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Disease on EC 5.4.2.1 - phosphoglycerate mutase

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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Abruptio Placentae
The association of factor V leiden and prothrombin gene mutation and placenta-mediated pregnancy complications: a systematic review and meta-analysis of prospective cohort studies.
Adenocarcinoma of Lung
Molecular typing of lung adenocarcinoma on cytological samples using a multigene next generation sequencing panel.
Use of the Ion PGM and the GeneReader NGS Systems in Daily Routine Practice for Advanced Lung Adenocarcinoma Patients: A Practical Point of View Reporting a Comparative Study and Assessment of 90 Patients.
Aggressive Periodontitis
Shifts of subgingival bacterial population after nonsurgical and pharmacological therapy of localized aggressive periodontitis, followed for 1 year by Ion Torrent PGM platform.
Alzheimer Disease
Mitophagy in degenerative joint diseases.
Organelle-specific autophagy in inflammatory diseases: a potential therapeutic target underlying the quality control of multiple organelles.
Amnesia
A Polysaccharide Extract from Maitake Culinary-Medicinal Mushroom, Grifola frondosa (Agaricomycetes) Ameliorates Learning and Memory Function in Aluminum Chloride-Induced Amnesia in Mice.
Amyotrophic Lateral Sclerosis
Organelle-specific autophagy in inflammatory diseases: a potential therapeutic target underlying the quality control of multiple organelles.
Anemia
[Chronic oral toxicity study of proglumetacin maleate in beagle dogs]
Anemia, Hemolytic
Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing.
Angina Pectoris
Phosphoglucomutase activity as a novel biomarker in patients with acute myocardial infarction.
Arthritis
[Pharmacological studies on proglumetacin maleate, a new non-steroidal anti-inflammatory drug. (2). Analgesic and antipyretic effects]
Arthritis, Experimental
[Pharmacological studies on proglumetacin maleate, a new non-steroidal anti-inflammatory drug. (1). Anti-inflammatory effects]
Aspergillosis
?-1,6-linked Galactofuranose- rich peptidogalactomannan of Fusarium oxysporum is important in the activation of macrophage mechanisms and as a potential diagnostic antigen.
Astrocytoma
Phosphoglycerate mutase, 2,3-bisphosphoglycerate phosphatase and creatine kinase activity and isoenzymes in human brain tumours.
Bacteremia
Emergence of Multidrug Resistant Hypervirulent ST23 Klebsiella pneumoniae: Multidrug Resistant Plasmid Acquisition Drives Evolution.
Brain Neoplasms
Phosphoglycerate mutase, 2,3-bisphosphoglycerate phosphatase and creatine kinase activity and isoenzymes in human brain tumours.
Breast Neoplasms
PALB2 mutations in BRCA1/2-mutation negative breast and ovarian cancer patients from Poland.
Phosphoglycerate mutase, 2,3-bisphosphoglycerate phosphatase, creatine kinase and enolase activity and isoenzymes in breast carcinoma.
Targeted next-generation sequencing detects a high frequency of potentially actionable mutations in metastatic breast cancers.
[Echogenic phospholipids-based gas-filled microbubbles as delivery system of antisense oligodeoxynucleotides]
Carcinoma
Advances and Applications of Ion Torrent Personal Genome Machine in Cutaneous Squamous Cell Carcinoma Reveal Novel Gene Mutations.
Antitumor and antimetastatic activity of the immunoadjuvant peptidoglycan monomer PGM in mice bearing MCa mammary carcinoma.
Effects of dimethyltriazenes combined with surgery and non-specific immunotherapy in mice bearing Lewis lung carcinoma lines.
Effects of L-(adamant-2-yl)glycyl-L-alanyl-d-isoglutamine on the antitumor action of cyclophosphamide, 5-fu, Cisplatin and dacarbazine on advanced carcinomas of the mouse.
Effects of postsurgical immunotherapy with PGM in mice bearing Lewis lung carcinoma treated with p-(3,3-dimethyl-1-triazeno) benzoic acid potassium salt.
