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Wu Lin

Showing results (651-660 of 660) with videos related to

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Plos One|March 21, 2015
Clinical and prognostic implications of Roundabout 4 (robo4) in adult patients with acute myeloid leukemiaYin-Kai Chen, Hsin-An Hou, Jih-Luh Tang, et al.
American Journal of Human Genetics|December 7, 2015
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin SyndromeLindsay C Burrage, Wu-Lin Charng, Mohammad K Eldomery, et al.
The Journal of Clinical Investigation|January 10, 2015
Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypesBo Yuan, Davut Pehlivan, Ender Karaca, et al.
American Journal of Human Genetics|December 27, 2016
Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial DysmorphismFrederike Leonie Harms, Katta M Girisha, Andrew A Hardigan, et al.
Genome Medicine|November 2, 2016
MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile deathMohammad K Eldomery, Zeynep C Akdemir, F-Nora Vögtle, et al.
Cell|September 27, 2014
A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseasesShinya Yamamoto, Manish Jaiswal, Wu-Lin Charng, et al.
The Journal of Physical Chemistry Letters|April 8, 2017
Performance Characterization of Dye-Sensitized Photovoltaics under Indoor LightingChia-Yuan Chen, Zih-Hong Jian, Shih-Han Huang, et al.
Nature Communications|December 26, 2022
Diverse monogenic subforms of human spermatogenic failureLiina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, et al.
American Journal of Human Genetics|July 27, 2021
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in DrosophilaLindsey D Goodman, Heidi Cope, Zelha Nil, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Pageof 66

Showing results (651-660 of 660) with videos related to

Sort By:
Pageof 66
You have reached the last page of results.This site can display upto 660 results.
Plos One|March 21, 2015
Clinical and prognostic implications of Roundabout 4 (robo4) in adult patients with acute myeloid leukemiaYin-Kai Chen, Hsin-An Hou, Jih-Luh Tang, et al.
American Journal of Human Genetics|December 7, 2015
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin SyndromeLindsay C Burrage, Wu-Lin Charng, Mohammad K Eldomery, et al.
The Journal of Clinical Investigation|January 10, 2015
Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypesBo Yuan, Davut Pehlivan, Ender Karaca, et al.
American Journal of Human Genetics|December 27, 2016
Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial DysmorphismFrederike Leonie Harms, Katta M Girisha, Andrew A Hardigan, et al.
Genome Medicine|November 2, 2016
MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile deathMohammad K Eldomery, Zeynep C Akdemir, F-Nora Vögtle, et al.
Cell|September 27, 2014
A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseasesShinya Yamamoto, Manish Jaiswal, Wu-Lin Charng, et al.
The Journal of Physical Chemistry Letters|April 8, 2017
Performance Characterization of Dye-Sensitized Photovoltaics under Indoor LightingChia-Yuan Chen, Zih-Hong Jian, Shih-Han Huang, et al.
Nature Communications|December 26, 2022
Diverse monogenic subforms of human spermatogenic failureLiina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, et al.
American Journal of Human Genetics|July 27, 2021
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in DrosophilaLindsey D Goodman, Heidi Cope, Zelha Nil, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Pageof 66