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Search results 1 to 100 out of 424 for Pah

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Category: Publication
Type Details Score
Publication
First Author: Lagler FB
Year: 2010
Journal: Biochem Pharmacol
Title: New insights into tetrahydrobiopterin pharmacodynamics from Pah enu1/2, a mouse model for compound heterozygous tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.
Volume: 80
Issue: 10
Pages: 1563-71
Publication
First Author: Spronk CA
Year: 2000
Journal: Nat Struct Biol
Title: The Mad1-Sin3B interaction involves a novel helical fold.
Volume: 7
Issue: 12
Pages: 1100-4
Publication
First Author: Swanson KA
Year: 2004
Journal: Nat Struct Mol Biol
Title: HBP1 and Mad1 repressors bind the Sin3 corepressor PAH2 domain with opposite helical orientations.
Volume: 11
Issue: 8
Pages: 738-46
Publication
First Author: van Ingen H
Year: 2004
Journal: Biochemistry
Title: Extension of the binding motif of the Sin3 interacting domain of the Mad family proteins.
Volume: 43
Issue: 1
Pages: 46-54
Publication
First Author: Sahu SC
Year: 2008
Journal: J Mol Biol
Title: Conserved themes in target recognition by the PAH1 and PAH2 domains of the Sin3 transcriptional corepressor.
Volume: 375
Issue: 5
Pages: 1444-56
Publication
First Author: Kumar GS
Year: 2011
Journal: J Mol Biol
Title: Solution structure of the mSin3A PAH2-Pf1 SID1 complex: a Mad1/Mxd1-like interaction disrupted by MRG15 in the Rpd3S/Sin3S complex.
Volume: 408
Issue: 5
Pages: 987-1000
Publication
First Author: Harding CO
Year: 1998
Journal: Gene Ther
Title: Metabolic engineering as therapy for inborn errors of metabolism--development of mice with phenylalanine hydroxylase expression in muscle.
Volume: 5
Issue: 5
Pages: 677-83
Publication
First Author: Brooks DL
Year: 2023
Journal: Nat Commun
Title: Rapid and definitive treatment of phenylketonuria in variant-humanized mice with corrective editing.
Volume: 14
Issue: 1
Pages: 3451
Publication
First Author: Brooks DL
Year: 2023
Journal: Am J Hum Genet
Title: Efficient in vivo prime editing corrects the most frequent phenylketonuria variant, associated with high unmet medical need.
Volume: 110
Issue: 12
Pages: 2003-2014
Publication
First Author: Gunasekera RS
Year: 2009
Journal: Mol Genet Metab
Title: In vivo regulation of phenylalanine hydroxylase in the genetic mutant hph-1 mouse model.
Volume: 98
Issue: 3
Pages: 264-72
Publication
First Author: Ledley FD
Year: 1990
Journal: Biochem J
Title: Mouse phenylalanine hydroxylase. Homology and divergence from human phenylalanine hydroxylase.
Volume: 267
Issue: 2
Pages: 399-405
Publication
First Author: Li Y
Year: 2021
Journal: Science
Title: A noncoding RNA modulator potentiates phenylalanine metabolism in mice.
Volume: 373
Issue: 6555
Pages: 662-673
Publication
First Author: Eichinger A
Year: 2018
Journal: Hum Mol Genet
Title: Secondary BH4 deficiency links protein homeostasis to regulation of phenylalanine metabolism.
Volume: 27
Issue: 10
Pages: 1732-1742
Publication
First Author: Aubi O
Year: 2021
Journal: Nat Commun
Title: The Pah-R261Q mouse reveals oxidative stress associated with amyloid-like hepatic aggregation of mutant phenylalanine hydroxylase.
Volume: 12
Issue: 1
Pages: 2073
Publication
First Author: Liu TJ
Year: 1992
Journal: Somat Cell Mol Genet
Title: Reconstitution of enzymatic activity in hepatocytes of phenylalanine hydroxylase-deficient mice.
Volume: 18
Issue: 1
Pages: 89-96
Publication
First Author: Sarkissian CN
Year: 2000
Journal: Mol Genet Metab
Title: A heteroallelic mutant mouse model: A new orthologue for human hyperphenylalaninemia.
Volume: 69
Issue: 3
Pages: 188-94
Publication
First Author: Singh K
Year: 2021
Journal: Sci Rep
Title: CRISPR/Cas9 generated knockout mice lacking phenylalanine hydroxylase protein as a novel preclinical model for human phenylketonuria.
Volume: 11
Issue: 1
Pages: 7254
Publication
First Author: Haefele MJ
Year: 2001
Journal: Mol Genet Metab
Title: Characterization of the mouse phenylalanine hydroxylase mutation Pah(enu3).
