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Hepatic toxicological responses of SiO2 nanoparticle on Oreochromis mossambicus

Environmental toxicology and pharmacology, 2020-08, Vol.78, p.103398, Article 103398

2020

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Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer‐associated variants

International journal of cancer, 2014-05, Vol.134 (10), p.2330-2341

2014

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Activity concentration of polonium-210 and lead-210 in tobacco products and annual committed effective dose to tobacco users in Tiruchirappalli District (Tamil Nadu, India)

Journal of radioanalytical and nuclear chemistry, 2020-03, Vol.323 (3), p.1425-1429

2020

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Growth Differentiation Factor 5 Regulates Cardiac Repair After Myocardial Infarction

Journal of the American College of Cardiology, 2010-01, Vol.55 (2), p.135-143

2010

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T cell‐inflamed gene expression profile is associated with favorable disease‐specific survival in non‐hypermutated microsatellite‐stable colorectal cancer patients

Cancer medicine (Malden, MA), 2023-03, Vol.12 (6), p.6583-6593

2023

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Haemato-immunological studies in ZnO and TiO2 nanoparticles exposed euryhaline fish, Oreochromis mossambicus

Environmental toxicology and pharmacology, 2019-02, Vol.66, p.55-61

2019

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A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1

Human genetics, 2015-11, Vol.134 (11-12), p.1249-1262

2015

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Histological alterations in the hepatic tissues of Al2O3 nanoparticles exposed freshwater fish Oreochromis mossambicus

Journal of trace elements in medicine and biology, 2017-12, Vol.44, p.125-131

2017

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Defective glycosylation of decorin and biglycan, altered collagen structure, and abnormal phenotype of the skin fibroblasts of an Ehlers-Danlos syndrome patient carrying the novel Arg270Cys substitution in galactosyltransferase I (beta4GalT-7)

Journal of molecular medicine (Berlin, Germany), 2006-07, Vol.84 (7), p.583-594

2006

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The effect of 5-fluorouracil/leucovorin chemotherapy on CpG methylation, or the confounding role of leukocyte heterogeneity: An illustration

Genomics (San Diego, Calif.), 2015-12, Vol.106 (6), p.340-347

2015

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Toxicological effect of Al2O3 nanoparticles on histoarchitecture of the freshwater fish Oreochromis mossambicus

Environmental toxicology and pharmacology, 2018-04, Vol.59, p.74-81

2018

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A novel non-sense mutation in the SLC2A10 gene of an arterial tortuosity syndrome patient of Kurdish origin

European journal of pediatrics, 2009-07, Vol.168 (7), p.867-870

2009

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Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci

Nature communications, 2015-02, Vol.6 (1), p.6326-6326, Article 6326

2015

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Effect of cobalt-60 gamma radiation on total hemocyte content and biochemical parameters in Macrobrachium rosenbergii (De Man, 1879)

International journal of radiation biology, 2019-06, Vol.95 (6), p.753-763

2019

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A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome

Atherosclerosis, 2009-04, Vol.203 (2), p.466-471

2009

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Clinical, neuroimaging, and genetic features of L-2-hydroxyglutaric aciduria in Arab kindreds

Annals of Saudi medicine, 2014-03, Vol.34 (2), p.107-114

2014

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A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations

European journal of pediatrics, 2010-06, Vol.169 (6), p.661-666

2010

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Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency

European journal of pediatrics, 2009-12, Vol.168 (12), p.1467-1471

2009

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Grebe-type chondrodysplasia: a novel missense mutation in a conserved cysteine of the growth differentiation factor 5

Journal of bone and mineral metabolism, 2008-11, Vol.26 (6), p.648-652

2008

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Ultrastructure abnormalities of collagen and elastin in Arab patients with arterial tortuosity syndrome

Journal of cutaneous pathology, 2022-07, Vol.49 (7), p.618-622

2022

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Novel and recurrent germline mutations in the VHL gene in 5 Arab patients with Von Hippel-Lindau disease

Cancer genetics, 2020-05, Vol.243, p.1-6

2020

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A Common Polymorphism in the Cannabinoid Receptor 1 (CNR1) Gene is Associated with Antipsychotic-Induced Weight Gain in Schizophrenia

Neuropsychopharmacology (New York, N.Y.), 2010-05, Vol.35 (6), p.1315-1324

2010

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Novel and Recurrent Mutations in the C1NH Gene of Arab Patients Affected with Hereditary Angioedema

International archives of allergy and immunology, 2010-01, Vol.151 (2), p.149-154

2010

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A Prospective Study of the Synergistic Effects of Arsenic Exposure and Smoking, Sun Exposure, Fertilizer Use, and Pesticide Use on Risk of Premalignant Skin Lesions in Bangladeshi Men

American journal of epidemiology, 2011-01, Vol.173 (2), p.183-191

2011

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Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation

Journal of pediatric endocrinology & metabolism : JPEM, 2018-08, Vol.31 (8), p.861

2018

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Hepatic toxicological responses of SiO2 nanoparticle on Oreochromis mossambicus

Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer‐associated variants

Activity concentration of polonium-210 and lead-210 in tobacco products and annual committed effective dose to tobacco users in Tiruchirappalli District (Tamil Nadu, India)

Growth Differentiation Factor 5 Regulates Cardiac Repair After Myocardial Infarction

T cell‐inflamed gene expression profile is associated with favorable disease‐specific survival in non‐hypermutated microsatellite‐stable colorectal cancer patients

Haemato-immunological studies in ZnO and TiO2 nanoparticles exposed euryhaline fish, Oreochromis mossambicus

A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1

Histological alterations in the hepatic tissues of Al2O3 nanoparticles exposed freshwater fish Oreochromis mossambicus

Defective glycosylation of decorin and biglycan, altered collagen structure, and abnormal phenotype of the skin fibroblasts of an Ehlers-Danlos syndrome patient carrying the novel Arg270Cys substitution in galactosyltransferase I (beta4GalT-7)

The effect of 5-fluorouracil/leucovorin chemotherapy on CpG methylation, or the confounding role of leukocyte heterogeneity: An illustration

Toxicological effect of Al2O3 nanoparticles on histoarchitecture of the freshwater fish Oreochromis mossambicus

A novel non-sense mutation in the SLC2A10 gene of an arterial tortuosity syndrome patient of Kurdish origin

Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci

Effect of cobalt-60 gamma radiation on total hemocyte content and biochemical parameters in Macrobrachium rosenbergii (De Man, 1879)

A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome

Clinical, neuroimaging, and genetic features of L-2-hydroxyglutaric aciduria in Arab kindreds

A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations

Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency

Grebe-type chondrodysplasia: a novel missense mutation in a conserved cysteine of the growth differentiation factor 5

Ultrastructure abnormalities of collagen and elastin in Arab patients with arterial tortuosity syndrome

Novel and recurrent germline mutations in the VHL gene in 5 Arab patients with Von Hippel-Lindau disease

A Common Polymorphism in the Cannabinoid Receptor 1 (CNR1) Gene is Associated with Antipsychotic-Induced Weight Gain in Schizophrenia

Novel and Recurrent Mutations in the C1NH Gene of Arab Patients Affected with Hereditary Angioedema

A Prospective Study of the Synergistic Effects of Arsenic Exposure and Smoking, Sun Exposure, Fertilizer Use, and Pesticide Use on Risk of Premalignant Skin Lesions in Bangladeshi Men

Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation

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