نتایج جستجو برای: dpp6

تعداد نتایج: 82  

2015
Ayush Giri Jennifer M. Wu Renee M. Ward Katherine E. Hartmann Amy J. Park Kari E. North Mariaelisa Graff Robert B. Wallace Gihan Bareh Lihong Qi Mary J. O'Sullivan Alexander P. Reiner Todd L. Edwards Digna R. Velez Edwards Dana C Crawford

Current evidence suggests a multifactorial etiology to pelvic organ prolapse (POP), including genetic predisposition. We conducted a genome-wide association study of POP in African American (AA) and Hispanic (HP) women from the Women's Health Initiative Hormone Therapy study. Cases were defined as any POP (grades 1-3) or moderate/severe POP (grades 2-3), while controls had grade 0 POP. We perfo...

Journal: :Neuroscience 2011
A D Whyment E Coderre J M M Wilson L P Renaud E O'Hare D Spanswick

Transient outward rectifying conductances or A-like conductances in sympathetic preganglionic neurons (SPN) are prolonged, lasting for hundreds of milliseconds to seconds and are thought to play a key role in the regulation of SPN firing frequency. Here, a multidisciplinary electrophysiological, pharmacological and molecular single-cell rt-PCR approach was used to investigate the kinetics, phar...

Journal: :Development 2006
Woo Chi Valerie Reinke

In Caenorhabditis elegans, EFL-1 (E2F), DPL-1 (DP) and LIN-35 (pRb) act coordinately in somatic tissues to inhibit ectopic cell division, probably by repressing the expression of target genes. EFL-1, DPL-1 and LIN-35 are also present in the germline, but do not always act together. Strong loss-of-function mutations in either efl-1 or dpl-1 cause defects in oogenesis that result in sterility, wh...

2014
Rakesh Chettier Kenneth Ward Hans M. Albertsen

Endometriosis is a complex gynecological condition that affects 6-10% of women in their reproductive years and is defined by the presence of endometrial glands and stroma outside the uterus. Twin, family, and genome-wide association (GWA) studies have confirmed a genetic role, yet only a small part of the genetic risk can be explained by SNP variation. Copy number variants (CNVs) account for a ...

2016
Chandra Shekhar Pareek Rafał Smoczyński Haja N. Kadarmideen Piotr Dziuba Paweł Błaszczyk Marcin Sikora Paulina Walendzik Tomasz Grzybowski Mariusz Pierzchała Jarosław Horbańczuk Agnieszka Szostak Magdalena Ogluszka Lech Zwierzchowski Urszula Czarnik Leyland Fraser Przemysław Sobiech Krzysztof Wąsowicz Brian Gelfand Yaping Feng Dibyendu Kumar

Examination of bovine pituitary gland transcriptome by strand-specific RNA-seq allows detection of putative single nucleotide polymorphisms (SNPs) within potential candidate genes (CGs) or QTLs regions as well as to understand the genomics variations that contribute to economic trait. Here we report a breed-specific model to successfully perform the detection of SNPs in the pituitary gland of y...

2012
Martin Kruse Gerald R.V. Hammond Bertil Hille

Phosphatidylinositol 4,5-bisphosphate (PI(4,5)P(2)) regulates activities of numerous ion channels including inwardly rectifying potassium (K(ir)) channels, KCNQ, TRP, and voltage-gated calcium channels. Several studies suggest that voltage-gated potassium (K(V)) channels might be regulated by PI(4,5)P(2). Wide expression of K(V) channels in different cells suggests that such regulation could ha...

Journal: :Cardiology journal 2012
Andrés Ricardo Pérez-Riera Luiz Carlos de Abreu Frank Yanowitz Raimundo Barbosa Barros Francisco Femenía William F McIntyre Adrian Baranchuk

In the great majority of cases the ECG pattern of early repolarization (ERP) is a benign phenomenon observed predominantly in teenagers, young adults, male athletes and the black race. The universally accepted criterion for its diagnosis is the presence, in at least two adjoining leads, of ≥ 1 mm or 0.1 mV ST segment elevation. In benign ERP reciprocal ST segment changes are possible only in le...

2015
O. A. Makeeva A. A. Sleptsov E. V. Kulish O. L. Barbarash A. M. Mazur E. B. Prokhorchuk N. N. Chekanov V. A. Stepanov V. P. Puzyrev

Comorbidity or a combination of several diseases in the same individual is a common and widely investigated phenomenon. However, the genetic background for non-random disease combinations is not fully understood. Modern technologies and approaches to genomic data analysis enable the investigation of the genetic profile of patients burdened with several diseases (polypathia, disease conglomerate...

2012
Hylke Merijn Blauw Hylke Blauw

We performed a genome-wide association study in sporadic ALS (2,323 patients and 9,013 controls) and evaluated all SNPs with P < 1.0 x 10-4 in a second, independent cohort of 2,532 patients and 5,940 controls. Analysis of the genome-wide data revealed genome-wide signifi cance for one SNP, rs12608932 with P = 1.30 x 10-9. This SNP demonstrated robust replication in the second cohort (P = 1.86 x...

Journal: :Journal of lipid research 2016
Fernando Martínez-Montañés Museer A Lone Fong-Fu Hsu Roger Schneiter

Long-chain bases (LCBs) are the precursors to ceramide and sphingolipids in eukaryotic cells. They are formed by the action of serine palmitoyl-CoA transferase (SPT), a complex of integral membrane proteins located in the endoplasmic reticulum. SPT activity is negatively regulated by Orm proteins to prevent the toxic overaccumulation of LCBs. Here we show that overaccumulation of LCBs in yeast ...

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