Ercan, Altan

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Ercan, Altan
Job Title
Email Address
Main Affiliation
01. Abdullah Gül University
Yaşam ve Doğa Bilimleri Fakültesi
Moleküler Biyoloji ve Genetik
Status
Former Staff
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ORCID ID
Scopus Author ID
Turkish CoHE Profile ID
Google Scholar ID
WoS Researcher ID

Sustainable Development Goals

NO POVERTY1
NO POVERTY
0
Research Products
ZERO HUNGER2
ZERO HUNGER
0
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GOOD HEALTH AND WELL-BEING3
GOOD HEALTH AND WELL-BEING
1
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QUALITY EDUCATION4
QUALITY EDUCATION
0
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GENDER EQUALITY5
GENDER EQUALITY
0
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CLEAN WATER AND SANITATION6
CLEAN WATER AND SANITATION
0
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AFFORDABLE AND CLEAN ENERGY7
AFFORDABLE AND CLEAN ENERGY
0
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DECENT WORK AND ECONOMIC GROWTH8
DECENT WORK AND ECONOMIC GROWTH
0
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INDUSTRY, INNOVATION AND INFRASTRUCTURE9
INDUSTRY, INNOVATION AND INFRASTRUCTURE
0
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REDUCED INEQUALITIES10
REDUCED INEQUALITIES
0
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SUSTAINABLE CITIES AND COMMUNITIES11
SUSTAINABLE CITIES AND COMMUNITIES
0
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RESPONSIBLE CONSUMPTION AND PRODUCTION12
RESPONSIBLE CONSUMPTION AND PRODUCTION
0
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CLIMATE ACTION13
CLIMATE ACTION
0
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LIFE BELOW WATER14
LIFE BELOW WATER
0
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LIFE ON LAND15
LIFE ON LAND
0
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PEACE, JUSTICE AND STRONG INSTITUTIONS16
PEACE, JUSTICE AND STRONG INSTITUTIONS
0
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PARTNERSHIPS FOR THE GOALS17
PARTNERSHIPS FOR THE GOALS
0
Research Products
This researcher does not have a Scopus ID.
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Scholarly Output

2

Articles

1

Views / Downloads

640/275

Supervised MSc Theses

1

Supervised PhD Theses

0

WoS Citation Count

6

Scopus Citation Count

6

Patents

0

Projects

0

WoS Citations per Publication

3.00

Scopus Citations per Publication

3.00

Open Access Source

2

Supervised Theses

1

JournalCount
Turkish Journal of Biology1
Current Page: 1 / 1

Scopus Quartile Distribution

Competency Cloud

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Scholarly Output Search Results

Now showing 1 - 2 of 2
  • Master Thesis
    COVID-19 Virüs Pandemisinde Haftalık Döngünün Kökeni ve Sosyo-Ekonomik Faktörlerle İlişkisinin Araştırılması
    (Abdullah Gül Üniversitesi, Fen Bilimleri Enstitüsü, 2024) Yağmur, İsmail Emre; Ercan, Altan
    The Covid-19 virus, which started in China in 2019 and affected the whole world, has caused a global pandemic. Looking at the worldwide data of this pandemic, the number of daily cases appears to have a weekly cycle that is underestimated as an artifact of the number of daily tests administered. In this thesis study, a new model is developed to calculate the daily infection numbers from daily case numbers by using the Weibull distribution and the natural characteristics of the COVID-19 virus. According to the results obtained, it is found that the number of daily cases has a real weekly cycle. It has been determined that the daily infection numbers calculated in this weekly cycle are minimum on weekdays. According to the analysis by the new methos, these weekly minimums are controlled by socio-economic factors such as human development index and annual national income per capita. During the ascending and descending phases of the pandemic, the weekly minimum shifts from Monday to Friday, exposing the presence of two separate environments for the transmission of the virus among people: working and social. Moreover, the data reveal a variable rather than a fixed reproduction number. As a result, the model we developed in this study successfully identifies the socio-economic factors as the effectors of the progression of the pandemic by taking into account the time of infection for the first time in the literature and is expected to guide the future pandemic studies and pandemic, itself.
  • Article
    Citation - WoS: 6
    Citation - Scopus: 6
    Sex Effect on the Correlation of Immunoglobulin G Glycosylation With Rheumatoid Arthritis Disease Activity
    (Tubitak Scientific & Technological Research Council Turkey, 2020) Ercan, Altan
    Rheumatoid arthritis (RA) is a chronic autoimmune disease which affects females more than males with a presence of autoantibodies. Immunoglobulin G (IgG) produced by adaptive arm has 2 functional domains, Fc and Fab. The Fc domain binds Fc gamma receptors and C1q proteins of the innate arm. Therefore, the IgG Fc domain serves as a bridge between the innate and adaptive arms and is regulated by an evolutionarily conserved N-glycosylation with variable structures. These glycans are classified as agalactosylated G0, monogalactosylated G1, and digalactosylated G2, which are further modified by core-fucosylation (F) and bisecting N-acetylglucosamine (B) moieties such as G0F and G0FB. Interestingly, proinflammatory G0F is shown to be regulated by estrogen in vivo. Here, it is hypothesized that the regulation of G0F by estrogen contributes to sex dichotomy in RA by setting up the level of IgG-dependent inflammation and therefore, RA disease activity (Das28-CRP3). To investigate this hypothesis, IgG glycosylation was characterized in serum samples from active RA patients (n = 232) and healthy controls (n = 232) by serum N-glycan analysis using the high performance liquid chromatography. According to the results, the IgG Fc glycan phenotype originates predominantly from the structure of G0F, and both G0F and G0FB correlate with Das28-CRP3 in females, but not in males. In conclusion, IgG G0F-dependent inflammation differs in males and females, and these differences point to the differential regulation of inflammation by sex hormone estrogen via IgG glycosylation.