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Health Knowledge of Outpatient Visitors at Mirjan Teaching Hospital in Al-Hilla city

Indian journal of public health research and development., 2019-05, Vol.10 (5), p.641

2019

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Reexpression of Cartilage-Specific Genes by Dedifferentiated Human Articular Chondrocytes Cultured in Alginate Beads

Experimental cell research, 1994-05, Vol.212 (1), p.97-104

1994

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Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy

American journal of human genetics, 2005-02, Vol.76 (2), p.334-339

2005

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Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

The Lancet (British edition), 2000-07, Vol.356 (9227), p.391-395

2000

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A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure

Nature genetics, 2001-09, Vol.29 (1), p.57-60

2001

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Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency

American journal of human genetics, 2001-06, Vol.68 (6), p.1344-1352

2001

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Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNA

Human molecular genetics, 2001-05, Vol.10 (11), p.1221-1228

2001

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Correlation between genotype, metabolic data, and clinical presentation in carnitine palmitoyltransferase 2 (CPT2) deficiency

Human mutation, 2003-05, Vol.21 (5), p.493-501

2003

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Substitution of aspartic acid for glycine at position 310 in type II collagen produces achondrogenesis II, and substitution of serine at position 805 produces hypochondrogenesis: analysis of genotype-phenotype relationships

Biochemical journal, 1995-05, Vol.307 ( Pt 3) (3), p.823-830

1995

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Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt-1) in the NDUFS4 gene in Leigh syndrome

Human genetics, 2003-05, Vol.112 (5-6), p.563-566

2003

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Molecular and Enzymatic Characterization of a Unique Carnitine Palmitoyltransferase 1A Mutation in the Hutterite Community

Molecular genetics and metabolism, 2001-05, Vol.73 (1), p.46-54

2001

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Caractérisation enzymatique et moléculaire d'un déficit en α-cétoglutarate déshydrogénase chez trois frères porteurs d'une encépahalopathie évolutive

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 1997-09, Vol.4 (9), p.907-908

1997

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Fructose-Induced Enhanced Mitogenicity of Diploid Human Cells: Possible Relationship with Cell Differentiation

In vitro cellular & developmental biology. Animal, 1994-04, Vol.30A (4), p.263-268

1994

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Periodic fluctuations in proliferation of SV-40 transformed human skin fibroblast lines with prolonged lifespan

Cell biology and toxicology, 1994-08, Vol.10 (4), p.247-254

1994

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Impaired hexose uptake by diploid skin fibroblasts from galactosaemic patients. Connection with cell growth and amino acid metabolism, and possible bearing on late‐onset clinical symptoms

Journal of inherited metabolic disease, 1993-01, Vol.16 (1), p.78-90

1993

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Glutamine dependency of human skin fibroblasts: Modulation by hexoses

Experimental cell research, 1989-08, Vol.183 (2), p.303-318

1989

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Cell complementation using Genebridge 4 human:rodent hybrids for physical mapping of novel mitochondrial respiratory chain deficiency genes

Human molecular genetics, 2002-12, Vol.11 (26), p.3273-3281

2002

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Human cultured skin fibroblasts survive profound inherited ubiquinone depletion

Free radical research, 2001-01, Vol.35 (1), p.11-21

2001

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Factor VIII procoagulant antigen in human tissues

Thrombosis and haemostasis, 1988-04, Vol.59 (2), p.289-294

1988

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Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiency

Biochemical genetics, 1989-04, Vol.27 (3-4), p.219-228

1989

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Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

The Lancet (British edition), 2000-07, Vol.356 (9227), p.391-395

2000

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Low Efficiency of [ 14C] Galactose Incorporation by Galactosemic Skin Fibroblasts: Relationship with Neurological Sequelae

Biochemical medicine and metabolic biology, 1994-08, Vol.52 (2), p.140-144

1994

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Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiency

Biochemical genetics, 1989-04, Vol.27 (3-4), p.219-228

1989

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Impact of project delivery method on geotechnical site conditions for implementing water treatment plants in Iraq

AIP Conference Proceedings, 2023, Vol.2651 (1)

2023

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Metabolic cooperation in cocultures of fibroblasts from patients with various abnormalities of galactose metabolism

Comptes rendus de l'Académie des sciences, Série III, Sciences de la vie, 1989, Vol.308 (17), p.453

1989

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Health Knowledge of Outpatient Visitors at Mirjan Teaching Hospital in Al-Hilla city

Reexpression of Cartilage-Specific Genes by Dedifferentiated Human Articular Chondrocytes Cultured in Alginate Beads

Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy

Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure

Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency

Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNA

Correlation between genotype, metabolic data, and clinical presentation in carnitine palmitoyltransferase 2 (CPT2) deficiency

Substitution of aspartic acid for glycine at position 310 in type II collagen produces achondrogenesis II, and substitution of serine at position 805 produces hypochondrogenesis: analysis of genotype-phenotype relationships

Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt-1) in the NDUFS4 gene in Leigh syndrome

Molecular and Enzymatic Characterization of a Unique Carnitine Palmitoyltransferase 1A Mutation in the Hutterite Community

Caractérisation enzymatique et moléculaire d'un déficit en α-cétoglutarate déshydrogénase chez trois frères porteurs d'une encépahalopathie évolutive

Fructose-Induced Enhanced Mitogenicity of Diploid Human Cells: Possible Relationship with Cell Differentiation

Periodic fluctuations in proliferation of SV-40 transformed human skin fibroblast lines with prolonged lifespan

Impaired hexose uptake by diploid skin fibroblasts from galactosaemic patients. Connection with cell growth and amino acid metabolism, and possible bearing on late‐onset clinical symptoms

Glutamine dependency of human skin fibroblasts: Modulation by hexoses

Cell complementation using Genebridge 4 human:rodent hybrids for physical mapping of novel mitochondrial respiratory chain deficiency genes

Human cultured skin fibroblasts survive profound inherited ubiquinone depletion

Factor VIII procoagulant antigen in human tissues

Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiency

Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

Low Efficiency of [ 14C] Galactose Incorporation by Galactosemic Skin Fibroblasts: Relationship with Neurological Sequelae

Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiency

Impact of project delivery method on geotechnical site conditions for implementing water treatment plants in Iraq

Metabolic cooperation in cocultures of fibroblasts from patients with various abnormalities of galactose metabolism

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