Type |
Details |
Score |
HT Experiment |
|
Experiment Type: |
RNA-Seq |
Study Type: |
WT vs. Mutant |
Source: |
GEO |
|
•
•
•
•
•
|
Publication |
First Author: |
Kitamoto T |
Year: |
2010 |
Journal: |
Stem Cells |
Title: |
Notch3 null mutation in mice causes muscle hyperplasia by repetitive muscle regeneration. |
Volume: |
28 |
Issue: |
12 |
Pages: |
2205-16 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
489
|
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
826
|
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
585
|
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
414
|
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
680
|
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
443
|
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
500
|
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
249
|
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
414
|
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Fryer CJ |
Year: |
2002 |
Journal: |
Genes Dev |
Title: |
Mastermind mediates chromatin-specific transcription and turnover of the Notch enhancer complex. |
Volume: |
16 |
Issue: |
11 |
Pages: |
1397-411 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
The Notch domain is also called the 'DSL' domain or the Lin-12/Notch repeat (LNR). The LNR region is present only in Notch related proteins C-terminal to EGF repeats. The lin-12/Notch proteins act as transmembrane receptors for intercellular signals that specify cell fates during animal development. In response to a ligand, proteolytic cleavages release the intracellular domain of Notch, which then gains access to the nucleus and acts as a transcriptional co-activator []. The LNR region is supposed to negatively regulate the Lin-12/Notch proteins activity. It is a triplication of an around 35-40 amino acids module present on the extracellular part of the protein [, ]. Each module contains six cysteine residues engaged in three disulphide bonds and three conserved aspartate and asparagine residues []. The biochemical characterisation of a recombinantly expressed LIN-12.1 module from the human Notch1 receptor indicate that the disulphide bonds are formed between the firstand fifth, second and fourth, and third and sixth cysteines. The formation of this particular disulphide isomer is favored by the presence of Ca2+,which is also required to maintain the structural integrity of the rLIN-12.1 module. The conserved aspartate and asparagine residues are likely to be important for Ca2+binding, and thereby contribute to the native fold. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Homologous_superfamily |
Description: |
This entry represents the N-terminal domain found in a family of neurogenic mastermind-like proteins (MAMLs), which act as critical transcriptional co-activators for Notch signaling [, , ]. Notch receptors are cleaved upon ligand engagement and the intracellular domain of Notch shuttles to the nucleus. MAMLs form a functional DNA-binding complex with the cleaved Notch receptor and the transcription factor CSL, thereby regulating transcriptional events that are specific to the Notch pathway. MAML proteins may also play roles as key transcriptional co-activators in other signal transduction pathways as well, including: muscle differentiation and myopathies (MEF2C) [], tumour suppressor pathway (p53) []and colon carcinoma survival (beta-catenin) []. MAML proteins could mediate cross-talk among the various signaling pathways and the diverse activities of the MAML proteins converge to impact normal biological processes and human diseases, including cancers.The N-terminal domain of MAML proteins adopt an elongated kinked helix that wraps around ANK and CSL forming one of the complexes in the build-up of the Notch transcriptional complex for recruiting general transcription factors []. This N-terminal domain is responsible for its interaction with the ankyrin repeat region of the Notch proteins NOTCH1 [], NOTCH2 [], NOTCH3 []and NOTCH4. It forms a DNA-binding complex with Notch proteins and RBPSUH/RBP-J kappa/CBF1, and also binds CREBBP/CBP []and CDK8 []. The C-terminal region is required for transcriptional activation. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
