Prof. Dr. Şefik GÜRAN

1. Uptake of high-dose folic acid decreases cell viability and proliferation via JAK/STAT pathway in human prostate cancer cells

GÜRAN Ş., Çoban Z. D., GÜNDEŞLİ H.

Gulhane Medical Journal , cilt.65, sa.1, ss.1-6, 2023 (Scopus, TRDizin)

2. Cell viability in SH-SY5Y neuroblastoma cells in folic acid application by using JACK-STAT pathway

GÜRAN Ş., Kaplan Z. Z., Kiliç Y. C., Çoban Z. D., Polat Y. E., Güleç K., et al.

Gulhane Medical Journal , cilt.61, sa.4, ss.157-161, 2020 (Scopus, TRDizin)

3. Melatonin hormone stimulates human clock genes on neuroblastoma (SH-SY5Y) cell line

GÜRAN Ş., Tunçbilek V., Baykara M. Z., Çoban Z. D., Polat Y. E., Kiliç Y. C., et al.

Gulhane Medical Journal , cilt.61, sa.4, ss.172-176, 2020 (Scopus, TRDizin)

4. Chitin increases the angiogenesis in chorioallantoic membrane model in the presence of testosterone and progesterone

Sağlam E. I., Kutlu I. C., Haberal O. E., YÜKSEKKAYA M., Kiliçarslan Ö., GÜRAN Ş.

Gulhane Medical Journal , cilt.61, sa.1, ss.20-24, 2019 (Scopus, TRDizin)

5. Folic acid and zinc inhibit angiogenesis in chicken chorioallontoic membrane model via angiogenic factor genes

GÜRAN Ş., Çoban Z. D., Fermanli O., Aydingöz E., Ipek E.

Gulhane Medical Journal , cilt.60, sa.3, ss.67-70, 2018 (Scopus, TRDizin)

6. Gene correction applications in cell replacement therapy and use in neurodegenerative diseases

GÜRAN Ş.

Gulhane Medical Journal , cilt.60, sa.2, ss.60-63, 2018 (Scopus, TRDizin)

7. Zinc increases nestin but not vimentin gene expression in mouse mesenchymal stem cells

GÜRAN Ş., Çoban Z. D., Elçi M. P., Sarper M., Avcu F.

Gulhane Medical Journal , cilt.60, sa.2, ss.56-59, 2018 (Scopus, TRDizin)

8. Dextrose solution used for prolotherapy decreases cell viability and increases gene expressions of angiogenic and apopitotic factors

GÜRAN Ş., Dilşad çoban Z., YENER Ö., Demirhan S., Karaağaç N., ÖRSÇELİK A., et al.

Gulhane Medical Journal , cilt.60, sa.2, ss.42-46, 2018 (Scopus, TRDizin)

9. MEFV gene mutation frequency and distribution of mutations in FMF patients: Analysis of a large group of patients from a single center FMF hastalarindaki MEFV gen mutasyon sikliği ve mutasyonlarin dağilimi: Tek bir merkezden geniş bir hasta grubunun analizi

TORUN D., TEKGÖZ E., Kavuş H., Öztuna A., Akar H., Çinar M., et al.

Gulhane Medical Journal , cilt.59, sa.1, ss.24-27, 2017 (Scopus, TRDizin)

10. Sorefenib inhibits the expressions of heat shock protein70 gene on multiple myeloma (RPMI-8226) and plasma cell leukemia (ARH-77) cell lines

Çoban Z. D., Kayir H., GÜRAN Ş.

Gulhane Medical Journal , cilt.59, sa.1, ss.6-10, 2017 (Scopus, TRDizin)

11. Farede östrus siklusu tayininde hızlı, kolay ve etkin bir yöntem

Çoban Z. D., GÜRAN Ş., Altaylı E., Kayır H., BAYKAL B.

