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Study of Endometritis Causing Repeat Breeding of Cycling Iraqi Buffalo Cows

Reproduction in domestic animals, 2008-12, Vol.43 (6), p.735-743

2008

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Clinical, Bacteriological, and Histopathological Study of Toxic Puerperal Metritis in Iraqi Buffalo

Journal of dairy science, 2007-10, Vol.90 (10), p.4654-4660

2007

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A Study on Postpartum Metritis in Iraqi Buffalo Cows: Bacterial Causes and Treatment

Reproduction in domestic animals, 2008-10, Vol.43 (5), p.556-565

2008

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Use of a high frequency transducer with real time B-mode ultrasound scanning to identify early pregnancy in cows

Veterinary record, 1988-07, Vol.123 (1), p.8-11

1988

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Ultrasonographic study of early embryonic loss induced by Actinomyces pyogenes in cattle

Veterinary record, 1992-07, Vol.131 (1), p.7-12

1992

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Evaluation of real time B-mode ultrasound scanning for detecting early pregnancy in cows

Veterinary record, 1990-10, Vol.127 (14), p.350-352

1990

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Preliminary observations of bovine ovarian structures using B-mode real time ultrasound

Veterinary record, 1988-05, Vol.122 (19), p.465-466

1988

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Role of nitric oxide in inflammatory diseases

Inflammopharmacology, 2007-12, Vol.15 (6), p.252-259

2007

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Design, Synthesis, and in Vitro Biological Evaluation of 14-Hydroxytylophorine-dichloroacetate Co-drugs as Antiproliferative Agents

Chemical and Pharmaceutical Bulletin, 2019/11/01, Vol.67(11), pp.1208-1210

2019

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Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome

Nature genetics, 2015-07, Vol.47 (7), p.809-813

2015

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SARS‐CoV‐2 targets neurons of 3D human brain organoids

The EMBO journal, 2020-10, Vol.39 (20), p.e106230-n/a

2020

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Cysteamine revisited: repair of arginine to cysteine mutations

Journal of inherited metabolic disease, 2017-07, Vol.40 (4), p.555-567

2017

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Cyclin O (Ccno) functions during deuterosome-mediated centriole amplification of multiciliated cells

The EMBO journal, 2015-04, Vol.34 (8), p.1078-1089

2015

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The Essential Autophagy Gene ATG7 Modulates Organ Fibrosis via Regulation of Endothelial-to-Mesenchymal Transition

The Journal of biological chemistry, 2015-01, Vol.290 (5), p.2547-2559

2015

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Homozygous nonsense mutation in SCHIP1/IQCJ‐SCHIP1 causes a neurodevelopmental brain malformation syndrome

Clinical genetics, 2018-02, Vol.93 (2), p.387-391

2018

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Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number

Neuron (Cambridge, Mass.), 2014-12, Vol.84 (6), p.1240-1257

2014

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Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation

Human molecular genetics, 2004-09, Vol.13 (18), p.2133-2141

2004

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The Preventive and Therapeutic Effects of Ajwa Date Fruit Extract Against Acute Diclofenac Toxicity-Induced Colopathy: An Experimental Study

Drug design, development and therapy, 2022-01, Vol.16, p.2601-2616

2022

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Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

Nature genetics, 2002-02, Vol.30 (2), p.143-144

2002

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To beat or not to beat: roles of cilia in development and disease

Human molecular genetics, 2003-04, Vol.12 (suppl-1), p.R27-R35

2003

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BRCA1 gene therapy reduces systemic inflammatory response and multiple organ failure and improves survival in experimental sepsis

Gene therapy, 2013-01, Vol.20 (1), p.51-61

2013

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Interleukin-1β and microRNA-146a in an immature rat model and children with mesial temporal lobe epilepsy

Epilepsia (Copenhagen), 2012-07, Vol.53 (7), p.1215-1224

2012

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Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration

Nature genetics, 2018-08, Vol.50 (8), p.1093-1101

2018

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Mutations in a novel gene, NPHP3 , cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis

Nature genetics, 2003-08, Vol.34 (4), p.455-459

2003

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Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia

American journal of human genetics, 2013-10, Vol.93 (4), p.672-686

2013

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Study of Endometritis Causing Repeat Breeding of Cycling Iraqi Buffalo Cows

Clinical, Bacteriological, and Histopathological Study of Toxic Puerperal Metritis in Iraqi Buffalo

A Study on Postpartum Metritis in Iraqi Buffalo Cows: Bacterial Causes and Treatment

Use of a high frequency transducer with real time B-mode ultrasound scanning to identify early pregnancy in cows

Ultrasonographic study of early embryonic loss induced by Actinomyces pyogenes in cattle

Evaluation of real time B-mode ultrasound scanning for detecting early pregnancy in cows

Preliminary observations of bovine ovarian structures using B-mode real time ultrasound

Role of nitric oxide in inflammatory diseases

Design, Synthesis, and in Vitro Biological Evaluation of 14-Hydroxytylophorine-dichloroacetate Co-drugs as Antiproliferative Agents

Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome

SARS‐CoV‐2 targets neurons of 3D human brain organoids

Cysteamine revisited: repair of arginine to cysteine mutations

Cyclin O (Ccno) functions during deuterosome-mediated centriole amplification of multiciliated cells

The Essential Autophagy Gene ATG7 Modulates Organ Fibrosis via Regulation of Endothelial-to-Mesenchymal Transition

Homozygous nonsense mutation in SCHIP1/IQCJ‐SCHIP1 causes a neurodevelopmental brain malformation syndrome

Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number

Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation

The Preventive and Therapeutic Effects of Ajwa Date Fruit Extract Against Acute Diclofenac Toxicity-Induced Colopathy: An Experimental Study

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

To beat or not to beat: roles of cilia in development and disease

BRCA1 gene therapy reduces systemic inflammatory response and multiple organ failure and improves survival in experimental sepsis

Interleukin-1β and microRNA-146a in an immature rat model and children with mesial temporal lobe epilepsy

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration

Mutations in a novel gene, NPHP3 , cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia

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