| Type |
Details |
Score |
| Strain |
| Attribute String: |
mutant strain, coisogenic, endonuclease-mediated mutation |
|
•
•
•
•
•
|
| Strain |
| Attribute String: |
mutant strain, coisogenic, endonuclease-mediated mutation |
|
•
•
•
•
•
|
| Strain |
| Attribute String: |
endonuclease-mediated mutation, coisogenic, mutant strain |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/Mcoln3<+> |
| Background: |
Not Specified |
| Zygosity: |
ht |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/Mcoln3 |
| Background: |
Not Specified |
| Zygosity: |
hm |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/Mcoln3 |
| Background: |
B6.Cg-Mcoln3 |
| Zygosity: |
hm |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/Mcoln3<+> |
| Background: |
B6C3Fe-a/a Hoxa13 Mcoln3/J |
| Zygosity: |
ht |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/Mcoln3 |
| Background: |
B6C3Fe-a/a Hoxa13 Mcoln3/J |
| Zygosity: |
hm |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/? |
| Background: |
involves: C3HeB/FeJLe * C57BL/6J |
| Zygosity: |
ot |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/? |
| Background: |
involves: A/J * C57BL/6J |
| Zygosity: |
ot |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/? |
| Background: |
involves: C57BL/6J * DBA/2J |
| Zygosity: |
ot |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/? |
| Background: |
involves: BALB/cByJ * C57BL/6J |
| Zygosity: |
ot |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/? |
| Background: |
involves: C57BL/6J * CZECHII/EiJ |
| Zygosity: |
ot |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Il7r/Il7r<+> |
| Background: |
involves: 129P2/OlaHsd * C57BL/6 |
| Zygosity: |
ht |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Ikzf1/Ikzf1 Il7r/Il7r<+> |
| Background: |
involves: 129P2/OlaHsd * C57BL/6 * SJL |
| Zygosity: |
cn |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Col16a1/Col16a1 |
| Background: |
C57BL/6NJ-Col16a1/J |
| Zygosity: |
hm |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Iqca1/Iqca1 |
| Background: |
C57BL/6NJ-Iqca1/J |
| Zygosity: |
hm |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Eftud2/Eftud2 Trp53/Trp53<+> |
| Background: |
involves: 129P2/OlaHsd * C57BL/6 * CD-1 |
| Zygosity: |
cx |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Genotype |
| Symbol: |
Mcoln3/Mcoln3 |
| Background: |
involves: C3HeB/FeJLe * C57BL/6J |
| Zygosity: |
hm |
| Has Mutant Allele: |
true |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Wen Z |
| Year: |
2021 |
| Journal: |
Biochem Biophys Res Commun |
| Title: |
Deficiency for Lcn8 causes epididymal sperm maturation defects in mice. |
| Volume: |
548 |
|
| Pages: |
7-13 |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE4818 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE5333 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE25768 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE21389 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE10067 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE41674 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE29192 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE67985 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE67009 |
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE55203 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE65754 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE51643 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE46584 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE52974 |
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
transcription profiling by array |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
WT vs. Mutant |
| Source: |
GEO |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Rodrigues PF |
| Year: |
2024 |
| Journal: |
Immunity |
| Title: |
Progenitors of distinct lineages shape the diversity of mature type 2 conventional dendritic cells. |
|
|
|
|
•
•
•
•
•
|
| Publication |
| First Author: |
Robles Luna G |
| Year: |
2018 |
| Journal: |
J Virol |
| Title: |
Citrus Psorosis Virus Movement Protein Contains an Aspartic Protease Required for Autocleavage and the Formation of Tubule-Like Structures at Plasmodesmata. |
| Volume: |
92 |
| Issue: |
21 |
|
|
•
•
•
•
•
|
| Publication |
| First Author: |
Bischoff V |
| Year: |
2010 |
| Journal: |
Plant Physiol |
| Title: |
TRICHOME BIREFRINGENCE and its homolog AT5G01360 encode plant-specific DUF231 proteins required for cellulose biosynthesis in Arabidopsis. |
| Volume: |
153 |
| Issue: |
2 |
| Pages: |
590-602 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Wang GG |
| Year: |
2009 |
| Journal: |
Nature |
| Title: |
Haematopoietic malignancies caused by dysregulation of a chromatin-binding PHD finger. |
| Volume: |
459 |
| Issue: |
7248 |
| Pages: |
847-51 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Ku DH |
| Year: |
1991 |
| Journal: |
Cell Growth Differ |
| Title: |
A new growth-regulated complementary DNA with the sequence of a putative trans-activating factor. |
| Volume: |
2 |
| Issue: |
4 |
| Pages: |
179-86 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Krautkramer KA |
| Year: |
2013 |
| Journal: |
Am J Physiol Endocrinol Metab |
| Title: |
Tcf19 is a novel islet factor necessary for proliferation and survival in the INS-1 β-cell line. |
| Volume: |
305 |
| Issue: |
5 |
| Pages: |
E600-10 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Kreft B |
| Year: |
1992 |
| Journal: |
Infect Immun |
| Title: |
Aggregation substance of Enterococcus faecalis mediates adhesion to cultured renal tubular cells. |
| Volume: |
60 |
| Issue: |
1 |
| Pages: |
25-30 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Bhatty M |
| Year: |
2015 |
| Journal: |
Mol Microbiol |
| Title: |
Enterococcus faecalis pCF10-encoded surface proteins PrgA, PrgB (aggregation substance) and PrgC contribute to plasmid transfer, biofilm formation and virulence. |
| Volume: |
95 |
| Issue: |
4 |
| Pages: |
660-77 |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Domain |
| Description: |
This entry describes an N-terminal domain found in Antigen I/II (also known antigen B, PAc or adhesin P1).The cariogenic bacterium Streptococcus mutans uses adhesin P1 to adhere to tooth surfaces, extracellular matrix components, and other bacteria. The N terminus forms a stabilizing scaffold by wrapping behind the base of P1's elongated stalk and physically 'locking' it into place. It is suggested that the N-terminal has a pronounced impact on P1 immunogenicity, antigenicity, folding, stability, and adherent function [].This domain can also found in aggregation substance (Asa1) from Enterococcus faecalis. It is a structural homologue of Streptococcus mutans Antigen I/II. It acts as an adhesin mediating cell-cell contact between different E. faecalis strains and also binding of E. faecalis to eukaryotic cells [, ]. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
The Ret finger protein-like (RFPL) protein family members includes RFPL1, RFPL2, RFPL3 and RFPL4. In humans, RFPL transcripts can be detected at the onset of neurogenesis in differentiating human embryonic stem cells, and in the developing human neocortex []. The human RFPL1, 2, 3 genes have a role in neocortex development. RFPL1 is a primate-specific target gene of Pax6, a key transcription factor for pancreas, eye and neocortex development. Human RFPL1, 2 and 3 are reported to impact on cell number, specifically through the RFPL-defining motif (RDM) and SPRY domains []. The RFPL4 (also known as RFPL4A) gene encodes a putative E3 ubiquitin-protein ligase expressed in adult germ cells and interacts with oocyte proteins of the ubiquitin-proteasome degradation pathway []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Family |
| Description: |
Arl2 (Arf-like 2) GTPases are members of the Arf family that bind GDP and GTP with very low affinity. Unlike most Arf family proteins, Arl2 is not myristoylated at its N-terminal helix. The protein PDE-delta, first identified in photoreceptor rod cells, binds specifically to Arl2 and is structurally very similar to RhoGDI. Despite the high structural similarity between Arl2 and Rho proteins and between PDE-delta and RhoGDI, the interactions between the GTPases and their effectors are very different. In its GTP bound form, Arl2 interacts with the protein Binder of Arl2 (BART), and thecomplex is believed to play a role in mitochondrial adenine nucleotide transport []. In its GDP bound form, Arl2 interacts with tubulin- folding Cofactor D; this interaction is believed to play a role in regulation of microtubule dynamics that impact the cytoskeleton, cell division, and cytokinesis [].This entry also includes Alp41 from fission yeasts which is essential for the cofactor-dependent biogenesis of microtubules []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Domain |
| Description: |
TCF-19, also termed transcription factor SC1, was identified as a putative trans-activating factor with expression beginning at the late G1-S boundary in dividing cells []. It also functions as a novel islet factor necessary for proliferation and survival in the INS-1 beta cell line. It plays an important role in susceptibility to both type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus (T2DM); it has been suggested that it may positively impact beta cell mass under conditions of beta cell stress and increased insulin demand [].TCF-19 contains an N-terminal fork head association domain (FHA), a proline rich region, and a C-terminal plant homeodomain (PHD) finger. The FHA domain may serve as a nuclear signaling domain or as a phosphoprotein binding domain. The proline rich region is a common characteristic of trans-activating factors. The PHD finger may allow TCF-19 to interact with chromatin via methylated histone H3 []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Domain |
| Description: |
This entry represents the C-terminal region found in viral movement proteins (MP) of the 30K type. This region has been suggested to be conserved in secondary structure in Ophioviruses Mps. It contains two parts, (i) a long segment with the potential to form an α-helix (alphaB), rich in charged residues, and (ii) a region highly variable in sequence downstream of alphaB.The C-terminal region corresponds to the protease domain which contains a strictly conserved DTG tripeptide, also found in related aspartic retroviral proteases. This protease is required for autocleavage of the Movement Protein of ophioviruses in an N-terminal part that supports movement of viral particles through the plant, and this C-terminal part which retains protease activity []. contains a strictly conserved DTG tripeptide which is probably conserved for functional, rather than structural reasons. Mutations in the aspartate residue in the core domain had an impact on cell to cell movement []. |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Kohlstaedt LA |