Gulhane Medical Journal , cilt.58, sa.1, ss.82-87, 2016 (Scopus, TRDizin)

12. Mesenchymal stem cells obtained from mouse represents high viability and steamness properties in the early phase of cell culture Fareden elde edilen mezenkimal kök hücre hücreler hücre kültüründe erken dönemde yüksek canlilik ve köklülük özellikleri gösterirler

Çoban Z. D., Güzel H., Demircan A., Arslan M., Demirhan F. S., Karaağaç N., et al.

Gulhane Medical Journal , cilt.58, sa.4, ss.389-393, 2016 (Scopus, TRDizin)

13. In mouse brain development the Notch and Sonic-Hedgehog signaling pathways have important role in the 3th trimester Fare beyin gelişiminde Notch ve Sonic-Hedgehog sinyal yolaklarinin özellikle 3. trimestirda önemli rolü vardir

Çoban Z. D., GÜRAN Ş., Altayli E., Sağaltici Ş. A.

Gulhane Medical Journal , cilt.58, sa.4, ss.417-421, 2016 (Scopus, TRDizin)

14. Importance of Myc-related microRNAs in induced pluripotency

Çağlayan E. S., GÜRAN Ş.

Cell Biology International , cilt.39, sa.9, ss.987-994, 2015 (SCI-Expanded, Scopus)

15. Anti-angiogenic role of Ankaferd on chick chorioallontoic membrane model

Gülşen M. R., Uzunay N. S., Fermanli O., Çoban Z. D., Öztürk D., Hamidi M., et al.

Gulhane Medical Journal , cilt.57, sa.3, ss.274-279, 2015 (Scopus, TRDizin)

16. Gorlin-chaudhry-moss syndrome revisited: Expanding the phenotype

Rosti R. O., Karaer K., KARAMAN B., TORUN D., GÜRAN Ş., Bahce M.

American Journal of Medical Genetics, Part A , cilt.161, sa.7, ss.1737-1742, 2013 (SCI-Expanded, Scopus)

17. Methylation of SOCS3 in myeloproliferative neoplasms and secondary erythrocytosis/thrombocythemia Miyeloproliferatif neoplazmlar ve sekonder eritrositoz/trombositemide SOCS3 metilasyonu

TORUN D., Nevruz O., AKYOL M., Kozan S., Bahçe M., GÜRAN Ş., et al.

Turkish Journal of Hematology , cilt.30, sa.1, ss.13-18, 2013 (SCI-Expanded, Scopus, TRDizin)

18. The affecting mechanisms in neural tube defects; The molecular biology and the genetics of these malformations: Review Nöral Tüp Defektinde Etkilenen Mekanizmalar, Hastalǧn Moleküler Biyolojisi ve Genetiǧi

GÜRAN Ş., Çoban Z. D.

Turkiye Klinikleri Pediatri , cilt.21, sa.4, ss.224-229, 2012 (Scopus)

19. Macrocephaly with multiple epiphyseal dysplasia: A second example of Al Gazali-Bakalinova syndrome?

Karaer K., Rosti R., TORUN D., SANAL H. T., GÜRAN Ş.

Genetic Counseling , cilt.23, sa.4, ss.457-463, 2012 (SCI-Expanded, Scopus)

20. BDNF and GAD 65 responses of primary auditory cortex and inferior colliculus to noise exposure and cochlear ablation

Erol U., SATAR B., Kozan S., Ates K., TORUN D., Goksoy C., et al.

Journal of International Advanced Otology , cilt.8, sa.2, ss.187-195, 2012 (SCI-Expanded, Scopus)

21. The sitotoxic effect of gemcitabine on multiple myeloma (RPMI-8226) and Ig G plasma cell leukemia (ARH 77) cell lines Gemsitabinin multipl myelom (RPMI-8226) ve Ig G plazma hücreli lösemi (ARH 77) hücre hatlari üzerindeki sitotoksik etkisi

Çoban Z. D., Avcu F., Ural A. U., Kuzhan O., GÜRAN Ş.

