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Search results 801 to 900 out of 913 for Bpi

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Categories

Hits by Pathway

Hits by Category

Hits by Strain

Type Details Score
Strain
MGI:6335604 | B6Dnk;B6Brd;B6N-Tyr<c-Brd> Bpifa3<tm1a(KOMP)Wtsi>/Wtsi
Attribute String: mutant strain, targeted mutation
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Strain
MGI:6343880 | C57BL/6N-A<tm1Brd> Bpifb1<tm1b(KOMP)Wtsi>/MbpMmucd
Attribute String: mutant strain, coisogenic, targeted mutation
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Strain
MGI:6343881 | C57BL/6N-A<tm1Brd> Bpifb5<tm2a(KOMP)Wtsi>/Mmucd
Attribute String: mutant strain, coisogenic, targeted mutation
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Strain
MGI:6343879 | C57BL/6N-A<tm1Brd> Bpifb1<tm1a(KOMP)Wtsi>/MbpMmucd
Attribute String: mutant strain, coisogenic, targeted mutation
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Strain
MGI:5557358 | C57BL/6N-A<tm1Brd> Bpifb5<tm2a(KOMP)Wtsi>/WtsiH
Attribute String: mutant strain, targeted mutation, coisogenic
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Strain
MGI:6361266 | STOCK Bpifa3<em1Osb>/OsbRbrc
Attribute String: mutant stock, endonuclease-mediated mutation
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Genotype
Genotype
Symbol: Bpifa3/Bpifa3
Background: involves: C57BL/6J * C57BL/6NSlc * DBA/2J
Zygosity: hm
Has Mutant Allele: true
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Publication
7835704 | J:22658
First Author: Huh C
Year: 1995
Journal: Gene
Title: Structural organization, expression and chromosomal mapping of the mouse cystatin-C-encoding gene (Cst3).
Volume: 152
Issue: 2
Pages: 221-6
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Publication
2300558 | J:10278
First Author: Joseph DR
Year: 1990
Journal: Proc Natl Acad Sci U S A
Title: Characterization and expression of the complementary DNA encoding rat histidine decarboxylase.
Volume: 87
Issue: 2
Pages: 733-7
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Publication
7751596 | J:24247
First Author: Siracusa LD
Year: 1995
Journal: J Hered
Title: Hypervariable yellow (Ahvy), a new murine agouti mutation: Ahvy displays the largest variation in coat color phenotypes of all known agouti alleles.
Volume: 86
Issue: 2
Pages: 121-8
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Publication
28852218 | J:256493
First Author: Vecchione C
Year: 2017
Journal: Sci Rep
Title: A rare genetic variant of BPIFB4 predisposes to high blood pressure via impairment of nitric oxide signaling.
Volume: 7
Issue: 1
Pages: 9706
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Publication
23470624 | J:211747
First Author: Britto CJ
Year: 2013
Journal: Am J Respir Cell Mol Biol
Title: Short palate, lung, and nasal epithelial clone-1 is a tightly regulated airway sensor in innate and adaptive immunity.
Volume: 48
Issue: 6
Pages: 717-24
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Publication
- | J:13827
 
