Identification of the gene ( BBS1 ) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome
Sheffield, Val C, Mykytyn, Kirk, Nishimura, Darryl Y, Searby, Charles C, Shastri, Mythreyi, Yen, Hsan-jan, Beck, John S, Braun, Terry, Streb, Luan M, Cornier, Alberto S, Cox, Gerald F, Fulton, Anne B, Carmi, Rivka, Lüleci, Güven, Chandrasekharappa, Settara C, Collins, Francis S, Jacobson, Samuel G, Heckenlively, John R, Weleber, Richard G, Stone, Edwin M
Published in Nature genetics (01.08.2002)
Published in Nature genetics (01.08.2002)
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Assessment of women who applied for the uterine transplant project as potential candidates for uterus transplantation
Erman Akar, Munire, Ozekinci, Murat, Alper, Ozgul, Demir, Durkadin, Cevikol, Can, Meric Bilekdemir, Asli, Daloglu, Aylin, Ongut, Gozde, Senol, Yesim, Ozdem, Sebahat, Uzun, Gulbahar, Luleci, Guven, Suleymanlar, Gultekin
Published in The journal of obstetrics and gynaecology research (01.01.2015)
Published in The journal of obstetrics and gynaecology research (01.01.2015)
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Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia
Demir Eksi, Durkadin, Shen, Yiping, Erman, Munire, Chorich, Lynn P, Sullivan, Megan E, Bilekdemir, Meric, Yılmaz, Elanur, Luleci, Guven, Kim, Hyung-Goo, Alper, Ozgul M, Layman, Lawrence C
Published in Molecular cytogenetics (03.02.2018)
Published in Molecular cytogenetics (03.02.2018)
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In Vivo and In Vitro Regulation of Akt Activation in Human Endometrial Cells Is Estrogen Dependent
Kayisli, Ozlem Guzeloglu, Kayisli, Umit A, Luleci, Guven, Arici, Aydin
Published in Biology of reproduction (01.09.2004)
Published in Biology of reproduction (01.09.2004)
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Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype
Bagci, Gulseren, Ph.D, Bisgin, Atil, M.D., Ph.D, Karauzum, Sibel Berker, Ph.D, Trak, Bilal, M.D, Luleci, Guven, Ph.D
Published in Fertility and sterility (01.04.2011)
Published in Fertility and sterility (01.04.2011)
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Effects of hormone replacement therapy on bone mineral density in Turkish patients with or without COL1A1 Sp1 binding site polymorphism
Simsek, Mehmet, Cetin, Zafer, Bilgen, Turker, Taskin, Omur, Luleci, Guven, Keser, Ibrahim
Published in The journal of obstetrics and gynaecology research (01.02.2008)
Published in The journal of obstetrics and gynaecology research (01.02.2008)
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Donor cell-derived acute myeloblastic leukemia after allogeneic peripheral blood hematopoietic stem cell transplantation for juvenile myelomonocytic leukemia
Cetin, Zafer, Tezcan, Gulsun, Karauzum, Sibel Berker, Kupesiz, Alphan, Manguoglu, Ayse Esra, Yesilipek, Akif, Luleci, Guven, Hazar, Volkan
Published in Journal of pediatric hematology/oncology (01.11.2006)
Published in Journal of pediatric hematology/oncology (01.11.2006)
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Lack of BCL-2 confers interferon-alpha sensitivity to B-cell lymphomas
Karauzum, Sibel Berker, Yasar, Duygu, Dirice, Ercument, Imir, Nilufer, Luleci, Guven, Ozes, Osman Nidai
Published in Growth factors (Chur, Switzerland) (01.01.2007)
Published in Growth factors (Chur, Switzerland) (01.01.2007)
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Triploidy in a growth discordant twin pregnancy after intracytoplasmic sperm injection treatment : Case report
MENDILCIOGLU, Inanc, OZCAN, Mualla, BAGCI, Gulseren, SIMSEK, Mehmet, KURSUN, Sinan, LULECI, Guven, TASKIN, Omur
Published in Fetal diagnosis and therapy (01.01.2006)
Published in Fetal diagnosis and therapy (01.01.2006)
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IMPACT and AIDIT: Strengthening Research Ties in Eastern Europe
Morgan, Sarah, Lubinski, Jan, Manguoglu, Esra, Luleci, Guven, Doherty, Rebecca, Christie, Margaret, Craven, Paul, Bancroft, Elizabeth, Mitra, Anita, Zieba, Karolina, Eeles, Ros
Published in Hereditary cancer in clinical practice (15.06.2006)
Published in Hereditary cancer in clinical practice (15.06.2006)
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A 5q12.1–5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement
Cetin, Zafer, Yakut, Sezin, Clark, Ozden Altiok, Mihci, Ercan, Berker, Sibel, Luleci, Guven
Published in Gene (01.03.2013)
Published in Gene (01.03.2013)
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A patient with Down syndrome with a de novo derivative chromosome 21
Cetin, Zafer, Yakut, Sezin, Mihci, Ercan, Manguoglu, Ayse Esra, Berker, Sibel, Keser, Ibrahim, Luleci, Guven
Published in Gene (10.10.2012)
Published in Gene (10.10.2012)
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Turkish population-based screening for first identified changes of BRCA1 and BRCA2 genes in breast and/or ovarian cancer patients
Semerci Sevimli, Tuğba, Sevimli, Murat, Manguoğlu, Ayşe Esra, Lüleci, Güven
Published in Egyptian Journal of Medical Human Genetics (01.12.2024)
Published in Egyptian Journal of Medical Human Genetics (01.12.2024)
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Journal Article
Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease
Yakut, Sezin, Cetin, Zafer, Arman, Mehmet, Akbas, Halide, Manguoglu, Ayse E., Luleci, Guven
Published in Rheumatology international (01.11.2013)
Published in Rheumatology international (01.11.2013)
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