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Items: 1 to 50 of 382

1.

Comparison of cytotoxic effects of calcium silicate-based materials on human pulp fibroblasts Mehmet.

Adıgüzel M, Ahmetoğlu F, Eldeniz AÜ, Tekin MG, Göğebakan B.

J Dent Res Dent Clin Dent Prospects. 2019 Fall;13(4):241-246. doi: 10.15171/joddd.2019.037.

2.

Evaluation Using Spectral-Domain Optical Coherence Tomography of the Effects of Malnutrition on Ocular Parameters in Pediatric Patients.

Tekin M, Simsek A, Bilak S, Konca C, Almis H, Bilen A.

Optom Vis Sci. 2020 Mar;97(3):154-161. doi: 10.1097/OPX.0000000000001490.

PMID:
32168237
3.

Genomics, Epigenetics, and Hearing Loss in Neurofibromatosis Type 2.

Dinh CT, Nisenbaum E, Chyou D, Misztal C, Yan D, Mittal R, Young J, Tekin M, Telischi F, Fernandez-Valle C, Liu XZ.

Otol Neurotol. 2020 Mar 6. doi: 10.1097/MAO.0000000000002613. [Epub ahead of print]

PMID:
32150022
4.

X-linked peripheral retinoschisis without macular involvement: a case series with RS1 genetic confirmation.

Smith LM, Cernichiaro-Espinosa LA, McKeown CA, Tekin M, Lam BL, Chiang J, Russell JF, Berrocal AM.

Ophthalmic Genet. 2020 Feb;41(1):57-62. doi: 10.1080/13816810.2020.1723115. Epub 2020 Mar 3.

PMID:
32124668
5.

Analyses of del(GJB6-D13S1830) and del(GJB6-D13S1834) deletions in a large cohort with hearing loss: Caveats to interpretation of molecular test results in multiplex families.

Pandya A, O'Brien A, Kovasala M, Bademci G, Tekin M, Arnos KS.

Mol Genet Genomic Med. 2020 Feb 17:e1171. doi: 10.1002/mgg3.1171. [Epub ahead of print]

6.

Novel OTOF pathogenic variant segregating with non-syndromic hearing loss in a consanguineous family from tribal Rajouri in Jammu and Kashmir.

Kuchay RAH, Mir YR, Zeng X, Hassan A, Namba K, Tekin M.

Int J Pediatr Otorhinolaryngol. 2020 Mar;130:109831. doi: 10.1016/j.ijporl.2019.109831. Epub 2019 Dec 16.

PMID:
31875531
7.

Autosomal dominant inheritance in a recently described ZMIZ1-related neurodevelopmental disorder: Case report of siblings and an affected parent.

Latchman K, Calder M, Morel D, Rhodes L, Juusola J, Tekin M.

Am J Med Genet A. 2020 Mar;182(3):548-552. doi: 10.1002/ajmg.a.61446. Epub 2019 Dec 12.

PMID:
31833199
8.

Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss.

Diaz-Horta O, Bademci G, Tokgoz-Yilmaz S, Guo S, Zafeer F, Sineni CJ, Duman D, Farooq A, Tekin M.

Clin Genet. 2019 Dec;96(6):575-578. doi: 10.1111/cge.13626. Epub 2019 Aug 27.

PMID:
31432506
9.

A unique case of vision loss in a patient with hypotrichosis and juvenile macular dystrophy and primary ciliary dyskinesia.

Fan KC, Patel NA, Yannuzzi NA, Prakhunhungsit S, Negron CI, Basora E, Colin AA, Tekin M, Berrocal AM.

Am J Ophthalmol Case Rep. 2019 Jun 5;15:100486. doi: 10.1016/j.ajoc.2019.100486. eCollection 2019 Sep.

10.

Concurrence of Two Rare Conditions: Simultaneous Bilateral Spontaneous Pneumothorax and Congenital Pulmonary Airway Malformation.

Konca C, Tekin M, Elmas OC.

J Pediatr Intensive Care. 2019 Sep;8(3):178-180. doi: 10.1055/s-0039-1677814. Epub 2019 Jan 25.

PMID:
31404456
11.

Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population.

Figueroa-Ildefonso E, Bademci G, Rajabli F, Cornejo-Olivas M, Villanueva RDC, Badillo-Carrillo R, Inca-Martinez M, Neyra KM, Sineni C, Tekin M.

Genes (Basel). 2019 Jul 31;10(8). pii: E581. doi: 10.3390/genes10080581.

12.

Adams-Oliver syndrome caused by mutations of the EOGT gene.

Schröder KC, Duman D, Tekin M, Schanze D, Sukalo M, Meester J, Wuyts W, Zenker M.

