Zaqout S - Search Results

1

Altered inhibition and excitation in neocortical circuits in congenital microcephaly.

Zaqout S, Blaesius K, Wu YJ, Ott S, Kraemer N, Becker LL, Rosário M, Rosenmund C, Strauss U, Kaindl AM. Zaqout S, et al. Neurobiol Dis. 2019 Sep;129:130-143. doi: 10.1016/j.nbd.2019.05.008. Epub 2019 May 15. Neurobiol Dis. 2019. PMID: 31102767

2

Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytes.

Kraemer N, Ravindran E, Zaqout S, Neubert G, Schindler D, Ninnemann O, Gräf R, Seiler AE, Kaindl AM. Kraemer N, et al. Among authors: zaqout s. Cell Cycle. 2015;14(13):2044-57. doi: 10.1080/15384101.2015.1044169. Cell Cycle. 2015. PMID: 25942099 Free PMC article.

3

Golgi-Cox Staining Step by Step.

Zaqout S, Kaindl AM. Zaqout S, et al. Front Neuroanat. 2016 Mar 31;10:38. doi: 10.3389/fnana.2016.00038. eCollection 2016. Front Neuroanat. 2016. PMID: 27065817 Free PMC article.

4

CDK5RAP2 Is Required to Maintain the Germ Cell Pool during Embryonic Development.

Zaqout S, Bessa P, Krämer N, Stoltenburg-Didinger G, Kaindl AM. Zaqout S, et al. Stem Cell Reports. 2017 Feb 14;8(2):198-204. doi: 10.1016/j.stemcr.2017.01.002. Epub 2017 Feb 2. Stem Cell Reports. 2017. PMID: 28162995 Free PMC article.

5

Autosomal Recessive Primary Microcephaly (MCPH): An Update.

Zaqout S, Morris-Rosendahl D, Kaindl AM. Zaqout S, et al. Neuropediatrics. 2017 Jun;48(3):135-142. doi: 10.1055/s-0037-1601448. Epub 2017 Apr 11. Neuropediatrics. 2017. PMID: 28399591 Review.

6

Congenital microcephaly-linked CDK5RAP2 affects eye development.

Zaqout S, Ravindran E, Stoltenburg-Didinger G, Kaindl AM. Zaqout S, et al. Ann Hum Genet. 2020 Jan;84(1):87-91. doi: 10.1111/ahg.12343. Epub 2019 Jul 29. Ann Hum Genet. 2020. PMID: 31355417

7

The murine ortholog of Kaufman oculocerebrofacial syndrome protein Ube3b regulates synapse number by ubiquitinating Ppp3cc.

Ambrozkiewicz MC, Borisova E, Schwark M, Ripamonti S, Schaub T, Smorodchenko A, Weber AI, Rhee HJ, Altas B, Yilmaz R, Mueller S, Piepkorn L, Horan ST, Straussberg R, Zaqout S, Jahn O, Dere E, Rosário M, Boehm-Sturm P, Borck G, Willig KI, Rhee J, Tarabykin V, Kawabe H. Ambrozkiewicz MC, et al. Among authors: zaqout s. Mol Psychiatry. 2021 Jun;26(6):1980-1995. doi: 10.1038/s41380-020-0714-8. Epub 2020 Apr 6. Mol Psychiatry. 2021. PMID: 32249816

8

Abnormal brain structure and behavior in MyD88-deficient mice.

Schroeder P, Rivalan M, Zaqout S, Krüger C, Schüler J, Long M, Meisel A, Winter Y, Kaindl AM, Lehnardt S. Schroeder P, et al. Among authors: zaqout s. Brain Behav Immun. 2021 Jan;91:181-193. doi: 10.1016/j.bbi.2020.09.024. Epub 2020 Sep 28. Brain Behav Immun. 2021. PMID: 33002631

9

Immunofluorescence Staining of Paraffin Sections Step by Step.

Zaqout S, Becker LL, Kaindl AM. Zaqout S, et al. Front Neuroanat. 2020 Nov 9;14:582218. doi: 10.3389/fnana.2020.582218. eCollection 2020. Front Neuroanat. 2020. PMID: 33240048 Free PMC article.

10

Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability.

Ravindran E, Gutierrez de Velazco C, Ghazanfar A, Kraemer N, Zaqout S, Waheed A, Hanif M, Mughal S, Prigione A, Li N, Fang X, Hu H, Kaindl AM. Ravindran E, et al. Among authors: zaqout s. J Med Genet. 2022 May;59(5):453-461. doi: 10.1136/jmedgenet-2020-107518. Epub 2021 May 31. J Med Genet. 2022. PMID: 34059554 Free PMC article.

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