First Author: Hjorth JP
Year: 1979
Journal: Mouse News Lett
Title: [Amy-1, Psp, Amy-2.]
Volume: 62
Pages: 41
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Publication
2570033 | J:9971
First Author: Barsh GS
Year: 1989
Journal: Genomics
Title: The long-range restriction map surrounding the mouse agouti locus reveals a disparity between physical and genetic distances.
Volume: 5
Issue: 1
Pages: 9-18
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Publication
6242882 | J:1872
First Author: Tada N
Year: 1980
Journal: Immunogenetics
Title: Ly-m11: the H-3 region of mouse chromosome 2 controls a new surface alloantigen.
Volume: 11
Issue: 5
Pages: 441-9
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Genotype
Genotype
Symbol: Bpifa1/Bpifa1 Scgb1a1/Scgb1a1
Background: involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Bpifb1/Bpifb1<+>
Background: C57BL/6N-Bpifb1/Ucd
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Bpifb3/Bpifb3<+>
Background: C57BL/6N-Bpifb3/H
Zygosity: ht
Has Mutant Allele: true
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Publication
16075367 | J:100122
First Author: Augustin M
Year: 2005
Journal: Mamm Genome
Title: Efficient and fast targeted production of murine models based on ENU mutagenesis.
Volume: 16
Issue: 6
Pages: 405-13
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Publication
6328281 | J:7461
First Author: Blatt C
Year: 1984
Journal: Mol Cell Biol
Title: Chromosomal mapping of murine c-fes and c-src genes.
Volume: 4
Issue: 5
Pages: 978-81
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Publication
2889668 | J:8880
First Author: D'Eustachio P
Year: 1987
Journal: Immunogenetics
Title: Interleukin-1 alpha and beta genes: linkage on chromosome 2 in the mouse.
Volume: 26
Issue: 6
Pages: 339-43
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Publication
7961761 | J:29026
First Author: Chang SC
Year: 1994
Journal: J Biol Chem
Title: Cartilage-derived morphogenetic proteins. New members of the transforming growth factor-beta superfamily predominantly expressed in long bones during human embryonic development.
Volume: 269
Issue: 45
Pages: 28227-34
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Protein Domain
IPR030675 | BPI/LBP
Type: Family
Description: This entry represents the bactericidal permeability-increasing protein (BPI) and the lipopolysaccharide-binding protein (LBP). The crystal structures of BPI and LBP are similar [], and they may represent a common gene family of lipid-binding proteins [].In mammals, LBP and BPI mediate the biological effects of LPS (lipopolysaccharide), a glycolipid present in the outer membrane of Gram-negative bacteria. LBP is a plasma protein that enhances the inflammatory response to LPS, whereas BPI is found in lysosomal granules of polymorphonuclear neutrophils, is bactericidal, and neutralises the toxic effects of LPS [, ]. LBP is an acute phase serum protein secreted mainly by the liver that modulates the LPS-induced immune response. LBP binds mainly to the lipid A moiety of LPS and acts as an affinity enhancer for CD14, facilitating its association with LPS [].
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Publication
2993648 | J:7991
First Author: Taylor BA
Year: 1985
Journal: J Virol
Title: Chromosomal assignment of two endogenous ecotropic murine leukemia virus proviruses of the AKR/J mouse strain.
Volume: 56
Issue: 1
Pages: 172-5
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Publication
2570027 | J:9964
First Author: Crosby JL
Year: 1989
Journal: Genomics
Title: The cardiac actin locus (Actc-1) is not on mouse chromosome 17 but is linked to beta 2-microglobulin on chromosome 2.
Volume: 5
Issue: 1
Pages: 19-23
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Publication
1450513 | J:3225
First Author: Pilz A
Year: 1992
Journal: Mamm Genome
Title: Mapping of the structural gene for S-adenosyl homocysteine hydrolase to mouse chromosome 2, and related sequences to chromosomes 8 and X.
Volume: 3
Issue: 11
Pages: 633-6
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Publication
- | J:20791
First Author: Liddell RA
Year: 1994
Journal: Mouse Genome
Title: Chromosomal localization and evolution of topoisomerase I sequences in the Mus genome
Volume: 92
Issue: 3
Pages: 520-22
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Protein Domain
IPR032942 | BPI/LBP/Plunc
Type: Family
Description: The BPI (bactericidal permeability-increasing proteins)/LBP (lipopolysaccharide-binding proteins)/PLUNC (palate, lung and nasal epithelium clone) family consists of proteins involved in host defence against bacteria, many acting in early recognition of bacteria in the upper respiratory tract [, , ]. They share homology with cholesterol ester transfer protein (CETP) and phospholipid transfer protein (PLTP), both of which are involved in lipid transport in blood plasma []. This entry also matches UPF0522 proteins from Dictyostelium (slime mold), whose function is unknown.
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Publication
8834448 | -
First Author: Su GL
Year: 1995
Journal: Crit Rev Immunol
Title: Lipopolysaccharide binding protein participation in cellular activation by LPS.
Volume: 15
Issue: 3-4
Pages: 201-14
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Publication
9441745 | -
First Author: Kirschning CJ
Year: 1997
Journal: Genomics
Title: Similar organization of the lipopolysaccharide-binding protein (LBP) and phospholipid transfer protein (PLTP) genes suggests a common gene family of lipid-binding proteins.
Volume: 46
Issue: 3
Pages: 416-25
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Publication
8835531 | J:31822
First Author: Charlier C
Year: 1996
Journal: Mamm Genome
Title: Microsatellite mapping of the bovine roan locus: a major determinant of White Heifer disease.
Volume: 7
Issue: 2
Pages: 138-42
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Publication
31201419 | J:279039
First Author: Lu Y
Year: 2019
Journal: Biol Reprod
Title: CRISPR/Cas9-mediated genome editing reveals 30 testis-enriched genes dispensable for male fertility in mice†.
Volume: 101
Issue: 2
Pages: 501-511
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Publication
24780629 | J:214665
First Author: Fuller K
Year: 2014
Journal: Dev Biol
Title: Rab23 regulates Nodal signaling in vertebrate left-right patterning independently of the Hedgehog pathway.
Volume: 391
Issue: 2
Pages: 182-95
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Publication
11307167 | J:81668
First Author: Menko AS
Year: 2001
Journal: Dev Dyn
Title: Loss of alpha3beta1 integrin function results in an altered differentiation program in the mouse submandibular gland.
Volume: 220
Issue: 4
Pages: 337-49
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Publication
2759422 | J:9913
First Author: Siracusa LD
Year: 1989
Journal: Genetics
Title: Recombinant inbred strain and interspecific backcross analysis of molecular markers flanking the murine agouti coat color locus.
Volume: 122
Issue: 3
Pages: 669-79
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Publication
1970329 | J:10439
First Author: Siracusa LD
Year: 1990
Journal: Genomics
Title: A molecular genetic linkage map of mouse chromosome 2.
Volume: 6
Issue: 3
Pages: 491-504
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Publication
35273595 | J:322001
 