Am J Med Genet A. 2019 Nov;179(11):2246-2251. doi: 10.1002/ajmg.a.61313. Epub 2019 Jul 31.

PMID:
31368252
13.

The Generation of Zebrafish Mariner Model Using the CRISPR/Cas9 System.

Zou B, Desmidt AA, Mittal R, Yan D, Richmond M, Tekin M, Liu XZ, Lu Z.

Anat Rec (Hoboken). 2020 Mar;303(3):556-562. doi: 10.1002/ar.24221. Epub 2019 Jul 18.

PMID:
31260171
14.

A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss.

Sineni CJ, Yildirim-Baylan M, Guo S, Camarena V, Wang G, Tokgoz-Yilmaz S, Duman D, Bademci G, Tekin M.

Hum Genet. 2019 Oct;138(10):1071-1075. doi: 10.1007/s00439-019-02037-1. Epub 2019 Jun 7.

PMID:
31175426
15.

Genetic Causes of Inner Ear Anomalies: a Review from the Turkish Study Group for Inner Ear Anomalies

Ocak E, Duman D, Tekin M.

Balkan Med J. 2019 Jul 11;36(4):206-211. doi: 10.4274/balkanmedj.galenos.2019.2019.4.66. Epub 2019 May 27. Review.

16.

The effect of luteolin in prevention of periodontal disease in Wistar rats.

Balci Yuce H, Toker H, Yildirim A, Tekin MB, Gevrek F, Altunbas N.

J Periodontol. 2019 Dec;90(12):1481-1489. doi: 10.1002/JPER.18-0584. Epub 2019 Jul 1.

PMID:
31115905
17.

Correction: ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.

DiStefano MT, Hemphill SE, Oza AM, Siegert RK, Grant AR, Hughes MY, Cushman BJ, Azaiez H, Booth KT, Chapin A, Duzkale H, Matsunaga T, Shen J, Zhang W, Kenna M, Schimmenti LA, Tekin M, Rehm HL, Tayoun ANA, Amr SS; ClinGen Hearing Loss Clinical Domain Working Group.

Genet Med. 2019 Oct;21(10):2409. doi: 10.1038/s41436-019-0553-7.

PMID:
31114025
18.

The effect of hyperlipidemia on bone graft regeneration of peri-implantal created defects in rabbits.

Tekin MB, Toker H.

Int J Implant Dent. 2019 May 15;5(1):18. doi: 10.1186/s40729-019-0170-x.

19.

Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia.

Ordonez J, Tekin M.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020.
2012 Sep 20 [updated 2019 Apr 4].

20.

ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.

DiStefano MT, Hemphill SE, Oza AM, Siegert RK, Grant AR, Hughes MY, Cushman BJ, Azaiez H, Booth KT, Chapin A, Duzkale H, Matsunaga T, Shen J, Zhang W, Kenna M, Schimmenti LA, Tekin M, Rehm HL, Tayoun ANA, Amr SS; ClinGen Hearing Loss Clinical Domain Working Group.

Genet Med. 2019 Oct;21(10):2239-2247. doi: 10.1038/s41436-019-0487-0. Epub 2019 Mar 21. Erratum in: Genet Med. 2019 May 22;:.

PMID:
30894701
21.

Risk Factors for Lingual Nerve Injury Associated With Suspension Laryngoscopy.

Ozdamar OI, Uzun L, Acar GO, Tekin M, Kokten N, Celik S.

Ann Otol Rhinol Laryngol. 2019 Jul;128(7):633-639. doi: 10.1177/0003489419835854. Epub 2019 Mar 6.

PMID:
30841712
22.

The effect of colchicine on alveolar bone loss in ligature-induced periodontitis.

Toker H, Yuce HB, Yildirim A, Tekin MB, Gevrek F.

Braz Oral Res. 2019 Feb 11;33:e001. doi: 10.1590/1807-3107bor-2019.vol33.0001.

23.
24.

Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss.

Li C, Bademci G, Subasioglu A, Diaz-Horta O, Zhu Y, Liu J, Mitchell TG, Abad C, Seyhan S, Duman D, Cengiz FB, Tokgoz-Yilmaz S, Blanton SH, Farooq A, Walz K, Zhai RG, Tekin M.

Proc Natl Acad Sci U S A. 2019 Jan 22;116(4):1347-1352. doi: 10.1073/pnas.1810951116. Epub 2019 Jan 4.

25.

FOXF2 is required for cochlear development in humans and mice.

Bademci G, Abad C, Incesulu A, Elian F, Reyahi A, Diaz-Horta O, Cengiz FB, Sineni CJ, Seyhan S, Atli EI, Basmak H, Demir S, Nik AM, Footz T, Guo S, Duman D, Fitoz S, Gurkan H, Blanton SH, Walter MA, Carlsson P, Walz K, Tekin M.