Volume: 72
Issue: 1
Pages: 27-30
Publication  
First Author: Oh HJ
Year: 2005
Journal: Mol Genet Metab
Title: Reversal of gene expression profile in the phenylketonuria mouse model after adeno-associated virus vector-mediated gene therapy.
Volume: 86 Suppl 1
Pages: S124-32
Publication
First Author: Bell SM
Year: 2017
Journal: PLoS One
Title: Formulation and PEGylation optimization of the therapeutic PEGylated phenylalanine ammonia lyase for the treatment of phenylketonuria.
Volume: 12
Issue: 3
Pages: e0173269
Publication
First Author: Manek R
Year: 2021
Journal: Sci Rep
Title: Blood phenylalanine reduction reverses gene expression changes observed in a mouse model of phenylketonuria.
Volume: 11
Issue: 1
Pages: 22886
Publication
First Author: Zagreda L
Year: 1999
Journal: J Neurosci
Title: Cognitive deficits in a genetic mouse model of the most common biochemical cause of human mental retardation.
Volume: 19
Issue: 14
Pages: 6175-82
Publication  
First Author: Richards DY
Year: 2020
Journal: Mol Ther Methods Clin Dev
Title: AAV-Mediated CRISPR/Cas9 Gene Editing in Murine Phenylketonuria.
Volume: 17
Pages: 234-245
Publication
First Author: Faust DM
Year: 1990
Journal: Differentiation
Title: Activation of phenylalanine hydroxylase expression following genomic DNA transfection of hepatoma cells.
Volume: 44
Issue: 1
Pages: 74-9
Publication
First Author: Kure S
Year: 2004
Journal: Mol Genet Metab
Title: Wild-type phenylalanine hydroxylase activity is enhanced by tetrahydrobiopterin supplementation in vivo: an implication for therapeutic basis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.
Volume: 83
Issue: 1-2
Pages: 150-6
Publication
First Author: Gersting SW
Year: 2010
Journal: Hum Mol Genet
Title: Pahenu1 is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivo.
Volume: 19
Issue: 10
Pages: 2039-49
Publication
First Author: Bode VC
Year: 1988
Journal: Genetics
Title: hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis.
Volume: 118
Issue: 2
Pages: 299-305
Publication
First Author: Ding Z
Year: 2006
Journal: Gene Ther
Title: Administration-route and gender-independent long-term therapeutic correction of phenylketonuria (PKU) in a mouse model by recombinant adeno-associated virus 8 pseudotyped vector-mediated gene transfer.
Volume: 13
Issue: 7
Pages: 587-93
Publication
First Author: McDonald JD
Year: 1990
Journal: Proc Natl Acad Sci U S A
Title: Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase.
Volume: 87
Issue: 5
Pages: 1965-7
Publication
First Author: Shedlovsky A
Year: 1993
Journal: Genetics
Title: Mouse models of human phenylketonuria.
Volume: 134
Issue: 4
Pages: 1205-10
Publication
First Author: Dyer CA
Year: 1996
Journal: J Neuropathol Exp Neurol
Title: Evidence for central nervous system glial cell plasticity in phenylketonuria.
Volume: 55
Issue: 7
Pages: 795-814
Publication  
First Author: Bruinenberg VM
Year: 2016
Journal: Front Behav Neurosci
Title: The Behavioral Consequence of Phenylketonuria in Mice Depends on the Genetic Background.
Volume: 10
Pages: 233
Publication
First Author: Mordhorst A
Year: 2021
Journal: FASEB J
Title: Phenylalanine hydroxylase contributes to serotonin synthesis in mice.
Volume: 35
Issue: 6
Pages: e21648
Publication
First Author: Thöny B
Year: 2004
Journal: FEBS Lett
Title: Tetrahydrobiopterin protects phenylalanine hydroxylase activity in vivo: implications for tetrahydrobiopterin-responsive hyperphenylalaninemia.
Volume: 577
Issue: 3
Pages: 507-11
Publication
First Author: Christensen R
Year: 2005
Journal: Exp Dermatol
Title: Characterization of transgenic mice with the expression of phenylalanine hydroxylase and GTP cyclohydrolase I in the skin.
Volume: 14
Issue: 7
Pages: 535-42
Publication
First Author: Hamman KJ
Year: 2011
Journal: Mol Genet Metab
Title: Hepatocytes from wild-type or heterozygous donors are equally effective in achieving successful therapeutic liver repopulation in murine phenylketonuria (PKU).
