نتائج البحث - "Filiz Geyik"

1

دورية أكاديمية

ACSL4 gen polimorfizminin (rs7886473) metabolik sendrom ve lipid düzeyleri üzerine etkisi

المؤلفون: Eren VURGUN, İrem Yağmur DİKER, Neslihan ÇOBAN, Filiz GEYİK, Gamze GÜVEN, Nihan ERGİNEL ÜNALTUNA

المصدر: Cukurova Medical Journal, Vol 43, Iss Ek 1, Pp 151-157 (2018)

مصطلحات موضوعية: acsl4, gen polimorfizmi, lipid, trigliserid, metabolik sendrom, snp, lipids, triglyceride, metabolic syndrome, Medicine (General), R5-920

وصف الملف: electronic resource

العلاقة: https://dergipark.org.tr/tr/pub/cumj/issue/38921/407589?publisher=cuTest; https://doaj.org/toc/2602-3040Test

الوصول الحر: https://doaj.org/article/8b26b0aeff934f3887d538aca7e7c8bdTest

View record in DOAJ

2

دورية أكاديمية

Negative results in screening for possible new sequence variations on ATP-binding cassette transporter A1 gene in Turkish adults with metabolic syndrome

المؤلفون: Neslihan Çoban, Altan Onat, Filiz Geyik, Nihan Erginel-ünaltuna

المصدر: Türk Kardiyoloji Derneği Arşivi, Vol 42, Iss 6, Pp 524-530 (2014)

مصطلحات موضوعية: atp binding cassette transporter 1, atherogenic dyslipidemia, hdl-c, metabolic syndrome x, turkish adults., Medicine, Internal medicine, RC31-1245, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

العلاقة: https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tkd&un=TKDA-64369Test; https://doaj.org/toc/1016-5169Test

الوصول الحر: https://doaj.org/article/7fb310983d834f1290eb94da198b7cd7Test

View record in DOAJ

3

Biallelic frameshift variants in

المؤلفون: Beyhan, Tuysuz, Dilek, Uludag Alkaya, Filiz, Geyik, Merve, Alaylıoğlu, Busra, Kasap, Sebuh, Kurugoğlu, Yunus Emre, Akman, Mehmet, Vural, Kaya, Bilguvar

المصدر: Journal of medical genetics.

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::609d7b6deedfcb34ece1cdb70b0ab31bTest
https://pubmed.ncbi.nlm.nih.gov/36543534Test

4

Neurofibromatosis type 1: Expanded variant spectrum with multiplex ligation‐dependent probe amplification and genotype–phenotype correlation in 138 Turkish patients

المؤلفون: Gozde Yesil, Nilay Güneş, Busra Kasap, Tiraje Celkan, Rejin Kebudi, Filiz Geyik, Beyhan Tüysüz

المساهمون: YEŞİL, Gözde

المصدر: Annals of Human Genetics. 85:155-165

مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Pathology, medicine.medical_specialty, Neurofibromatosis 1, Adolescent, Turkey, Expanded variant spectrum with multiplex ligation-dependent probe amplification and genotype-phenotype correlation in 138 Turkish patients-, ANNALS OF HUMAN GENETICS, 2021 [Gunes N., YEŞİL G., Geyik F., Kasap B., Celkan T., Kebudi R., TÜYSÜZ B., -Neurofibromatosis type 1], Genotype phenotype, Correlation, Young Adult, 03 medical and health sciences, Age groups, Genetics, Humans, Medicine, In patient, Multiplex, Multiplex ligation-dependent probe amplification, Neurofibromatosis, Child, neoplasms, Genetic Association Studies, Genetics (clinical), Retrospective Studies, 030304 developmental biology, 0303 health sciences, business.industry, 030305 genetics & heredity, Infant, medicine.disease, Phenotype, eye diseases, nervous system diseases, Child, Preschool, population characteristics, Female, business, Multiplex Polymerase Chain Reaction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::245de901af46dc132487b061e1be4b4fTest
https://doi.org/10.1111/ahg.12422Test

5

The Methylation Status in the Chromosome 11p15.5 Region and Metabolic Disorders in Children with Syndromic and Nonsyndromic Intrauterine Growth Restriction

المؤلفون: Zeynep Alp Ünkar, Beyhan Tüysüz, Emre Özer, Filiz Geyik, Oya Ercan

المصدر: Mol Syndromol

مصطلحات موضوعية: Genetics, business.industry, medicine, Intrauterine growth restriction, Chromosome, Original Article, Methylation, medicine.disease, business, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f95d4f957ab3e34434495af89941783Test
https://europepmc.org/articles/PMC8928180Test/