Hum Mol Genet. 2019 Apr 15;28(8):1286-1297. doi: 10.1093/hmg/ddy431.

PMID:
30561639
26.

Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability.

McSherry M, Masih KE, Elcioglu NH, Celik P, Balci O, Cengiz FB, Nunez D, Sineni CJ, Seyhan S, Kocaoglu D, Guo S, Duman D, Bademci G, Tekin M.

PLoS One. 2018 Nov 30;13(11):e0208324. doi: 10.1371/journal.pone.0208324. eCollection 2018.

27.

Tympanogram Findings in Hemodialysis Patients.

Aksit AM, Pektas E, Kalcioglu MT, Ozkok A, Tuysuz O, Tekin M.

J Craniofac Surg. 2019 Jan;30(1):e49-e52. doi: 10.1097/SCS.0000000000004960.

PMID:
30480629
28.

Facial canal dehiscence rate: a retrospective analysis of 372 chronic otitis media cases.

Kalcioglu MT, Kilic O, Tuysuz O, Serifler S, Tekin M.

Eur Arch Otorhinolaryngol. 2019 Jan;276(1):79-83. doi: 10.1007/s00405-018-5198-7. Epub 2018 Nov 12.

PMID:
30421175
29.

Thrombocytopenia in Infants: CMV-Related ITP or CMV-Related Thrombocytopenia?

Isleyen F, Tekin M, Konca C.

Indian J Hematol Blood Transfus. 2018 Oct;34(4):774-775. doi: 10.1007/s12288-018-0945-x. Epub 2018 Mar 6. No abstract available.

30.

Comparing Spontaneous Closure and Paper Patching in Traumatic Tympanic Membrane Perforations.

Hanege FM, Karaca S, Kalcioglu MT, Tekin M.

J Craniofac Surg. 2018 Oct;29(7):1922-1924. doi: 10.1097/SCS.0000000000005047.

PMID:
30290584
31.

Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientation.

Diaz-Horta O, Abad C, Cengiz FB, Bademci G, Blackwelder P, Walz K, Tekin M.

J Mol Med (Berl). 2018 Nov;96(11):1227-1238. doi: 10.1007/s00109-018-1694-x. Epub 2018 Oct 3.

32.

Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies.

Su M, Benke PJ, Bademci G, Cengiz FB, Ouyang X, Peng J, Casas CE, Tekin M, Fan YS.

Mol Cytogenet. 2018 Aug 1;11:43. doi: 10.1186/s13039-018-0390-4. eCollection 2018.

33.

MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss.

Bademci G, Abad C, Incesulu A, Rad A, Alper O, Kolb SM, Cengiz FB, Diaz-Horta O, Silan F, Mihci E, Ocak E, Najafi M, Maroofian R, Yilmaz E, Nur BG, Duman D, Guo S, Sant DW, Wang G, Monje PV, Haaf T, Blanton SH, Vona B, Walz K, Tekin M.

Hum Genet. 2018 Jul;137(6-7):479-486. doi: 10.1007/s00439-018-1901-4. Epub 2018 Jul 7.

34.

Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure.

Clavijo RI, Arora H, Gibbs E, Cohen S, Griswold A, Bakircioglu E, Bademci G, Tekin M, Ramasamy R.

Urology. 2018 Oct;120:86-89. doi: 10.1016/j.urology.2018.06.031. Epub 2018 Jun 30.

PMID:
29966603
35.

Anti-inflammatory and antibacterial evaluation of Thymus sipyleus Boiss. subsp. sipyleus var. sipyleus essential oil against rhinosinusitis pathogens.

Demirci F, Karaca N, Tekin M, Demirci B.

Microb Pathog. 2018 Sep;122:117-121. doi: 10.1016/j.micpath.2018.06.025. Epub 2018 Jun 19.

PMID:
29908309
36.

KBG Syndrome.

Morel Swols D, Tekin M.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020.
2018 Mar 22.

37.

In vivo activity assessment of some Tanacetum species used as traditional wound healer along with identification of the phytochemical profile by a new validated HPLC method.

Özbilgin S, Akkol EK, Ergene Öz B, Ilhan M, Saltan G, Acıkara ÖB, Tekin M, Keleş H, Süntar I.

Iran J Basic Med Sci. 2018 Feb;21(2):145-152. doi: 10.22038/IJBMS.2018.24258.6055.

38.

An Early Finding of Keratoconus: Increase in Corneal Densitometry.

Koc M, Tekin K, Tekin MI, Uzel MM, Kosekahya P, Ozulken K, Yilmazbas P.

Cornea. 2018 May;37(5):580-586. doi: 10.1097/ICO.0000000000001537.

PMID:
29384807
39.

Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations.

Regalado ES, Mellor-Crummey L, De Backer J, Braverman AC, Ades L, Benedict S, Bradley TJ, Brickner ME, Chatfield KC, Child A, Feist C, Holmes KW, Iannucci G, Lorenz B, Mark P, Morisaki T, Morisaki H, Morris SA, Mitchell AL, Ostergaard JR, Richer J, Sallee D, Shalhub S, Tekin M; Montalcino Aortic Consortium, Estrera A, Musolino P, Yetman A, Pyeritz R, Milewicz DM.

Genet Med. 2018 Oct;20(10):1206-1215. doi: 10.1038/gim.2017.245. Epub 2018 Jan 4.

40.

Electrophysiological and Histopathological Evaluation of Effects of Sodium-2 Mercaptoethanesulfonate Used for Middle Ear Surgery on Facial Nerve Functions.

Eğilmez OK, Kökten N, Baran M, Kalcıoğlu MT, Doğan Ekici I, Tekin M.

J Int Adv Otol. 2018 Aug;14(2):239-244. doi: 10.5152/iao.2017.3888.

41.

KBG syndrome.

Morel Swols D, Foster J 2nd, Tekin M.

Orphanet J Rare Dis. 2017 Dec 19;12(1):183. doi: 10.1186/s13023-017-0736-8. Review.

42.

A Case With Short Stature, Growth Hormone Deficiency and 46, XX, Xq27-qter Deletion.

Yıldırım Ş, Topaloğlu N, Tekin M, Sılan F.

Acta Med Iran. 2017 Oct;55(10):661-663.

43.

A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure.

Hung CY, Volkmar B, Baker JD, Bauer JW, Gussoni E, Hainzl S, Klausegger A, Lorenzo J, Mihalek I, Rittinger O, Tekin M, Dallman JE, Bodamer OA.

PLoS One. 2017 Dec 11;12(12):e0189324. doi: 10.1371/journal.pone.0189324. eCollection 2017.

44.

A rare ANOS1 variant in siblings with Kallmann syndrome identified by whole exome sequencing.

Lopategui DM, Griswold AJ, Arora H, Clavijo RI, Tekin M, Ramasamy R.

Andrology. 2018 Jan;6(1):53-57. doi: 10.1111/andr.12432. Epub 2017 Dec 6.

45.

A MECOM variant in an African American child with radioulnar synostosis and thrombocytopenia.

Lord SV, Jimenez JE, Kroeger ZA, Patrick CS, Sanchez-Pena I, Ziga E, Bademci G, Tekin M.

Clin Dysmorphol. 2018 Jan;27(1):9-11. doi: 10.1097/MCD.0000000000000200. No abstract available.

PMID:
29200407
46.

The effects of chemoradiotherapy on recurrence and survival in locally advanced rectal cancers with curative total mesorectal excision: a prospective, nonrandomized study.

Akgun E, Ozkok S, Tekin M, Yoldas T, Caliskan C, Kose T, Karabulut B, Sezak M, Elmas N, Ozutemiz O.

World J Surg Oncol. 2017 Nov 22;15(1):205. doi: 10.1186/s12957-017-1275-4.

47.

Molecular and agro-morphological characterization of ancient wheat landraces of turkey.

Gurcan K, Demirel F, Tekin M, Demirel S, Akar T.

BMC Plant Biol. 2017 Nov 14;17(Suppl 1):171. doi: 10.1186/s12870-017-1133-0.

48.

Variants in CIB2 cause DFNB48 and not USH1J.

Booth KT, Kahrizi K, Babanejad M, Daghagh H, Bademci G, Arzhangi S, Zareabdollahi D, Duman D, El-Amraoui A, Tekin M, Najmabadi H, Azaiez H, Smith RJ.

Clin Genet. 2018 Apr;93(4):812-821. doi: 10.1111/cge.13170. Epub 2018 Feb 12.

49.

LPS-induced Src family kinases activity mediates IL-10 production through activation of STAT3 in peripheral blood mononuclear cells of patients with Behçet's Disease.

Irtegun Kandemir S, Tekin MA, Bozkurt M, Dagli AZ, Kalkanli-Tas S.

Cell Mol Biol (Noisy-le-grand). 2017 Oct 31;63(10):116-121. doi: 10.14715/cmb/2017.63.10.18.

PMID:
29096751
50.

Research of genetic bases of hereditary non-syndromic hearing loss.

Subaşıoğlu A, Duman D, Sırmacı A, Bademci G, Carkıt F, Somdaş MA, Erkan M, Tekin M, Dündar M.

Turk Pediatri Ars. 2017 Sep 1;52(3):122-132. doi: 10.5152/TurkPediatriArs.2017.4254. eCollection 2017 Sep.

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