Zaqout S - Search Results

1

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.

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

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

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

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

8

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.

9

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.

10

Autosomal Recessive Primary Microcephaly: Not Just a Small Brain.

Zaqout S, Kaindl AM. Zaqout S, et al. Front Cell Dev Biol. 2022 Jan 17;9:784700. doi: 10.3389/fcell.2021.784700. eCollection 2021. Front Cell Dev Biol. 2022. PMID: 35111754 Free PMC article. Review.

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

21 results

Search Page

Filters