Search Results - "Ku, J L"
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Complex chromosomal rearrangements by single catastrophic pathogenesis in NUT midline carcinoma
Published in Annals of oncology (01-04-2017)“…Nuclear protein in testis (NUT) midline carcinoma (NMC) is a rare aggressive malignancy often occurring in the tissues of midline anatomical structures. Except…”
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2
Screening of Fracture Risk and Osteoporosis Among Older Long-term Care Residents: A Prospective Study
Published in The Journal of nutrition, health & aging (01-12-2023)“…This prospective study assessed the effectiveness of screening older long-term care residents (LTCRs) for fracture risk and osteoporosis in Taiwan. Fracture…”
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3
Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population
Published in Gut (01-06-2011)“…Colorectal cancer (CRC) is a multifactorial disease with both environmental and genetic factors contributing to its development. The incidence of CRC is…”
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4
Galectin-3 stabilizes heterogeneous nuclear ribonucleoprotein Q to maintain proliferation of human colon cancer cells
Published in Cellular and molecular life sciences : CMLS (01-01-2009)“…Comparative analysis of proteomes using 5-fluorouracil (5-FU)-resistant human colon cancer cell line revealed that decreased galectin-3 expression was…”
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5
Mutational analysis of OGG1, MYH, MTH1 in FAP, HNPCC and sporadic colorectal cancer patients: R154H OGG1 polymorphism is associated with sporadic colorectal cancer patients
Published in Human genetics (01-11-2004)“…MYH, OGG1 and MTH1 are members of base excision repair (BER) families, and MYH germline mutations were recently identified in patients with multiple adenomas…”
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6
Establishment and characterisation of six human biliary tract cancer cell lines
Published in British journal of cancer (15-07-2002)“…Human cell lines established from biliary tract cancers are rare, and only five have been reported previously. We report the characterisation of six new six…”
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7
Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients
Published in British journal of cancer (01-04-2000)“…Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by hamartomatous gastrointestinal polyps and mucocutaneous…”
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8
Impact of Caring for Grandchildren on the Health of Grandparents in Taiwan
Published in The journals of gerontology. Series B, Psychological sciences and social sciences (01-11-2013)“…To understand how caring for grandchildren affects the physical and mental health of grandparents in Taiwan. Grandparents aged 50 and older from 4 waves of the…”
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9
A novel germline mutation in the MET extracellular domain in a Korean patient with the diffuse type of familial gastric cancer
Published in Journal of medical genetics (01-08-2003)“…7 Most of the MET mutations associated with HPRC or sporadic papillary renal carcinomas 7 were missense mutations in the tyrosine kinase domain, 10, 11 and…”
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10
Clinical characteristics of Peutz-Jeghers syndrome in Korean polyposis patients
Published in International journal of colorectal disease (01-02-2000)“…Peutz-Jeghers syndrome is an autosomal dominant inherited disorder characterized by hamartomatous polyps in the small bowel and mucocutaneous pigmentation…”
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11
Mutations in hMSH6 alone are not sufficient to cause the microsatellite instability in colorectal cancer cell lines
Published in European journal of cancer (1990) (01-11-1999)“…Microsatellite instability (MSI) at simple repeated sequences characterises a distinct mechanism of carcinogenesis in hereditary nonpolyposis colorectal cancer…”
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12
Identification of a novel BMPR1A germline mutation in a Korean juvenile polyposis patient without SMAD4 mutation
Published in Clinical genetics (01-02-2003)“…Juvenile polyposis (JP) is characterized by the development of multiple hamartomatous polyps and is inherited as an autosomal dominant trait. Germline…”
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13
Germline Mutations of hMLH1 and hMSH2 Genes in Korean Hereditary Nonpolyposis Colorectal Cancer
Published in JNCI : Journal of the National Cancer Institute (18-09-1996)“…One of the most common autosomal dominantly inherited diseases, affecting as many as one in every 200-400 individuals in the Western world, is hereditary…”
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14
Mutations of the Birt-Hogg-Dubé (BHD) gene in sporadic colorectal carcinomas and colorectal carcinoma cell lines with microsatellite instability
Published in Journal of medical genetics (01-05-2003)“…Thirteen of these cell lines (SNU-175, SNU-407, SNU-769A, SNU-769B, SNU-1040, SNU-1047, SNU-C2A, SNU-C4, HCT-116, LoVo, LS174T, HCT-8, and DLD-1) are MMR…”
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15
Germline mutations of E-cadherin gene in Korean familial gastric cancer patients
Published in Journal of human genetics (01-01-1999)“…Gastric cancer is the most common cancer in Korea. Germline mutations of the E-cadherin gene have recently been identified in familial gastric cancer patients…”
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16
Germline mutations of the dpc4 gene in Korean juvenile polyposis patients
Published in International journal of cancer (15-05-2000)“…Juvenile polyposis is an uncommon condition characterized by the development of multiple (usually more than 5) juvenile polyps in the gastrointestinal tract,…”
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17
Establishment and characterization of seven human renal cell carcinoma cell lines
Published in BJU international (01-01-2000)“…Objective To establish human renal cell carcinoma (RCC) cell lines, and to investigate the cell phenotypes and molecular characteristics of human RCC cell…”
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18
Alpha-tocopheryl succinate, in contrast to alpha-tocopherol and alpha-tocopheryl acetate, inhibits prostaglandin E2 production in human lung epithelial cells
Published in Carcinogenesis (New York) (01-11-2006)“…The production of prostaglandin E2 (PGE2), a key proinflammatory mediator, is regulated by the availability of its substrate, arachidonic acid (AA), and the…”
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19
Promoter hypermethylation downregulates RUNX3 gene expression in colorectal cancer cell lines
Published in Oncogene (02-09-2004)“…It was recently reported that RUNX3 gene expression is significantly downregulated in human gastric cancer cells due to hypermethylation of its promoter region…”
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Germline mutations in a polycytosine repeat of the hMSH6 gene in Korean hereditary nonpolyposis colorectal cancer
Published in Journal of human genetics (1999)“…Somatic mutations within a mononucleotide repeat sequence present in the hMSH6 and hMSH3 coding regions have been frequently observed in various human cancer…”
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