Ahrens-Nicklas RC - Search Results

1

Postnatal Arx transcriptional activity regulates functional properties of PV interneurons.

Joseph DJ, Von Deimling M, Hasegawa Y, Cristancho AG, Ahrens-Nicklas RC, Rogers SL, Risbud R, McCoy AJ, Marsh ED. Joseph DJ, et al. iScience. 2020 Dec 28;24(1):101999. doi: 10.1016/j.isci.2020.101999. eCollection 2021 Jan 22. iScience. 2020. PMID: 33490907 Free PMC article.

2

NeuroTri2-VISDOT: An open-access tool to harness the power of second trimester human single cell data to inform models of Mendelian neurodevelopmental disorders.

Clark KJ, Lubin EE, Gonzalez EM, Sangree AK, Layo-Carris DE, Durham EL, Ahrens-Nicklas RC, Nomakuchi TT, Bhoj EJ. Clark KJ, et al. bioRxiv [Preprint]. 2024 Feb 4:2024.02.01.578438. doi: 10.1101/2024.02.01.578438. bioRxiv. 2024. PMID: 38352329 Free PMC article. Preprint.

3

Lmod2 is necessary for effective skeletal muscle contraction.

Larrinaga TM, Farman GP, Mayfield RM, Yuen M, Ahrens-Nicklas RC, Cooper ST, Pappas CT, Gregorio CC. Larrinaga TM, et al. Among authors: ahrens nicklas rc. Sci Adv. 2024 Mar 15;10(11):eadk1890. doi: 10.1126/sciadv.adk1890. Epub 2024 Mar 13. Sci Adv. 2024. PMID: 38478604 Free PMC article.

4

Molecular annotation of integrative feeding neural circuits.

Pérez CA, Stanley SA, Wysocki RW, Havranova J, Ahrens-Nicklas R, Onyimba F, Friedman JM. Pérez CA, et al. Cell Metab. 2011 Feb 2;13(2):222-32. doi: 10.1016/j.cmet.2010.12.013. Cell Metab. 2011. PMID: 21284989 Free PMC article.

5

Leiomodin 2 neonatal dilated cardiomyopathy mutation results in altered actin gene signatures and cardiomyocyte dysfunction.

Iwanski JB, Pappas CT, Mayfield RM, Farman GP, Ahrens-Nicklas R, Churko JM, Gregorio CC. Iwanski JB, et al. NPJ Regen Med. 2024 Sep 16;9(1):21. doi: 10.1038/s41536-024-00366-y. NPJ Regen Med. 2024. PMID: 39285234 Free PMC article.

6

Precision therapy for a new disorder of AMPA receptor recycling due to mutations in ATAD1.

Ahrens-Nicklas RC, Umanah GK, Sondheimer N, Deardorff MA, Wilkens AB, Conlin LK, Santani AB, Nesbitt A, Juulsola J, Ma E, Dawson TM, Dawson VL, Marsh ED. Ahrens-Nicklas RC, et al. Neurol Genet. 2017 Feb 1;3(1):e130. doi: 10.1212/NXG.0000000000000130. eCollection 2017 Feb. Neurol Genet. 2017. PMID: 28180185 Free PMC article.

7

Neuronal network dysfunction precedes storage and neurodegeneration in a lysosomal storage disorder.

Ahrens-Nicklas RC, Tecedor L, Hall AF, Lysenko E, Cohen AS, Davidson BL, Marsh ED. Ahrens-Nicklas RC, et al. JCI Insight. 2019 Nov 1;4(21):e131961. doi: 10.1172/jci.insight.131961. JCI Insight. 2019. PMID: 31573978 Free PMC article.

8

Neuronal genetic rescue normalizes brain network dynamics in a lysosomal storage disorder despite persistent storage accumulation.

Ahrens-Nicklas RC, Tecedor L, Hall AF, Kane O, Chung RJ, Lysenko E, Marsh ED, Stein CS, Davidson BL. Ahrens-Nicklas RC, et al. Mol Ther. 2022 Jul 6;30(7):2464-2473. doi: 10.1016/j.ymthe.2022.03.025. Epub 2022 Apr 5. Mol Ther. 2022. PMID: 35395398 Free PMC article.

9

ECHS1 Deficiency as a Cause of Severe Neonatal Lactic Acidosis.

Ganetzky RD, Bloom K, Ahrens-Nicklas R, Edmondson A, Deardorff MA, Bennett MJ, Ficicioglu C. Ganetzky RD, et al. JIMD Rep. 2016;30:33-37. doi: 10.1007/8904_2016_538. Epub 2016 Feb 27. JIMD Rep. 2016. PMID: 26920905 Free PMC article.

10

Utility of genetic evaluation in infants with congenital heart defects admitted to the cardiac intensive care unit.

Ahrens-Nicklas RC, Khan S, Garbarini J, Woyciechowski S, D'Alessandro L, Zackai EH, Deardorff MA, Goldmuntz E. Ahrens-Nicklas RC, et al. Am J Med Genet A. 2016 Dec;170(12):3090-3097. doi: 10.1002/ajmg.a.37891. Epub 2016 Sep 8. Am J Med Genet A. 2016. PMID: 27605484

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

70 results

Search Page

Filters