Gulhane Medical Journal , cilt.54, sa.4, ss.263-266, 2012 (Scopus, TRDizin)

22. The use of induced pluripotent stem cells in medicine Uyarılmış pluripotent kök hücrelerin tıpta kullanımı

GÜRAN Ş., Çoban Z. D.

Erciyes Tip Dergisi , cilt.34, sa.4, ss.184-187, 2012 (Scopus, TRDizin)

23. Rheumatic and autoimmune diseases may have a role in disease progression of myelodysplastic syndrome Ramatolojik ve otoimmün hastalıkların myelodisplastik sendromun progresyonunda rolü olabilir

Kozan S., TORUN D., TUNCA Y., Beyan C., Ifran A., Kaptan M. K., et al.

Turkiye Klinikleri Journal of Medical Sciences , cilt.32, sa.4, ss.910-916, 2012 (Scopus)

24. New phenotype with generalized platyspondyly, large mandible, hypoplastic teeth, strabismus, hyperopia and low cholesterol levels

Koç A., Bahce M., SANAL H. T., ULUDAĞ A., Kozan S., TORUN D., et al.

Genetic Counseling , cilt.22, sa.2, ss.129-134, 2011 (SCI-Expanded, Scopus)

25. A case with oto-spondylo-mega-epiphyseal-dysplasia (OSMED): The clinical recognition and differential diagnosis

Karaer K., Rosti R. Ö., TORUN D., SANAL H. T., Bahçe M., GÜRAN Ş.

Turkish Journal of Pediatrics , cilt.53, sa.3, ss.346-351, 2011 (SCI-Expanded, Scopus)

26. I(17q) in a case with myelodysplastic syndrome: An important and rarely seen chromosomal anomaly Miyelodisplastik sendromlu olguda i(17q): Nadir görülen önemli bir kromozomal anomali

Bahçe M., Beyan C., Erdem G., Ateş Ö., Kozan S., TORUN D., et al.

Gulhane Medical Journal , cilt.53, sa.4, ss.301-303, 2011 (Scopus, TRDizin)

27. Cytotoxic effect of docetaxel on multiple myeloma cell lines (RPMI-8226) as a chemotherapotic agent Kemoterapötik ajan olarak dosetaksel'in multipl miyelom Hücre hatti (RPMI-8226) üzerindeki sitotoksik etkisi

Çoban Z. D., Avcu F., Ural A. U., AKYOL M., GÜRAN Ş.

Gulhane Medical Journal , cilt.53, sa.4, ss.258-263, 2011 (Scopus, TRDizin)

28. Proceeded diagnosis and therapy in eye diseases under the light of developments in molecular biology and genetics Moleküler biyoloji ve genetikteki gelişmelerin işiǧında göz hastaliklarinda ileri tani ve tedavi

GÜRAN Ş.

Gulhane Medical Journal , cilt.53, sa.1, ss.74-76, 2011 (Scopus, TRDizin)

29. The effect of cytogenetic analysis results on prognosis in cases with myelodysplastic syndrome Miyelodisplastik sendrom olgularinda sitogenetik analiz sonuçlarinin hasta prognozuna etkisi

GÜRAN Ş., Beyan C., TUNCA Y., Kozan S., TORUN D., Ifran A., et al.

Gulhane Medical Journal , cilt.53, sa.2, ss.104-106, 2011 (Scopus, TRDizin)

30. Germline mutations of BRCA1 and BRCA2 genes in Turkish breast, ovarian, and prostate cancer patients

Manguoĝlu E., GÜRAN Ş., Yamaç D., Çolak T., ŞİMŞEK M., Baykara M., et al.

Cancer Genetics and Cytogenetics , cilt.203, sa.2, ss.230-237, 2010 (SCI-Expanded, Scopus)

31. Rare chromosomal complement of trisomy 21 in a boy conceived only by IVF

GÜRAN Ş., Rosti R. O., Sarici S. Ü., TORUN D., Kozan S., Bahe M.

