Lozic B - Search Results

1

Bardet-Biedl syndrome caused by compound heterozygosity in BBS12 gene: a case report of one family with three affected members.

Simičić Majce A, Tudor D, Simunovic M, Todorovic M, Parlov M, Lozic B, Saraga-Babić M, Saraga M, Arapović A. Simičić Majce A, et al. Among authors: lozic b. Front Pediatr. 2023 Jul 4;11:1226595. doi: 10.3389/fped.2023.1226595. eCollection 2023. Front Pediatr. 2023. PMID: 37469681 Free PMC article.

2

Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia.

Sansović I, Meašić AM, Bobinec A, Morožin Pohovski L, Odak L, Vulin K, Lozić B, Kero M, Huljev Frković S, Pušeljić S. Sansović I, et al. Among authors: lozic b. Croat Med J. 2024 Jun 13;65(3):198-208. doi: 10.3325/cmj.2024.65.198. Croat Med J. 2024. PMID: 38868966 Free PMC article.

3

Correction: SPRTN is involved in hepatocellular carcinoma development through the ER stress response.

Batel A, Polović M, Glumac M, Šuman O, Jadrijević S, Lozić B, Petrović M, Samardžija B, Bradshaw NJ, Skube K, Palada V, Acman M, Marinović Terzić I. Batel A, et al. Among authors: lozic b. Cancer Gene Ther. 2024 May;31(5):802-804. doi: 10.1038/s41417-024-00772-w. Cancer Gene Ther. 2024. PMID: 38600122 No abstract available.

4

SPRTN is involved in hepatocellular carcinoma development through the ER stress response.

Batel A, Polović M, Glumac M, Šuman O, Jadrijević S, Lozić B, Petrović M, Samardžija B, Bradshaw NJ, Skube K, Palada V, Acman M, Marinović Terzić I. Batel A, et al. Among authors: lozic b. Cancer Gene Ther. 2024 Mar;31(3):376-386. doi: 10.1038/s41417-023-00708-w. Epub 2023 Dec 12. Cancer Gene Ther. 2024. PMID: 38086993

5

Oculo-facio-cardio-dental syndrome in three succeeding generations: genotypic data and phenotypic features.

Lozić B, Ljubković J, Pandurić DG, Saltvig I, Kutsche K, Krželj V, Zemunik T. Lozić B, et al. Braz J Med Biol Res. 2012 Dec;45(12):1315-9. doi: 10.1590/s0100-879x2012007500150. Epub 2012 Sep 18. Braz J Med Biol Res. 2012. PMID: 22983184 Free PMC article.

6

A Novel SETBP1 Gene Disruption by a De Novo Balanced Translocation in a Patient with Speech Impairment, Intellectual, and Behavioral Disorder.

Vrkić Boban I, Sekiguchi F, Lozić M, Miyake N, Matsumoto N, Lozić B. Vrkić Boban I, et al. Among authors: lozic b, lozic m. J Pediatr Genet. 2020 Aug 31;11(2):135-138. doi: 10.1055/s-0040-1715639. eCollection 2022 Jun. J Pediatr Genet. 2020. PMID: 35769969 Free PMC article.

7

Endobronchial ALK+ anaplastic large-cell lymphoma resembling asthma in a 13-year-old girl.

Pavlov N, Pavlov V, Culić S, Armanda V, Siebert R, Lozić B, Forempoher G, Lukšić B, Perić I, Goic-Barisic I. Pavlov N, et al. Among authors: lozic b. J Pediatr Hematol Oncol. 2013 Jan;35(1):e4-6. doi: 10.1097/MPH.0b013e31827076c4. J Pediatr Hematol Oncol. 2013. PMID: 23042012

8

The OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal death.

Lozić B, Krželj V, Kuzmić-Prusac I, Kuzmanić-Šamija R, Čapkun V, Lasan R, Zemunik T. Lozić B, et al. Med Sci Monit. 2014 Aug 28;20:1531-8. doi: 10.12659/MSM.890916. Med Sci Monit. 2014. PMID: 25164089 Free PMC article.

9

Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1.

Karadža-Lapić L, Korošec P, Šilar M, Košnik M, Cikojević D, Lozić B, Rijavec M. Karadža-Lapić L, et al. Among authors: lozic b. Ann Med. 2016 Nov;48(7):485-491. doi: 10.1080/07853890.2016.1185144. Epub 2016 May 17. Ann Med. 2016. PMID: 27187751 Free article.

10

Spatio-Temporal Expression Pattern of CAKUT Candidate Genes DLG1 and KIF12 during Human Kidney Development.

Veljačić Visković D, Lozić M, Vukoja M, Šoljić V, Vukojević K, Glavina Durdov M, Filipović N, Lozić B. Veljačić Visković D, et al. Among authors: lozic b. Biomolecules. 2023 Feb 9;13(2):340. doi: 10.3390/biom13020340. Biomolecules. 2023. PMID: 36830709 Free PMC article.

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