This family includes the neurogenic mastermind-like proteins 1-3 (MAML1-3) from chordates, which act as critical transcriptional co-activators for Notch signaling [, ]. Notch receptors are cleaved upon ligand engagement and the intracellular domain of Notch shuttles to the nucleus. MAMLs form a functional DNA-binding complex with the cleaved Notch receptor and the transcription factor CSL, thereby regulating transcriptional events that are specific to the Notch pathway. MAML proteins may also play roles as key transcriptional co-activators in other signal transduction pathways as well, including: muscle differentiation and myopathies (MEF2C) [], tumour suppressor pathway (p53) []and colon carcinoma survival (beta-catenin) []. MAML proteins could mediate cross-talk among the various signaling pathways and the diverse activities of the MAML proteins converge to impact normal biological processes and human diseases, including cancers.They consist of an N-terminal domain which adopt an elongated kinked helix that wraps around ANK and CSL forming one of the complexes in the build-up of the Notch transcriptional complex for recruiting general transcription factors [, ]]. This N-terminal domain is responsible for its interaction with the ankyrin repeat region of the Notch proteins NOTCH1 [], NOTCH2 [], NOTCH3 []and NOTCH4. It forms a DNA-binding complex with Notch proteins and RBPSUH/RBP-J kappa/CBF1, and also binds CREBBP/CBP []and CDK8 []. The C-terminal region is required for transcriptional activation. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
This entry represents the N-terminal domain found in a family of neurogenic mastermind-like proteins (MAMLs), which act as critical transcriptional co-activators for Notch signaling [, , ]. Notch receptors are cleaved upon ligand engagement and the intracellular domain of Notch shuttles to the nucleus. MAMLs form a functional DNA-binding complex with the cleaved Notch receptor and the transcription factor CSL, thereby regulating transcriptional events that are specific to the Notch pathway. MAML proteins may also play roles as key transcriptional co-activators in other signal transduction pathways as well, including: muscle differentiation and myopathies (MEF2C) [], tumour suppressor pathway (p53) []and colon carcinoma survival (beta-catenin) []. MAML proteins could mediate cross-talk among the various signaling pathways and the diverse activities of the MAML proteins converge to impact normal biological processes and human diseases, including cancers.The N-terminal domain of MAML proteins adopt an elongated kinked helix that wraps around ANK and CSL forming one of the complexes in the build-up of the Notch transcriptional complex for recruiting general transcription factors []. This N-terminal domain is responsible for its interaction with the ankyrin repeat region of the Notch proteins NOTCH1 [], NOTCH2 [], NOTCH3 []and NOTCH4. It forms a DNA-binding complex with Notch proteins and RBPSUH/RBP-J kappa/CBF1, and also binds CREBBP/CBP []and CDK8 []. The C-terminal region is required for transcriptional activation. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Homologous_superfamily |
Description: |
The Notch domain is also called the 'DSL' domain or the Lin-12/Notch repeat (LNR). The LNR region is present only in Notch related proteins C-terminal to EGF repeats. The lin-12/Notch proteins act as transmembrane receptors for intercellular signals that specify cell fates during animal development. In response to a ligand, proteolytic cleavages release the intracellular domain of Notch, which then gains access to the nucleus and acts as a transcriptional co-activator []. The LNR region is supposed to negatively regulate the Lin-12/Notch proteins activity. It is a triplication of an around 35-40 amino acids module present on the extracellular part of the protein [, ]. Each module contains six cysteine residues engaged in three disulphide bonds and three conserved aspartate and asparagine residues []. The biochemical characterisation of a recombinantly expressed LIN-12.1 module from the human Notch1 receptor indicate that the disulphide bonds are formed between the firstand fifth, second and fourth, and third and sixth cysteines. The formation of this particular disulphide isomer is favored by the presence of Ca2+, which is also required to maintain the structural integrity of the rLIN-12.1 module. The conserved aspartate and asparagine residues are likely to be important for Ca2+binding, and thereby contribute to the native fold. |
|
•
•
•
•
•
|
Publication |
First Author: |
Tang H |
Year: |
2008 |
Journal: |
Development |
Title: |
Notch signaling maintains Leydig progenitor cells in the mouse testis. |
Volume: |
135 |
Issue: |
22 |
Pages: |
3745-53 |
|
•
•
•
•
•
|
Publication |
First Author: |
McGovern MM |
Year: |
2018 |
Journal: |
Front Cell Neurosci |
Title: |
Spontaneous Hair Cell Regeneration Is Prevented by Increased Notch Signaling in Supporting Cells. |
Volume: |
12 |
|
Pages: |
120 |
|
•
•
•
•
•
|
Publication |
First Author: |
Grassmeyer J |
Year: |
2017 |
Journal: |
Dev Biol |
Title: |
Elf5 is a principal cell lineage specific transcription factor in the kidney that contributes to Aqp2 and Avpr2 gene expression. |
Volume: |
424 |
Issue: |
1 |
Pages: |
77-89 |
|
•
•
•
•
•
|
Publication |
First Author: |
Saito T |
Year: |
2003 |
Journal: |
Immunity |
Title: |
Notch2 is preferentially expressed in mature B cells and indispensable for marginal zone B lineage development. |
Volume: |
18 |
Issue: |
5 |
Pages: |
675-85 |
|
•
•
•
•
•
|
Publication |
First Author: |
Jeon HM |
Year: |
2008 |
Journal: |
Genes Dev |
Title: |
Inhibitor of differentiation 4 drives brain tumor-initiating cell genesis through cyclin E and notch signaling. |
Volume: |
22 |
Issue: |
15 |
Pages: |
2028-33 |
|
•
•
•
•
•
|
Publication |
First Author: |
Mallo M |
Year: |
1995 |
Journal: |
Dev Dyn |
Title: |
Protein characterization and targeted disruption of Grg, a mouse gene related to the groucho transcript of the Drosophila Enhancer of split complex. |
Volume: |
204 |
Issue: |
3 |
Pages: |
338-47 |
|
•
•
•
•
•
|
Publication |
First Author: |
Rathinam C |
Year: |
2011 |
Journal: |
Nat Immunol |
Title: |
The E3 ligase Itch is a negative regulator of the homeostasis and function of hematopoietic stem cells. |
Volume: |
12 |
Issue: |
5 |
Pages: |
399-407 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lefort K |
Year: |
2004 |
Journal: |
Semin Cancer Biol |
Title: |
Notch signaling in the integrated control of keratinocyte growth/differentiation and tumor suppression. |
Volume: |
14 |
Issue: |
5 |
Pages: |
374-86 |
|
•
•
•
•
•
|
Publication |
First Author: |
Grabher C |
Year: |
2006 |
Journal: |
Nat Rev Cancer |
Title: |
Notch 1 activation in the molecular pathogenesis of T-cell acute lymphoblastic leukaemia. |
Volume: |
6 |
Issue: |
5 |
Pages: |
347-59 |
|
•
•
•
•
•
|
Publication |
First Author: |
Mori M |
Year: |
2015 |
Journal: |
Development |
Title: |
Notch3-Jagged signaling controls the pool of undifferentiated airway progenitors. |
Volume: |
142 |
Issue: |
2 |
Pages: |
258-67 |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