Volume: 104
Issue: 3
Pages: 235-40
Publication
First Author: McDonald JD
Year: 1997
Journal: Genomics
Title: Characterization of mutations at the mouse phenylalanine hydroxylase locus.
Volume: 39
Issue: 3
Pages: 402-5
Publication
First Author: Solverson P
Year: 2012
Journal: Am J Physiol Endocrinol Metab
Title: Glycomacropeptide, a low-phenylalanine protein isolated from cheese whey, supports growth and attenuates metabolic stress in the murine model of phenylketonuria.
Volume: 302
Issue: 7
Pages: E885-95
Publication
First Author: Sawin EA
Year: 2014
Journal: Mol Genet Metab
Title: Differential effects of low-phenylalanine protein sources on brain neurotransmitters and behavior in C57Bl/6-Pah(enu2) mice.
Volume: 111
Issue: 4
Pages: 452-61
Publication
First Author: Joseph B
Year: 2003
Journal: J Neurochem
Title: Relationship between myelin production and dopamine synthesis in the PKU mouse brain.
Volume: 86
Issue: 3
Pages: 615-26
Publication      
First Author: Siggs OM
Year: 2009
Journal: MGI Direct Data Submission
Title: Record for bronze, updated 15 Sept 2009 (Accessed 2 Oct 2009)
Publication
First Author: Pascucci T
Year: 2002
Journal: Neuroreport
Title: Deficits in brain serotonin synthesis in a genetic mouse model of phenylketonuria.
Volume: 13
Issue: 18
Pages: 2561-4
Publication
First Author: Sidell N
Year: 2009
Journal: PLoS One
Title: Carcinogenic effects in a phenylketonuria mouse model.
Volume: 4
Issue: 1
Pages: e4292
Publication
First Author: Ney DM
Year: 2008
Journal: J Nutr
Title: Dietary glycomacropeptide supports growth and reduces the concentrations of phenylalanine in plasma and brain in a murine model of phenylketonuria.
Volume: 138
Issue: 2
Pages: 316-22
Publication
First Author: Winn SR
Year: 2018
Journal: Mol Genet Metab
Title: Blood phenylalanine reduction corrects CNS dopamine and serotonin deficiencies and partially improves behavioral performance in adult phenylketonuric mice.
Volume: 123
Issue: 1
Pages: 6-20
Publication
First Author: Lu L
Year: 2011
Journal: Mol Genet Metab
Title: Mechanisms regulating superoxide generation in experimental models of phenylketonuria: an essential role of NADPH oxidase.
Volume: 104
Issue: 3
Pages: 241-8
Publication
First Author: Crook N
Year: 2019
Journal: Cell Host Microbe
Title: Adaptive Strategies of the Candidate Probiotic E. coli Nissle in the Mammalian Gut.
Volume: 25
Issue: 4
Pages: 499-512.e8
Publication
First Author: Bruinenberg VM
Year: 2019
Journal: PLoS One
Title: Long-term dietary intervention with low Phe and/or a specific nutrient combination improve certain aspects of brain functioning in phenylketonuria (PKU).
Volume: 14
Issue: 3
Pages: e0213391
Publication
First Author: Embury JE
Year: 2007
Journal: Brain Res
Title: PKU is a reversible neurodegenerative process within the nigrostriatum that begins as early as 4 weeks of age in Pah(enu2) mice.
Volume: 1127
Issue: 1
Pages: 136-50
Publication
First Author: Ercal N
Year: 2002
Journal: Free Radic Biol Med
Title: Oxidative stress in a phenylketonuria animal model.
Volume: 32
Issue: 9
Pages: 906-11
Publication
First Author: Gropper SS
Year: 2004
Journal: Mol Genet Metab
Title: Plasma phenylalanine concentrations are associated with hepatic iron content in a murine model for phenylketonuria.
Volume: 82
Issue: 1
Pages: 76-82
Publication
First Author: Cabib S
Year: 2003
Journal: Behav Genet
Title: The behavioral profile of severe mental retardation in a genetic mouse model of phenylketonuria.
Volume: 33
Issue: 3
Pages: 301-10
Publication
First Author: Winn SR
Year: 2016
Journal: Mol Genet Metab
Title: High dose sapropterin dihydrochloride therapy improves monoamine neurotransmitter turnover in murine phenylketonuria (PKU).
Volume: 117
Issue: 1
Pages: 5-11
Publication
First Author: Solverson P
Year: 2012
Journal: PLoS One
Title: Low bone strength is a manifestation of phenylketonuria in mice and is attenuated by a glycomacropeptide diet.
