and feasibility for antibody therapy targeting REG4
• Identification of C2orf18, termed ANT2BP (ANT2-binding protein), as one of the key molecules involved in pancreatic carcinogenesis
• Over-expression of cysteine proteinase inhibitor cystatin 6 promotes pancreatic cancer growth
• Microarray Analysis of Gene-expression Profiles in Diffuse Large B-cell Lymphoma : Identification of Genes Related to Disease Progression
• Distinct pattern of gene expression in pyothorax-associated lymphoma (PAL), a lymphoma developing in long-standing inflammation
• Molecular cloning, mapping, and characterization of a novel human gene, MTA1-L1, showing homology to a metastasis-associated gene, MTA1
• Critical roles of T-LAK cell-originated protein kinase in cytokinesis
• Enhanced SMYD3 expression is essential for the growth of breast cancer cells
• Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease
• Combined hepatocellular/cholangiocellular carcinoma with sarcomatoid features : genetic analysis for histogenesis
• Accumulation of β-catenin in the cytoplasm and the nuclei during the early hepatic tumorigenesis
• Molecular cloning, expression, and mapping of a novel human cDNA, GRP17, highly homologous to human gadd45 and murine MyD118
• Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia
• Association of the RIP2 Gene with Childhood Atopic Asthma
• Association between genetic variation in the gene for death-associated protein-3 (DAP3) and adult asthma
• Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B_1 and B_2
• Functional and Morphological Abnormalities of Mitochondria in Human Cells Containing Mitochondrial DNA with Pathogenic Point Mutations in tRNA Genes
• Alendronate and pharmacological doses of 1α OHD_3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia
• A patient with Shiga toxin-associated hemolytic uremic syndrome who developed hyperkalemia in the recovery period
• Hypophosphatemic rickets accompanying McCune-Albright syndrome : evidence that a humoral factor causes hypophosphatemia
• Blunted effect of parathyroid hormone on adenosine 3',5'-cyclic monophosphate production is derived from ATP depletion in proximal convoluted tubules of hypophosphatemic mice
• The role of IGF-I in phosphate therapy for the short stature of patients with hypophosphatemic vitamin D-resistant rickets
• An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway
• Isolation and Characterization of Human NBL4, a Gene Involved in the β-Catenin/Tcf Signaling Pathway
• Frameshift Mutation of the STK11 Gene in a Sporadic Gastrointestinal Cancer with Microsatellite Instability
• Overexpression of the Wilms' tumor gene WT1 in primary astrocytic tumors
• Overexpression of the Wilms' tumor gene WT1 in primary thyroid cancer
• Stanniocalcin 2 overexpression in castration-resistant prostate cancer and aggressive prostate cancer
• Oncogenic role of NALP7 in testicular seminomas
• Novel 5α-steroid reductase (SRD5A3, type-3) is overexpressed in hormone-refractory prostate cancer
• Overexpression of the Wilms' tumor gene WT1 in human bone and soft-tissue sarcomas
• Fibroblast growth factor receptor 1 oncogene partner as a novel prognostic biomarker and therapeutic target for lung cancer
• Characterization of SEZ6L2 cell-surface protein as a novel prognostic marker for lung cancer
• Overexpression of the Wilms' tumor gene WT1 in colorectal adenocarcinoma
• Difficulty in differential diagnosis of atypical absence seizures and complex partial seizures in childhood
• Infrequent Mutations in the PTEN/MMAC1 Gene among Primary Breast Cancers
• Mutation analysis of Japanese patient with fucosidosis
• Potential involvement of p53 in ischemia/reperfusion-induced osteonecrosis
• Frequent β-Catenin Abnormalities in Bone and Soft-tissue Tumors
• Expression profiles of two types of human knee-joint cartilage
• Identification of human leukocyte antigen-A24-restricted epitope peptides derived from gene products upregulated in lung and esophageal cancers as novel targets for immunotherapy
• Identification of secernin 1 as a novel immunotherapy target for gastric cancer using the expression profiles of cDNA microarray
• Identification of novel polymorphisms in the AXIN1 and CDX-2 genes
• Isolation and characterization of a human cDNA homologous to the Xenopus laevis XCAP-C gene belonging to the structural maintenance of chromosomes (SMC) family
• Detection of novel cancer-testis antigen-specific T-cell responses in TIL, regional lymph nodes, and PBL in patients with esophageal squamous cell carcinoma
• Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss
• Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplification
• Low Grade Amplification of MDM2 Gene in a Subset of Human Breast Cancers without p53 Alterations
• Overexpression of the Wilms′tumor gene WT1 in head and neck squamous cell carcinoma
• Overexpression of the potential kinase serine/threonine/tyrosine kinase 1 (STYK 1) in castration-resistant prostate cancer
• Zonisamide Monotherapy in Newly Diagnosed Infantile Spasms
• Human herpesvirus-6 infection in neonates : Not protected by only humoral immunity
• Decreased frequency of seizures in infantile spasms associated with lissencephaly by human herpes virus 7 infection
• Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome
• Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence
• Ictal Video-EEG Recording of Three Partial Seizures in a Patient with the Benign Infantile Convulsions Associated with Mild Gastroenteritis
• Remission of progressive multifocal leukoencephalopathy following highly active antiretroviral therapy in a patient with HIV infection
• Isolated Iissencephaly sequence with balanced chromosome translocation involving 17p13.3
• Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome
• Novel polymorphisms in the βig-h3 gene
• Fukuyama-type congenital muscular dystrophy (FCMD) and α-dystroglycanopathy
• Isolation and characterization of a novel serine threonine kinase gene on chromosome 3p22-21.3
• AN EcoRI RFLP IN HUMAN APC GENE
• A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia
• DUAL-COLOR FISH ANALYSIS OF BREAKPOINTS ON ROBERTSONIAN TRANSLOCATIONS
• Mutations in Zinc-binding Domains of p53 as a Prognostic Marker of Esophageal-cancer Patients
• Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome
• Significantly elevated expression of PF4 (platelet factor 4) and eotaxin in the NOA mouse, a model for atopic dermatitis
• Secretion of Thrips VIII : Secretions of the Two Ponticulothrips Species (Thysanoptera: Phlaeothripidae)
• Vaccination with multiple peptides derived from novel cancer-testis antigens can induced specific T-cell responses and clinical responses in advanced esophageal cancer
• 5αDH-DOC (5α-dihydro-deoxycorticosterone) activates androgen receptor in castration-resistant prostate cancer
• ALLELE FREQUENCIES OF INTRAGENIC, AND 5' AND 3' MARKERS OF THE DYSTROPHIN GENE IN JAPANESE FAMILIES AFFLICTED WITH DUCHENNE OR BECKER MUSCULAR DYSTROPHY
• A case of chronic infantile type of fucosidosis : clinical and magnetic resonance in image findings
• Validation of the histone methyltransferase EZH2 as a therapeutic target for various types of human cancer and as a prognostic marker
• A novel tumor-associated antigen, cell division cycle 45-like can induce cytotoxic T-lymphocytes reactive to tumor cells
• Screening of genes involved in chromosome segregation during meiosis I : toward the identification of genes responsible for infertility in humans
• Recent advance in our understanding of the molecular nature of chromosomal abnormalities
• Screening of genes involved in chromosome segregation during meiosis I : in vitro gene transfer to mouse fetal oocytes

もっと見る 閉じる

スポンサーリンク