نتایج جستجو برای: electrolyte csw eos

تعداد نتایج: 30817  

Journal: :Cell 1996
Ronald Herbst Pamela M Carroll John D Allard James Schilling Thomas Raabe Michael A Simon

The SH2 domain-containing phosphotyrosine phosphatase Corkscrew (CSW) is an essential component of the signaling pathway initiated by the activation of the sevenless receptor tyrosine kinase (SEV) during Drosophila eye development. We have used genetic and biochemical approaches to identify a substrate for CSW. Expression of a catalytically inactive CSW was used to trap CSW in a complex with a ...

1996
Nelson R. Manohar Atul Prakash

This paper presents a novel and exible architecture to support the asynchronous sharing of computer-supported workspaces (CSWs), or simply replayable workspaces. Such workspaces are composed of multiple, interacting tools. Through the capture, re-execution, and manipulation of a session with a CSW, it is possible to reuse valuable collaborative information, (e.g., the how-to process). The sessi...

Journal: :Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering 2011
Y Yang L Zhang Y Q Zhao S P Wang X C Guo Y Guo L Wang Y X Ren X C Wang

This study was conducted to examine the possibility of using construction solid waste (CSW), an inevitable by-product of the construction and demolition process, as the main substrate in a laboratory scale multi-stage constructed wetland system (CWs) to improve phosphorus (P) removal from secondary sewage effluent. A tidal-flow operation strategy was employed to enhance the wetland aeration. Th...

Journal: :Neurosurgery clinics of North America 2010
Alan H Yee Joseph D Burns Eelco F M Wijdicks

Cerebral salt wasting (CSW) is a syndrome of hypovolemic hyponatremia caused by natriuresis and diuresis. The mechanisms underlying CSW have not been precisely delineated, although existing evidence strongly implicates abnormal elevations in circulating natriuretic peptides. The key in diagnosis of CSW lies in distinguishing it from the more common syndrome of inappropriate secretion of antidiu...

Journal: :Journal of the American Society of Nephrology : JASN 2008
Richard H Sterns Stephen M Silver

The term cerebral salt wasting (CSW) was introduced before the syndrome of inappropriate antidiuretic hormone secretion was described in 1957. Subsequently, CSW virtually vanished, only to reappear a quarter century later in the neurosurgical literature. A valid diagnosis of CSW requires evidence of inappropriate urinary salt losses and reduced "effective arterial blood volume." With no gold st...

Journal: :Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research 1996
J A Cooper M A Simon S J Kussick

Vertebrate Src can be activated by specific mutations to become oncogenic. Analogous mutations in Drosophila Src64 (DSrc) induce abnormal differentiation of photoreceptor cells when expressed ectopically in the developing Drosophila adult eye. We have investigated the roles that the adapter protein, Downstream of receptor kinases (Drk), and the SH2 domain-containing tyrosine phosphatase, Corksc...

صابر ساعتی, , علیرضا شایسته, ,

Data envelopment analysis (DEA) does not provide more information about the efficient decision making units (DMUs). A method to rank efficient DMUs is common set of weights (CSW). This research proposes some simple methods to find common set of weights CSW for the performance indices of DEA efficient DMUs. These methods use the results of the standard DEA models to determine the CSW. Unlike the...

Journal: :Surgical neurology 2008
Daniel C Lu Devin K Binder Bonnie Chien Alan Maisel Geoffrey T Manley

BACKGROUND Historically, hyponatremia in patients with varying brain diseases was termed cerebral salt wasting. Hyponatremia secondary to CSW was reported to be a distinct entity from SIADH, with the distinguishing feature of decreased extracellular fluid volume. Brain natriuretic peptide, a peptide with natriuretic, vasorelaxant, and aldosterone-inhibiting properties, was recently implicated i...

Journal: :Human molecular genetics 2006
Kimihiko Oishi Konstantin Gaengel Srinivasan Krishnamoorthy Kenichi Kamiya In-Kyong Kim Huiwen Ying Ursula Weber Lizabeth A Perkins Marco Tartaglia Marek Mlodzik Leslie Pick Bruce D Gelb

Mutations in the PTPN11 gene, which encodes the protein tyrosine phosphatase SHP-2, causes Noonan syndrome (NS), an autosomal dominant disorder with pleomorphic developmental abnormalities. Certain germline and somatic PTPN11 mutations cause leukemias. Mutations have gain-of-function (GOF) effects with the commonest NS allele, N308D, being weaker than the leukemia-causing mutations. To study th...

2004
Mingxing Luo

One-loop maximal helicity violating (MHV) amplitudes in N = 4 super YangMills (SYM) theories are analyzed, using the prescription of Cachazo, Svrcek, and Witten (CSW). The relations between leading Nc amplitudes An;1 and sub-leading amplitudes An;c obtained by the CSW prescription are found to be identical to those obtained from conventional field theory calculations. Combining with existing re...

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