المؤلفون: Manguoğlu E, Akdeniz S, Dündar N, Duman Ö, Aktekin B, Haspolat Ş, Bilge U, Özel D, Lüleci G

المصدر: Balkan Journal of Medical Genetics, Vol 14, Iss 1, Pp 25-30 (2011)

مصطلحات موضوعية: epilepsy, neuropharmacology, pharmacogenetics, polymorphism, rlip76 gene, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1311-0160

URL الوصول: https://doaj.org/article/8b2358ff1820473caab914abf8fca0a9

المؤلفون: Manguoglu, E., Akdeniz, S., Dündar, N., Duman, Ö., Aktekin, B., Haspolat, Ş., Lüleci, G.

المساهمون: Manguoglu, E., Akdeniz, S., Dündar, N., Duman, Ö., Aktekin, B., Haspolat, Ş., Lüleci, G., Yeditepe Üniversitesi

مصطلحات موضوعية: Epilepsy, Neuropharmacology, Pharmacogenetics, Polymorphism, RLIP76 gene

Relation: Balkan Journal of Medical Genetics; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; 25; 30; 14; https://hdl.handle.net/20.500.11831/4049

الاتاحة: https://hdl.handle.net/20.500.11831/4049

المؤلفون: Doherty R, Lubinski J, Manguoglu E, Luleci G, Christie M, Craven P, Bancroft E, Mitra A, Morgan S, Eeles R

المصدر: Hereditary Cancer in Clinical Practice, Vol 5, Iss 1, Pp 53-55 (2007)

مصطلحات موضوعية: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470

Relation: http://www.hccpjournal.com/content/5/1/53; https://doaj.org/toc/1897-4287; https://doaj.org/article/a1c2e83c95ee4ccd80d2d49e248f3bf7

الاتاحة: https://doi.org/10.1186/1897-4287-5-1-53
https://doaj.org/article/a1c2e83c95ee4ccd80d2d49e248f3bf7

المؤلفون: Doherty, R, Lubinski, J, Manguoglu, E, Luleci, G, Christie, M, Craven, P, Bancroft, E, Mitra, A, Morgan, S, Eeles, R, the IMPACT steering committee†, collaborators*

Relation: http://www.hccpjournal.com/content/5/1/53

الاتاحة: http://www.hccpjournal.com/content/5/1/53

المؤلفون: MARSHALL CR, YOUNG EJ, PANI AM, FRECKMANN ML, LACASSIE Y, HOWALD C, FITZGERALD KK, PEIPPO M, MORRIS CA, SHANE K, PRIOLO M, MORIMOTO M, KONDO I, MANGUOGLU E, BERKER KARAUZUM S, EDERY P, HOBART HH, MERVIS CB, REYMOND A, KAPLAN P, TASSABEHJI M, GREGG RG, SCHERER SW, OSBORNE LR, ZUFFARDI, ORSETTA

المساهمون: Marshall, Cr, Young, Ej, Pani, Am, Freckmann, Ml, Lacassie, Y, Howald, C, Fitzgerald, Kk, Peippo, M, Morris, Ca, Shane, K, Priolo, M, Morimoto, M, Kondo, I, Manguoglu, E, BERKER KARAUZUM, S, Edery, P, Hobart, Hh, Mervis, Cb, Zuffardi, Orsetta, Reymond, A, Kaplan, P, Tassabehji, M, Gregg, Rg, Scherer, Sw, Osborne, Lr

مصطلحات موضوعية: "EPILESSIA", "GENI", "DELEZIONI CRIPTICHE"

وصف الملف: STAMPA

Relation: volume:83; firstpage:106; lastpage:111; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11571/118980

الاتاحة: http://hdl.handle.net/11571/118980

المؤلفون: Marshall, C.R., Young, E.J., Pani, A.M., Freckmann, M.L., Lacassie, Y., Howald, C., Fitzgerald, K.K., Peippo, M., Morris, C.A., Shane, K., Priolo, M., Morimoto, M., Kondo, I., Manguoglu, E., Berker-Karauzum, S., Edery, P., Hobart, H.H., Mervis, C.B., Zuffardi, O., Reymond, A., Kaplan, P., Tassabehji, M., Gregg, R.G., Scherer, S.W., Osborne, L.R.

