نتایج جستجو برای: pndm

تعداد نتایج: 79  

2016
Jingnan Lv Xiuqin Qi Dan Zhang Zhou Zheng Yuehui Chen Yinjuan Guo Shanshan Wang Liang Chen Barry N. Kreiswirth Yi-Wei Tang Zengqiang Chen Longhua Hu Liangxing Wang Fangyou Yu

Since the first report of blaNDM-1, 16 blaNDM variants have been identified among Gram-negative bacteria worldwide. Recently, a novel blaNDM variant, blaNDM-13, was identified in the chromosome of an ST101 Escherichia coli isolate from Nepal. Here we first reported plasmid-mediated blaNDM-13 in a carbapenem-resistant E. coli ST5138 clinical isolate associated with hospital-acquired urinary trac...

Journal: :Human molecular genetics 2004
Maki Inoue Yoshiyuki Sakuraba Hiromi Motegi Naoto Kubota Hideaki Toki Junko Matsui Yukiyasu Toyoda Ichitomo Miwa Yasuo Terauchi Takashi Kadowaki Yutaka Shigeyama Masato Kasuga Takashi Adachi Naomi Fujimoto Rie Matsumoto Keiko Tsuchihashi Tomoko Kagami Ayako Inoue Hideki Kaneda Junko Ishijima Hiroshi Masuya Tomohiro Suzuki Shigeharu Wakana Yoichi Gondo Osamu Minowa Toshihiko Shiroishi Tetsuo Noda

Mutant mouse models are indispensable tools for clarifying the functions of genes and for elucidating the underlying pathogenic mechanisms of human diseases. Currently, several large-scale mutagenesis projects that employ the chemical mutagen N-ethyl-N-nitrosourea (ENU) are underway worldwide. One specific aim of our ENU mutagenesis project is to generate diabetic mouse models. We screened 9375...

2012
Sameer K. Salih S. A. Aljunid Abid Yahya Khalid Ghailan

In this study, an automatic approach for detecting QRS complexes and evaluating related R-R intervals of ECG signals (PNDM) is proposed. It reliably recognizes QRS complexes based on the deflection occurred between R & S waves as a large positive and negative interval with respect to other ECG signal waves. The proposed detection method follows new fast direct algorithm applied to the entire EC...

2015
Fengjun Sun Zhe Yin Jiao Feng Yefeng Qiu Defu Zhang Wenbo Luo Huiying Yang Wenhui Yang Jie Wang Weijun Chen Peiyuan Xia Dongsheng Zhou

Raoultella ornithinolytica YNKP001 and Leclercia adecarboxylata P10164, which harbor conjugative plasmids pYNKP001-NDM and pP10164-NDM, respectively, were isolated from two different Chinese patients, and their complete nucleotide sequences were determined. Production of NDM-1 enzyme by these plasmids accounts for the carbapenem resistance of these two strains. This is the first report of bla N...

Journal: :American journal of physiology. Endocrinology and metabolism 2010
Savita Dhanvantari

DIABETES MELLITUS can be described as a collection of metabolic diseases characterized by fasting hyperglycemia. Although the most prevalent forms of diabetes mellitus are the polygenic forms that result in -cell destruction or dysfunction, there exist monogenic forms that are diagnosed within the first six months of life, termed neonatal diabetes mellitus. This is a rare condition, occurring i...

2013
Abdelhadi M. Habeb

Background Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis. The frequency of this rare syndrome is largely unknown. Objectives To define the frequency and spectrum of WRS in the Kingdom of Saudi Arabia (KSA) based on published data. Methods The Medline database was ...

Journal: :Diabetes 2008
Benjamin Glaser

Studies of monogenic disorders of -cell function have yielded important information on -cell physiology and have improved the diagnosis and treatment of patients with these rare diseases. These disorders include defects associated with increased insulin secretion, causing hypoglycemia, and decreased insulin secretion, resulting in diabetes. The most common form of monogenic diabetes is so-calle...

Journal: :Diabetes Care 2009
Oscar Rubio-Cabezas Jayne A.L. Minton Richard Caswell Julian P. Shield Dorothee Deiss Zdenek Sumnik Amely Cayssials Mathias Herr Anja Loew Vaughan Lewis Sian Ellard Andrew T. Hattersley

OBJECTIVE Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is caused by FOXP3 mutations. We aimed to determine the prevalence, genetics, and clinical phenotype of FOXP3 mutations in a large cohort with permanent neonatal diabetes (PNDM). RESEARCH DESIGN AND METHODS The 11 coding exons and the polyadenylation region of FOXP3 were sequenced in 26 male subjects wit...

2017
Ja Hyang Cho Eungu Kang Beom Hee Lee Gu Hwan Kim Jin Ho Choi Han Wook Yoo

Permanent neonatal diabetes mellitus (PNDM) is caused by mutations in the ATP-sensitive potassium channel (KATP channel) subunits. Developmental delay, epilepsy, and neonatal diabetes (DEND) syndrome is the most severe form of PNDM and is characterized by various neurologic features. We report on a patient with DEND syndrome following initial misdiagnosis with type 1 DM, who was successfully sw...

Journal: :Diabetes 2006
Kenju Shimomura Christophe A J Girard Peter Proks Joanna Nazim Jonathan D Lippiat Franco Cerutti Renata Lorini Sian Ellard Andrew T Hattersley Fabrizio Barbetti Frances M Ashcroft

Heterozygous mutations in the human Kir6.2 gene (KCNJ11), the pore-forming subunit of the ATP-sensitive K(+) channel (K(ATP) channel), are a common cause of neonatal diabetes. We identified a novel KCNJ11 mutation, R50Q, that causes permanent neonatal diabetes (PNDM) without neurological problems. We investigated the functional effects this mutation and another at the same residue (R50P) that l...

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