OpenAlex topic

Porphyrin Metabolism and Disorders

This page lists works and academicians tagged with an OpenAlex topic. It is not a YÖKSİS primary or secondary field.

OpenAlex 590 works 4 author topics

Works

590 works

Endoplasmic Reticulum Stress and Homeostasis in Reproductive Physiology and Pathology 2017
OpenAlex top 10% OpenAlex 98.5%
The endoplasmic reticulum (ER), comprises 60% of the total cell membrane and interacts directly or indirectly with several cell organelles i.e., Golgi bodies, mitochondria and proteasomes. The ER is usually associated with large numbers of attached ribosomes. During evolution, ER developed as the specific cellular sit…
The Stone Clinic Effect in Patients with Idiopathic Calcium Urolithiasis 1985
OpenAlex top 10% OpenAlex 98.6%
No abstract yet.
Kinetics of excision of purine lesions from DNA by Escherichia coli Fpg protein 1997
OpenAlex top 10% OpenAlex 95.9%
The kinetics of excision of damaged purine bases from oxidatively damaged DNA by Escherichia coli Fpg protein were investigated. DNA substrates, prepared by treatment with H2O2/Fe(III)-EDTA or by gamma-irradiation under N2O or air, were incubated with Fpg protein, followed by precipitation of DNA. Precipitated DNA and…
The Association of Nephrolithiasis and Autosomal Dominant Polycystic Kidney Disease 1988
OpenAlex 85.1%
No abstract yet.
Water soluble quaternized mercaptopyridine substituted zinc phthalocyanines Synthesis photophysical photochemical and bovine serum albumin binding properties 2011
YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 95.5%
No abstract yet.
- MAHMUT DURMUŞ
Water soluble quaternized mercaptopyridine substituted zinc phthalocyanines Synthesis photophysical photochemical and bovine serum albumin binding properties 2011
YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 95.5%
No abstract yet.
- CEM GÖL
Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients 2005
YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 92.0%
Xeroderma pigmentosum group C (XP-C) is a rare autosomal recessive disorder. Patients with two mutant alleles of the XPC DNA repair gene have sun sensitivity and a 1000-fold increase in skin cancers. Clinically normal parents of XP-C patients have one mutant allele and one normal allele. As a step toward evaluating ca…
- AHMET METİN
Xeroderma Pigmentosum-Variant Patients from America, Europe, and Asia 2008
YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 91.3%
No abstract yet.
- AHMET METİN
Xeroderma Pigmentosum Variant Patients from America Europe and Asia 2008
YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 91.7%
No abstract yet.
- AHMET METİN
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: Founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East 2004
OpenAlex 85.4%
Selective intestinal malabsorption of vitamin B(12) causing juvenile megaloblastic anemia (MGA; MIM# 261100) is a recessively inherited disorder that is believed to be rare except for notable clusters of cases in Finland, Norway, and the Eastern Mediterranean region. The disease can be caused by mutations in either th…
Update on transcobalamin deficiency clinical presentation treatment and outcome 2014
YÖKSİS SJR Q2 JCR Q2 OpenAlex top 10% OpenAlex 90.3%
Transcobalamin (TC) transports cobalamin from blood into cells. TC deficiency is a rare autosomal recessive disorder usually presenting in early infancy with failure to thrive, weakness, diarrhoea, pallor, anemia, and pancytopenia or agammaglobulinemia. It can sometimes resemble neonatal leukemia or severe combined im…
- MUSTAFA BÜYÜKAVCI
Hexachlorobenzene episode in Turkey. 1989
OpenAlex 38.4%
During the period 1955-1959, approximately 4000 people in southeast Anatolia developed porphyria due to the ingestion of hexachlorobenzene (HCB), a fungicide added to wheat seedlings. These HCB exposures subsequently led to the development of bullae on sun-exposed areas, hyperpigmentation, hypertrichosis, and porphyri…

Academicians

4 academicians