109-44-4

应用筛选条件

关键词:'109-44-4'

显示 1-15 共 15 条结果关于 "109-44-4" 范围论文

Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.

G Jayandharan et al.

Haemophilia : the official journal of the World Federation of Hemophilia, 11(5), 481-491 (2005-09-01)

Haemophilia A (HA) is an X-linked bleeding disorder caused by diverse mutations in the human coagulation factor VIII (FVIII) gene. We have analysed DNA from 109 unrelated Indian patients with HA for their FVIII gene defects. Among these patients 89

Novel mutations of the ATP7B gene among 109 Hungarian patients with Wilson's disease.

Aniko Folhoffer et al.

European journal of gastroenterology & hepatology, 19(2), 105-111 (2007-02-03)

Diagnosis of Wilson's disease may be difficult in patients presenting with liver disease and in asymptomatic siblings. The aim of the present study was to assess the impact of genetic testing for diagnosis of the disease in a large cohort

Cometabolism of 3,4-dichlorobenzoate by Acinetobacter sp. strain 4-CB1.

P Adriaens et al.

Applied and environmental microbiology, 57(1), 173-179 (1991-01-01)

When Acinetobacter sp. strain 4-CB1 was grown on 4-chlorobenzoate (4-CB), it cometabolized 3,4-dichlorobenzoate (3,4-DCB) to 3-chloro-4-hydroxybenzoate (3-C-4-OHB), which could be used as a growth substrate. No cometabolism of 3,4-DCB was observed when Acinetobacter sp. strain 4-CB1 was grown on benzoate.

Demonstration of a functional motilin receptor in TE671 cells from human cerebellum.

L Thielemans et al.

Brain research, 895(1-2), 119-128 (2001-03-22)

Our laboratory has described the presence of motilin receptors in the rabbit cerebellum. We discovered its presence in the human TE671 cell line, which is of cerebellar origin. Cytosolic Ca(2+) fluxes were monitored on a confocal microscope in cells loaded

Alterations in the expression of p53, KLF4, and p21 in neuroendocrine lung tumors.

José Manuel Naranjo Gómez et al.

Archives of pathology & laboratory medicine, 138(7), 936-942 (2014-07-01)

Neuroendocrine lung neoplasms are a heterogeneous group of tumors with different clinical behavior and prognosis. To evaluate the expression of p53, KLF4, and p21 in neuroendocrine lung neoplasms and to analyze the influence that expression has on the prognosis of

Genome Analysis of Staphylococcus capitis TE8 Reveals Repertoire of Antimicrobial Peptides and Adaptation Strategies for Growth on Human Skin.

Rohit Kumar et al.

Scientific reports, 7(1), 10447-10447 (2017-09-07)

Staphylococcus capitis TE8 was isolated from skin surface of a healthy human foot, and exhibited a strong antibacterial activity against Gram-positive bacteria, including Staphylococcus aureus. Whole genome sequence of S. capitis TE8 was obtained by shotgun and paired-end pyrosequencing with

Residual feed intake is repeatable for lactating Holstein dairy cows fed high and low starch diets.

S B Potts et al.

Journal of dairy science, 98(7), 4735-4747 (2015-05-20)

Residual feed intake (RFI) is a tool to quantify feed efficiency in livestock and is commonly used to assess feed efficiency independent of production level, body weight (BW), or BW change. Lactating Holstein cows (n=109; 44 primiparous and 65 multiparous)

Impact of VKORC1 gene polymorphism on interindividual and interethnic warfarin dosage requirement--a systematic review and meta analysis.

Limei Yang et al.

Thrombosis research, 125(4), e159-e166 (2009-11-28)

Warfarin is the most widely used oral anticoagulant. It has been suggested that anticoagulation effect of warfarin is significantly associated with the polymorphism of certain genes, including Cytochrome P450 complex subunit 2C9 (CYP2C9), Vitamin K Epoxide Reductase Complex Subunit 1

Twelve novel single nucleotide polymorphisms in ABCB1/MDR1 among Japanese patients with ventricular tachycardia who were administered amiodarone.

Masaya Itoda et al.

Drug metabolism and pharmacokinetics, 17(6), 566-571 (2004-12-25)

Twelve novel single nucleotide polymorphisms (SNPs) were found in the gene encoding the ATP-binding cassette transporter, P-glycoprotein, from 60 Japanese individuals who were administered the anti-antiarrythmic drug, amiodarone. The detected SNPs were as follows: 1) SNP, MPJ6_AB1017 (IVS6-109); GENE NAME

Acute and chronic nephropathy induced by fluindione must be addressed.

Gérard Cam et al.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 27(4), 1554-1558 (2011-09-21)

Among the vitamin K antagonists (VKA), indanedione-derived VKA is suspected to induce an immunoallergic risk. One indanedione-derived VKA, fluindione, is still being used in France. The aim of this study was to evaluate the contribution of VKA to acute and

Müllerian inhibiting substance type II receptor (MISIIR): a novel, tissue-specific target expressed by gynecologic cancers.

Jamie N Bakkum-Gamez et al.

Gynecologic oncology, 108(1), 141-148 (2007-11-09)

Müllerian inhibiting substance type II receptor (MISIIR) is expressed by ovarian, breast, and prostate cancers [Masiakos PT, et al. Human ovarian cancer, cell lines, and primary ascites cells express the human Mullerian inhibiting substance (MIS) Type II Receptor, bind, and

Angiography for renal artery stenosis: no additional impairment of renal function by angioplasty.

Volkmar Lufft et al.

European radiology, 12(4), 804-809 (2002-04-18)

The aim of this study was to compare renal function between patients with renal angiography and patients with renal angiography and angioplasty (AP) for renal artery stenosis (RAS). Forty-seven patients with suspected RAS were prospectively investigated by digital subtraction angiography

Association of loss-of-function mutations in the ABCA1 gene with high-density lipoprotein cholesterol levels and risk of ischemic heart disease.

Ruth Frikke-Schmidt et al.

JAMA, 299(21), 2524-2532 (2008-06-05)

Low levels of high-density lipoprotein (HDL) cholesterol are inversely related to cardiovascular risk. Whether this is a causal effect is unclear. To determine whether genetically reduced HDL cholesterol due to heterozygosity for 4 loss-of-function mutations in ABCA1 cause increased risk

Multi-Biomarkers for Early Detection of Type 2 Diabetes, Including 10- and 12-(Z,E)-Hydroxyoctadecadienoic Acids, Insulin, Leptin, and Adiponectin.

Aya Umeno et al.

PloS one, 10(7), e0130971-e0130971 (2015-07-02)

We have previously found that fasting plasma levels of totally assessed 10- and 12-(Z,E)-hydroxyoctadecadienoic acid (HODE) correlated well with levels of glycated hemoglobin (HbA1c) and glucose during oral glucose tolerance tests (OGTT); these levels were determined via liquid chromatography-mass spectrometry

Delayed polarization of mononuclear phagocyte transcriptional program by type I interferon isoforms.

David F Stroncek et al.

Journal of translational medicine, 3, 24-24 (2005-06-15)

Interferon (IFN)-alpha is considered a key modulator of immunopathological processes through a signature-specific activation of mononuclear phagocytes (MPs). This study utilized global transcript analysis to characterize the effects of the entire type I IFN family in comparison to a broad

1/1