Published in Endoscopy on January 01, 1991
Alprazolam as Conscious Sedation for Upper Gastrointestinal Endoscopy | NCT01949038
Is premedication necessary in diagnostic endoscopy of the upper gastrointestinal tract? Endoscopy (1991) 0.75
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature (1994) 8.04
BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing. J Med Genet (2004) 2.75
Endoscopic diagnosis of submucosal gastric lesions. The results after routine endoscopy. Surg Endosc (1991) 2.38
Integration of FGF and TWIST in calvarial bone and suture development. Development (2000) 2.15
Cbfa1 is required for epithelial-mesenchymal interactions regulating tooth development in mice. Development (1999) 2.03
Molecular basis of HNPCC: mutations of MMR genes. Hum Mutat (1997) 1.88
Frameshift-mutation-derived peptides as tumor-specific antigens in inherited and spontaneous colorectal cancer. Proc Natl Acad Sci U S A (2001) 1.80
A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers. Genes Chromosomes Cancer (1998) 1.79
The life history of an embryonic signaling center: BMP-4 induces p21 and is associated with apoptosis in the mouse tooth enamel knot. Development (1998) 1.77
The enamel knot as a signaling center in the developing mouse tooth. Mech Dev (1996) 1.71
COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer. Br J Cancer (2009) 1.62
Evaluation of a surveillance strategy for early detection of adenovirus by PCR of peripheral blood in hematopoietic SCT recipients: incidence and outcome. Bone Marrow Transplant (2010) 1.59
Distinct and overlapping ligand specificities of the alpha 3A beta 1 and alpha 6A beta 1 integrins: recognition of laminin isoforms. Mol Biol Cell (1994) 1.56
Optimal structure of a congenital heart surgery department in Europe. Eur J Cardiothorac Surg (2003) 1.52
Colorectal cancer with and without microsatellite instability involves different genes. Genes Chromosomes Cancer (1999) 1.44
Association of developmental regulatory genes with the development of different molar tooth shapes in two species of rodents. Dev Genes Evol (1998) 1.41
Transventricular aortic cannulation for repair of aortic dissection. Ann Thorac Surg (2001) 1.39
Recommendations to improve identification of hereditary and familial colorectal cancer in Europe. Fam Cancer (2009) 1.38
Adenoma prevalence and cancer risk in familial non-polyposis colorectal cancer. Gut (2002) 1.38
Permeability of intestinal mucosa from urinary reservoirs in man and rat. BJU Int (2000) 1.37
Microsatellite instability in sporadic colorectal cancer is not an independent prognostic factor. Br J Cancer (1999) 1.36
Colorectal carcinogenesis is associated with stromal expression of COL11A1 and COL5A2. Carcinogenesis (2001) 1.36
Epithelial-mesenchymal signaling during tooth development. Connect Tissue Res (1995) 1.34
High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium. Genes Chromosomes Cancer (1995) 1.34
Differential expression of aquaporin 8 in human colonic epithelial cells and colorectal tumors. BMC Physiol (2001) 1.32
Association studies on 11 published colorectal cancer risk loci. Br J Cancer (2010) 1.31
A rare CYP19 (aromatase) variant may increase the risk of breast cancer. Pharmacogenetics (1998) 1.30
Results from a large multinational clinical trial (guardian™1) using prophylactic treatment with turoctocog alfa in adolescent and adult patients with severe haemophilia A: safety and efficacy. Haemophilia (2013) 1.27
Apoptosis in the developing tooth: association with an embryonic signaling center and suppression by EGF and FGF-4. Development (1996) 1.25
TNF signaling via the ligand-receptor pair ectodysplasin and edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis. Dev Biol (2001) 1.24
Peptide-containing nerve fibers in the stomach wall of rat and mouse. Gastroenterology (1985) 1.23
Cleansing of the colon without enemas. Radiologe (1975) 1.23
The role of hPMS1 and hPMS2 in predisposing to colorectal cancer. Cancer Res (2001) 1.20
Microsatellite Instability and hMLH1 and hMSH2 expression analysis in familial and sporadic colorectal cancer. Lab Invest (2001) 1.19
Linkage analysis in a large Swedish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 9q22.32-31.1. J Med Genet (2006) 1.18
Nerve fibers in the gut and pancreas of the rat displaying neuropeptide-Y immunoreactivity. Intrinsic and extrinsic origin. Cell Tissue Res (1983) 1.17
Vein invasion in renal cell carcinoma: impact on metastatic behavior and survival. J Urol (1995) 1.17
Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families. Cancer Res (1995) 1.17
Anticholinergic medication in diagnostic endoscopy of the upper gastrointestinal tract. Endoscopy (1991) 1.16
Hyperplastic polyposis coli syndrome and colorectal carcinoma. Endoscopy (2006) 1.16
The effect of metastasectomy: fact or fiction? Ann Thorac Surg (1980) 1.16
The role of ataxia-telangiectasia heterozygotes in familial breast cancer. Cancer Res (1998) 1.14
Various mutation screening techniques in the DNA mismatch repair genes hMSH2 and hMLH1. Genet Test (1999) 1.14
The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC)--results of an international collaborative study. Fam Cancer (2001) 1.13
Aortopulmonary window: a new operative approach. Ann Thorac Surg (1978) 1.13
Consortium study on 1280 breast carcinomas: allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters. Cancer Res (1998) 1.12
A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants. Br J Cancer (2010) 1.11
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome. J Med Genet (2008) 1.11
