ATCC American Type Culture Collection

Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors

Varderidou-Minasian, Suzy
Hinz, Lisa
Hagemans, Dominique
Posthuma, Danielle
Altelaar, Maarten
Heine, Vivi M

May 2020

BACKGROUND: Rett syndrome (RTT) is a progressive neurodevelopmental disease that is characterized by...

Quantitative proteomic analysis identifies proteins and pathways related to neuronal development in differentiated SH-SY5Y neuroblastoma cells

Murillo, Jimmy Rodriguez
Goto-Silva, Livia
Sánchez, Aniel
Nogueira, Fábio C.S.
Domont, Gilberto B.
Junqueira, Magno

September 2017

SH-SY5Y neuroblastoma cells are susceptible to differentiation using retinoic acid (RA) and brain-de...

NeuroLINCS Proteomics: Defining human-derived iPSC proteomes and protein signatures of pluripotency

Matlock, Andrea D
Vaibhav, Vineet
Holewinski, Ronald
Venkatraman, Vidya
Dardov, Victoria
Manalo, Danica-Mae
Shelley, Brandon
Ornelas, Loren
Banuelos, Maria
Mandefro, Berhan
Escalante-Chong, Renan
Li, Jonathan
Finkbeiner, Steve
Fraenkel, Ernest
Rothstein, Jeffrey
Thompson, Leslie
Sareen, Dhruv
Svendsen, Clive N
Van Eyk, Jennifer E

January 2023

The National Institute of Health (NIH) Library of integrated network-based cellular signatures (LINC...

Deep proteomic evaluation of primary and cell line motoneuron disease models delineates major differences in neuronal characteristics.

Hornburg, D.
Drepper, C.
Butter, F.
Meissner, F.
Sendtner, M.
Mann, M.

January 2014

The fatal neurodegenerative disorders amyotrophic lateral sclerosis and spinal muscular atrophy are,...

Deep Proteomic Evaluation of Primary and Cell Line Motoneuron Disease Models Delineates Major Differences in Neuronal Characteristics*

Hornburg, Daniel
Drepper, Carsten
Butter, Falk
Meissner, Felix
Sendtner, Michael
Mann, Matthias

January 2014

The fatal neurodegenerative disorders amyotrophic lateral sclerosis and spinal muscular atrophy are,...

Deep Proteomic Evaluation of Primary and Cell Line Motoneuron Disease Models Delineates

Michael Sendtner
Matthias Mann

October 2016

The fatal neurodegenerative disorders amyotrophic lat-eral sclerosis and spinal muscular atrophy are...

2-DE proteomic profiling of neuronal stem cells

Hoffrogge, Raimund
Beyer, Susanne
Völker, Uwe
Uhrmacher, Adelinde
Rolfs, Arndt

January 2006

Hoffrogge R, Beyer S, Völker U, Uhrmacher A, Rolfs A. 2-DE proteomic profiling of neuronal stem cell...

Proteomic analysis of muscle affected by motor neuron degeneration: The wobbler mouse model of amyotrophic lateral sclerosis

Staunton, Lisa
Jockusch, Harald
Ohlendieck, Kay

January 2011

Staunton L, Jockusch H, Ohlendieck K. Proteomic analysis of muscle affected by motor neuron degenera...

Early signs of motoneuron vulnerability in a disease model system: characterization of transverse slice cultures of spinal cord isolated from embryonic ALS mice.

Avossa, D.
Grandolfo, M.
Mazzarol, F.
Zatta, M.
Ballerini, L.

January 2006

Cell types within the G93A slice underwent maturation and slices could be maintained in culture for ...

2-DE proteome analysis of a proliferating and differentiating human neuronal stem cell line (ReNcell VM)

Hoffrogge, Raimund
Mikkat, Stefan
Scharf, Christian
Christoph, Hilmar
Beyer, Susanne
Pahnke, Jens
Mix, Eilhard
Berth, Mathias
Uhrmacher, Adelinde
Zubrzycki, Igor Z.
Miljan, Eric
Völker, Uwe
Rolfs, Arndt

January 2006

Hoffrogge R, Mikkat S, Scharf C, et al. 2-DE proteome analysis of a proliferating and differentiatin...

Quantitative mass spectrometry-based proteomics in the study of iPSC-derived neurons and disease modeling: A study in neurodevelopment and neurological disorders

Varderidou, Souzanna
Dep Farmaceutische wetenschappen

November 2019

In this thesis we applied mass spectrometry-based proteomics to study neuronal differentiation deriv...

Proteomic analysis of muscle affected by motor neuron degeneration: The wobbler mouse model of amyotrophic lateral sclerosis

Staunton, Lisa
Jockusch, Harald
Ohlendieck, Kay

January 2011

Amyotrophic lateral sclerosis is the most common form of motor neuron disease in adult patients and ...