المصدر: American Journal of Human Genetics, vol. 83, no. 1, pp. 106-111

مصطلحات موضوعية: Chromosome Breakage, Chromosomes, Human, Pair 17, Female, Gene Deletion, Genetic Markers, Humans, In Situ Hybridization, Fluorescence, Infant, Male, Microsatellite Repeats, Oligonucleotide Array Sequence Analysis, Physical Chromosome Mapping, Polymorphism, Single Nucleotide, Proteins/genetics, Spasms, Infantile/diagnosis, Infantile/genetics

Relation: info:eu-repo/semantics/altIdentifier/pmid/18565486; info:eu-repo/semantics/altIdentifier/pissn/1537-6605[electronic]; https://serval.unil.ch/notice/serval:BIB_74562E3FC31E

الاتاحة: https://serval.unil.ch/notice/serval:BIB_74562E3FC31E
https://doi.org/10.1016/j.ajhg.2008.06.001

المؤلفون: Manguoğlu, E, Berker-Karaüzüm, S, Baumer Wolz, Alessandra, Mihci, Ercan, Taçoy, S, Lüleci, Güven, Schinzel, Albert

المصدر: Manguoğlu, E; Berker-Karaüzüm, S; Baumer Wolz, Alessandra; Mihci, Ercan; Taçoy, S; Lüleci, Güven; Schinzel, Albert (2005). A case with de novo interstitial deletion of chromosome 7q21.1-q22. Genetic Counseling, 16(2):155-9.

مصطلحات موضوعية: Institute of Medical Genetics, 610 Medicine & health, 570 Life sciences, biology, Genetics, Genetics (clinical)

Relation: https://www.zora.uzh.ch/237918; info:pmid/16080295; urn:issn:1015-8146

الاتاحة: https://www.zora.uzh.ch/id/eprint/237918/
https://www.zora.uzh.ch/237918

المؤلفون: Bozkurt, B, Kontogianni, E, Ozcelik, T, Yulug, IG, Karakaya, AE, Kocabas, NA, Florentin, L, Papadopoulou, E, Nasioulas, G, Gerassimos, V, Sayek, I, Tez, M, Colakoglu, G, AKYERLİ BOYLU, Cemaliye, Colak, T, Luleci, G, Manguoglu, E, Konstantopoulou, I, Yannoukakos, D, Sevinc, A

الاتاحة: https://avesis.hacettepe.edu.tr/publication/details/c2bbb120-d61e-4f65-bc63-45d81c973079/oai

المؤلفون: Papadopoulou, E, Kontogianni, E, Bozkurt, B, Florentin, L, Sevinc, A, Yannoukakos, D, Konstantopoulou, I, Manguoglu, E, Luleci, G, Colak, T, AKYERLİ BOYLU, Cemaliye, Colakoglu, G, Tez, M, Sayek, I, Gerassimos, V, Nasioulas, G, Kocabas, NA, Karakaya, AE, Yulug, IG, Ozcelik, T

Relation: c2bbb120-d61e-4f65-bc63-45d81c973079; https://avesis.gazi.edu.tr/publication/details/c2bbb120-d61e-4f65-bc63-45d81c973079/oai

الاتاحة: https://avesis.gazi.edu.tr/publication/details/c2bbb120-d61e-4f65-bc63-45d81c973079/oai

المؤلفون: Sevinç, A., Yannoukakos, D., Konstantopoulou I., Manguoglu, E., Lüleci G., Çolak, T., Akyerli, C., Çolakoglu G., Tez, M., Sayek I., Gerassimos V., Nasioulas G., Papadopoulou, E., Florentin L., Kontogianni, E., Bozkurt, B., Kocabas, N.A., Karakaya, A.E., Yulug I.G., Özçelik, T.

المصدر: Anticancer Research

مصطلحات موضوعية: Breast cancer, RNASEL, arginine, glutamine, ribonuclease L, adolescent, aged, amino acid sequence, amplification refractory mutation system, article, cancer risk, controlled study, disease association, female, gene amplification, gene mutation, genotype, Greece, human, human tissue, major clinical study, pleiotropy, priority journal, protein variant, risk factor, Turkey (republic), Adult, 80 and over, Alleles, Breast Neoplasms

وصف الملف: application/pdf

Relation: 2507005; http://hdl.handle.net/11693/24266

الاتاحة: http://hdl.handle.net/11693/24266

المؤلفون: Keser, I., Sanlioglu, A.D., Manguoglu, E., Guzeloglu Kayisli, O., Nal, N., Sargin, F., Yesilipek, A., Simsek, M., Mendilcioglu, I., Canatan, D., Luleci, G.

المصدر: Acta Haematologica ; volume 111, issue 4, page 205-210 ; ISSN 0001-5792 1421-9662

الاتاحة: http://dx.doi.org/10.1159/000077567
https://www.karger.com/Article/Pdf/77567

المؤلفون: Morgan Sarah, Lubinski Jan, Manguoglu Esra, Luleci Guven, Doherty Rebecca, Christie Margaret, Craven Paul, Bancroft Elizabeth, Mitra Anita, Zieba Karolina, Eeles Ros

المصدر: Hereditary Cancer in Clinical Practice, Vol 4, Iss 2, Pp 111-112 (2006)

مصطلحات موضوعية: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://www.hccpjournal.com/content/4/2/111; https://doaj.org/toc/1897-4287

URL الوصول: https://doaj.org/article/eea82286151749e8b2720debc7b88f15