2412
|
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Yanger K |
Year: |
2013 |
Journal: |
Genes Dev |
Title: |
Robust cellular reprogramming occurs spontaneously during liver regeneration. |
Volume: |
27 |
Issue: |
7 |
Pages: |
719-24 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lin Y |
Year: |
2018 |
Journal: |
Front Immunol |
Title: |
Notch Signaling Modulates Macrophage Polarization and Phagocytosis Through Direct Suppression of Signal Regulatory Protein α Expression. |
Volume: |
9 |
|
Pages: |
1744 |
|
•
•
•
•
•
|
Publication |
First Author: |
Nakamura M |
Year: |
2015 |
Journal: |
J Immunol |
Title: |
A genome-wide analysis identifies a notch-RBP-Jκ-IL-7Rα axis that controls IL-17-producing γδ T cell homeostasis in mice. |
Volume: |
194 |
Issue: |
1 |
Pages: |
243-51 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chen S |
Year: |
2013 |
Journal: |
J Bone Miner Res |
Title: |
Notch gain of function inhibits chondrocyte differentiation via Rbpj-dependent suppression of Sox9. |
Volume: |
28 |
Issue: |
3 |
Pages: |
649-59 |
|
•
•
•
•
•
|
Strain |
Attribute String: |
congenic, mutant stock, transgenic |
|
•
•
•
•
•
|
Publication |
First Author: |
Maddaluno L |
Year: |
2013 |
Journal: |
Nature |
Title: |
EndMT contributes to the onset and progression of cerebral cavernous malformations. |
Volume: |
498 |
Issue: |
7455 |
Pages: |
492-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Fujimura S |
Year: |
2010 |
Journal: |
J Am Soc Nephrol |
Title: |
Notch2 activation in the embryonic kidney depletes nephron progenitors. |
Volume: |
21 |
Issue: |
5 |
Pages: |
803-10 |
|
•
•
•
•
•
|
Allele |
Name: |
gene trap ROSA 26, Philippe Soriano; targeted mutation 8, Rui Benedito |
Allele Type: |
Targeted |
Attribute String: |
Conditional ready, Epitope tag, Inserted expressed sequence, Reporter |
|
•
•
•
•
•
|
Allele |
Name: |
gene trap ROSA 26, Philippe Soriano; targeted mutation 9, Rui Benedito |
Allele Type: |
Targeted |
Attribute String: |
Conditional ready, Epitope tag, Inserted expressed sequence, Reporter |
|
•
•
•
•
•
|
Allele |
Name: |
notch 4; targeted mutation 1, Tom Gridley |
Allele Type: |
Targeted |
|
|
•
•
•
•
•
|
Genotype |
Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Tg(Pdx1-cre)89.1Dam/? |
Background: |
involves: 129S4/SvJae * C57BL/6 * ICR |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(Nes-cre)1Kln/? Tg(ACTB-NOTCH1)1Shn/? |
Background: |
B6.Cg-Tg(Nes-cre)1Kln Tg(ACTB-NOTCH1)1Shn |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(Actb-NOTCH1)2Shn/? Tg(Nes-cre)1Kln/? |
Background: |
involves: C57BL/6J * SJL |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(ACTB-NOTCH1)1Shn/? Tg(Syn1-cre)671Jxm/? |
Background: |
involves: C57BL/6J |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(ACTB-NOTCH1)1Shn/? Tg(Nes-cre/Esr1*)4Ynj/? |
Background: |
involves: C57BL/6 * C57BL/6J |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Mesp1/Mesp1<+> Rbpj/Rbpj Tg(CAG-cat,-Notch1)1Ysa/? |
Background: |
involves: 129P2/OlaHsd * C3H * C57BL/6 * CBA |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Mesp1/Mesp1<+> Pofut1/Pofut1 Tg(CAG-cat,-Notch1)1Ysa/? |
Background: |
involves: C3H * C57BL/6 * CBA * SJL |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Kras/Kras Tg(Pdx1-cre/Esr1*)35.10Dam/? |
Background: |
involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6 * CBA |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Kras/Kras Tg(Cela1-cre/ERT)1Dam/? |
Background: |
involves: 129S4/SvJae * 129S4/SvJaeSor |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Tg(Pdx1-cre)89.1Dam/? |
Background: |
involves: 129S4/SvJaeSor * C57BL/6 * CBA |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Tg(Neurod1-cre)1Able/? |
Background: |
involves: 129S4/SvJaeSor * C57BL/6 * DBA/2 |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Tg(Neurog3-cre)C1Able/? |
Background: |
involves: 129S4/SvJaeSor |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Ndor1/? |
Background: |
involves: 129S/SvEv * C57BL/6 |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Alb/Alb<+> Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> |
Background: |
involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Notch1/Notch1<+> Notch2/Notch2 |
Background: |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Notch1/Notch1<+> Notch2/Notch2 Tg(Pax3-cre)1Joe/? |
Background: |
involves: 129S1/Sv * C57BL/6 * SJL |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Notch1/Notch1 Notch2/Notch2 Tg(Pax3-cre)1Joe/? |
Background: |
involves: 129S1/Sv * C57BL/6 * SJL |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Rbpj/Rbpj Tg(Col1a1-cre)1Kry/? |
Background: |
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * FVB/N |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Adam10/Adam10 Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Tg(Six3-cre)69Frty/? |
Background: |
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * DBA/2 |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Notch1/Notch1 |
Background: |
involves: 129X1/SvJ * C57BL/6NTac |
Zygosity: |
ht |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Tax FE |
Year: |
1994 |
Journal: |
Nature |
Title: |
Sequence of C. elegans lag-2 reveals a cell-signalling domain shared with Delta and Serrate of Drosophila. |
Volume: |
368 |
Issue: |
6467 |
Pages: |
150-4 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1072
|
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Hozumi K |
Year: |
2004 |
Journal: |
Nat Immunol |
Title: |
Delta-like 1 is necessary for the generation of marginal zone B cells but not T cells in vivo. |
Volume: |
5 |
Issue: |
6 |
Pages: |
638-44 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hu QD |
Year: |
2003 |
Journal: |
Cell |
Title: |
F3/contactin acts as a functional ligand for Notch during oligodendrocyte maturation. |
Volume: |
115 |
Issue: |
2 |
Pages: |
163-75 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hodson DJ |
Year: |
2010 |
Journal: |
Nat Immunol |
Title: |
Deletion of the RNA-binding proteins ZFP36L1 and ZFP36L2 leads to perturbed thymic development and T lymphoblastic leukemia. |
Volume: |
11 |
Issue: |
8 |
Pages: |
717-24 |
|
•
•
•
•
•
|
Publication |
First Author: |
Choi HY |
Year: |
2020 |
Journal: |
Nat Commun |
Title: |
p53 destabilizing protein skews asymmetric division and enhances NOTCH activation to direct self-renewal of TICs. |
Volume: |
11 |
Issue: |
1 |
Pages: |
3084 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kostrzewski T |
Year: |
2018 |
Journal: |
J Immunol |
Title: |
Multiple Levels of Control Determine How E4bp4/Nfil3 Regulates NK Cell Development. |
Volume: |
200 |
Issue: |
4 |
Pages: |
1370-1381 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ettersperger J |
Year: |
2016 |
Journal: |
Immunity |
Title: |
Interleukin-15-Dependent T-Cell-like Innate Intraepithelial Lymphocytes Develop in the Intestine and Transform into Lymphomas in Celiac Disease. |
Volume: |
45 |
Issue: |
3 |
Pages: |
610-625 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lu H |
Year: |
2023 |
Journal: |
Nat Commun |
Title: |
Angiotensin-converting enzyme inhibitor promotes angiogenesis through Sp1/Sp3-mediated inhibition of notch signaling in male mice. |
Volume: |
14 |
Issue: |
1 |
Pages: |
731 |
|
•
•
•
•
•
|
Publication |
First Author: |
García-Ojeda ME |
Year: |
2013 |
Journal: |
Blood |
Title: |
GATA-3 promotes T-cell specification by repressing B-cell potential in pro-T cells in mice. |
Volume: |
121 |
Issue: |
10 |
Pages: |
1749-59 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hauer J |
Year: |
2011 |