Motoneurons derived from induced pluripotent stem cells develop mature phenotypes typical of endogenous spinal motoneurons

Toma, J. S.
Shettar, B. C.
Chipman, P. H.
Pinto, D. M.
Borowska, J. P.
Ichida, J. K.
Fawcett, J. P.
Zhang, Y.
Eggan, K.
Rafuse, V. F.

January 2015

Induced pluripotent cell-derived motoneurons (iPSCMNs) are sought for use in cell replacement therap...

Proteomic identification of muscle-associated biomarkers of amyotrophic lateral sclerosis using the wobbler mouse model of primary motor neuronopathy

Ashling Holland
Kay Ohlendieck

December 2014

Motor neuron disease is a major group of inherited or spontaneous disorders that are associated with...

Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia

Miedema, Suzanne S.M.
Mol, Merel O.
Koopmans, Frank T.W.
Hondius, David C.
van Nierop, Pim
Menden, Kevin
de Veij Mestdagh, Christina F.
van Rooij, Jeroen
Ganz, Andrea B.
Paliukhovich, Iryna
Melhem, Shamiram
Li, Ka Wan
Holstege, Henne
Rizzu, Patrizia
van Kesteren, Ronald E.
van Swieten, John C.
Heutink, Peter
Smit, August B.

December 2022

Frontotemporal dementia is characterized by progressive atrophy of frontal and/or temporal cortices ...

Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors

Varderidou-Minasian, Suzy
Hinz, Lisa
Hagemans, Dominique
Posthuma, Danielle
Altelaar, Maarten
Heine, Vivi M

May 2020

BACKGROUND: Rett syndrome (RTT) is a progressive neurodevelopmental disease that is characterized by...

Quantitative proteomic analysis identifies proteins and pathways related to neuronal development in differentiated SH-SY5Y neuroblastoma cells

Murillo, Jimmy Rodriguez
Goto-Silva, Livia
Sánchez, Aniel
Nogueira, Fábio C.S.
Domont, Gilberto B.
Junqueira, Magno

September 2017

SH-SY5Y neuroblastoma cells are susceptible to differentiation using retinoic acid (RA) and brain-de...

NeuroLINCS Proteomics: Defining human-derived iPSC proteomes and protein signatures of pluripotency

Matlock, Andrea D
Vaibhav, Vineet
Holewinski, Ronald
Venkatraman, Vidya
Dardov, Victoria
Manalo, Danica-Mae
Shelley, Brandon
Ornelas, Loren
Banuelos, Maria
Mandefro, Berhan
Escalante-Chong, Renan
Li, Jonathan
Finkbeiner, Steve
Fraenkel, Ernest
Rothstein, Jeffrey
Thompson, Leslie
Sareen, Dhruv
Svendsen, Clive N
Van Eyk, Jennifer E

January 2023

The National Institute of Health (NIH) Library of integrated network-based cellular signatures (LINC...

Deep proteomic evaluation of primary and cell line motoneuron disease models delineates major differences in neuronal characteristics.

Hornburg, D.
Drepper, C.
Butter, F.
Meissner, F.
Sendtner, M.
Mann, M.

January 2014

The fatal neurodegenerative disorders amyotrophic lateral sclerosis and spinal muscular atrophy are,...

Deep Proteomic Evaluation of Primary and Cell Line Motoneuron Disease Models Delineates Major Differences in Neuronal Characteristics*

Hornburg, Daniel
Drepper, Carsten
Butter, Falk
Meissner, Felix
Sendtner, Michael
Mann, Matthias

January 2014

The fatal neurodegenerative disorders amyotrophic lateral sclerosis and spinal muscular atrophy are,...

Deep Proteomic Evaluation of Primary and Cell Line Motoneuron Disease Models Delineates

Michael Sendtner
Matthias Mann

October 2016

The fatal neurodegenerative disorders amyotrophic lat-eral sclerosis and spinal muscular atrophy are...

2-DE proteomic profiling of neuronal stem cells

Hoffrogge, Raimund
Beyer, Susanne
Völker, Uwe
Uhrmacher, Adelinde
Rolfs, Arndt

January 2006

Hoffrogge R, Beyer S, Völker U, Uhrmacher A, Rolfs A. 2-DE proteomic profiling of neuronal stem cell...

Proteomic analysis of muscle affected by motor neuron degeneration: The wobbler mouse model of amyotrophic lateral sclerosis

Staunton, Lisa
Jockusch, Harald
Ohlendieck, Kay

January 2011

Staunton L, Jockusch H, Ohlendieck K. Proteomic analysis of muscle affected by motor neuron degenera...