6

ACSL4 gen polimorfizminin (rs7886473) metabolik sendrom ve lipid düzeyleri üzerine etkisi

المؤلفون: Nihan Erginel Ünaltuna, I.Y. Diker, Gamze Guven, Eren Vurgun, Neslihan Çoban, Filiz Geyik

المصدر: Cukurova Medical Journal. 43:151-157

مصطلحات موضوعية: 0301 basic medicine, 03 medical and health sciences, 030104 developmental biology, General Earth and Planetary Sciences, General Environmental Science

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::fca8d44e2328075321c661a206a1edc5Test
https://doi.org/10.17826/cumj.407589Test

7

Seven patients with Smith-McCort dysplasia 2: Four novel nonsense variants in RAB33B and follow-up findings

المؤلفون: Dilek Uludağ Alkaya, Sabine Sharifova, Ali Metin Kafadar, Filiz Geyik, Beyhan Tüysüz, Timur Yildirim

المصدر: European journal of medical genetics. 64(7)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1781912870a0dd0eaa03734fcd5d52e5Test
https://pubmed.ncbi.nlm.nih.gov/34000439Test

8

Investigation of (epi)genotype causes and follow-up manifestations in the patients with classical and atypical phenotype of Beckwith-Wiedemann spectrum

المؤلفون: Gozde Yesil, Mehmet Vural, Beyhan Tüysüz, Tiraje Celkan, Filiz Geyik, Nilay Güneş

المصدر: American journal of medical genetics. Part AREFERENCES. 185(6)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::042a6e7c5038f30902ce9fca3eb8f961Test
https://pubmed.ncbi.nlm.nih.gov/33704912Test

9

CONTRIBUTION OF SARCOMERIC GENE VARIANTS TO THE PREDICTION OF SUDDEN CARDIAC DEATH RISK IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY

المؤلفون: Filiz Geyik, Evrim Kömürcü Bayrak, Gökhan Kahveci, Fatih Bayrak

المساهمون: Acibadem University Dspace

المصدر: Volume: 83, Issue: 4 345-354
Journal of Istanbul Faculty of Medicine

مصطلحات موضوعية: medicine.medical_specialty, Familial Hypertrophic Cardiomyopathy, business.industry, familial hypertrophic cardiomyopathy, medicine.disease, sudden cardiac death, Sarcomeric gene variant,familial hypertrophic cardiomyopathy,sudden cardiac death, Sudden cardiac death, Sarcomeric gene variant, Health Care Sciences and Services, Internal medicine, medicine, Cardiology, cardiovascular system, cardiovascular diseases, Sarkomerik gen varyantı,ailesel hipertrofik kardiyomiyopati,ani kardiyak ölüm, Sağlık Bilimleri ve Hizmetleri, business, Gene

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::683c36efa8db5ca25e6e6e065a85314aTest
https://dergipark.org.tr/tr/pub/iuitfd/issue/57333/805397Test

10

Negative results in screening for possible new sequence variations on ATP-binding cassette transporter A1 gene in Turkish adults with metabolic syndrome

المؤلفون: Filiz Geyik, Altan Onat, Neslihan Çoban, Erginel Ünaltuna N

المصدر: Türk Kardiyoloji Derneği Arşivi, Vol 42, Iss 6, Pp 524-530 (2014)

مصطلحات موضوعية: Male, medicine.medical_specialty, lcsh:Internal medicine, lcsh:Diseases of the circulatory (Cardiovascular) system, Turkey, lcsh:Medicine, White People, Exon, atherogenic dyslipidemia, Internal medicine, atp binding cassette transporter 1, ABCA1 Gene, Medicine, Humans, Genetic Testing, Prospective Studies, Risk factor, lcsh:RC31-1245, Gene, DNA Primers, Metabolic Syndrome, biology, business.industry, hdl-c, metabolic syndrome x, turkish adults, Reverse cholesterol transport, Cholesterol, HDL, lcsh:R, Middle Aged, medicine.disease, Endocrinology, Cyclic nucleotide-binding domain, lcsh:RC666-701, ABCA1, Mutation, biology.protein, Female, lipids (amino acids, peptides, and proteins), Metabolic syndrome, Cardiology and Cardiovascular Medicine, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::000166f09c8a4b227bfee0c25195a5d0Test
https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tkd&un=TKDA-64369Test

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