| Year: |
1992 |
| Journal: |
Science |
| Title: |
Crystal structure at 3.5 A resolution of HIV-1 reverse transcriptase complexed with an inhibitor. |
| Volume: |
256 |
| Issue: |
5065 |
| Pages: |
1783-90 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Hamilton BA |
| Year: |
2001 |
| Journal: |
Cell |
| Title: |
Of mice and genome sequence. |
| Volume: |
107 |
| Issue: |
1 |
| Pages: |
13-6 |
|
•
•
•
•
•
|
| Publication |
| First Author: |
Roberts J |
| Year: |
2023 |
| Journal: |
J Immunol |
| Title: |
Retinoic Acid-Related Orphan Receptor α Is Required for Generation of Th2 Cells in Type 2 Pulmonary Inflammation. |
| Volume: |
211 |
| Issue: |
4 |
| Pages: |
626-632 |
|
•
•
•
•
•
|
| HT Experiment |
| Series Id: |
GSE32935 |
| Experiment Type: |
transcription profiling by array |
| Study Type: |
Baseline |
| Source: |
ArrayExpress |
|
•
•
•
•
•
|
| HT Experiment |
|
| Experiment Type: |
RNA-Seq |
| Study Type: |
Baseline |
| Source: |
GEO |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
1020
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
1135
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
739
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
1170
 |
| Fragment?: |
false |
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•
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| Publication |
| First Author: |
Nam Y |
| Year: |
2006 |
| Journal: |
Cell |
| Title: |
Structural basis for cooperativity in recruitment of MAML coactivators to Notch transcription complexes. |
| Volume: |
124 |
| Issue: |
5 |
| Pages: |
973-83 |
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•
•
•
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| Publication |
| First Author: |
Kovall RA |
| Year: |
2008 |
| Journal: |
Oncogene |
| Title: |
More complicated than it looks: assembly of Notch pathway transcription complexes. |
| Volume: |
27 |
| Issue: |
38 |
| Pages: |
5099-109 |
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•
•
•
•
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| Publication |
| First Author: |
Shen H |
| Year: |
2006 |
| Journal: |
Genes Dev |
| Title: |
The Notch coactivator, MAML1, functions as a novel coactivator for MEF2C-mediated transcription and is required for normal myogenesis. |
| Volume: |
20 |
| Issue: |
6 |
| Pages: |
675-88 |
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•
•
•
•
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| Publication |
| First Author: |
Zhao Y |
| Year: |
2007 |
| Journal: |
J Biol Chem |
| Title: |
The notch regulator MAML1 interacts with p53 and functions as a coactivator. |
| Volume: |
282 |
| Issue: |
16 |
| Pages: |
11969-81 |
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•
•
•
•
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| Publication |
| First Author: |
Alves-Guerra MC |
| Year: |
2007 |
| Journal: |
Cancer Res |
| Title: |
Mastermind-like 1 Is a specific coactivator of beta-catenin transcription activation and is essential for colon carcinoma cell survival. |
| Volume: |
67 |
| Issue: |
18 |
| Pages: |
8690-8 |
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•
•
•
•
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| Publication |
| First Author: |
Chiang MY |
| Year: |
2006 |
| Journal: |
Mol Cell Biol |
| Title: |
Identification of a conserved negative regulatory sequence that influences the leukemogenic activity of NOTCH1. |
| Volume: |
26 |
| Issue: |
16 |
| Pages: |
6261-71 |
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•
•
•
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| Publication |
| First Author: |
Wu L |
| Year: |
2007 |
| Journal: |
Blood |
| Title: |
The transcriptional coactivator Maml1 is required for Notch2-mediated marginal zone B-cell development. |
| Volume: |
110 |
| Issue: |
10 |
| Pages: |
3618-23 |
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•
•
•
•
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| Publication |
| First Author: |
Liu H |
| Year: |
2009 |
| Journal: |
Circ Res |
| Title: |
NOTCH3 expression is induced in mural cells through an autoregulatory loop that requires endothelial-expressed JAGGED1. |
| Volume: |
104 |
| Issue: |
4 |
| Pages: |
466-75 |
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•
•
•
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| Publication |
| First Author: |
Wu L |
| Year: |
2005 |
| Journal: |
EMBO J |
| Title: |
Transforming activity of MECT1-MAML2 fusion oncoprotein is mediated by constitutive CREB activation. |
| Volume: |
24 |
| Issue: |
13 |
| Pages: |
2391-402 |
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•
•
•
•
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| Publication |
| First Author: |
Fryer CJ |
| Year: |
2004 |
| Journal: |
Mol Cell |
| Title: |
Mastermind recruits CycC:CDK8 to phosphorylate the Notch ICD and coordinate activation with turnover. |
| Volume: |
16 |
| Issue: |
4 |
| Pages: |
509-20 |
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