نتایج جستجو برای: kid

تعداد نتایج: 1589  

Journal: :Cancer Biology & Therapy 2008

Journal: :Synthese 2014
Sjur Dyrkolbotn Michal Walicki

A novel normal form for propositional theories underlies the logic pdl, which captures some essential features of natural discourse, independent from any particular subject matter and related only to its referential structure. In particular, pdl allows to distinguish vicious circularity from the innocent one, and to reason in the presence of inconsistency using a minimal number of extraneous as...

2012
Mary S. Varaschin Christian Hirsch Flademir Wouters Karen Y. Nakagaki Antônio M. Guimarães Domingos S. Santos Pedro S. Bezerra Rafael C. Costa Ana P. Peconick Ingeborg M. Langohr

Congenital Neospora caninum infection was diagnosed in two Saanen goat kids from two distinct herds with a history of abortion and weak newborn goat kids in the Southern region of the State of Minas Gerais, Brazil. The first kid was weak at birth, had difficulty to rise and was unable to nurse. Gross lesions of porencephaly and hydrocephalus ex vacuo were seen. Multifocal necrosis, gliosis and ...

Journal: :Pediatrics 2012
Craig W Lillehei Kimberlee Gauvreau Kathy J Jenkins

OBJECTIVE To develop a risk-adjustment method for evaluation of in-hospital mortality after noncardiac neonatal surgery regardless of gestational age. METHODS Infants ≤ 30 days old undergoing noncardiac surgical procedures were identified by using the Kids' Inpatient Database (KID) 2000 + 2003. Neonates were included regardless of gestational age. International Classification of Disease, Nint...

Journal: :The Journal of investigative dermatology 2009
Jack R Lee Adam M Derosa Thomas W White

Mutations in the GJB2 gene-encoding connexin 26 (Cx26) have been linked to skin disorders and genetic deafness. However, the severity and type of the skin disorders caused by Cx26 mutations are heterogeneous. Here we explored the effect of Cx26 KID syndrome-associated mutations, G12R, S17F, and D50N on channel function. The Cx26 N14K mutation was also examined that is associated with deafness b...

2017
Sanna Gudmundsson Maria Wilbe Sara Ekvall Adam Ameur Nicola Cahill Ludmil B. Alexandrov Marie Virtanen Maritta Hellström Pigg Anders Vahlquist Hans Törmä Marie-Louise Bondeson

Revertant mosaicism (RM) is a naturally occurring phenomenon where the pathogenic effect of a germline mutation is corrected by a second somatic event. Development of healthy-looking skin due to RM has been observed in patients with various inherited skin disorders, but not in connexin-related disease. We aimed to clarify the underlying molecular mechanisms of suspected RM in the skin of a pati...

2015
Elaine W. Flagg Hillard Weinstock

Methods The MarketScan Commercial Claims and Encounters (CCAE) data from Truven Health Analytics contains annual beneficiary enrollment information and inpatient admissions, outpatient encounters, and outpatient pharmacy dispensing claims from approximately 100 employee-sponsored private insurance plans. The 2012 CCAE contains 1.1 billion inpatient and outpatient claims records for 53 million e...

2012
Andrew B. Smith Juan López-Villarejo Elizabeth Diago-Navarro Lesley A. Mitchenall Arjan Barendregt Albert J. Heck Marc Lemonnier Anthony Maxwell Ramón Díaz-Orejas

Bacterial toxin-antitoxin (TA) systems encode two proteins, a potent inhibitor of cell proliferation (toxin) and its specific antidote (antitoxin). Structural data has revealed striking similarities between the two model TA toxins CcdB, a DNA gyrase inhibitor encoded by the ccd system of plasmid F, and Kid, a site-specific endoribonuclease encoded by the parD system of plasmid R1. While a commo...

Journal: :Journal of animal science 2010
K Sidler-Lauff A Boos M Kraenzlin A Liesegang

The purpose of this study was to investigate whether diets differing in Ca concentration would have an influence on vitamin D (VitD) receptor (VDR) and calbindin D9k (Calb9k) immunoreactivities in the gastrointestinal tract of growing goats. In addition, the effect of a single VitD injection was studied, to clarify whether exogenous VitD would further increase the active Ca absorption mechanism...

2016
Elizabeth de Wolf Joseph van de Wiel Jonathan Cook Nicholas Dale

Connexin26 (Cx26) mutations underlie human pathologies ranging from hearing loss to keratitis ichthyosis deafness (KID) syndrome. Cx26 hemichannels are directly gated by CO2 and contribute to the chemosensory regulation of breathing. The KID syndrome mutation A88V is insensitive to CO2, and has a dominant negative action on the CO2 sensitivity of Cx26WT hemichannels, and reduces respiratory dri...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید