Menke C - Search Results

1

Differential requirements of tubulin genes in mammalian forebrain development.

Bittermann E, Abdelhamed Z, Liegel RP, Menke C, Timms A, Beier DR, Stottmann RW. Bittermann E, et al. Among authors: menke c. PLoS Genet. 2019 Aug 6;15(8):e1008243. doi: 10.1371/journal.pgen.1008243. eCollection 2019 Aug. PLoS Genet. 2019. PMID: 31386652 Free PMC article.

2

The mouse MC13 mutant is a novel ENU mutation in collagen type II, alpha 1.

Cionni M, Menke C, Stottmann RW. Cionni M, et al. Among authors: menke c. PLoS One. 2014 Dec 26;9(12):e116104. doi: 10.1371/journal.pone.0116104. eCollection 2014. PLoS One. 2014. PMID: 25541700 Free PMC article.

3

Grhl2 is required in nonneural tissues for neural progenitor survival and forebrain development.

Menke C, Cionni M, Siggers T, Bulyk ML, Beier DR, Stottmann RW. Menke C, et al. Genesis. 2015 Sep;53(9):573-582. doi: 10.1002/dvg.22875. Epub 2015 Jul 22. Genesis. 2015. PMID: 26177923 Free PMC article.

4

Novel genetic tools facilitate the study of cortical neuron migration.

Cionni M, Menke C, Stottmann RW. Cionni M, et al. Among authors: menke c. Mamm Genome. 2016 Feb;27(1-2):8-16. doi: 10.1007/s00335-015-9615-6. Epub 2015 Dec 12. Mamm Genome. 2016. PMID: 26662625 Free PMC article.

5

A Novel Mutation in Cse1l Disrupts Brain and Eye Development with Specific Effects on Pax6 Expression.

Blizzard LE, Menke C, Patel SD, Waclaw RR, Lachke SA, Stottmann RW. Blizzard LE, et al. Among authors: menke c. J Dev Biol. 2021 Jul 7;9(3):27. doi: 10.3390/jdb9030027. J Dev Biol. 2021. PMID: 34287339 Free PMC article.

6

Successful therapeutic intervention in new mouse models of frizzled 2-associated congenital malformations.

Liegel RP, Michalski MN, Vaidya S, Bittermann E, Finnerty E, Menke CA, Diegel CR, Zhong ZA, Williams BO, Stottmann RW. Liegel RP, et al. Among authors: menke ca. Development. 2023 Feb 1;150(3):dev201038. doi: 10.1242/dev.201038. Epub 2023 Feb 15. Development. 2023. PMID: 36789910 Free PMC article.

7

Understanding and interpretation of a variant of uncertain significance (VUS) genetic test result by pediatric providers who do not specialize in genetics.

Menke C, Nagaraj CB, Dawson B, He H, Tawde S, Wakefield EG. Menke C, et al. J Genet Couns. 2021 Dec;30(6):1559-1569. doi: 10.1002/jgc4.1422. Epub 2021 May 9. J Genet Couns. 2021. PMID: 33969574

8

rAAVrh74.MCK.GALGT2 Demonstrates Safety and Widespread Muscle Glycosylation after Intravenous Delivery in C57BL/6J Mice.

Zygmunt DA, Xu R, Jia Y, Ashbrook A, Menke C, Shao G, Yoon JH, Hamilton S, Pisharath H, Bolon B, Martin PT. Zygmunt DA, et al. Among authors: menke c. Mol Ther Methods Clin Dev. 2019 Oct 21;15:305-319. doi: 10.1016/j.omtm.2019.10.005. eCollection 2019 Dec 13. Mol Ther Methods Clin Dev. 2019. PMID: 31890730 Free PMC article.

9

Clinical genetic counselors' use of people- and identity-first language in regard to patients' identification with disability.

Lepard T, Dugan M, Cleveland E, Menke C. Lepard T, et al. Among authors: menke c. J Genet Couns. 2024 Sep 11. doi: 10.1002/jgc4.1972. Online ahead of print. J Genet Couns. 2024. PMID: 39262055

10

Pull-Out Strength of Orthodontic Miniscrews in the Temporal Bone.

Menke C, Kluge M, Welke B, Lenarz T, Majdani O, S Rau T. Menke C, et al. J Otolaryngol Head Neck Surg. 2024 Jan-Dec;53:19160216241248669. doi: 10.1177/19160216241248669. J Otolaryngol Head Neck Surg. 2024. PMID: 38903014 Free PMC article.

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