21. A fruitless upstream region that defines the species specificity in the male-specific muscle patterning in Drosophila. (March 2015) Authors: Takayanagi, Sakino; Toba, Gakuta; Lukacsovich, Tamas; Ote, Manabu; Sato, Kosei; Yamamoto, Daisuke Journal: Journal of neurogenetics Issue: Volume 29:Number 1(2015) Page Start: 23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
22. A gain-of-function mutation in the GRIK2 gene causes neurodevelopmental deficits. (February 2017) Authors: Guzmán, Yomayra F.; Ramsey, Keri; Stolz, Jacob R.; Craig, David W.; Huentelman, Mathew J.; Narayanan, Vinodh; Swanson, Geoffrey T. Journal: Neurology Issue: Volume 3:Number 1(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
23. A journey to 'tame a small metazoan organism', ‡ seen through the artistic eyes of C. elegans researchers. (1st October 2020) Authors: Gourgou, Eleni; Willis, Alexandra R.; Giunti, Sebastian; De Rosa, Maria J.; Charlesworth, Amanda G.; Hernandez Lima, Mirella; Glater, Elizabeth; Soo, Sonja; Pereira, Bianca; Akbaş, Kübra; Deb, Anushka; Kamak, Madhushree; Moyle, Mark W.; Traa, Annika; Singhvi, Aakanksha; Sural, Surojit; Jin, Eugen... Journal: Journal of neurogenetics Issue: Volume 34:Number 3/4(2020) Page Start: 549 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
24. A latitudinal cline in a courtship song character of Drosophila melanogaster. (3rd July 2021) Authors: Stanley, Rosamund A.; Kyriacou, Charalambos P. Journal: Journal of neurogenetics Issue: Volume 35:Number 3(2021) Page Start: 333 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
25. A look inside the Atwood lab. (3rd July 2018) Authors: Dason, Jeffrey S.; Hegström-Wojtowicz, Marianne; Sokolowski, Marla B. Journal: Journal of neurogenetics Issue: Volume 32:Number 3(2018) Page Start: 279 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
26. A lot of nexts: Next-generation sequencing, databases, and neurologists. (August 2015) Authors: Pulst, Stefan M. Journal: Neurology Issue: Volume 1:Number 2(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
27. A New Case With Cortical Malformation Caused by Biallelic Variants in LAMC3. (9th June 2022) Authors: Abe, Kazuo; Ando, Kumiko; Kato, Mitsuhiro; Saitsu, Hirotomo; Nakashima, Mitsuko; Aoki, Shintaro; Kimura, Takashi Journal: Neurology Issue: Volume 8:Number 3(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
28. A new dawn for genetic association studies in multiple sclerosis. (August 2016) Authors: Kantarci, Orhun H. Journal: Neurology Issue: Volume 2:Number 4(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
29. A novel de novo mutation in the TSC2 gene in a Chinese patient with tuberous sclerosis complex. (1st October 2016) Authors: Li, Wenzao; Zhou, Peng; Zhao, Congmin; Zhang, Yuping Journal: Journal of neurogenetics Issue: Volume 31:Number 1/2(2017) Page Start: 285 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
30. A novel DYNC1H1 mutation causing spinal muscular atrophy with lower extremity predominance. (August 2015) Authors: Niu, Qi; Wang, Xingxia; Shi, Mingchao; Jin, Qingwen Journal: Neurology Issue: Volume 1:Number 2(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