Volume: 7
Issue: 9
Pages: e45165
Publication
First Author: Smith CB
Year: 2000
Journal: Proc Natl Acad Sci U S A
Title: Cerebral protein synthesis in a genetic mouse model of phenylketonuria.
Volume: 97
Issue: 20
Pages: 11014-9
Publication
First Author: Dobrowolski SF
Year: 2014
Journal: Mol Genet Metab
Title: Methylome repatterning in a mouse model of Maternal PKU Syndrome.
Volume: 113
Issue: 3
Pages: 194-9
Publication
First Author: Puglisi-Allegra S
Year: 2000
Journal: Neuroreport
Title: Dramatic brain aminergic deficit in a genetic mouse model of phenylketonuria.
Volume: 11
Issue: 6
Pages: 1361-4
Publication
First Author: Goldfinger M
Year: 2017
Journal: Mol Genet Metab
Title: Partial rescue of neuropathology in the murine model of PKU following administration of recombinant phenylalanine ammonia lyase (pegvaliase).
Volume: 122
Issue: 1-2
Pages: 33-35
Publication  
First Author: Pascucci T
Year: 2008
Journal: Brain Res
Title: Reduced availability of brain amines during critical phases of postnatal development in a genetic mouse model of cognitive delay.
Volume: 1217
Pages: 232-8
Publication
First Author: Sawin EA
Year: 2015
Journal: Am J Physiol Gastrointest Liver Physiol
Title: Glycomacropeptide is a prebiotic that reduces Desulfovibrio bacteria, increases cecal short-chain fatty acids, and is anti-inflammatory in mice.
Volume: 309
Issue: 7
Pages: G590-601
Publication
First Author: Pascucci T
Year: 2013
Journal: PLoS One
Title: Behavioral and neurochemical characterization of new mouse model of hyperphenylalaninemia.
Volume: 8
Issue: 12
Pages: e84697
Publication
First Author: Durrer KE
Year: 2017
Journal: PLoS One
Title: Genetically engineered probiotic for the treatment of phenylketonuria (PKU); assessment of a novel treatment in vitro and in the PAHenu2 mouse model of PKU.
Volume: 12
Issue: 5
Pages: e0176286
Publication
First Author: Seagraves NJ
Year: 2012
Journal: Mol Genet Metab
Title: Cardiac teratogenicity in mouse maternal phenylketonuria: defining phenotype parameters and genetic background influences.
Volume: 107
Issue: 4
Pages: 650-8
Publication
First Author: Embury JE
Year: 2005
Journal: Pediatr Res
Title: Pathologic and immunohistochemical findings in hypothalamic and mesencephalic regions in the pah(enu2) mouse model for phenylketonuria.
Volume: 58
Issue: 2
Pages: 283-7
Publication
First Author: Cho S
Year: 2001
Journal: Mol Genet Metab
Title: Effect of maternal blood phenylalanine level on mouse maternal phenylketonuria offspring.
Volume: 74
Issue: 4
Pages: 420-5
Publication
First Author: McDonald JD
Year: 2000
Journal: Contemp Top Lab Anim Sci
Title: Postnatal growth in a mouse genetic model of classical phenylketonuria.
Volume: 39
Issue: 6
Pages: 54-6
Publication
First Author: Kornguth S
Year: 1994
Journal: Neuroimage
Title: Near-microscopic magnetic resonance imaging of the brains of phenylalanine hydroxylase-deficient mice, normal littermates, and of normal BALB/c mice at 9.4 Tesla.
Volume: 1
Issue: 3
Pages: 220-9
Publication  
First Author: Nardecchia F
Year: 2018
Journal: Front Neurosci
Title: Targeting mGlu5 Metabotropic Glutamate Receptors in the Treatment of Cognitive Dysfunction in a Mouse Model of Phenylketonuria.
Volume: 12
Pages: 154
Publication  
First Author: Bruinenberg VM
Year: 2017
Journal: Front Neurol
Title: Sleep Disturbances in Phenylketonuria: An Explorative Study in Men and Mice.
Volume: 8
Pages: 167
Publication
First Author: Dahl HH
Year: 1986
Journal: J Biol Chem
Title: Isolation and sequence of a cDNA clone which contains the complete coding region of rat phenylalanine hydroxylase. Structural homology with tyrosine hydroxylase, glucocorticoid regulation, and use of alternate polyadenylation sites.
Volume: 261
Issue: 9
Pages: 4148-53
Publication
First Author: Hommes FA
Year: 1992
Journal: J Inherit Metab Dis
Title: Myelin turnover in hyperphenylalaninaemia. A re-evaluation with the HPH-5 mouse.