First Author: Gao H
Year: 2022
Journal: Front Immunol
Title: The Lineage Differentiation and Dynamic Heterogeneity of Thymic Epithelial Cells During Thymus Organogenesis.
Volume: 13
Pages: 805451
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Protein
Q8VEH9
Organism: Mus musculus/domesticus
Length: 490  
Fragment?: false
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Protein
Q0VGU8
Organism: Mus musculus/domesticus
Length: 367  
Fragment?: false
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Protein
Q61805
Organism: Mus musculus/domesticus
Length: 481  
Fragment?: false
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Protein
P55065
Organism: Mus musculus/domesticus
Length: 493  
Fragment?: false
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Protein
A2A5K2
Organism: Mus musculus/domesticus
Length: 441  
Fragment?: false
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Protein
Q3UFS5
Organism: Mus musculus/domesticus
Length: 493  
Fragment?: false
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Protein
Q4FJT5
Organism: Mus musculus/domesticus
Length: 493  
Fragment?: false
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Protein
Q3UE59
Organism: Mus musculus/domesticus
Length: 377  
Fragment?: true
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Protein Domain
IPR017943 | Bactericidal_perm-incr_a/b_dom
Type: Homologous_superfamily
Description: This superfamily represents a structural domain with a core structure consisting of two layers, alpha/beta. These homologous structural domains can show little sequence identity with each other. A number of mammalian lipid-binding serum glycoproteins contain one or more such structural domains, including:Bactericidal permeability-increasing protein (BPI)Lipopolysaccharide-binding protein (LBP)Cholesteryl ester transfer protein (CETP)Phospholipid transfer protein (PLTP)Palate, lung and nasal epithelium carcinoma-associated protein (PLUNC)Bactericidal permeability-increasing protein (BPI) is a potent antimicrobial protein of 456 residues that binds to and neutralises lipopolysaccharides from the outer membrane of Gram-negative bacteria []. BPI contains two domains that adopt the same structural fold, even though they have little sequence similarity []. Lipopolysaccharide-binding protein (LBP) is an endotoxin-binding protein that is closely related to, and functions in a co-ordinated manner with BPI to facilitate an integrated host response to invading Gram-negative bacteria [].Cholesteryl ester transfer protein (CETP) is a glycoprotein that facilitates the transfer of lipids (cholesteryl esters and triglycerides) between the different lipoproteins that transport them through plasma, including HDL, LDL, VLDL and chylomicrons. These lipoproteins shield the lipids from water by encapsulating them within a coating of polar lipids and proteins [].Phospholipid transfer protein (PLTP) exchanges phospholipids between lipoproteins and remodels high-density lipoproteins (HDLs) [].Palate, lung and nasal epithelium carcinoma-associated protein (PLUNC) is a potential host defensive protein that is secreted from the submucosal gland to the saliva and nasal lavage fluid. PLUNC appears to be a secreted product of neutrophil granules that participates in an aspect of the inflammatory response that contributes to host defence []. Short palate, lung and nasal epithelium clone 1 (SPLUNC1) may bind the lipopolysaccharide of Gram-negative nanobacteria, thereby playing an important role in the host defence of nasopharyngeal epithelium [].
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Protein Domain
IPR017942 | Lipid-bd_serum_glycop_N
Type: Domain