Genetic profiling of thymic carcinoma using targeted next-generation sequencing.
Insulin/IGF1-PI3K-dependent nucleolar localization of a glycolytic enzyme--phosphoglycerate mutase 2, is necessary for proper structure of nucleolus and RNA synthesis.
Next generation sequencing in lung cancer: An initial experience from India.
Transcriptomic comparison of primary bovine horn core carcinoma culture and parental tissue at early stage.
Carcinoma, Hepatocellular
Targeted deep DNA methylation analysis of circulating cell-free DNA in plasma using massively parallel semiconductor sequencing.
Carcinoma, Lewis Lung
Effects of dimethyltriazenes combined with surgery and non-specific immunotherapy in mice bearing Lewis lung carcinoma lines.
Effects of L-(adamant-2-yl)glycyl-L-alanyl-d-isoglutamine on the antitumor action of cyclophosphamide, 5-fu, Cisplatin and dacarbazine on advanced carcinomas of the mouse.
Effects of postsurgical immunotherapy with PGM in mice bearing Lewis lung carcinoma treated with p-(3,3-dimethyl-1-triazeno) benzoic acid potassium salt.
Carcinoma, Non-Small-Cell Lung
Predictive efficacy of low burden EGFR mutation detected by next-generation sequencing on response to EGFR tyrosine kinase inhibitors in non-small-cell lung carcinoma.
Carcinoma, Squamous Cell
Advances and Applications of Ion Torrent Personal Genome Machine in Cutaneous Squamous Cell Carcinoma Reveal Novel Gene Mutations.
Genetic profiling of thymic carcinoma using targeted next-generation sequencing.
Insulin/IGF1-PI3K-dependent nucleolar localization of a glycolytic enzyme--phosphoglycerate mutase 2, is necessary for proper structure of nucleolus and RNA synthesis.
Transcriptomic comparison of primary bovine horn core carcinoma culture and parental tissue at early stage.
Cardiomyopathies
Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathies.
Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.
Targeted next-generation sequencing (NGS) of nine candidate genes with custom AmpliSeq in patients and a cardiomyopathy risk group.
Cataract
Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri Lanka.
Cholera
[Multilocus sequence-typing of vibrio cholerae strains with various epidemic importance].
Colitis, Collagenous
Multilocus sequence typing of Campylobacter concisus from Danish diarrheic patients.
Colitis, Ulcerative
Clinicopathologic Features and Diagnostic Implications of Pyloric Gland Metaplasia in Intestinal Specimens.
Colorectal Neoplasms
The utility of the Ion Torrent PGM next generation sequencing for analysis of the most commonly mutated genes among patients with colorectal cancer in India.
Validation of targeted next-generation sequencing for RAS mutation detection in FFPE colorectal cancer tissues: comparison with Sanger sequencing and ARMS-Scorpion real-time PCR.
Validation of the Ion Torrent PGM sequencing for the prospective routine molecular diagnostic of colorectal cancer.
Communicable Diseases
Infectious disease 1947-1987. A PGM retrospective.
Congenital Abnormalities
Evaluating the abnormal ossification in tibiotarsi of developing chick embryos exposed to 1.0ppm doses of platinum group metals by spectroscopic techniques.
Cough
Influence of simulated mucus on cough sounds in cats.
Cystic Fibrosis
Mucus penetrating properties of soft, distensible lipid nanocapsules.
Cysts
Prenatal pseudocysts of the germinal matrix in preterm infants.
Deafness
Clinical Application of a Custom AmpliSeq Library and Ion Torrent PGM Sequencing to Comprehensive Mutation Screening for Deafness Genes.
Dementia
[Indicators of early Alzheimer dementia in family practice. Development and validation of the Observation List of Early Symptoms of Dementia (OLD)]
Dengue
Isolation and characterization of dengue virus serotype 2 from the large dengue outbreak in Guangdong, China in 2014.
Dermatitis, Atopic
Genetic investigations in atopic dermatitis.
