Additional file 6: Video 4. of MUNC18–1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development

Additional file 1:Â Supplementary information: of Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model

Denise Haslinger (5940275)
Regina Waltes (184878)
Afsheen Yousaf (5940278)
Silvia Lindlar (5940281)
Ines Schneider (5940284)
Chai Lim (1783117)
Meng-Miao Tsai (5940287)
Boyan Garvalov (5940290)
Amparo Acker-Palmer (3173001)
Nicolas Krezdorn (2573719)
BjĂśrn Rotter (5162456)
Till Acker (4091635)
Gilles Guillemin (3523148)
Simone Fulda (106002)
Christine Freitag (314982)
Andreas Chiocchetti (184869)

November 2018

Supplementary methods, supplementary results, supplementary table S1, supplementary figures S1-S6. (...

Additional file 1: of A novel SLC6A8 mutation associated with intellectual disabilities in a Chinese family exhibiting creatine transporter deficiency: case report

Qin Wang (109812)
Jingxin Yang (5940116)
Yang Liu (4829)
Xingping Li (5940119)
Fuwei Luo (5940122)
Jiansheng Xie (105263)

November 2018

Figure S1. A. Gesell developmental scale evaluated the proband as severely developmentally delayed. ...

Additional file 3: of Modeling hallmark pathology using motor neurons derived from the family and sporadic amyotrophic lateral sclerosis patient-specific iPS cells

Xuejiao Sun (391248)
Jianyuan Song (5980739)
Hailong Huang (1449589)
Hong Chen (108084)
Kun Qian (62517)

November 2018

Video S1. NF-LGFP40X_7_ch1.AVI. NF inclusions in NF-L-GFP merge MN neurites in light microscope (Ăâ...

Additional file 7: of Mutations in dock1 disrupt early Schwann cell development

Rebecca Cunningham (793883)
Amy Herbert (5614991)
Breanne Harty (5614994)
Sarah Ackerman (5614997)
Kelly Monk (4164241)

August 2018

Movie S2. Grayscale single channel movie of Lifeact as seen in Additional file 6: Movie S1. (AVI 648...

Additional file 4: Video 4. of Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex

Nanako Hamada (541246)
Hidenori Ito (637706)
Ikuko Iwamoto (3534455)
Rika Morishita (201737)
Hidenori Tabata (3534458)
Koh-ichi Nagata (538350)

October 2015

Time-lapse imaging of Rbfox1-iso2-defcient neurons migrating in CP.Â The deficient cells exhibited c...

Additional file 1: of Mutations in dock1 disrupt early Schwann cell development

Rebecca Cunningham (793883)
Amy Herbert (5614991)
Breanne Harty (5614994)
Sarah Ackerman (5614997)
Kelly Monk (4164241)

August 2018

Figure S1. A-C) Lateral view of WISH for mbp. Arrowheads indicate the PLLn. Asterisks indicate the C...

Additional file 9: of Mutations in dock1 disrupt early Schwann cell development

Rebecca Cunningham (793883)
Amy Herbert (5614991)
Breanne Harty (5614994)
Sarah Ackerman (5614997)
Kelly Monk (4164241)

August 2018

Movie S4. Grayscale single channel movie of Lifeact as seen in Additional file 8: Movie S3. (AVI 281...

Additional file 6: of Modeling hallmark pathology using motor neurons derived from the family and sporadic amyotrophic lateral sclerosis patient-specific iPS cells

Xuejiao Sun (391248)
Jianyuan Song (5980739)
Hailong Huang (1449589)
Hong Chen (108084)
Kun Qian (62517)

November 2018

Video S4. NF-LGFP40X_7_ch4.AVI. Some mitochondria moved into, rather out of NF inclusions. (AVI 4590...

Additional file 6: of Genetic deletion of genes in the cerebellar rhombic lip lineage can stimulate compensation through adaptive reprogramming of ventricular zone-derived progenitors

Alexandre Wojcinski (6340172)
Morgane Morabito (6340175)
Andrew Lawton (6340178)
Daniel Stephen (6340181)
Alexandra Joyner (3501674)

February 2019

Video S2. PCL NEPs migrate toward the EGL in Atoh1-Gli2 CKO CB at P8. Detection of native CFP fluore...