Journal: |
Blood |
Title: |
Loss of p19Arf in a Rag1(-/-) B-cell precursor population initiates acute B-lymphoblastic leukemia. |
Volume: |
118 |
Issue: |
3 |
Pages: |
544-53 |
|
•
•
•
•
•
|
Publication |
First Author: |
Pasut A |
Year: |
2016 |
Journal: |
Cell Rep |
Title: |
Notch Signaling Rescues Loss of Satellite Cells Lacking Pax7 and Promotes Brown Adipogenic Differentiation. |
Volume: |
16 |
Issue: |
2 |
Pages: |
333-43 |
|
•
•
•
•
•
|
Publication |
First Author: |
Vanderluit JL |
Year: |
2004 |
Journal: |
J Cell Biol |
Title: |
p107 regulates neural precursor cells in the mammalian brain. |
Volume: |
166 |
Issue: |
6 |
Pages: |
853-63 |
|
•
•
•
•
•
|
Publication |
First Author: |
Berquam-Vrieze KE |
Year: |
2012 |
Journal: |
Genesis |
Title: |
Characterization of transgenic mice expressing cancer-associated variants of human NOTCH1. |
Volume: |
50 |
Issue: |
2 |
Pages: |
112-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yoshizaki K |
Year: |
2014 |
Journal: |
PLoS One |
Title: |
Ablation of coactivator Med1 switches the cell fate of dental epithelia to that generating hair. |
Volume: |
9 |
Issue: |
6 |
Pages: |
e99991 |
|
•
•
•
•
•
|
Publication |
First Author: |
Fiorini E |
Year: |
2008 |
Journal: |
J Immunol |
Title: |
Cutting edge: thymic crosstalk regulates delta-like 4 expression on cortical epithelial cells. |
Volume: |
181 |
Issue: |
12 |
Pages: |
8199-203 |
|
•
•
•
•
•
|
Publication |
First Author: |
Engin F |
Year: |
2008 |
Journal: |
Nat Med |
Title: |
Dimorphic effects of Notch signaling in bone homeostasis. |
Volume: |
14 |
Issue: |
3 |
Pages: |
299-305 |
|
•
•
•
•
•
|
Publication |
First Author: |
Schmid RS |
Year: |
2003 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Neuregulin 1-erbB2 signaling is required for the establishment of radial glia and their transformation into astrocytes in cerebral cortex. |
Volume: |
100 |
Issue: |
7 |
Pages: |
4251-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kasahara A |
Year: |
2013 |
Journal: |
Science |
Title: |
Mitochondrial fusion directs cardiomyocyte differentiation via calcineurin and Notch signaling. |
Volume: |
342 |
Issue: |
6159 |
Pages: |
734-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Schnell SA |
Year: |
2015 |
Journal: |
Blood |
Title: |
Therapeutic targeting of HES1 transcriptional programs in T-ALL. |
Volume: |
125 |
Issue: |
18 |
Pages: |
2806-14 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kalucka J |
Year: |
2018 |
Journal: |
Cell Metab |
Title: |
Quiescent Endothelial Cells Upregulate Fatty Acid β-Oxidation for Vasculoprotection via Redox Homeostasis. |
Volume: |
28 |
Issue: |
6 |
Pages: |
881-894.e13 |
|
•
•
•
•
•
|
Publication |
First Author: |
King B |
Year: |
2013 |
Journal: |
Cell |
Title: |
The ubiquitin ligase FBXW7 modulates leukemia-initiating cell activity by regulating MYC stability. |
Volume: |
153 |
Issue: |
7 |
Pages: |
1552-66 |
|
•
•
•
•
•
|
Publication |
First Author: |
Okuyama K |
Year: |
2012 |
Journal: |
Biochem Biophys Res Commun |
Title: |
A checkpoint in B-lymphopoiesis related to Notch resistance. |
Volume: |
417 |
Issue: |
1 |
Pages: |
141-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Weber BN |
Year: |
2011 |
Journal: |
Nature |
Title: |
A critical role for TCF-1 in T-lineage specification and differentiation. |
Volume: |
476 |
Issue: |
7358 |
Pages: |
63-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Rupec RA |
Year: |
2005 |
Journal: |
Immunity |
Title: |
Stroma-mediated dysregulation of myelopoiesis in mice lacking I kappa B alpha. |
Volume: |
22 |
Issue: |
4 |
Pages: |
479-91 |
|
•
•
•
•
•
|
Publication |
First Author: |
Tanaka T |
Year: |
2017 |
Journal: |
J Exp Med |
Title: |
Internal deletion of BCOR reveals a tumor suppressor function for BCOR in T lymphocyte malignancies. |