Extensively Drug-Resistant Tuberculosis
An optimized genomic VCF workflow for precise identification of Mycobacterium tuberculosis cluster from cross-platform whole genome sequencing data.
Eye Diseases
Galloyl Carbohydrates with Antiangiogenic Activity Mediated by Capillary Morphogenesis Gene 2 (CMG2) Protein Binding.
Fetal Death
Prepartum changes of plasma concentrations of prostaglandin F and 13,14-dihydro-15-ketoprostaglandin metabolites in pregnant animals exposed to Sarcocystis cruzi or Campylobacter fetus.
Frontotemporal Dementia
Organelle-specific autophagy in inflammatory diseases: a potential therapeutic target underlying the quality control of multiple organelles.
Galactosemias
Using a Personal Glucose Meter and Alkaline Phosphatase for Point-of-Care Quantification of Galactose-1-Phosphate Uridyltransferase in Clinical Galactosemia Diagnosis.
Gallstones
[A study on the mechanism of the choleretic effect of proglumide]
[The effect of proglumide on gallstone formation in guinea pigs]
Genetic Diseases, Inborn
Molecular diagnostics of the HBB gene in an Omani cohort using bench-top DNA Ion Torrent PGM technology.
[Detection of pathogenic mutations for methylmalonic acidemia using new-generation semiconductor targeted sequencing].
Glioblastoma
Phosphoglycerate mutase, 2,3-bisphosphoglycerate phosphatase and creatine kinase activity and isoenzymes in human brain tumours.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Red cell phosphoglucomutase (PGM)-deficiency: hereditary defect of the PGM1-locus.
Glucosephosphate Dehydrogenase Deficiency
Red cell phosphoglucomutase (PGM)-deficiency: hereditary defect of the PGM1-locus.
Glycogen Storage Disease
CARM1/PRMT4 is necessary for the glycogen gene expression programme in skeletal muscle cells.
Muscle phosphoglycerate mutase deficiency revisited.
Hearing Loss
Deafness gene variations in a 1120 nonsyndromic hearing loss cohort: molecular epidemiology and deafness mutation spectrum of patients in Japan.
Heart Diseases
Potential contribution of erythrocyte microRNA to secondary erythrocytosis and thrombocytopenia in congenital heart disease.
Hemochromatosis
Hereditary hemochromatosis restores the virulence of plague vaccine strains.
Hemoglobinopathies
Molecular diagnostics of the HBB gene in an Omani cohort using bench-top DNA Ion Torrent PGM technology.
Hepatitis
[Phosphoglyceromutase activity of the blood in human viral hepatitis.]
Hepatitis B
Comparison of error correction algorithms for Ion Torrent PGM data: application to hepatitis B virus.
Hepatitis, Viral, Human
[Phosphoglyceromutase activity of the blood in human viral hepatitis.]
Hypersensitivity
Allergy and immunology 1947-1987. A PGM retrospective.
Hypertension, Renovascular
Duplex ultrasound for identifying renal artery stenosis: direct criteria re-evaluated.
Illusions
Comparisons of flashILM, transformational apparent motion, and polarized gamma motion indicate these are three independent and separable illusions.
Infections
Absence of inflammation and pneumonia during infection with non-pigmented Yersinia pestis reveals new role for the pgm locus in pathogenesis.
Capsule Production and Glucose Metabolism Dictate Fitness during Serratia marcescens Bacteremia.
Host and MTB genome encoded miRNA markers for diagnosis of tuberculosis.
Hybrids between Schistosoma haematobium and S. mattheei and their identification by isoelectric focusing of enzymes.
Longitudinal cerebral metabolic changes in pig-tailed macaques infected with the neurovirulent virus SIVsmmFGb.
Prepartum changes of plasma concentrations of prostaglandin F and 13,14-dihydro-15-ketoprostaglandin metabolites in pregnant animals exposed to Sarcocystis cruzi or Campylobacter fetus.
Seroprevalence in Household Raised Pigs Indicate High Exposure to GII Noroviruses in Rural Nicaragua.
The enzyme phosphoglucomutase (Pgm) is required by Salmonella enterica serovar Typhimurium for O-antigen production, resistance to antimicrobial peptides and in vivo fitness.
Venezuelan Equine Encephalitis Virus Induces Apoptosis through the Unfolded Protein Response Activation of EGR1.
Influenza, Human
Analysis of the genetic diversity of influenza A viruses using next-generation DNA sequencing.
Insulin Resistance
Partial deficiency of phosphoglycerate mutase with diabetic polyneuropathy: the first Japanese patient.
Intervertebral Disc Degeneration
Mitophagy in degenerative joint diseases.
Leishmaniasis, Visceral
A preliminary isoenzyme study on five species of phlebotomine sandflies in China.
Leishmaniasis in Brazil. XXII: Characterization of Leishmania from man, dogs and the sandfly Lutzomyia longipalpis (Lutz & Neiva, 1912) isolated during an outbreak of visceral leishmaniasis in Santarém, Pará State.
[The identification of Leishmania isolates obtained from patients and dogs with visceral leishmaniasis in the Turkmen SSR]
Leukemia
Regulation of phosphoglucomutase 1 phosphorylation and activity by a signaling kinase.
Lung Neoplasms
Assessment of the clinical application of detecting EGFR, KRAS, PIK3CA and BRAF mutations in patients with non-small cell lung cancer using next-generation sequencing.
Non-small cell lung cancers with isocitrate dehydrogenase 1 or 2 (IDH1/2) mutations.
Predictive efficacy of low burden EGFR mutation detected by next-generation sequencing on response to EGFR tyrosine kinase inhibitors in non-small-cell lung carcinoma.
Lymphoma
Inbreeding, heterozygosity, and lymphoma risk among the baboons (Papio hamadryas) of Sukhumi, USSR.
Malaria
A Method for Amplicon Deep Sequencing of Drug Resistance Genes in Plasmodium falciparum Clinical Isolates from India.
Maxillofacial Injuries
[The role of the genotype in the development of suppurative inflammatory complications in trauma to the facial bones]
Melanoma
A Case of Primary Gastric Melanoma Exhibiting a Rare BRAF V600R Mutation.
Immunotherapy of B-16 melanoma with peptidoglycan monomer.
Mutational concordance between primary and metastatic melanoma: a next-generation sequencing approach.
Primary gastric melanoma: A case report with imaging findings and 5-year follow-up.
Meningioma
Phosphoglycerate mutase, 2,3-bisphosphoglycerate phosphatase and creatine kinase activity and isoenzymes in human brain tumours.
Menkes Kinky Hair Syndrome
A phosphoglycerate mutase brain isoform (PGAM 1) pseudogene is localized within the human Menkes disease gene (ATP7 A).
Mouth Neoplasms
Genome-wide mitochondrial DNA sequence variations and lower expression of OXPHOS genes predict mitochondrial dysfunction in oral cancer tissue.
Muscle Cramp
Partial deficiency of phosphoglycerate mutase with diabetic polyneuropathy: the first Japanese patient.
Phosphoglycerate mutase deficiency with tubular aggregates in a patient from Panama.
Muscular Diseases
Decreased oxidative phosphorylation and PGAM deficiency in horses suffering from atypical myopathy associated with acquired MADD.
Molecular genetic studies in muscle phosphoglycerate mutase (PGAM-M) deficiency.
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene.
Muscular Dystrophies
Plasma phosphoglycerate mutase as a marker of muscular dystrophy.
Myocardial Infarction
Activity of phosphoglycerate mutase and its isoenzymes in serum after acute myocardial infarction.
Association of venous thromboembolism and myocardial infarction with Factor V Leiden and Factor II gene mutations among Libyan patients.
Phosphoglucomutase activity as a novel biomarker in patients with acute myocardial infarction.
Myocardial Ischemia
Phosphoglucomutase activity as a novel biomarker in patients with acute myocardial infarction.
Myoglobinuria
Metabolic causes of myoglobinuria.
Phosphoglycerate mutase deficiency with tubular aggregates in a patient from Panama.
Neoplasm Metastasis
Effects of L-(adamant-2-yl)glycyl-L-alanyl-d-isoglutamine on the antitumor action of cyclophosphamide, 5-fu, Cisplatin and dacarbazine on advanced carcinomas of the mouse.
Immunotherapy of B-16 melanoma with peptidoglycan monomer.
Targeted next-generation sequencing detects a high frequency of potentially actionable mutations in metastatic breast cancers.
Neoplasms
Antitumor and antimetastatic activity of the immunoadjuvant peptidoglycan monomer PGM in mice bearing MCa mammary carcinoma.
Basal Cell Carcinoma With Matrical Differentiation: Clinicopathologic, Immunohistochemical, and Molecular Biological Study of 22 Cases.
Clinical Evaluation of a Novel Nine-Gene Panel for Ion Torrent PGM Sequencing of Myeloid Malignancies.
Connecting the dots between different networks: miRNAs associated with bladder cancer risk and progression.
Deacetylation of phosphoglycerate mutase in its distinct central region by SIRT2 down-regulates its enzymatic activity.
Dual cascade isothermal amplification reaction based glucometer sensors for point-of-care diagnostics of cancer-related microRNAs.
Effects of dimethyltriazenes combined with surgery and non-specific immunotherapy in mice bearing Lewis lung carcinoma lines.
Effects of L-(adamant-2-yl)glycyl-L-alanyl-d-isoglutamine on the antitumor action of cyclophosphamide, 5-fu, Cisplatin and dacarbazine on advanced carcinomas of the mouse.
Effects of postsurgical immunotherapy with PGM in mice bearing Lewis lung carcinoma treated with p-(3,3-dimethyl-1-triazeno) benzoic acid potassium salt.
G-6-PD and PGM phenotypes of 16 continuous human tumor cell lines. Evidence against cross-contamination and contamination by HeLa cells.
Galloyl Carbohydrates with Antiangiogenic Activity Mediated by Capillary Morphogenesis Gene 2 (CMG2) Protein Binding.
Genetic profiling of thymic carcinoma using targeted next-generation sequencing.
Identification of Circulating Genomic and Metabolic Biomarkers in Intrahepatic Cholangiocarcinoma.
Identification of novel BRCA1 large genomic rearrangements by a computational algorithm of amplicon-based Next-Generation Sequencing data.
Immunohistochemical expression of chromogranins A and B, prohormone convertases 2 and 3, and amidating enzyme in carcinoid tumors and pancreatic endocrine tumors.
Immunotherapy of B-16 melanoma with peptidoglycan monomer.
Improving Adequacy of Small Biopsy and Fine-Needle Aspiration Specimens for Molecular Testing by Next-Generation Sequencing in Patients With Lung Cancer: A Quality Improvement Study at Dartmouth-Hitchcock Medical Center.
Individualized Mutation Detection in Circulating Tumor DNA for Monitoring Colorectal Tumor Burden Using a Cancer-Associated Gene Sequencing Panel.
Mitophagy in degenerative joint diseases.
Molecular diagnostics of a single multifocal non-small cell lung cancer case using targeted next generation sequencing.
Next generation sequencing in lung cancer: An initial experience from India.
Next-generation sequencing of BRCA1 and BRCA2 genes for rapid detection of germline mutations in hereditary breast/ovarian cancer.
Non-small cell lung cancers with isocitrate dehydrogenase 1 or 2 (IDH1/2) mutations.
Oxidative stress activates SIRT2 to deacetylate and stimulate phosphoglycerate mutase.
Phosphoglycerate Mutase Cooperates with Chk1 Kinase to Regulate Glycolysis.
Phosphoglycerate mutase-derived polypeptide inhibits glycolytic flux and induces cell growth arrest in tumor cell lines.
Primary gastric melanoma: A case report with imaging findings and 5-year follow-up.
Pulmonary Langerhans Cell Histiocytosis: Profiling of Multifocal Tumors Using Next-Generation Sequencing Identifies Concordant Occurrence of BRAF V600E Mutations.
Quality control material for the detection of somatic mutations in fixed clinical specimens by next-generation sequencing.
Serial Next-Generation Sequencing of Circulating Cell-Free DNA Evaluating Tumor Clone Response To Molecularly Targeted Drug Administration.
Study of Preanalytic and Analytic Variables for Clinical Next-Generation Sequencing of Circulating Cell-Free Nucleic Acid.
Targeted deep sequencing of mucinous ovarian tumors reveals multiple overlapping RAS-pathway activating mutations in borderline and cancerous neoplasms.
Targeted Next Generation Sequencing as a Reliable Diagnostic Assay for the Detection of Somatic Mutations in Tumours Using Minimal DNA Amounts from Formalin Fixed Paraffin Embedded Material.
Targeted next-generation sequencing detects a high frequency of potentially actionable mutations in metastatic breast cancers.
Towards a Next-Generation Sequencing Diagnostic Service for Tumour Genotyping: A Comparison of Panels and Platforms.
TP53, PIK3CA, FBXW7 and KRAS Mutations in Esophageal Cancer Identified by Targeted Sequencing.
Two roles for Ia in antigen-specific T lymphocyte activation.
Validation of quantitative PCR-based assays for detection of gene copy number aberrations in formalin-fixed, paraffin embedded solid tumor samples.
Variant call concordance between two laboratory-developed, solid tumor targeted genomic profiling assays using distinct workflows and sequencing instruments.
Versatile ion S5XL sequencer for targeted next generation sequencing of solid tumors in a clinical laboratory.
Neoplastic Syndromes, Hereditary
Next-generation sequencing of BRCA1 and BRCA2 genes for rapid detection of germline mutations in hereditary breast/ovarian cancer.
Neurofibromatoses
Fast and Robust Next-Generation Sequencing Technique Using Ion Torrent Personal Genome Machine for the Screening of Neurofibromatosis Type 1 (NF1) Gene.
Neurofibromatosis 1
Fast and Robust Next-Generation Sequencing Technique Using Ion Torrent Personal Genome Machine for the Screening of Neurofibromatosis Type 1 (NF1) Gene.
Obesity
Adherence to the Healthy Eating Index-2015 across Generations Is Associated with Birth Outcomes and Weight Status at Age 5 in the Lifeways Cross-Generation Cohort Study.
Osteoarthritis
Mitophagy in degenerative joint diseases.
Otitis Media with Effusion
Role of sialic acid and complex carbohydrate biosynthesis in biofilm formation by nontypeable Haemophilus influenzae in the chinchilla middle ear.
Ovarian Hyperstimulation Syndrome
Factor V Leiden and prothrombin gene G20210A mutation and in vitro fertilization: prospective cohort study.
Ovarian Neoplasms
New recurrent BRCA1/2 mutations in Polish patients with familial breast/ovarian cancer detected by next generation sequencing.
PALB2 mutations in BRCA1/2-mutation negative breast and ovarian cancer patients from Poland.
Synthesis and evaluation of new polynuclear organometallic Ru(II), Rh(III) and Ir(III) pyridyl ester complexes as in vitro antiparasitic and antitumor agents.
Paralysis
Paralysis of innervated cultured human muscle fibers affects enzymes differentially.
Parasitemia
Deep sequencing to detect diversity of Trypanosoma cruzi infection in patients co-infected with HIV and Chagas disease.
Parkinson Disease
Mitophagy in degenerative joint diseases.
Organelle-specific autophagy in inflammatory diseases: a potential therapeutic target underlying the quality control of multiple organelles.
phosphoglycerate mutase deficiency
Decreased oxidative phosphorylation and PGAM deficiency in horses suffering from atypical myopathy associated with acquired MADD.
Exercise-induced cramp, myoglobinuria, and tubular aggregates in phosphoglycerate mutase deficiency.
Hereditary thrombophilia and recurrent pregnancy loss: a systematic review and meta-analysis.
Inactivation of the phosphoglucomutase gene pgm in Paenibacillus polymyxa leads to overproduction of fusaricidin.
Infantile muscle glycogen storage disease: phosphoglucomutase deficiency with decreased muscle and serum carnitine levels.
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) gene.
Metabolic causes of myoglobinuria.
Molecular genetic studies in muscle phosphoglycerate mutase (PGAM-M) deficiency.
Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and 31P-MR spectroscopy.
Muscle phosphoglycerate mutase (PGAM) deficiency: a second case.
Muscle phosphoglycerate mutase deficiency revisited.
Partial deficiency of phosphoglycerate mutase with diabetic polyneuropathy: the first Japanese patient.
Phosphoglycerate mutase deficiency with tubular aggregates in a patient from Panama.
Physiologic assessment of phosphoglycerate mutase deficiency: incremental exercise test.
Red cell phosphoglucomutase (PGM)-deficiency: hereditary defect of the PGM1-locus.
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene.
[A case of adult onset phosphoglucomutase deficiency]
phosphorylase kinase deficiency
Metabolic causes of myoglobinuria.
Plague
Absence of inflammation and pneumonia during infection with non-pigmented Yersinia pestis reveals new role for the pgm locus in pathogenesis.
Genetic variations in the pgm locus among natural isolates of Yersinia pestis.
Hereditary hemochromatosis restores the virulence of plague vaccine strains.
Modification of the Pulmonary MyD88 Inflammatory Response Underlies the Role of the Yersinia pestis Pigmentation Locus in Primary Pneumonic Plague.
Septic shock and nonpulmonary organ dysfunction in pneumonic plague: The role of Yersinia pestis pCD1- vs. pgm- virulence factors.
The yersiniabactin transport system is critical for the pathogenesis of bubonic and pneumonic plague.
Yersinia pestis YbtU and YbtT are involved in synthesis of the siderophore yersiniabactin but have different effects on regulation.
Yersiniabactin production requires the thioesterase domain of HMWP2 and YbtD, a putative phosphopantetheinylate transferase.
Pleurisy
[Pharmacological studies on proglumetacin maleate, a new non-steroidal anti-inflammatory drug. (1). Anti-inflammatory effects]
Pneumonia
Absence of inflammation and pneumonia during infection with non-pigmented Yersinia pestis reveals new role for the pgm locus in pathogenesis.
Septic shock and nonpulmonary organ dysfunction in pneumonic plague: The role of Yersinia pestis pCD1- vs. pgm- virulence factors.
Polycystic Kidney Diseases
Functional alterations due to amino acid changes and evolutionary comparative analysis of ARPKD and ADPKD genes.
Polycystic Kidney, Autosomal Recessive
Functional alterations due to amino acid changes and evolutionary comparative analysis of ARPKD and ADPKD genes.
Next-generation sequencing for molecular diagnosis of autosomal recessive polycystic kidney disease.
Polyneuropathies
Partial deficiency of phosphoglycerate mutase with diabetic polyneuropathy: the first Japanese patient.
Pouchitis
Is Pyloric Gland Metaplasia in Ileal Pouch Biopsies a Marker for Crohn's Disease?
Pyloric gland metaplasia: Potential histologic predictor of severe pouch disease including Crohn's disease of the pouch in ulcerative colitis.
Pre-Eclampsia
The association of factor V leiden and prothrombin gene mutation and placenta-mediated pregnancy complications: a systematic review and meta-analysis of prospective cohort studies.
Pregnancy Complications
The association of factor V leiden and prothrombin gene mutation and placenta-mediated pregnancy complications: a systematic review and meta-analysis of prospective cohort studies.
Pulmonary Disease, Chronic Obstructive
Organelle-specific autophagy in inflammatory diseases: a potential therapeutic target underlying the quality control of multiple organelles.
