E-LIB Suche - Ergebnisse für: Tischfield, Max A.

1

Human mutations in high-confidence Tourette disorder genes ..:

Nasello, Cara ; Poppi, Lauren A. ; Wu, Junbing...
Proceedings of the National Academy of Sciences. 121 (2024) 19 - p. , 2024

Link: https://doi.org/10.1073/..

2

Mapping the neuroethological signatures of pain, analgesia,..:

Bohic, Manon ; Pattison, Luke A. ; Jhumka, Z. Anissa...
Neuron. 111 (2023) 18 - p. 2811-2830.e8 , 2023

Link: https://doi.org/10.1016/..

3

Piezo1 agonist restores meningeal lymphatic vessels, draina..:

Matrongolo, Matt J. ; Ang, Phillip S. ; Wu, Junbing...
Journal of Clinical Investigation. 134 (2023) 4 - p. , 2023

Link: https://doi.org/10.1172/..

4

Understanding the development, pathogenesis, and injury res..:

Jain, Aditya ; Ang, Phillip S. ; Matrongolo, Matthew J..
Cellular and Molecular Life Sciences. 80 (2023) 11 - p. , 2023

Link: https://doi.org/10.1007/..

5

TWIST1, a gene associated with Saethre-Chotzen syndrome, re..:

Whitman, Mary C. ; Gilette, Nicole M. ; Bell, Jessica L....
Developmental Biology. 490 (2022) - p. 126-133 , 2022

Link: https://doi.org/10.1016/..

6

Planar cell polarity and the pathogenesis of Tourette Disor..:

Wu, Junbing ; Poppi, Lauren A. ; Tischfield, Max A.
Developmental Biology. 489 (2022) - p. 14-20 , 2022

Link: https://doi.org/10.1016/..

7

Recurrent Implication of Striatal Cholinergic Interneurons ..:

Poppi, Lauren A. ; Ho-Nguyen, Khue Tu ; Shi, Anna..
Cells. 10 (2021) 4 - p. 907 , 2021

Link: https://doi.org/10.3390/..

8

Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal..:

Latremoliere, Alban ; Cheng, Long ; DeLisle, Michelle...
Cell Reports. 24 (2018) 7 - p. 1865-1879.e9 , 2018

Link: https://doi.org/10.1016/..

9

Transient Opening of the Mitochondrial Permeability Transit..:

Agarwal, Amit ; Wu, Pei-Hsun ; Hughes, Ethan G....
Neuron. 93 (2017) 3 - p. 587-605.e7 , 2017

Link: https://doi.org/10.1016/..

10

Two unique TUBB3 mutations cause both CFEOM3 and malformati..:

Whitman, Mary C. ; Andrews, Caroline ; Chan, Wai‐Man...
American Journal of Medical Genetics Part A. 170 (2015) 2 - p. 297-305 , 2015

Link: https://doi.org/10.1002/..

11

An inherited TUBB2B mutation alters a kinesin-binding site ..:

Cederquist, Gustav Y. ; Luchniak, Anna ; Tischfield, Max A....
Human Molecular Genetics. 21 (2012) 26 - p. 5484-5499 , 2012

Link: https://doi.org/10.1093/..

12

Phenotypic spectrum of the tubulin-related disorders and fu..:

Tischfield, Max A ; Cederquist, Gustav Y ; Gupta Jr, Mohan L.
Current Opinion in Genetics & Development. 21 (2011) 3 - p. 286-294 , 2011

Link: https://doi.org/10.1016/..

13

Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin..:

Tischfield, Max A. ; Baris, Hagit N. ; Wu, Chen...
Cell. 140 (2010) 1 - p. 74-87 , 2010

Link: https://doi.org/10.1016/..

14

The clinical spectrum of homozygous HOXA1 mutations:

Bosley, Thomas M. ; Alorainy, Ibrahim A. ; Salih, Mustafa A....
American Journal of Medical Genetics Part A. 146A (2008) 10 - p. 1235-1240 , 2008

Link: https://doi.org/10.1002/..

15

HOXA1 mutations are not a common cause of Duane anomaly:

Tischfield, Max A. ; Chan, Wai-Man ; Grunert, Jann-Frederik..
American Journal of Medical Genetics Part A. 140A (2006) 8 - p. 900-902 , 2006

Link: https://doi.org/10.1002/..