Reproductive BioMedicine Online , cilt.21, sa.5, ss.721-722, 2010 (SCI-Expanded, Scopus)

32. The progeny of homozygous identical reciprocal translocation carrier mother

Koç A., GÜRAN Ş., Bahce M.

American Journal of Medical Genetics, Part A , cilt.152, sa.11, ss.2886-2887, 2010 (SCI-Expanded, Scopus)

33. A case with neurosensorial hearing loss and anodonty findings: Is this a variant of otodental syndrome? Nörosensoryal işitme kaybı ve anodonti bulgular? Olan bir olgu: Otodental sendromun bir varyantı mı?

TORUN D., GÜRAN Ş., Karahatay S., Öncel Torun Z., GEREK M., Bahçe M.

Turkiye Klinikleri Journal of Medical Sciences , cilt.30, sa.1, ss.387-391, 2010 (SCI-Expanded, Scopus)

34. Coexistence of cytogenetic findings of trisomy 8, trisomy 9 and trisomy 21 in a case with acute myeloblastic leukemia Akut miyeloblastik lösemili olguda trizomi 8, trizomi 9 ve trizomi 21 sitogenetik bulgularının birlikteliǧi

Kozan S., Öztürk E., TORUN D., Bahçe M., Kaya H., Beyan C., et al.

Gulhane Medical Journal , cilt.52, sa.4, ss.287-289, 2010 (Scopus, TRDizin)

35. Specific polymorphisms of IL-1β genes (-511, +3953) and their probable effects on IL-1β production in idiopatic hypogonadotropic hypogonadism Idiopatik hipogonadotropik hipogonadizm hastalarinda IL-1β genlerindeki spesifik (-511, +3953) polimorfizmler ve bunlarin IL-1β üretimindeki olasi etkileri

Muşabak U., Bolu E., ILIKÇI SAĞKAN R., TUNCA Y., GÜRAN Ş., Gül D., et al.

Turkiye Klinikleri Journal of Medical Sciences , cilt.30, sa.6, ss.1814-1819, 2010 (SCI-Expanded, Scopus)

36. Hyperhomocysteinemia and homozygous MTHFR 677C>T mutation finding in an Alzheimer's disease case with metabolic syndrome diagnosis

GÜRAN Ş., Kozan S., Bahçe M.

Folia Neuropathologica , cilt.48, sa.1, ss.64-65, 2010 (SCI-Expanded, Scopus)

37. Co-occurrence of inversion 16 and trisomy 22 cytogenetic abnormalities in a relapse phase acute non-lymphocytic leukemia case Bir Relaps Akut Non-Lenfositer Lösemi Olgusunda İnversiyon 16 ve Trizomi 22 Sitogenetik Anomalilerinin Birlikteliǧi

Kozan S., Ateş Ö., GÜRAN Ş., Bahçe M., Beyan C.

Turkiye Klinikleri Journal of Medical Sciences , cilt.30, sa.6, ss.2037-2040, 2010 (SCI-Expanded, Scopus)

38. A new syndrome associated with absence of lower lid lacrimal punctum, ptosis, elevation deficiency of both eyes and mild facial dysmorphism

GÜRAN Ş., TORUN D., MUTLU F. M., UYSAL Y., Ugurel M. S., Bahce M.

Ophthalmic Genetics , cilt.30, sa.3, ss.146-151, 2009 (SCI-Expanded, Scopus)

39. Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: Importance of genetic counseling

Terzi Y., Oguzkan-Balci S., Anlar B., Aysun S., GÜRAN Ş., Ayter S.

Genetic Counseling , cilt.20, sa.2, ss.195-202, 2009 (SCI-Expanded, Scopus)

40. Imatinib mesylate therapy may cause additional chromosomal instability by a feedback mechanism in chronic myeloid leukemia treatment

GÜRAN Ş.

