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Modelling of a direct evaporative air cooler using artificial neural network

International journal of energy research, 2008-01, Vol.32 (1), p.83-89

2008

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A simple mathematical model to analyse a fluidyne heat machine

Proceedings of the Institution of Mechanical Engineers. Part A, Journal of power and energy, 2003-01, Vol.217 (1), p.91-100

2003

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Natural convection in a vertical porous enclosure with internal heat generation

International journal of heat and mass transfer, 1984-01, Vol.27 (10), p.1893-1902

1984

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Estimation of heat transfer in oscillating annular flow using artifical neural networks

Advances in engineering software (1992), 2009-09, Vol.40 (9), p.864-870

2009

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Porosity variation and determination of REV in porous medium of screen meshes

International communications in heat and mass transfer, 1997-11, Vol.24 (7), p.955-964

1997

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Forced convective heat transfer in porous medium of wire screen meshes

Heat and mass transfer, 1997, Vol.33 (1-2), p.129-136

1997

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Experimental study of topology optimized, additively manufactured microchannel heat sinks designed using a homogenization approach

International journal of heat and mass transfer, 2023-08, Vol.209, p.124108, Article 124108

2023

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Active Latitude Oscillations Observed on the Sun

Solar physics, 2016-04, Vol.291 (4), p.1077-1087

2016

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Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis

Human molecular genetics, 2004-10, Vol.13 (20), p.2473-2482

2004

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Comparison of early and on-demand maternal feeding after Caesarean delivery: a prospective randomised trial

Singapore medical journal, 2021-10, Vol.62 (10), p.542-545

2021

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Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1

Human molecular genetics, 2002-01, Vol.11 (1), p.107-113

2002

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l-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1

Human molecular genetics, 2004-11, Vol.13 (22), p.2803-2811

2004

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Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome

American journal of human genetics, 2001-11, Vol.69 (5), p.1002-1012

2001

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Relationships between markers of inflammation, severity of injury, and clinical outcomes in hemorrhagic shock

Advances in therapy, 2007-09, Vol.24 (5), p.955-962

2007

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Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12-q12 and Evidence for Further Genetic Heterogeneity

American journal of human genetics, 2000-03, Vol.66 (3), p.904-913

2000

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Serial analysis of gene expression in the hippocampus of patients with mesial temporal lobe epilepsy

Neuroscience, 2006, Vol.138 (2), p.457-474

2006

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Ogilvie's syndrome following bilateral knee arthroplasty: a case report

Acta orthopaedica et traumatologica turcica, 2012, Vol.46 (3), p.220-222

2012

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Androgen receptor immunostaining and androgen receptor messenger ribonucleic acid expression are increased in cremaster muscles associated with undescended testis

Urology (Ridgewood, N.J.), 2006-04, Vol.67 (4), p.855-858

2006

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Neurotrophin receptor immunoreactivity in the hippocampus of patients with mesial temporal lobe epilepsy

Neuropathology and applied neurobiology, 2004-12, Vol.30 (6), p.651-664

2004

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Evidence for genetic susceptibility to thrombosis in idiopathic intracranial hypertension

Thrombosis research, 2003, Vol.111 (6), p.389-395

2003

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Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population

Eye (London), 2001-04, Vol.15 (2), p.183-188

2001

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Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1

Human molecular genetics, 2002, Vol.11 (1), p.107-113

2002

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Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families

Neuropediatrics, 2001-06, Vol.32 (3), p.142

2001

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An Animation System for Fracturing of Rigid Objects

Computer and Information Sciences - ISCIS 2005, 2005, p.688-697

2005

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MICA EXON 5 microsatellite alleles in Turkish patients with FMF

Human immunology, 2004-09, Vol.65 (9), p.S105-S105

2004

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Modelling of a direct evaporative air cooler using artificial neural network

A simple mathematical model to analyse a fluidyne heat machine

Natural convection in a vertical porous enclosure with internal heat generation

Estimation of heat transfer in oscillating annular flow using artifical neural networks

Porosity variation and determination of REV in porous medium of screen meshes

Forced convective heat transfer in porous medium of wire screen meshes

Experimental study of topology optimized, additively manufactured microchannel heat sinks designed using a homogenization approach

Active Latitude Oscillations Observed on the Sun

Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis

Comparison of early and on-demand maternal feeding after Caesarean delivery: a prospective randomised trial

Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1

l-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1

Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome

Relationships between markers of inflammation, severity of injury, and clinical outcomes in hemorrhagic shock

Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12-q12 and Evidence for Further Genetic Heterogeneity

Serial analysis of gene expression in the hippocampus of patients with mesial temporal lobe epilepsy

Ogilvie's syndrome following bilateral knee arthroplasty: a case report

Androgen receptor immunostaining and androgen receptor messenger ribonucleic acid expression are increased in cremaster muscles associated with undescended testis

Neurotrophin receptor immunoreactivity in the hippocampus of patients with mesial temporal lobe epilepsy

Evidence for genetic susceptibility to thrombosis in idiopathic intracranial hypertension

Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population

Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1

Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families

An Animation System for Fracturing of Rigid Objects

MICA EXON 5 microsatellite alleles in Turkish patients with FMF

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