Pyometra
Increased concentrations of C-reactive protein but not high-mobility group box 1 in dogs with naturally occurring sepsis.
Quadriplegia
Associations between inherited thrombophilias, gestational age, and cerebral palsy.
Retinitis Pigmentosa
[Identification of a novel RHO mutation in a pedigree affected with retinitis pigmentosa].
Sarcoma
Sheep gene mapping: additional DNA markers included (CASB, CASK, LALBA, IGF-1 and AMH).
The NAB2-STAT6 gene fusion in solitary fibrous tumor can be reliably detected by anchored multiplexed PCR for targeted next-generation sequencing.
Seizures
Ameliorating effects of proglumide on neurobehavioral and biochemical deficits in animal model of status epilepticus.
Sepsis
First report of Burkholderia pseudomallei ST412 and ST734 clones harbouring blaOXA-57 but susceptible to imipenem in India.
Increased concentrations of C-reactive protein but not high-mobility group box 1 in dogs with naturally occurring sepsis.
Septic shock and nonpulmonary organ dysfunction in pneumonic plague: The role of Yersinia pestis pCD1- vs. pgm- virulence factors.
Sexually Transmitted Diseases
Population genetics of Neisseria gonorrhoeae in a high-prevalence community using a hypervariable outer membrane porB and 13 slowly evolving housekeeping genes.
Splenic Infarction
Autosomal-dominant inheritance of the prothrombin gene mutation in a Puerto Rican family: A case study.
Starvation
The novel PII-interactor PirC identifies phosphoglycerate mutase as key control point of carbon storage metabolism in cyanobacteria.
Stroke
A new stroke marker as detected by serum phosphoglycerate mutase B-type isozyme.
Suppuration
[The role of the genotype in the development of suppurative inflammatory complications in trauma to the facial bones]
Thrombocytopenia
Molecular diagnosis of thrombocytopenia-absent radius syndrome using next-generation sequencing.
Thrombophilia
Association between in vitro fertilization outcomes and inherited thrombophilias: a meta-analysis.
Genetic Testing for Thrombophilia-Related Genes: Observations of Testing Patterns for Factor V Leiden (G1691A) and Prothrombin Gene "Mutation" (G20210A).
Hereditary thrombophilia and recurrent pregnancy loss: a systematic review and meta-analysis.
Thrombosis
Association of venous thromboembolism and myocardial infarction with Factor V Leiden and Factor II gene mutations among Libyan patients.
Autosomal-dominant inheritance of the prothrombin gene mutation in a Puerto Rican family: A case study.
Factor V Leiden and prothrombin gene G20210A mutation and in vitro fertilization: prospective cohort study.
Phosphoglucomutase activity as a novel biomarker in patients with acute myocardial infarction.
Tuberculosis
An optimized genomic VCF workflow for precise identification of Mycobacterium tuberculosis cluster from cross-platform whole genome sequencing data.
Host and MTB genome encoded miRNA markers for diagnosis of tuberculosis.
[A genotypic study of children ill with tuberculosis and of healthy BCG-revaccinated ones of Tuvinian nationality]
Tuberculosis, Pulmonary
Host and MTB genome encoded miRNA markers for diagnosis of tuberculosis.
Venous Thrombosis
Association of venous thromboembolism and myocardial infarction with Factor V Leiden and Factor II gene mutations among Libyan patients.
Autosomal-dominant inheritance of the prothrombin gene mutation in a Puerto Rican family: A case study.
Virus Diseases
Comparison of third-generation sequencing approaches to identify viral pathogens under public health emergency conditions.
von Willebrand Disease, Type 3
Variants p.Pro2063Ser and p.Arg324* co-segregate in type 3 von Willebrand disease patients from Southern Brazil.
Whooping Cough
Genetic Diversity of Clinical Bordetella Pertussis ST2 Strains in comparison with Vaccine Reference Strains of India.
Xerostomia
Incorporation of Dosimetric Gradients and Parotid Gland Migration Into Xerostomia Prediction.