Bioscience Hypotheses , cilt.2, sa.6, ss.396-398, 2009 (Scopus)

41. Three hemifascial microsomia patients and the review of the literature Üç adet hemifasiyal mikrosomia hastasi ve literatürün gözden geçirilmesi

ULUDAĞ A., Tepeli E., Koç A., Kozan S., TORUN D., GÜRAN Ş., et al.

Anatolian Journal of Clinical Investigation , cilt.3, sa.4, ss.252-255, 2009 (Scopus)

42. Genetic appoproch in cases with disorders of sexual development Cinsel farklılaşma bozukluǧu olan olgularda genetik yaklaşım

Bahçe M., TUNCA Y., Gül D., Imirzalioǧlu N., Emre Taşçilar M., Bolu E., et al.

Gulhane Medical Journal , cilt.51, sa.4, ss.223-228, 2009 (Scopus, TRDizin)

43. JAK2 V617F mutation in cases with chronic myeloproliferative disorders and myelodysplastic syndrome Kronik miyeloproliferatif hastalık ve miyelodisplastik sendrom olgularında Jak2 V617F mutasyonu

Kozan S., GÜRAN Ş., Bahçe M., Kaptan K., Ifran A., Avni Atay A., et al.

Gulhane Medical Journal , cilt.51, sa.3, ss.137-140, 2009 (Scopus, TRDizin)

44. Deletion in 3P21.3 region in a multiple myeloma case with poor prognosis: Letter to the editor 3P21.3 bölgesinde delesyon ile karakterize kötü prognozla giden bir multipl miyeloma olgusu

GÜRAN Ş., Ateş Ö., TORUN D., Kozan S., Nevruz O., Avcu F., et al.

Turkiye Klinikleri Journal of Medical Sciences , cilt.29, sa.6, ss.1795-1796, 2009 (SCI-Expanded, Scopus)

45. Cancer diagnosis from circulating nucleic acids: Review Kanda Dolaşan Nükleik Asitten Kanser Tanisi

GÜRAN Ş., Yurdakul H.

Turkiye Klinikleri Journal of Medical Sciences , cilt.29, sa.2, ss.488-491, 2009 (SCI-Expanded, Scopus)

46. Familial multiple myeloma associated with disorders of chronic inflammation: First report from Turkey

Özet A., GÜRAN Ş., Beksac M.

Clinical Lymphoma and Myeloma , cilt.8, sa.4, ss.246-248, 2008 (SCI-Expanded, Scopus)

47. Prenatal diagnosis of Cri-du chat syndrome following high maternal serum human chorionic gonodotrophin and choroid plexus cysts

TORUN D., Bahce M., Alanbay I., GÜRAN Ş., Baser I.

Prenatal Diagnosis , cilt.29, sa.5, ss.536-537, 2008 (SCI-Expanded, Scopus)

48. A breast cancer patient with pelvic and gastric malignancy after adjuvant tamoxifen treatment for breast cancer

Dede M., Gezginç K., Ulubay M., Alanbay I., GÜRAN Ş., Yenen M.

European Journal of Gynaecological Oncology , cilt.29, sa.2, ss.200, 2008 (SCI-Expanded, Scopus)

49. Unilateral tubal ectopic twin pregnancy

Dede M., Gezginç K., Yenen M., Ulubay M., Kozan S., GÜRAN Ş., et al.

Taiwanese Journal of Obstetrics and Gynecology , cilt.47, sa.2, ss.226-228, 2008 (Scopus)

50. Persistent mullerian duct syndrome with transverse testicular ectopia

Boleken M. E., KAYA M., GÜRAN Ş., Memetoǧlu M. E., Kanmaz T., Yücesan S.

International Urology and Nephrology , cilt.39, sa.4, ss.1173-1175, 2007 (SCI-Expanded, Scopus)

51. A papillary thyroid carcinoma case associated with hereditary colon carcinoma due to familial adenomatous polyposis with no hereditary mutation finding [4]

Yagci G., Dede M., GÜRAN Ş., Yenen M. C., DURUKAN A. H., Safali M.

