نتایج جستجو برای: de novo programming

تعداد نتایج: 1852646  

Journal: :The Journal of biological chemistry 2008
Francisco Leocata Nieto Lucila G Pescio Nicolás O Favale Ana M Adamo Norma B Sterin-Speziale

The present report was addressed to study the influence of sphingolipid metabolism in determining cellular fate. In nonstimulated proliferating Madin-Darby canine kidney (MDCK) cells, sphingolipid de novo synthesis is branched mainly to a production of sphingomyelin and ceramide, with a minor production of sphingosylphosphocholine, ceramide 1-phosphate, and sphingosine 1-phosphate. Experiments ...

2017
Shi-Yan Wang Ting-Ting Cao Run-Zhi Wang Xin Yang Xiu-Li Sun Jian-Liu Wang

BACKGROUND Some patients with pelvic organ prolapse may suffer from lower urinary tract symptoms (LUTS), especially stress urinary incontinence (SUI) named de novo SUI after pelvic floor reconstruction. This study aimed to investigate the incidence and risk factors of de novo SUI. METHODS This is a nested case-control study of 533 patients who underwent pelvic floor reconstruction due to pelv...

Bashir N, Bashir Y, Bhat Sh, Geelani S, Manzoor F, Rasool J,

Background: Acute Myeloid Leukemia (AML) with translocation (3,3) is a form of AML that may present de novo or may arise from a previous myelodysplastic syndrome. It is often associated with normal or elevated peripheral blood platelet count and increased bone marrow megakaryocytes with associated multi lineage dysplasia. A subset of patients present with hepatosplenomegaly while a few cases h...

2017
Jonathan F Schmitz Erich Bornberg-Bauer

Over the last few years, there has been an increasing amount of evidence for the de novo emergence of protein-coding genes, i.e. out of non-coding DNA. Here, we review the current literature and summarize the state of the field. We focus specifically on open questions and challenges in the study of de novo protein-coding genes such as the identification and verification of de novo-emerged genes...

Journal: :Human molecular genetics 2015
Lan Yu Ashley D Sawle Julia Wynn Gudrun Aspelund Charles J Stolar Marc S Arkovitz Douglas Potoka Kenneth S Azarow George B Mychaliska Yufeng Shen Wendy K Chung

Congenital diaphragmatic hernia (CDH) is a serious birth defect that accounts for 8% of all major birth anomalies. Approximately 40% of cases occur in association with other anomalies. As sporadic complex CDH likely has a significant impact on reproductive fitness, we hypothesized that de novo variants would account for the etiology in a significant fraction of cases. We performed exome sequenc...

Journal: :The American journal of clinical nutrition 2001
R M McDevitt S J Bott M Harding W A Coward L J Bluck A M Prentice

BACKGROUND The results of previous studies suggest that de novo lipogenesis may play an important role in the etiology of obesity, particularly during overconsumption of different carbohydrates. OBJECTIVE We hypothesized that de novo lipogenesis would increase during overfeeding, would vary depending on the type of carbohydrate consumed, and would be greater in obese than in lean women. DES...

Journal: :The Journal of clinical investigation 1983
M E King J M Honeysett S B Howell

In previous studies from this laboratory, human bone marrow hypoxanthine concentrations were found to average 7.1 microM, three times higher than plasma hypoxanthine concentrations measured simultaneously. To assess the significance of this finding, the relationship between hypoxanthine concentration and the rate of purine nucleotide synthesis by the de novo pathway was studied in normal human ...

Journal: :Stroke 2016
Antti E Lindgren Sari Räisänen Joel Björkman Hanna Tattari Jukka Huttunen Terhi Huttunen Mitja I Kurki Juhana Frösen Timo Koivisto Juha E Jääskeläinen Mikael von Und Zu Fraunberg

BACKGROUND AND PURPOSE Formation of new (de novo) aneurysms in patients carrying saccular intracranial aneurysm (sIA) disease has been published, but data from population-based cohorts are scarce. METHODS Kuopio sIA database (http://www.uef.fi/ns) contains all unruptured and ruptured sIA patients admitted to Kuopio University Hospital from its Eastern Finnish catchment population. We studied ...

2017
Suzanne C E H Sallevelt Christine E M de Die-Smulders Alexandra T M Hendrickx Debby M E I Hellebrekers Irenaeus F M de Coo Charlotte L Alston Charlotte Knowles Robert W Taylor Robert McFarland Hubert J M Smeets

BACKGROUND Severe, disease-causing germline mitochondrial (mt)DNA mutations are maternally inherited or arise de novo. Strategies to prevent transmission are generally available, but depend on recurrence risks, ranging from high/unpredictable for many familial mtDNA point mutations to very low for sporadic, large-scale single mtDNA deletions. Comprehensive data are lacking for de novo mtDNA poi...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید