نتایج جستجو برای: pgm1

تعداد نتایج: 107  

2013
Jiri Jablonsky Martin Hagemann Doreen Schwarz Olaf Wolkenhauer

Phosphoglycerate-mutase (PGM) is an ubiquitous glycolytic enzyme, which in eukaryotic cells can be found in different compartments. In prokaryotic cells, several PGMs are annotated/localized in one compartment. The identification and functional characterization of PGMs in prokaryotes is therefore important for better understanding of metabolic regulation. Here we introduce a method, based on a ...

Journal: :Human reproduction 2009
Marina Berbic Lauren Schulke Robert Markham Natsuko Tokushige Peter Russell Ian S Fraser

BACKGROUND Endometriosis is an inflammatory condition, characterized by the presence of endometrial-like tissue outside the uterus. The immune system provides a defence mechanism in response to foreign pathogens, and macrophages play important roles in this response. Activation of macrophages has been reported in peritoneal fluid and ectopic endometriotic lesions; however, controversy exists re...

2015
Periyasamy Govindaraj Sheikh Nizamuddin Anugula Sharath Vuskamalla Jyothi Harish Rotti Ritu Raval Jayakrishna Nayak Balakrishna K. Bhat B. V. Prasanna Pooja Shintre Mayura Sule Kalpana S. Joshi Amrish P. Dedge Ramachandra Bharadwaj G. G. Gangadharan Sreekumaran Nair Puthiya M. Gopinath Bhushan Patwardhan Paturu Kondaiah Kapaettu Satyamoorthy Marthanda Varma Sankaran Valiathan Kumarasamy Thangaraj

The practice of Ayurveda, the traditional medicine of India, is based on the concept of three major constitutional types (Vata, Pitta and Kapha) defined as "Prakriti". To the best of our knowledge, no study has convincingly correlated genomic variations with the classification of Prakriti. In the present study, we performed genome-wide SNP (single nucleotide polymorphism) analysis (Affymetrix, ...

Journal: :Human biology 1993
A G Novoradovsky V A Spitsyn R Duggirala M H Crawford

Genetic polymorphisms of blood groups, serum proteins, red cell enzymes, PTC tasting, and cerumen types are reported for five Mongoloid populations of Buryats from the Lake Baikal region of Siberia (Russia). These groups are characterized by relatively high frequencies of alleles ABO*B, RH*D, cerumen D, GC*1F, ACP1*B, ESD*2, and PGD*C. Significant genetic heterogeneity between populations was d...

Journal: :Journal of Carcinogenesis 2006
Saied Hosseini-Asl Mohammad H Modarressi Morteza Atri Mohamed Salhab Kefah Mokbel Parvin Mehdipour

Telomerase is a ribonucleoprotein enzyme that compensates for the telomere length shortening which occurs during the cell cycle. Telomerase activity has been detected in most tumours but not in somatic cells. However, hTR; the RNA component of telomerase; has been reported to be universally expressed in both cancerous and non-cancerous tissues. Tumour samples from 50 patients with primary invas...

Journal: :Blood 2014
Jorge Galvez Silva Michael Rytting

A 13-month-old boy with recurrent upper respiratory infections, persistent fevers, and chronic rash presented to our facility. The patient had been treated with several months of antibiotics and topical creams with no improvement. In the emergency room, he had a prominent rash (panel A), jaundice, and tachypnea. Complete blood count showed white blood cells 3.5 3 10/mL, absolute neutrophils 0.3...

2017
Hüseyin Demirbilek Khalid Hussain

Pancreatic β-cells are finely tuned to secrete insulin so that plasma glucose levels are maintained within a narrow physiological range (3.5-5.5 mmol/L). Hyperinsulinaemic hypoglycaemia (HH) is the inappropriate secretion of insulin in the presence of low plasma glucose levels and leads to severe and persistent hypoglycaemia in neonates and children. Mutations in 12 different key genes (ABCC8, ...

Journal: :Plant, cell & environment 2013
Ianis G Matsoukas Andrea J Massiah Brian Thomas

The physiology and genetics underlying juvenility is poorly understood. Here, we exploit Arabidopsis as a system to understand the mechanisms that regulate floral incompetence during juvenility. Using an experimental assay that allows the length of juvenility to be estimated and mutants impaired in different pathways, we show that multiple inputs influence juvenility. Juvenile phase lengths of ...

Journal: :The New England journal of medicine 2014
Laura C Tegtmeyer Stephan Rust Monique van Scherpenzeel Bobby G Ng Marie-Estelle Losfeld Sharita Timal Kimiyo Raymond Ping He Mie Ichikawa Joris Veltman Karin Huijben Yoon S Shin Vandana Sharma Maciej Adamowicz Martin Lammens Janine Reunert Anika Witten Esther Schrapers Gert Matthijs Jaak Jaeken Daisy Rymen Tanya Stojkovic Pascal Laforêt François Petit Olivier Aumaître Elzbieta Czarnowska Monique Piraud Teodor Podskarbi Charles A Stanley Reuben Matalon Patricie Burda Soraya Seyyedi Volker Debus Piotr Socha Jolanta Sykut-Cegielska Francjan van Spronsen Linda de Meirleir Pietro Vajro Terry DeClue Can Ficicioglu Yoshinao Wada Ron A Wevers Dieter Vanderschaeghe Nico Callewaert Ralph Fingerhut Emile van Schaftingen Hudson H Freeze Eva Morava Dirk J Lefeber Thorsten Marquardt

BACKGROUND Congenital disorders of glycosylation are genetic syndromes that result in impaired glycoprotein production. We evaluated patients who had a novel recessive disorder of glycosylation, with a range of clinical manifestations that included hepatopathy, bifid uvula, malignant hyperthermia, hypogonadotropic hypogonadism, growth retardation, hypoglycemia, myopathy, dilated cardiomyopathy,...

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