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Development (Cambridge, England)
|
July 8, 2005
Mind bomb 1 is essential for generating functional Notch ligands to activate Notch
Bon-Kyoung Koo, Hyoung-Soo Lim, Ran Song, et al.
Molecular Psychiatry
|
September 29, 2020
Regulation of habenular G-protein gamma 8 on learning and memory via modulation of the central acetylcholine system
Hyun-Ju Lee, Tae-Ik Choi, Yong-Min Kim, et al.
The Journal of Biological Chemistry
|
January 21, 2011
Crystal structure of the human N-Myc downstream-regulated gene 2 protein provides insight into its role as a tumor suppressor
Jungwon Hwang, Yoonjeong Kim, Ho Bum Kang, et al.
Gastroenterology
|
July 31, 2012
Inhibition of MKK7-JNK by the TOR signaling pathway regulator-like protein contributes to resistance of HCC cells to TRAIL-induced apoptosis
In Sung Song, Soo Young Jun, Hee-Jun Na, et al.
Nature Biotechnology
|
September 15, 2015
Optogenetic control of endogenous Ca(2+) channels in vivo
Taeyoon Kyung, Sangkyu Lee, Jung Eun Kim, et al.
EMBO Reports
|
December 22, 2017
WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome
Yeon-Joo Kim, Daniel Ps Osborn, Ji-Young Lee, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
October 5, 2024
RFC2 may contribute to the pathogenicity of Williams syndrome revealed in a zebrafish model
Ji-Won Park, Tae-Ik Choi, Tae-Yoon Kim, et al.
Molecular Autism
|
October 13, 2017
Zebrafish knockout of Down syndrome gene, <i>DYRK1A</i>, shows social impairments relevant to autism
Oc-Hee Kim, Hyun-Ju Cho, Enna Han, et al.
Research Square
|
April 10, 2023
A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome
Afif Ben-Mahmoud, Shotaro Kishikawa, Vijay Gupta, et al.
Human Mutation
|
April 14, 2025
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of <i>PGAP2</i> Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)
Seda Susgun, Afif Ben-Mahmoud, Franz Rüschendorf, et al.
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Search research articles
Search
Showing results (191-200 of 225) with videos related to
Sort By:
Page
of 23
Development (Cambridge, England)
|
July 8, 2005
Mind bomb 1 is essential for generating functional Notch ligands to activate Notch
Bon-Kyoung Koo, Hyoung-Soo Lim, Ran Song, et al.
Molecular Psychiatry
|
September 29, 2020
Regulation of habenular G-protein gamma 8 on learning and memory via modulation of the central acetylcholine system
Hyun-Ju Lee, Tae-Ik Choi, Yong-Min Kim, et al.
The Journal of Biological Chemistry
|
January 21, 2011
Crystal structure of the human N-Myc downstream-regulated gene 2 protein provides insight into its role as a tumor suppressor
Jungwon Hwang, Yoonjeong Kim, Ho Bum Kang, et al.
Gastroenterology
|
July 31, 2012
Inhibition of MKK7-JNK by the TOR signaling pathway regulator-like protein contributes to resistance of HCC cells to TRAIL-induced apoptosis
In Sung Song, Soo Young Jun, Hee-Jun Na, et al.
Nature Biotechnology
|
September 15, 2015
Optogenetic control of endogenous Ca(2+) channels in vivo
Taeyoon Kyung, Sangkyu Lee, Jung Eun Kim, et al.
EMBO Reports
|
December 22, 2017
WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome
Yeon-Joo Kim, Daniel Ps Osborn, Ji-Young Lee, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
October 5, 2024
RFC2 may contribute to the pathogenicity of Williams syndrome revealed in a zebrafish model
Ji-Won Park, Tae-Ik Choi, Tae-Yoon Kim, et al.
Molecular Autism
|
October 13, 2017
Zebrafish knockout of Down syndrome gene, <i>DYRK1A</i>, shows social impairments relevant to autism
Oc-Hee Kim, Hyun-Ju Cho, Enna Han, et al.
Research Square
|
April 10, 2023
A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome
Afif Ben-Mahmoud, Shotaro Kishikawa, Vijay Gupta, et al.
Human Mutation
|
April 14, 2025
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of <i>PGAP2</i> Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)
Seda Susgun, Afif Ben-Mahmoud, Franz Rüschendorf, et al.
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of 23