Abad C - Search Results

1

Fatal septicemia in 2 South American camelids with caudal C3-pyloric-duodenal adenocarcinoma.

Abad C, Fritz H, Gonzales-Viera O. Abad C, et al. J Vet Diagn Invest. 2024 May;36(3):473-476. doi: 10.1177/10406387241239920. Epub 2024 Mar 23. J Vet Diagn Invest. 2024. PMID: 38520120

2

Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development.

Bademci G, Abad C, Cengiz FB, Seyhan S, Incesulu A, Guo S, Fitoz S, Atli EI, Gosstola NC, Demir S, Colbert BM, Seyhan GC, Sineni CJ, Duman D, Gurkan H, Morton CC, Dykxhoorn DM, Walz K, Tekin M. Bademci G, et al. Among authors: abad c. J Clin Invest. 2020 Aug 3;130(8):4213-4217. doi: 10.1172/JCI136951. J Clin Invest. 2020. PMID: 32369452 Free PMC article.

3

Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning.

Abad C, Robayo MC, Muñiz-Moreno MDM, Bernardi MT, Otero MG, Kosanovic C, Griswold AJ, Pierson TM, Walz K, Young JI. Abad C, et al. Transl Psychiatry. 2024 Jan 18;14(1):33. doi: 10.1038/s41398-023-02678-x. Transl Psychiatry. 2024. PMID: 38238293 Free PMC article.

4

SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights.

Rebelo AP, Abad C, Dohrn MF, Li JJ, Tieu EK, Medina J, Yanick C, Huang J, Zotter B, Young JI, Saporta M, Scherer SS, Walz K, Zuchner S. Rebelo AP, et al. Among authors: abad c. Brain. 2024 Mar 27:awae079. doi: 10.1093/brain/awae079. Online ahead of print. Brain. 2024. PMID: 38538210

5

Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction.

Foster J 2nd, Kapoor S, Diaz-Horta O, Singh A, Abad C, Rastogi A, Moharana R, Tekeli O, Walz K, Tekin M. Foster J 2nd, et al. Among authors: abad c. Clin Genet. 2014 Dec;86(6):589-91. doi: 10.1111/cge.12321. Epub 2013 Dec 27. Clin Genet. 2014. PMID: 24372406 No abstract available.

6

Bromodomain Protein BRD4 Is Essential for Hair Cell Function and Survival.

Kannan-Sundhari A, Abad C, Maloof ME, Ayad NG, Young JI, Liu XZ, Walz K. Kannan-Sundhari A, et al. Among authors: abad c. Front Cell Dev Biol. 2020 Sep 8;8:576654. doi: 10.3389/fcell.2020.576654. eCollection 2020. Front Cell Dev Biol. 2020. PMID: 33015071 Free PMC article.

7

Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2.

Ramzan M, Zafeer MF, Abad C, Guo S, Owrang D, Alper O, Mutlu A, Atik T, Duman D, Bademci G, Vona B, Kalcioglu MT, Walz K, Tekin M. Ramzan M, et al. Among authors: abad c. Eur J Hum Genet. 2024 Feb 19. doi: 10.1038/s41431-024-01562-6. Online ahead of print. Eur J Hum Genet. 2024. PMID: 38374469

8

Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome.

Camarena V, Cao L, Abad C, Abrams A, Toledo Y, Araki K, Araki M, Walz K, Young JI. Camarena V, et al. Among authors: abad c. EMBO Mol Med. 2014 Aug;6(8):1003-15. doi: 10.15252/emmm.201404044. EMBO Mol Med. 2014. PMID: 25001218 Free PMC article.

9

Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice.

Rao NR, Abad C, Perez IC, Srivastava AK, Young JI, Walz K. Rao NR, et al. Among authors: abad c. Biology (Basel). 2017 Apr 27;6(2):25. doi: 10.3390/biology6020025. Biology (Basel). 2017. PMID: 28448442 Free PMC article.

10

FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing.

Diaz-Horta O, Subasioglu-Uzak A, Grati M, DeSmidt A, Foster J 2nd, Cao L, Bademci G, Tokgoz-Yilmaz S, Duman D, Cengiz FB, Abad C, Mittal R, Blanton S, Liu XZ, Farooq A, Walz K, Lu Z, Tekin M. Diaz-Horta O, et al. Among authors: abad c. Proc Natl Acad Sci U S A. 2014 Jul 8;111(27):9864-8. doi: 10.1073/pnas.1401950111. Epub 2014 Jun 23. Proc Natl Acad Sci U S A. 2014. PMID: 24958875 Free PMC article.

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