International Journal of Colorectal Disease , cilt.22, sa.6, ss.725-726, 2007 (SCI-Expanded, Scopus)

52. Development of secondary myelodysplastic syndrome in a patient with previous bladder carcinoma [5]

Ifran A., Nevruz O., Avcu F., GÜRAN Ş., Ural A. U.

American Journal of Hematology , cilt.81, sa.7, ss.560, 2006 (SCI-Expanded, Scopus)

53. The importance of results of MEFV gene analysis in cases prediagnosed as "familial mediterranean fever" Ai̇lesel akdeni̇z ateşi̇ ön tanisi alan olgularda MEFV gen mutasyon anali̇z sonuçlarinin önemi̇

YALÇINKAYA E., GÜRAN Ş., Nas B. G., Dursun A., Imirzalioǧlu N.

Erciyes Tip Dergisi , cilt.28, sa.1, ss.19-24, 2006 (Scopus, TRDizin)

54. Donor cell leukemia in a patient developing 11 months after an allogeneic bone marrow transplantation for chronic myeloid leukemia

Ataergin S., Arpaci F., Cetin T., GÜRAN Ş., Yakicier C., BEYZADEOĞLU M. M., et al.

American Journal of Hematology , cilt.81, sa.5, ss.370-373, 2006 (SCI-Expanded, Scopus)

55. Synchronous double malignancies of renal cell carcinoma and acute myeloid leukemia: An unreported co-existence [1]

Beyan C., Kaptan K., TUNCA Y., Ifran A., GÜRAN Ş.

American Journal of Hematology , cilt.80, sa.2, ss.164, 2005 (SCI-Expanded, Scopus)

56. Identification of polymorphisms on the MDR1 gene among Turkish population and their effects on multidrug resistance in acute leukemia patients

Kaya P., Gündüz U., Arpaci F., Ural A. U., GÜRAN Ş.

American Journal of Hematology , cilt.80, sa.1, ss.26-34, 2005 (Scopus)

57. Hereditary breast cancer syndromes in a Turkish population. Results of molecular germline analysis

GÜRAN Ş., Özet A., Dede M., Gille J. J., Yenen M. C.

Cancer Genetics and Cytogenetics , cilt.160, sa.2, ss.164-168, 2005 (Scopus)

58. Periodontal status in two siblings with severe congenital neutropenia: Diagnosis and mutational analysis of the cases

Hakki S. S., Aprikyan A. A., Yildirim S., Aydinbelge M., Gokalp A., Ucar C., et al.

Journal of Periodontology , cilt.76, sa.5, ss.837-844, 2005 (Scopus)

59. A chronic myeloid leukemia-like syndrome case with del (12) (p12) in a Li-Fraumeni syndrome family

GÜRAN Ş., Beyan C., Nevruz O., Yakicier C., TUNCA Y.

Clinical and Laboratory Haematology , cilt.27, sa.2, ss.135-138, 2005 (Scopus)

60. Trisomy 8 finding treatment of imatinib mesylate in chronic myeloid leukemia cases

TUNCA Y., GÜRAN Ş.

Experimental Hematology , cilt.33, sa.2, ss.151, 2005 (SCI-Expanded, Scopus)

61. Development of squamous cell carcinoma of the tongue during induction chemotherapy for acute myeloid leukemia

Ural A. U., Avcu F., Yilmaz M. I., Guden M., Ozturk B., Ozcan A., et al.

Tumori , cilt.91, sa.1, ss.81-83, 2005 (SCI-Expanded, Scopus)

62. New diagnostic approaches into diseases: Protein chip technology Hastaliklara yeni bir tani yaklaşimi: Protein-çip teknolojisi

GÜRAN Ş.

Gulhane Medical Journal , cilt.47, sa.3, ss.243-245, 2005 (Scopus, TRDizin)

63. The importance of molecular biology and biotechnology in national defence Ulusal savunmada moleküler biyoloji ve biyoteknolojinin önemi

GÜRAN Ş.