Early signs of motoneuron vulnerability in a disease model system: characterization of transverse slice cultures of spinal cord isolated from embryonic ALS mice.

Avossa, D.
Grandolfo, M.
Mazzarol, F.
Zatta, M.
Ballerini, L.

January 2006

Cell types within the G93A slice underwent maturation and slices could be maintained in culture for ...

2-DE proteome analysis of a proliferating and differentiating human neuronal stem cell line (ReNcell VM)

Hoffrogge, Raimund
Mikkat, Stefan
Scharf, Christian
Christoph, Hilmar
Beyer, Susanne
Pahnke, Jens
Mix, Eilhard
Berth, Mathias
Uhrmacher, Adelinde
Zubrzycki, Igor Z.
Miljan, Eric
Völker, Uwe
Rolfs, Arndt

January 2006

Hoffrogge R, Mikkat S, Scharf C, et al. 2-DE proteome analysis of a proliferating and differentiatin...

Quantitative mass spectrometry-based proteomics in the study of iPSC-derived neurons and disease modeling: A study in neurodevelopment and neurological disorders

Varderidou, Souzanna
Dep Farmaceutische wetenschappen

November 2019

In this thesis we applied mass spectrometry-based proteomics to study neuronal differentiation deriv...

Proteomic analysis of muscle affected by motor neuron degeneration: The wobbler mouse model of amyotrophic lateral sclerosis

Staunton, Lisa
Jockusch, Harald
Ohlendieck, Kay

January 2011

Amyotrophic lateral sclerosis is the most common form of motor neuron disease in adult patients and ...

Motoneurons derived from induced pluripotent stem cells develop mature phenotypes typical of endogenous spinal motoneurons

Toma, J. S.
Shettar, B. C.
Chipman, P. H.
Pinto, D. M.
Borowska, J. P.
Ichida, J. K.
Fawcett, J. P.
Zhang, Y.
Eggan, K.
Rafuse, V. F.

January 2015

Induced pluripotent cell-derived motoneurons (iPSCMNs) are sought for use in cell replacement therap...

Proteomic identification of muscle-associated biomarkers of amyotrophic lateral sclerosis using the wobbler mouse model of primary motor neuronopathy

Ashling Holland
Kay Ohlendieck

December 2014

Motor neuron disease is a major group of inherited or spontaneous disorders that are associated with...

Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia

Miedema, Suzanne S.M.
Mol, Merel O.
Koopmans, Frank T.W.
Hondius, David C.
van Nierop, Pim
Menden, Kevin
de Veij Mestdagh, Christina F.
van Rooij, Jeroen
Ganz, Andrea B.
Paliukhovich, Iryna
Melhem, Shamiram
Li, Ka Wan
Holstege, Henne
Rizzu, Patrizia
van Kesteren, Ronald E.
van Swieten, John C.
Heutink, Peter
Smit, August B.

December 2022

Frontotemporal dementia is characterized by progressive atrophy of frontal and/or temporal cortices ...

Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors

Varderidou-Minasian, Suzy
Hinz, Lisa
Hagemans, Dominique
Posthuma, Danielle
Altelaar, Maarten
Heine, Vivi M

May 2020

BACKGROUND: Rett syndrome (RTT) is a progressive neurodevelopmental disease that is characterized by...

Quantitative proteomic analysis identifies proteins and pathways related to neuronal development in differentiated SH-SY5Y neuroblastoma cells

Murillo, Jimmy Rodriguez
Goto-Silva, Livia
Sánchez, Aniel
Nogueira, Fábio C.S.
Domont, Gilberto B.
Junqueira, Magno

September 2017

SH-SY5Y neuroblastoma cells are susceptible to differentiation using retinoic acid (RA) and brain-de...

NeuroLINCS Proteomics: Defining human-derived iPSC proteomes and protein signatures of pluripotency

Matlock, Andrea D
Vaibhav, Vineet
Holewinski, Ronald
Venkatraman, Vidya
Dardov, Victoria
Manalo, Danica-Mae
Shelley, Brandon
Ornelas, Loren
Banuelos, Maria
Mandefro, Berhan
Escalante-Chong, Renan
Li, Jonathan
Finkbeiner, Steve
Fraenkel, Ernest
Rothstein, Jeffrey
Thompson, Leslie
Sareen, Dhruv
Svendsen, Clive N
Van Eyk, Jennifer E

January 2023

The National Institute of Health (NIH) Library of integrated network-based cellular signatures (LINC...

ATCC American Type Culture Collection

Abstract

Extracted data

ATCC American Type Culture Collection

Abstract

Extracted data

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