Sakizli M - Search Results

1

Analysis of cytotoxic T lymphocyte antigen-4 (CTLA-4) exon 1 polymorphism in patients with type 1 diabetes mellitus in a Turkish population.

Genc S, Genc K, Sercan O, Kizildag S, Gulay Z, Atay T, Dundar B, Sakizli M, Büyükgebiz A. Genc S, et al. Among authors: sakizli m. J Pediatr Endocrinol Metab. 2004 May;17(5):731-5. doi: 10.1515/jpem.2004.17.5.731. J Pediatr Endocrinol Metab. 2004. PMID: 15237707

2

Microsatellite instability in early-onset breast cancer.

Ozer E, Yuksel E, Kizildag S, Sercan O, Ozen E, Canda T, Sakizli M. Ozer E, et al. Among authors: sakizli m. Pathol Res Pract. 2002;198(8):525-30. doi: 10.1078/0344-0338-00296. Pathol Res Pract. 2002. PMID: 12389995

3

Two brothers with a 7.0 kb gene deletion associated with isolated growth hormone deficiency type 1A.

Sercan OH, Korkmaz KS, Yazicioğlu MV, Sakizli M, Büyükgebiz A. Sercan OH, et al. Among authors: sakizli m. J Pediatr Endocrinol Metab. 1996 May-Jun;9(3):423-7. doi: 10.1515/jpem.1996.9.3.423. J Pediatr Endocrinol Metab. 1996. PMID: 8887154

4

A Turkish family with 6.7 Kb deletion associated with isolated growth hormone deficiency type 1A.

Korkmaz KS, Sercan OH, Yazicioğlu MV, Sakizli M, Darcan S, Büyükgebiz A. Korkmaz KS, et al. Among authors: sakizli m. Turk J Pediatr. 1997 Jan-Mar;39(1):99-104. Turk J Pediatr. 1997. PMID: 10868200

5

Hyperbilirubinemic serum is cytotoxic and induces apoptosis in murine astrocytes.

Kumral A, Genc S, Genc K, Duman N, Tatli M, Sakizli M, Ozkan H. Kumral A, et al. Among authors: sakizli m. Biol Neonate. 2005;87(2):99-104. doi: 10.1159/000081969. Epub 2004 Nov 9. Biol Neonate. 2005. PMID: 15539765

6

TLR-2 Arg753Gln, TLR-4 Asp299Gly, and TLR-4 Thr399Ile polymorphisms in Henoch Schonlein purpura with and without renal involvement.

Soylu A, Kizildağ S, Kavukçu S, Cingöz S, Türkmen M, Demir BK, Sakizli M. Soylu A, et al. Among authors: sakizli m. Rheumatol Int. 2010 Mar;30(5):667-70. doi: 10.1007/s00296-009-1052-y. Epub 2009 Jul 12. Rheumatol Int. 2010. PMID: 19597734

7

Microsatellite instability is not a common feature in medullary breast cancer.

Yuksel E, Ozer E, Kizildag S, Sercan O, Canda T, Sakizli M. Yuksel E, et al. Among authors: sakizli m. Breast. 2002 Dec;11(6):473-7. doi: 10.1054/brst.2002.0479. Breast. 2002. PMID: 14965712

8

A case of mixed gonadal dysgenesis with 45 X/46 XY karyotype and aortic coarctation.

Büyükgebiz A, Oren H, Unsal E, Akçoral A, Ozen E, Sakizli M. Büyükgebiz A, et al. Among authors: sakizli m. J Pediatr Endocrinol. 1993 Apr-Jun;6(2):191-6. J Pediatr Endocrinol. 1993. PMID: 8348224

9

beta-catenin gene mutation in invasive ductal breast cancer.

Kizildag S, Zengel B, Vardar E, Sakizli M. Kizildag S, et al. Among authors: sakizli m. J BUON. 2008 Oct-Dec;13(4):533-6. J BUON. 2008. PMID: 19145675

10

Consistent loss of heterozygosity at 14Q32 in lymphoid blast crisis of chronic myeloid leukemia.

Sercan HO, Sercan ZY, Kizildag S, Undar B, Soydan S, Sakizli M. Sercan HO, et al. Among authors: sakizli m. Leuk Lymphoma. 2000 Oct;39(3-4):385-90. doi: 10.3109/10428190009065838. Leuk Lymphoma. 2000. PMID: 11342319

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

34 results

Search Page

Filters