Results from a large multinational clinical trial (guardian™3) using prophylactic treatment with turoctocog alfa in paediatric patients with severe haemophilia A: safety, efficacy and pharmacokinetics. Haemophilia (2013) 1.11
COL11A1 in FAP polyps and in sporadic colorectal tumors. BMC Cancer (2001) 1.10
A study of the PTEN/MMAC1 gene in 136 breast cancer families. Hum Genet (1998) 1.10
High incidence of skewed X chromosome inactivation in young patients with familial non-BRCA1/BRCA2 breast cancer. J Med Genet (2005) 1.10
Germline mutations in the MYH gene in Swedish familial and sporadic colorectal cancer. Genet Test (2005) 1.10
Runx2 (Cbfa1) inhibits Shh signaling in the lower but not upper molars of mouse embryos and prevents the budding of putative successional teeth. J Dent Res (2005) 1.09
ATM mutations in cancer families. Cancer Res (1996) 1.09
Topography of somatostatin cells in the stomach of the rat: possible functional significance. Cell Tissue Res (1979) 1.08
MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancer. Cancer Res (2001) 1.06
Tumorigenesis in colorectal tumors from patients with hereditary non-polyposis colorectal cancer. Hum Genet (1997) 1.06
Prevalence and incidence of hyperplastic polyps and adenomas in familial colorectal cancer: correlation between the two types of colon polyps. Gut (2003) 1.06
Virtual reality colonoscopy simulation: a compulsory practice for the future colonoscopist? Endoscopy (2005) 1.05
Adverse effects on the brain in cardiac operations as assessed by biochemical, psychometric, and radiologic methods. J Thorac Cardiovasc Surg (1984) 1.05
A germline E-cadherin mutation in a family with gastric and colon cancer. Int J Mol Med (2001) 1.04
Argyrophil carcinoid tumors of the lung. Incidence, clinical study, and follow-up of 46 patients. Chest (1980) 1.04
Low frequency of E-cadherin alterations in familial breast cancer. Breast Cancer Res (2001) 1.04
Microsatellite instability as a predictor of a mutation in a DNA mismatch repair gene in familial colorectal cancer. Genes Chromosomes Cancer (2000) 1.04
Classification of colorectal polyps: guidelines for the endoscopist. Endoscopy (2002) 1.03
Molecular regulation of tooth development. Bone (1999) 1.03
Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC. J Med Genet (2004) 1.03
Association of the E23K polymorphism in the KCNJ11 gene with gestational diabetes mellitus. Diabetologia (2005) 1.02
Germline BRCA1 and HMLH1 mutations in a family with male and female breast carcinoma. Int J Cancer (2000) 1.01
Gene expression patterns associated with suppression of odontogenesis in mouse and vole diastema regions. Dev Genes Evol (1999) 1.00
Ki-ras mutations and prognosis in colorectal cancer. Eur J Cancer (1998) 0.99
Hereditary breast cancer: a review. Semin Cancer Biol (2000) 0.99
Missense mutations in hMLH1 associated with colorectal cancer. Hum Genet (1999) 0.97
FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium. Br J Cancer (2014) 0.96
Quality of survival in patients with surgically treated bronchial carcinoma. Thorax (1980) 0.96
Individuals with an increased risk of colorectal cancer: perceived benefits and psychological aspects of surveillance by means of regular colonoscopies. J Clin Oncol (2004) 0.95
Selection mechanisms as major determinants of survival after pulmonary metastasectomy. Ann Thorac Surg (1997) 0.94
The vagus exerts trophic control of the stomach in the rat. Gastroenterology (1984) 0.94
Cerebral protection during open-heart surgery. Thorax (1977) 0.94
The choice of operation for bronchial carcinoids. Ann Thorac Surg (1981) 0.93
Mucosal in vitro permeability in the intestinal tract of the pig, the rat, and man: species- and region-related differences. Scand J Gastroenterol (2000) 0.92
Appropriateness of referral of coronary angiography patients in Sweden. SECOR/SBU Project Group. Heart (1999) 0.91
Quality assurance in clinical perfusion. Eur J Cardiothorac Surg (1998) 0.91
Calcium binding to tandem repeats of EGF-like modules. Expression and characterization of the EGF-like modules of human Notch-1 implicated in receptor-ligand interactions. Protein Sci (1997) 0.91
TGFBR1 variants TGFBR1(*)6A and Int7G24A are not associated with an increased familial colorectal cancer risk. Br J Cancer (2009) 0.90
Germline mutation screening of the STK11/LKB1 gene in familial breast cancer with LOH on 19p. Clin Genet (2000) 0.90
Gastrin and the vagus interact in the trophic control of the rat oxyntic mucosa. Regul Pept (1988) 0.90
TGFBR1(*)6A and Int7G24A variants of transforming growth factor-beta receptor 1 in Swedish familial and sporadic breast cancer. Br J Cancer (2007) 0.90
Formation of the Scandinavian Obesity Surgery Registry, SOReg. Obes Surg (2015) 0.90
Release of adenylate kinase into cerebrospinal fluid during open-heart surgery and its relation to postoperative intellectual function. Lancet (1982) 0.89
Intestinal permeability in humans is increased after radiation therapy. Dis Colon Rectum (2000) 0.89
Quantification of adenovirus DNA in unrelated donor hematopoietic stem cell transplant recipients. J Clin Virol (2008) 0.89
Increased colonic permeability in patients with ulcerative colitis: an in vitro study. Scand J Gastroenterol (1998) 0.88
Flucloxacillin-induced cholestatic liver damage. Scand J Infect Dis (1985) 0.88
Influence of pericardial suction blood retransfusion on memory function and release of protein S100B. Perfusion (2004) 0.87
Prevailing effectiveness of the 2009 influenza A(H1N1)pdm09 vaccine during the 2010/11 season in Sweden. Euro Surveill (2013) 0.87
Effect of open heart surgery on intellectual function. Scand J Thorac Cardiovasc Surg Suppl (1974) 0.87