Search Results

1 - 4 of 4 items :

  • Clinical Medicine, other x
  • Education, other x
Clear All
Genetic, Genomic and Epigenomic Studies of Balkan Endemic Nephropathy (Ben)

, HSPG2 and KCNK5 as candida te-genes for predisposition to Balkan Endemic Nephropathy. BioMed Res Int. 2014; 1-7, doi: 10.1155/2014/920723 19. Shen, L, et al. Genome-wide profiling of DNA methylation reveals a class of normally methylated CpG island promoters. PLoS Genet. 2007; 3(10): p. 2023-36. 20. Weinhold B. Epigenetics: the science of change. Environ Health Perspect. 2006; 114(3): p. A160-7. 21. Bjornsson H.T, et al. Intra-individual change over time in DNA methylation with familial clustering. JAMA, 2008; 299

Open access
in PRILOZI
Emanuel Syndrome (Es): New Case-Report and Review of the Literature/ Емануел Синдром (Es): Презентација На Нов Случај И Преглед На Литературата

(1): 46-51. 3. Liehr T, Claussen U, Starke H. Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res. 2004; 107: 55-67. 4. Fraccaro M, Lindsten J, Ford C. E, Iselius L. The 11q;22q translocation: a European collaborative analysis of 43 cases. Human Genetics.1980; 56(1): 21-51. 5. Zackai E. H, Emanuel B. S. Site-specific reciprocal translocation, t(11;22)(q23;q11), in several unrelated families with 3:1 meiotic disjunction. Am J Med Genet. 1980; 7: 507-21. 6. Medne L, Zackai E. H

Open access
in PRILOZI
Obesity in Childhood and Adolescence, Genetic Factors

;2014(1):21. 33. Turan S, Bastepe M. GNAS spectrum of disorders. Curr Osteoporos Rep. 2015;13(3):146-158. 34. Levine MA. An update on the clinical and molecular characteristics of pseudohypoparathyroidism. Curr Opi Endocrinol Diabetes Obes. 2012;19(6):443-451. 35. Rivera-Brugues N, Albrecht B, Wieczorek D, et al. Cohen syndrome diagnosis using whole genome arrays. J Med Genet. 2011;48(2):136-140. 36. Kolehmainen J, Black GC, Saarinen A, et al. Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in

Open access
in PRILOZI
Expression of p53 Protein Product in Triple Negative Breast Cancers and Relation with Clinical and Histopathological Parameters/ Експресија На Р53 Протеинскиот Продукт Кај Тројно Негативните Карциноми На Дојка Во Сооднос Со Клиничките И Хистопатолошките Параметри

, Earp HS, Millikan RC. Race, breast cancer subtypes, and survival in the Carolina Breast cancer Study. JAMA. 2006; 295(21): 2492-2502. 15. Voduc KD, Cheang MC, Tyldesley S, Gelmon K, Nielsen TO, Kennecke H. Breast cancer subtypes and the risk of local and regional relapse. J Clin Oncol. 2010; 28(10): 1684-1691. 16. Carey LA. Molecular intrinsic subtypes of breast cancer. In: UpToDate. Hayes DF, Dizon DS, eds. Waltham, MA: UpToDate; 2012. p. 77-84. 17. Cancer Genome Atlas Network. Comprehensive molecular portraits of

Open access
in PRILOZI