E-LIB Suche - Ergebnisse für: Lehmann, Ordan J.

1

FoxC1 activates limbal epithelial stem cells following corn..:

Yang, Wending ; Lee, Sun Kyong ; Lehmann, Ordan J....
Experimental Eye Research. 234 (2023) - p. 109599 , 2023

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

2

BMP3 is a novel locus involved in the causality of ocular c..:

Fox, Sabrina C. ; Widen, Sonya A. ; Asai-Coakwell, Mika...
Human Genetics. 141 (2022) 8 - p. 1385-1407 , 2022

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

3

The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left..:

Chrystal, Paul W. ; French, Curtis R. ; Jean, Francesca...
Genes. 12 (2021) 2 - p. 170 , 2021

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

4

Genetics and therapy for pediatric eye diseases:

Chen, Holly.Y. ; Lehmann, Ordan J. ; Swaroop, Anand
EBioMedicine. 67 (2021) - p. 103360 , 2021

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

5

Ocular coloboma: Genetic variants reveal a dynamic model of..:

Yoon, Kevin H. ; Fox, Sabrina C. ; Dicipulo, Renée..
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184 (2020) 3 - p. 590-610 , 2020

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

6

foxc1 is required for embryonic head vascular smooth muscle..:

Whitesell, Thomas R. ; Chrystal, Paul W. ; Ryu, Jae-Ryeon...
Developmental Biology. 453 (2019) 1 - p. 34-47 , 2019

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

7

Non-Synonymous variants in premelanosome protein (PMEL) cau..:

Lahola-Chomiak, Adrian A ; Footz, Tim ; Nguyen-Phuoc, Kim...
Human Molecular Genetics. 28 (2018) 8 - p. 1298-1311 , 2018

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

8

Morphogenetic defects underlie Superior Coloboma, a newly i..:

Hocking, Jennifer C. ; Famulski, Jakub K. ; Yoon, Kevin H....
PLOS Genetics. 14 (2018) 3 - p. e1007246 , 2018

Link: https://doi.org/10.1371/..

9

Genetic background-dependent role ofEgr1for eyelid developm..:

Oh, Jangsuk ; Wang, Yujuan ; Chen, Shida...
Proceedings of the National Academy of Sciences. 114 (2017) 34 - p. , 2017

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

10

Genetic background-dependent role of Egr1 for eyelid develo..:

Oh, Jangsuk ; Wang, Yujuan ; Chen, Shida...
Proceedings of the National Academy of Sciences of the United States of America. 114 (2017) 34 - p. E7131-E7139 , 2017

Link: https://www.jstor.org/st..

11

Expanding the ciliopathy spectrum:

Lehmann, Ordan ; Chrystal, Paul ; Waskieiwicz, Andrew.
Mechanisms of Development. 145 (2017) - p. S32-S33 , 2017

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

12

A secreted WNT-ligand-binding domain of FZD5 generated by a..:

Liu, Chunqiao ; Widen, Sonya A. ; Williamson, Kathleen A....
Human Molecular Genetics. 25 (2016) 7 - p. 1382-1391 , 2016

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

13

Sox11 Is Required to Maintain Proper Levels of Hedgehog Sig..:

Pillai-Kastoori, Lakshmi ; Wen, Wen ; Wilson, Stephen G....
PLoS Genetics. 10 (2014) 7 - p. e1004491 , 2014

Link: https://doi.org/10.1371/..

14

Mutations in PIK3R1 Cause SHORT Syndrome:

Dyment, David A. ; Smith, Amanda C. ; Alcantara, Diana...
The American Journal of Human Genetics. 93 (2013) 1 - p. 158-166 , 2013

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

15

Contribution of growth differentiation factor 6-dependent c..:

Asai-Coakwell, Mika ; March, Lindsey ; Dai, Xiao Hua...
Human Molecular Genetics. 22 (2013) 7 - p. 1432-1442 , 2013

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