Additional file 1: of Autism-associated CHD8 deficiency impairs axon development and migration of cortical neurons

Qiong Xu (204847)
Yuan-yuan Liu (2575882)
Xiaoming Wang (187053)
Guo-he Tan (6105170)
Hui-ping Li (6105173)
Samuel Hulbert (6105176)
Chun-yang Li (5049653)
Chun-chun Hu (5049647)
Zhi-qi Xiong (6105179)
Xiu Xu (498635)
Yong-hui Jiang (243375)

December 2018

Validation of rescued constructs against shRNA-mediated knockdown of mouse Chd8 in transfected neuro...

MUNC18–1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development

Nanako Hamada
Ikuko Iwamoto
Hidenori Tabata
Koh-ichi Nagata

November 2017

Abstract While Munc18–1 interacts with Syntaxin1 and controls the formation of soluble N-ethylmaleim...

Additional file 6: of Genome-wide target analysis of NEUROD2 provides new insights into regulation of cortical projection neuron migration and differentiation

Efil Bayam (3519806)
Gulcan Sahin (3519818)
Gizem Guzelsoy (3519809)
Gokhan Guner (3519812)
Alkan Kabakcioglu (3519815)
Gulayse Ince-Dunn (3519821)

September 2015

In this file we provide the list of most significantly represented pathways among NEUROD2 target gen...

Additional file 2: Video 2. of Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex

Nanako Hamada (541246)
Hidenori Ito (637706)
Ikuko Iwamoto (3534455)
Rika Morishita (201737)
Hidenori Tabata (3534458)
Koh-ichi Nagata (538350)

October 2015

Time-lapse imaging of Rbfox1-iso2-defcient neurons stranded in upper IZ to lower CP.Â The deficient ...

Additional file 8: of Microtubule-associated protein 1b is required for shaping the neural tube

Pradeepa Jayachandran (3555338)
Valerie Olmo (3555344)
Stephanie Sanchez (3555326)
Rebecca McFarland (3555341)
Eudorah Vital (3555347)
Jonathan M. Werner (3555332)
Elim Hong (40249)
Neus Sanchez-Alberola (3555335)
Aleksey Molodstov (3555329)
Rachel Brewster (40251)

January 2016

Time lapse imaging of NC in a WT embryo. Time-lapse movie (1 min intervals) of a control, mGFP-label...

Additional file 2: of Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

Hugh McMillan (5280101)
Aida Telegrafi (5520248)
Amanda Singleton (5520269)
Megan Cho (5520251)
Daniel Lelli (5520242)
Francis Lynn (5520272)
Julie Griffin (5520233)
Alexander Asamoah (5520254)
Tuula Rinne (243480)
Corrie Erasmus (5520236)
David Koolen (4706029)
Charlotte Haaxma (5520260)
Boris Keren (374547)
Diane Doummar (1777717)
Cyril Mignot (3416648)
Islay Thompson (5520239)
Lea Velsher (5520257)
Mohammadreza Dehghani (4446685)
Mohammad Vahidi Mehrjardi (5520266)
Reza Maroofian (5237852)
Michel Tchan (5520224)
Cas Simons (36269)
John Christodoulou (450398)
Elena MartĂn-HernĂĄndez (5520302)
Maria Guillen Sacoto (5520227)
Lindsay Henderson (4446877)
Heather McLaughlin (5520263)
Laurie Molday (5520230)
Robert Molday (4167616)
Grace Yoon (802408)

May 2018

Video S1. Patient 1 (age 4Â years old) demonstrates chorea of her head, upper and lower extremities ...

Additional file 1:Â Supplementary information: of Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model

Denise Haslinger (5940275)
Regina Waltes (184878)
Afsheen Yousaf (5940278)
Silvia Lindlar (5940281)
Ines Schneider (5940284)
Chai Lim (1783117)
Meng-Miao Tsai (5940287)
Boyan Garvalov (5940290)
Amparo Acker-Palmer (3173001)
Nicolas Krezdorn (2573719)
BjĂśrn Rotter (5162456)
Till Acker (4091635)
Gilles Guillemin (3523148)
Simone Fulda (106002)
Christine Freitag (314982)
Andreas Chiocchetti (184869)

November 2018

Supplementary methods, supplementary results, supplementary table S1, supplementary figures S1-S6. (...

Additional file 1: of A novel SLC6A8 mutation associated with intellectual disabilities in a Chinese family exhibiting creatine transporter deficiency: case report

Qin Wang (109812)
Jingxin Yang (5940116)
Yang Liu (4829)
Xingping Li (5940119)
Fuwei Luo (5940122)
Jiansheng Xie (105263)

November 2018

Figure S1. A. Gesell developmental scale evaluated the proband as severely developmentally delayed. ...

Additional file 3: of Modeling hallmark pathology using motor neurons derived from the family and sporadic amyotrophic lateral sclerosis patient-specific iPS cells

Xuejiao Sun (391248)
Jianyuan Song (5980739)
Hailong Huang (1449589)
Hong Chen (108084)
Kun Qian (62517)

November 2018

Video S1. NF-LGFP40X_7_ch1.AVI. NF inclusions in NF-L-GFP merge MN neurites in light microscope (Ăâ...

Additional file 7: of Mutations in dock1 disrupt early Schwann cell development

Rebecca Cunningham (793883)
Amy Herbert (5614991)
Breanne Harty (5614994)
Sarah Ackerman (5614997)
Kelly Monk (4164241)

August 2018

Movie S2. Grayscale single channel movie of Lifeact as seen in Additional file 6: Movie S1. (AVI 648...

Additional file 4: Video 4. of Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex

Nanako Hamada (541246)
Hidenori Ito (637706)
Ikuko Iwamoto (3534455)
Rika Morishita (201737)
Hidenori Tabata (3534458)
Koh-ichi Nagata (538350)

October 2015

Time-lapse imaging of Rbfox1-iso2-defcient neurons migrating in CP.Â The deficient cells exhibited c...

Additional file 1: of Mutations in dock1 disrupt early Schwann cell development

Rebecca Cunningham (793883)
Amy Herbert (5614991)
Breanne Harty (5614994)
Sarah Ackerman (5614997)
Kelly Monk (4164241)

August 2018

Figure S1. A-C) Lateral view of WISH for mbp. Arrowheads indicate the PLLn. Asterisks indicate the C...

Additional file 9: of Mutations in dock1 disrupt early Schwann cell development

Rebecca Cunningham (793883)
Amy Herbert (5614991)
Breanne Harty (5614994)
Sarah Ackerman (5614997)
Kelly Monk (4164241)

August 2018

Movie S4. Grayscale single channel movie of Lifeact as seen in Additional file 8: Movie S3. (AVI 281...

Additional file 6: of Modeling hallmark pathology using motor neurons derived from the family and sporadic amyotrophic lateral sclerosis patient-specific iPS cells

Xuejiao Sun (391248)
Jianyuan Song (5980739)
Hailong Huang (1449589)
Hong Chen (108084)
Kun Qian (62517)

November 2018

Video S4. NF-LGFP40X_7_ch4.AVI. Some mitochondria moved into, rather out of NF inclusions. (AVI 4590...

Additional file 6: of Genetic deletion of genes in the cerebellar rhombic lip lineage can stimulate compensation through adaptive reprogramming of ventricular zone-derived progenitors

Alexandre Wojcinski (6340172)
Morgane Morabito (6340175)
Andrew Lawton (6340178)
Daniel Stephen (6340181)
Alexandra Joyner (3501674)

February 2019

Video S2. PCL NEPs migrate toward the EGL in Atoh1-Gli2 CKO CB at P8. Detection of native CFP fluore...

Additional file 1: of Autism-associated CHD8 deficiency impairs axon development and migration of cortical neurons

Qiong Xu (204847)
Yuan-yuan Liu (2575882)
Xiaoming Wang (187053)
Guo-he Tan (6105170)
Hui-ping Li (6105173)
Samuel Hulbert (6105176)
Chun-yang Li (5049653)
Chun-chun Hu (5049647)
Zhi-qi Xiong (6105179)
Xiu Xu (498635)
Yong-hui Jiang (243375)

December 2018

Validation of rescued constructs against shRNA-mediated knockdown of mouse Chd8 in transfected neuro...

MUNC18–1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development

Nanako Hamada
Ikuko Iwamoto
Hidenori Tabata
Koh-ichi Nagata

November 2017

Abstract While Munc18–1 interacts with Syntaxin1 and controls the formation of soluble N-ethylmaleim...

Additional file 6: of Genome-wide target analysis of NEUROD2 provides new insights into regulation of cortical projection neuron migration and differentiation

Efil Bayam (3519806)
Gulcan Sahin (3519818)
Gizem Guzelsoy (3519809)
Gokhan Guner (3519812)
Alkan Kabakcioglu (3519815)
Gulayse Ince-Dunn (3519821)

September 2015

In this file we provide the list of most significantly represented pathways among NEUROD2 target gen...

Additional file 2: Video 2. of Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex

Nanako Hamada (541246)
Hidenori Ito (637706)
Ikuko Iwamoto (3534455)
Rika Morishita (201737)
Hidenori Tabata (3534458)
Koh-ichi Nagata (538350)

October 2015

Time-lapse imaging of Rbfox1-iso2-defcient neurons stranded in upper IZ to lower CP.Â The deficient ...

Additional file 8: of Microtubule-associated protein 1b is required for shaping the neural tube

Pradeepa Jayachandran (3555338)
Valerie Olmo (3555344)
Stephanie Sanchez (3555326)
Rebecca McFarland (3555341)
Eudorah Vital (3555347)
Jonathan M. Werner (3555332)
Elim Hong (40249)
Neus Sanchez-Alberola (3555335)
Aleksey Molodstov (3555329)
Rachel Brewster (40251)

January 2016

Time lapse imaging of NC in a WT embryo. Time-lapse movie (1 min intervals) of a control, mGFP-label...

Additional file 2: of Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

Hugh McMillan (5280101)
Aida Telegrafi (5520248)
Amanda Singleton (5520269)
Megan Cho (5520251)
Daniel Lelli (5520242)
Francis Lynn (5520272)
Julie Griffin (5520233)
Alexander Asamoah (5520254)
Tuula Rinne (243480)
Corrie Erasmus (5520236)
David Koolen (4706029)
Charlotte Haaxma (5520260)
Boris Keren (374547)
Diane Doummar (1777717)
Cyril Mignot (3416648)
Islay Thompson (5520239)
Lea Velsher (5520257)
Mohammadreza Dehghani (4446685)
Mohammad Vahidi Mehrjardi (5520266)
Reza Maroofian (5237852)
Michel Tchan (5520224)
Cas Simons (36269)
John Christodoulou (450398)
Elena MartĂn-HernĂĄndez (5520302)
Maria Guillen Sacoto (5520227)
Lindsay Henderson (4446877)
Heather McLaughlin (5520263)
Laurie Molday (5520230)
Robert Molday (4167616)
Grace Yoon (802408)

May 2018

Video S1. Patient 1 (age 4Â years old) demonstrates chorea of her head, upper and lower extremities ...

Additional file 1:Â Supplementary information: of Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model

Denise Haslinger (5940275)
Regina Waltes (184878)
Afsheen Yousaf (5940278)
Silvia Lindlar (5940281)
Ines Schneider (5940284)
Chai Lim (1783117)
Meng-Miao Tsai (5940287)
Boyan Garvalov (5940290)
Amparo Acker-Palmer (3173001)
Nicolas Krezdorn (2573719)
BjĂśrn Rotter (5162456)
Till Acker (4091635)
Gilles Guillemin (3523148)
Simone Fulda (106002)
Christine Freitag (314982)
Andreas Chiocchetti (184869)

November 2018

Supplementary methods, supplementary results, supplementary table S1, supplementary figures S1-S6. (...

Additional file 1: of A novel SLC6A8 mutation associated with intellectual disabilities in a Chinese family exhibiting creatine transporter deficiency: case report

Qin Wang (109812)
Jingxin Yang (5940116)
Yang Liu (4829)
Xingping Li (5940119)
Fuwei Luo (5940122)
Jiansheng Xie (105263)

November 2018

Figure S1. A. Gesell developmental scale evaluated the proband as severely developmentally delayed. ...

Additional file 3: of Modeling hallmark pathology using motor neurons derived from the family and sporadic amyotrophic lateral sclerosis patient-specific iPS cells

Xuejiao Sun (391248)
Jianyuan Song (5980739)
Hailong Huang (1449589)
Hong Chen (108084)
Kun Qian (62517)

November 2018

Video S1. NF-LGFP40X_7_ch1.AVI. NF inclusions in NF-L-GFP merge MN neurites in light microscope (Ăâ...

Additional file 6: Video 4. of MUNC18–1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development

Abstract

Extracted data

Additional file 6: Video 4. of MUNC18–1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development

Abstract

Extracted data

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