Description: This entry represents the N-terminal domain found in several lipid-binding serum glycoproteins. The N- and C-terminal domains share a similar two-layer alpha/beta structure, but they show little sequence identity. Proteins containing this N-terminal domain include:Bactericidal permeability-increasing protein (BPI)Lipopolysaccharide-binding protein (LBP)Cholesteryl ester transfer protein (CETP)Phospholipid transfer protein (PLTP)Palate, lung and nasal epithelium carcinoma-associated protein (PLUNC)Bactericidal permeability-increasing protein (BPI) is a potent antimicrobial protein of 456 residues that binds to and neutralises lipopolysaccharides from the outer membrane of Gram-negative bacteria []. BPI contains two domains that adopt the same structural fold, even though they have little sequence similarity []. Lipopolysaccharide-binding protein (LBP) is an endotoxin-binding protein that is closely related to, and functions in a co-ordinated manner with BPI to facilitate an integrated host response to invading Gram-negative bacteria [].Cholesteryl ester transfer protein (CETP) is a glycoprotein that facilitates the transfer of lipids (cholesteryl esters and triglycerides) between the different lipoproteins that transport them through plasma, including HDL, LDL, VLDL and chylomicrons. These lipoproteins shield the lipids from water by encapsulating them within a coating of polar lipids and proteins [].Phospholipid transfer protein (PLTP) exchanges phospholipids between lipoproteins and remodels high-density lipoproteins (HDLs) [].Palate, lung and nasal epithelium carcinoma-associated protein (PLUNC) is a potential host defensive protein that is secreted from the submucosal gland to the saliva and nasal lavage fluid. PLUNC appears to be a secreted product of neutrophil granules that participates in an aspect of the inflammatory response that contributes to host defence []. Short palate, lung and nasal epithelium clone 1 (SPLUNC1) may bind the lipopolysaccharide of Gram-negative nanobacteria, thereby playing an important role in the host defence of nasopharyngeal epithelium [].
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Protein Domain
IPR001124 | Lipid-bd_serum_glycop_C
Type: Domain
Description: This entry represents the C-terminal domain found in several lipid-binding serum glycoproteins. The N- and C-terminal domains share a similar two-layer alpha/beta structure, but they show little sequence identity. Proteins containing this C-terminal domain include:Bactericidal permeability-increasing protein (BPI)Lipopolysaccharide-binding protein (LBP)Cholesteryl ester transfer protein (CETP)Phospholipid transfer protein (PLTP)Palate, lung and nasal epithelium carcinoma-associated protein (PLUNC)Bactericidal permeability-increasing protein (BPI) is a potent antimicrobial protein of 456 residues that binds to and neutralises lipopolysaccharides from the outer membrane of Gram-negative bacteria []. BPI contains two domains that adopt the same structural fold, even though they have little sequence similarity []. Lipopolysaccharide-binding protein (LBP) is an endotoxin-binding protein that is closely related to, and functions in a co-ordinated manner with BPI to facilitate an integrated host response to invading Gram-negative bacteria [].Cholesteryl ester transfer protein (CETP) is a glycoprotein that facilitates the transfer of lipids (cholesteryl esters and triglycerides) between the different lipoproteins that transport them through plasma, including HDL, LDL, VLDL and chylomicrons. These lipoproteins shield the lipids from water by encapsulating them within a coating of polar lipids and proteins [].Phospholipid transfer protein (PLTP) exchanges phospholipids between lipoproteins and remodels high-density lipoproteins (HDLs) [].Palate, lung and nasal epithelium carcinoma-associated protein (PLUNC) is a potential host defensive protein that is secreted from the submucosal gland to the saliva and nasal lavage fluid. PLUNC aapears to be a secreted product of neutrophil granules that participates in an aspect of the inflammatory response that contributes to host defence []. Short palate, lung and nasal epithelium clone 1 (SPLUNC1) may bind the lipopolysaccharide of Gram-negative nanobacteria, thereby playing an important role in the host defence of nasopharyngeal epithelium [].
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Publication
30898767 | J:274882
 
First Author: Del-Pozo J
Year: 2019
Journal: Dis Model Mech
Title: Chronic otitis media is initiated by a bulla cavitation defect in the FBXO11 mouse model.
Volume: 12
Issue: 3
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Publication
18981480 | J:140928
First Author: Furtado MB
Year: 2008
Journal: Genes Dev
Title: BMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4.
Volume: 22
Issue: 21
Pages: 3037-49
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Publication
22627279 | J:185535
First Author: Saund RS
Year: 2012
Journal: Development
Title: Gut endoderm is involved in the transfer of left-right asymmetry from the node to the lateral plate mesoderm in the mouse embryo.
Volume: 139
Issue: 13
Pages: 2426-35
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Publication
23789091 | J:201080
First Author: Nelson DA
Year: 2013
Journal: Biol Open
Title: Quantitative single cell analysis of cell population dynamics during submandibular salivary gland development and differentiation.
Volume: 2
Issue: 5
Pages: 439-47
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Protein
A2A5K3
Organism: Mus musculus/domesticus
Length: 147  
Fragment?: true
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Protein
A2AC65
Organism: Mus musculus/domesticus
Length: 123  
Fragment?: false
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Protein
Q14AS4
Organism: Mus musculus/domesticus
Length: 462  
Fragment?: false
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Protein
Q14AV3
Organism: Mus musculus/domesticus
Length: 462  
Fragment?: false
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Publication
10843855 | -
First Author: Kleiger G
Year: 2000
Journal: J Mol Biol
Title: The 1.7 A crystal structure of BPI: a study of how two dissimilar amino acid sequences can adopt the same fold.
Volume: 299
Issue: 4
Pages: 1019-34
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Publication
12887306 | -
First Author: Weiss J
Year: 2003
Journal: Biochem Soc Trans
Title: Bactericidal/permeability-increasing protein (BPI) and lipopolysaccharide-binding protein (LBP): structure, function and regulation in host defence against Gram-negative bacteria.
Volume: 31
Issue: Pt 4
Pages: 785-90
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Publication
17277799 | -
First Author: Hamilton JA
Year: 2007
Journal: Nat Struct Mol Biol
Title: Crystal structure of CETP: new hopes for raising HDL to decrease risk of cardiovascular disease?
Volume: 14
Issue: 2
Pages: 95-7
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Publication
18245229 | -
First Author: Bartlett JA
Year: 2008
Journal: J Leukoc Biol
Title: PLUNC is a secreted product of neutrophil granules.
Volume: 83
Issue: 5
Pages: 1201-6
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Publication
16364440 | -
First Author: Zhou HD
Year: 2006
Journal: Mol Immunol
Title: Intracellular co-localization of SPLUNC1 protein with nanobacteria in nasopharyngeal carcinoma epithelia HNE1 cells depended on the bactericidal permeability increasing protein domain.
Volume: 43
Issue: 11
Pages: 1864-71
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Publication
12693940 | -
First Author: Ponsin G
Year: 2003
Journal: Biochemistry
Title: Structural and functional determinants of human plasma phospholipid transfer protein activity as revealed by site-directed mutagenesis of charged amino acids.
Volume: 42
Issue: 15
Pages: 4444-51
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Protein
F6XKX9
Organism: Mus musculus/domesticus
Length: 145  
Fragment?: true
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Protein
A2A5K4
Organism: Mus musculus/domesticus
Length: 165  
Fragment?: true
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Publication
37838739 | J:341713
First Author: Aure MH
Year: 2023
Journal: Nat Commun
Title: FGFR2 is essential for salivary gland duct homeostasis and MAPK-dependent seromucous acinar cell differentiation.
Volume: 14
Issue: 1
Pages: 6485
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Publication
8858346 | J:34960
First Author: Chambers DM
Year: 1996
Journal: Genome Res
Title: Isolation and mapping of novel mouse brain cDNA clones containing trinucleotide repeats, and demonstration of novel alleles in recombinant inbred strains.
Volume: 6
Issue: 8
Pages: 715-23
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Publication
33305192 | J:306806
First Author: Hauser BR
Year: 2020
Journal: iScience
Title: Generation of a Single-Cell RNAseq Atlas of Murine Salivary Gland Development.
Volume: 23
Issue: 12
Pages: 101838
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Protein Domain
IPR017954 | Lipid-bd_serum_glycop_CS
Type: Conserved_site
Description: This entry represents a conserved sequence region found in the N-terminal domain of several lipid-binding serum glycoproteins. The N- and C-terminal domains of these proteins share a similar two-layer alpha/beta structure, but they show little sequence identity. Proteins containing this N-terminal domain include:Bactericidal permeability-increasing protein (BPI)Lipopolysaccharide-binding protein (LBP)Cholesteryl ester transfer protein (CETP)Phospholipid transfer protein (PLTP)Palate, lung and nasal epithelium carcinoma-associated protein (PLUNC)Bactericidal permeability-increasing protein (BPI) is a potent antimicrobial protein of 456 residues that binds to and neutralises lipopolysaccharides from the outer membrane of Gram-negative bacteria []. BPI contains two domains that adopt the same structural fold, even though they have little sequence similarity []. Lipopolysaccharide-binding protein (LBP) is an endotoxin-binding protein that is closely related to BPI, and functions with it to facilitate an integrated host response to invading Gram-negative bacteria [].Cholesteryl ester transfer protein (CETP) is a glycoprotein that facilitates the transfer of lipids (cholesteryl esters and triglycerides) between the different lipoproteins that transport them through plasma, including HDL, LDL, VLDL and chylomicrons. These lipoproteins shield the lipids from water by encapsulating them within a coating of polar lipids and proteins [].Phospholipid transfer protein (PLTP) exchanges phospholipids between lipoproteins and remodels high-density lipoproteins (HDLs) [].Palate, lung and nasal epithelium carcinoma-associated protein (PLUNC) is a potential host defensive protein that is secreted from the submucosal gland to the saliva and nasal lavage fluid. PLUNC aapears to be a secreted product of neutrophil granules that participates in an aspect of the inflammatory response that contributes to host defence []. Short palate, lung and nasal epithelium clone 1 (SPLUNC1) may bind the lipopolysaccharide of Gram-negative nanobacteria, thereby playing an important role in the host defence of nasopharyngeal epithelium [].
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Publication
- | J:103485
     