Volume: |
214 |
Issue: |
10 |
Pages: |
2901-2913 |
|
•
•
•
•
•
|
Publication |
First Author: |
Roderick JE |
Year: |
2014 |
Journal: |
Blood |
Title: |
c-Myc inhibition prevents leukemia initiation in mice and impairs the growth of relapsed and induction failure pediatric T-ALL cells. |
Volume: |
123 |
Issue: |
7 |
Pages: |
1040-50 |
|
•
•
•
•
•
|
Publication |
First Author: |
Robey E |
Year: |
1996 |
Journal: |
Cell |
Title: |
An activated form of Notch influences the choice between CD4 and CD8 T cell lineages. |
Volume: |
87 |
Issue: |
3 |
Pages: |
483-92 |
|
•
•
•
•
•
|
Publication |
First Author: |
Endo Y |
Year: |
2020 |
Journal: |
FASEB J |
Title: |
Loss of ARNT in skeletal muscle limits muscle regeneration in aging. |
Volume: |
34 |
Issue: |
12 |
Pages: |
16086-16104 |
|
•
•
•
•
•
|
Publication |
First Author: |
Guinea-Viniegra J |
Year: |
2012 |
Journal: |
J Clin Invest |
Title: |
Differentiation-induced skin cancer suppression by FOS, p53, and TACE/ADAM17. |
Volume: |
122 |
Issue: |
8 |
Pages: |
2898-910 |
|
•
•
•
•
•
|
Publication |
First Author: |
Espinosa L |
Year: |
2010 |
Journal: |
Cancer Cell |
Title: |
The Notch/Hes1 pathway sustains NF-κB activation through CYLD repression in T cell leukemia. |
Volume: |
18 |
Issue: |
3 |
Pages: |
268-81 |
|
•
•
•
•
•
|
Publication |
First Author: |
Janas ML |
Year: |
2011 |
Journal: |
J Immunol |
Title: |
Interaction of Ras with p110γ is required for thymic β-selection in the mouse. |
Volume: |
187 |
Issue: |
9 |
Pages: |
4667-75 |
|
•
•
•
•
•
|
Publication |
First Author: |
Malcolm TI |
Year: |
2016 |
Journal: |
Nat Commun |
Title: |
Anaplastic large cell lymphoma arises in thymocytes and requires transient TCR expression for thymic egress. |
Volume: |
7 |
|
Pages: |
10087 |
|
•
•
•
•
•
|
Publication |
First Author: |
Saint Fleur-Lominy S |
Year: |
2018 |
Journal: |
Cell Rep |
Title: |
STIM1 and STIM2 Mediate Cancer-Induced Inflammation in T Cell Acute Lymphoblastic Leukemia. |
Volume: |
24 |
Issue: |
11 |
Pages: |
3045-3060.e5 |
|
•
•
•
•
•
|
Publication |
First Author: |
Majumder S |
Year: |
2016 |
Journal: |
Cell Rep |
Title: |
G-Protein-Coupled Receptor-2-Interacting Protein-1 Controls Stalk Cell Fate by Inhibiting Delta-like 4-Notch1 Signaling. |
Volume: |
17 |
Issue: |
10 |
Pages: |
2532-2541 |
|
•
•
•
•
•
|
Publication |
First Author: |
Pan F |
Year: |
2017 |
Journal: |
Nat Commun |
Title: |
Tet2 loss leads to hypermutagenicity in haematopoietic stem/progenitor cells. |
Volume: |
8 |
|
Pages: |
15102 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bertout JA |
Year: |
2009 |
Journal: |
Cancer Res |
Title: |
Heterozygosity for hypoxia inducible factor 1alpha decreases the incidence of thymic lymphomas in a p53 mutant mouse model. |
Volume: |
69 |
Issue: |
7 |
Pages: |
3213-20 |
|
•
•
•
•
•
|
Publication |
First Author: |
Satoh Y |
Year: |
2013 |
Journal: |
Immunity |
Title: |
The Satb1 protein directs hematopoietic stem cell differentiation toward lymphoid lineages. |
Volume: |
38 |
Issue: |
6 |
Pages: |
1105-15 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hozumi K |
Year: |
2008 |
Journal: |
Eur J Immunol |
Title: |
Notch signaling is necessary for GATA3 function in the initiation of T cell development. |
Volume: |
38 |
Issue: |
4 |
Pages: |
977-85 |
|
•
•
•
•
•
|
Publication |
First Author: |
Schober A |
Year: |
2014 |
Journal: |
Nat Med |
Title: |
MicroRNA-126-5p promotes endothelial proliferation and limits atherosclerosis by suppressing Dlk1. |
Volume: |
20 |
Issue: |
4 |
Pages: |
368-76 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wang J |
Year: |
2019 |
Journal: |
Nat Neurosci |
Title: |
Invasion of white matter tracts by glioma stem cells is regulated by a NOTCH1-SOX2 positive-feedback loop. |
Volume: |
22 |
Issue: |
1 |
Pages: |
91-105 |
|
•
•
•
•
•
|