Gulhane Medical Journal , cilt.47, sa.2, ss.153-155, 2005 (Scopus, TRDizin)

64. Prevention from cancer Kanserden korunma

GÜRAN Ş.

Gulhane Medical Journal , cilt.47, sa.4, ss.324-326, 2005 (Scopus, TRDizin)

65. A case of neurofibromatosis and breast cancer: Loss of heterozygosity of NF1 in breast cancer

GÜRAN Ş., Safali M.

Cancer Genetics and Cytogenetics , cilt.156, sa.1, ss.86-88, 2005 (SCI-Expanded, Scopus)

66. The cytogenetic results of the cases who had chronic myeloproliferative disorders except chronic myeloid leukemia Kroni̇k mi̇yelosi̇ter lösemi̇ dişi kroni̇k mi̇yeloproli̇ferati̇f hastaliǧi olan olgularimizda si̇togeneti̇k i̇nceleme sonuçlari

Nevruz O., GÜRAN Ş., Beyan C., Ifran A., TUNCA Y., Kaptan K., et al.

Gulhane Medical Journal , cilt.47, sa.1, ss.11-13, 2005 (Scopus, TRDizin)

67. The role of secondary chromosomal abnormalities in the progression of chronic myeloid leukemia cases Kronik miyelositer lösemi olgularinda philadelphia kromozomu haricindeki sitogenetik anomalilerin prognoza etkisi

Nevruz O., GÜRAN Ş., Beyan C., Ifran A., TUNCA Y., Kaptan K., et al.

Turkiye Klinikleri Journal of Medical Sciences , cilt.25, sa.2, ss.174-177, 2005 (Scopus, TRDizin)

68. Prenatal diagnosis history of a Li-Fraumeni syndrome family [3]

GÜRAN Ş., TUNCA Y.

Cancer Genetics and Cytogenetics , cilt.157, sa.2, ss.191, 2005 (SCI-Expanded, Scopus)

69. Overexpression of p16INK4A and p14ARF in haematological malignancies (Lee et al., 2003) [2]

GÜRAN Ş., Beyan C.

Clinical and Laboratory Haematology , cilt.26, sa.4, ss.303, 2004 (Scopus)

70. Our treatment results in patients with ANNL over 60 years old 60 Yaş üzeri̇ akut nonlenfosi̇ter lösemi̇ olgularimizda tedavi̇ sonuçlari

Nevruz O., Beyan C., GÜRAN Ş., Ifran A., TUNCA Y., Kaptan K., et al.

Gulhane Medical Journal , cilt.46, sa.4, ss.276-279, 2004 (Scopus, TRDizin)

71. A case of Zellweger syndrome with clonal 46, XX, t(1;2) (q43;q21) cytogenetic abnormality Klonal 46XX, t(1;2) (q43;q21) si̇togeneti̇k anomali̇si̇ i̇le karakteri̇ze Zellweger sendromu olgusu

GÜRAN Ş., Bal F., TUNCA Y.

Erciyes Tip Dergisi , cilt.26, sa.3, ss.145-148, 2004 (Scopus, TRDizin)

72. Angiogenesis and gene therapy in heart failure Kalp yetmezli̇ǧi̇nde anji̇yogenezis ve gen tedavi̇si̇

GÜRAN Ş.

Gulhane Medical Journal , cilt.46, sa.1, ss.84-87, 2004 (Scopus, TRDizin)

73. The results of analyses for common MEFV gene mutation in 110 patients in whom was considered FMF and their correlation with clinical findings Ai̇lesel akdeni̇z ateşi̇ düşc̈nülen 110 vakada sik görülen MEFV gen mutasyonlari anali̇z sonuçlari ve kli̇ni̇k bulgularla korelasyonu

Tüzün A., Dursun A., Ateş Y., Kataş B., GÜRAN Ş., UYGUN A., et al.