First Author: Lexicon Genetics Inc
Year: 2005
Journal: MGI Direct Data Submission
Title: NIH initiative supporting placement of Lexicon Genetics, Inc. mice into public repositories
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Publication
30728831 | J:304253
 
First Author: Jones MR
Year: 2018
Journal: Front Genet
Title: A Comprehensive Analysis of Fibroblast Growth Factor Receptor 2b Signaling on Epithelial Tip Progenitor Cells During Early Mouse Lung Branching Morphogenesis.
Volume: 9
Pages: 746
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Publication
20562862 | J:161922
First Author: Tang T
Year: 2010
Journal: Nat Biotechnol
Title: A mouse knockout library for secreted and transmembrane proteins.
Volume: 28
Issue: 7
Pages: 749-55
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Publication
- | J:171883
     
First Author: Lexicon Genetics, Inc
Year: 2011
Journal: Database Download
Title: MGI download of Lexicon knockout data
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Publication
- | J:104881
     
First Author: The RIKEN BioResource Center
Year: 2006
Journal: Unpublished
Title: Information obtained from The RIKEN BioResource Center
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Publication
- | J:157064
     
First Author: University of California, Davis
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by the University of California, Davis
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Publication
- | J:237616
     
First Author: MGI and IMPC
Year: 2017
Journal: MGI Direct Data Submission
Title: MGI Curation of Endonuclease-Mediated Alleles (CRISPR) from the International Mouse Phenotyping Consortium (IMPC)
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Publication
12477932 | J:82808
First Author: Strausberg RL
Year: 2002
Journal: Proc Natl Acad Sci U S A
Title: Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
Volume: 99
Issue: 26
Pages: 16899-903
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Publication
- | J:109762
     
First Author: Mouse Genome Informatics and VEGA Genome Database Project
Year: 2006
Journal: Database Release
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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