Gulhane Medical Journal , cilt.46, sa.3, ss.238-241, 2004 (Scopus, TRDizin)

74. Nonfunctioning adrenocortical carcinoma in a child

Kanmaz T., Demirbilek S., Ozardali I., Safali M., GÜRAN Ş., Yucesan S.

Pediatric Pathology and Molecular Medicine , cilt.22, sa.5, ss.405-410, 2003 (Scopus)

75. Dystraphin gene mutations in cases diagnosed as muscular dystrophia and the correlations with the clinical findings Musküler di̇strofi̇ tanisi almiş olgularda di̇strofi̇n gen mutasyon anali̇z sonuçlari ve kli̇ni̇k bulgular i̇le korelasyonu

Imirzaliǧlu N., SOYSAL Y., Akin R., Gül D., ÜNAY B., GÜRAN Ş.

Gulhane Medical Journal , cilt.45, sa.1, ss.25-28, 2003 (Scopus, TRDizin)

76. A DIDMOAD syndrome family with juvenile glaucoma and myopia findings

Bekir N. A., Güngör K., GÜRAN Ş.

Acta Ophthalmologica Scandinavica , cilt.78, sa.4, ss.480-482, 2000 (SCI-Expanded, Scopus)

77. Chronic myelomonocytic leukemia developed 2 years after the onset of immune thrombocytopenic purpura like syndrome

Ural A. U., Kaptan K., Avcu F., GÜRAN Ş., Beyan C., Durmuş Ö., et al.

Haematologia , cilt.30, sa.3, ss.221-224, 2000 (SCI-Expanded, Scopus)

78. Association of sets of alleles of genes encoding β3-adrenoreceptor, uncoupling protein 1 and lipoprotein lipase with increased risk of metabolic complications in obesity

Proenza A., Poissonnet C., Ozata M., Ozen S., GÜRAN Ş., Palou A., et al.

International Journal of Obesity , cilt.24, sa.1, ss.93-100, 2000 (SCI-Expanded, Scopus)

79. Hereditary TP53 codon 292 and somatic P16(INK4A) codon 94 mutations in a Li-Fraumeni syndrome family

GÜRAN Ş., TUNCA Y., Imirzalioglu N.

Cancer Genetics and Cytogenetics , cilt.113, sa.2, ss.145-151, 1999 (SCI-Expanded, Scopus)

80. Cumulation of TP53 mutations and p16(INK4A)/p15(INK4B) homozygous deletions in human papilloma virus type 16 positive scrotal cancer

GÜRAN Ş., Pak I.

Cancer Genetics and Cytogenetics , cilt.109, sa.2, ss.108-113, 1999 (SCI-Expanded, Scopus)

81. p53 and p16(INK4A) mutations during the progression of glomus tumor

GÜRAN Ş., TALI E. T.

Pathology and Oncology Research , cilt.5, sa.1, ss.41-45, 1999 (Scopus)

82. P53, p15INK4B, p16INK4A and p57KIP2 mutations during the progression of chronic myeloid leukemia

GÜRAN Ş., Bahçe M., Beyan C., Korkmaz K., Yalçin A.

Haematologia , cilt.29, sa.3, ss.181-193, 1998 (Scopus)

83. The Δccr5 mutation conferring protection against HIV-1 in Caucasian populations has a single and recent origin in Northeastern Europe

Libert F., Cochaux P., Beckman G., Samson M., Aksenova M., Cao A., et al.

Human Molecular Genetics , cilt.7, sa.3, ss.399-406, 1998 (SCI-Expanded, Scopus)

84. Application of the 'apt test' in prenatal diagnosis to evaluate the fetal origin of blood obtained by cordocentesis: Results of 30 pregnancies

Ogur G., Gül D., Özen S., Imirzalioglu N., Cankus G., TUNCA Y., et al.

Prenatal Diagnosis , cilt.17, sa.9, ss.879-882, 1997 (SCI-Expanded, Scopus)

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