Volume: 15
Issue: 2
Pages: 243-51
Publication
First Author: Hommes FA
Year: 1993
Journal: J Inherit Metab Dis
Title: The effect of hyperphenylalaninaemia on the muscarinic acetylcholine receptor in the HPH-5 mouse brain.
Volume: 16
Issue: 6
Pages: 962-74
Publication
First Author: Faust DM
Year: 1996
Journal: Mol Cell Biol
Title: The activity of the highly inducible mouse phenylalanine hydroxylase gene promoter is dependent upon a tissue-specific, hormone-inducible enhancer.
Volume: 16
Issue: 6
Pages: 3125-37
Publication  
First Author: Belanger AM
Year: 2018
Journal: JCI Insight
Title: Inhibiting neutral amino acid transport for the treatment of phenylketonuria.
Volume: 3
Issue: 14
Publication
First Author: Ledley FD
Year: 1988
Journal: Cytogenet Cell Genet
Title: Localization of mouse phenylalanine hydroxylase locus on chromosome 10.
Volume: 47
Issue: 3
Pages: 125-6
Publication
First Author: Keller SA
Year: 1990
Journal: Proc Natl Acad Sci U S A
Title: Transgene-induced mutation of the murine steel locus.
Volume: 87
Issue: 24
Pages: 10019-22
Publication
First Author: Apte SS
Year: 1994
Journal: Dev Dyn
Title: Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP-3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10.
Volume: 200
Issue: 3
Pages: 177-97
Publication
First Author: Surendran S
Year: 2005
Journal: Neurochem Int
Title: Expression of calpastatin, minopontin, NIPSNAP1, rabaptin-5 and neuronatin in the phenylketonuria (PKU) mouse brain: possible role on cognitive defect seen in PKU.
Volume: 46
Issue: 8
Pages: 595-9
Publication
First Author: MacLaren DC
Year: 1992
Journal: Genomics
Title: The L-isoaspartyl/D-aspartyl protein methyltransferase gene (PCMT1) maps to human chromosome 6q22.3-6q24 and the syntenic region of mouse chromosome 10.
Volume: 14
Issue: 4
Pages: 852-6
Publication
First Author: Zhao GQ
Year: 1994
Journal: Mech Dev
Title: The gene for the homeodomain-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development.
Volume: 48
Issue: 3
Pages: 245-54
Publication
First Author: Okano HJ
Year: 1997
Journal: J Neurosci
Title: A hierarchy of Hu RNA binding proteins in developing and adult neurons.
Volume: 17
Issue: 9
Pages: 3024-37
Publication
First Author: Zhang N
Year: 2000
Journal: Genomics
Title: Cloning, expression, and chromosomal localization of a mouse gene homologous to the germ cell migration regulator wunen and to type 2 phosphatidic acid phosphatases.
Volume: 63
Issue: 1
Pages: 142-4
Publication
First Author: Matalon R
Year: 2005
Journal: Int J Immunopathol Pharmacol
Title: Abnormal expression of genes associated with development and inflammation in the heart of mouse maternal phenylketonuria offspring.
Volume: 18
Issue: 3
Pages: 557-65
Publication
First Author: Dobrowolski SF
Year: 2016
Journal: Mol Genet Metab
Title: DNA methylation in the pathophysiology of hyperphenylalaninemia in the PAH(enu2) mouse model of phenylketonuria.
Volume: 119
Issue: 1-2
Pages: 1-7
Publication
First Author: Simon-Chazottes D
Year: 1992
Journal: Mamm Genome
Title: Chromosomal localization of two cell surface-associated molecules of potential importance in development: midkine (Mdk) and basigin (Bsg).
Volume: 2
Issue: 4
Pages: 269-71
Publication
First Author: Tamai Y
Year: 1995
Journal: Genomics
Title: Mouse Elk oncogene maps to chromosome X and a novel Elk oncogene (Elk3) maps to chromosome 10.
Volume: 26
Issue: 2
Pages: 414-6
Publication
First Author: Copeland NG
Year: 1990
Journal: Cell
Title: Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel alleles.
Volume: 63
Issue: 1
Pages: 175-83
Publication
First Author: Buckle VJ
Year: 1990
Journal: Hum Genet
Title: Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus.
Volume: 85
Issue: 3
Pages: 324-6
Publication
First Author: Shimizu A
Year: 1992
Journal: Biochem Genet
Title: A molecular genetic linkage map of mouse chromosome 10, including the Myb, S100b, Pah, Sl, and Ifg genes.
Volume: 30
Issue: 9-10
Pages: 529-35
Publication
First Author: Valk PJ
Year: 1999
Journal: J Virol
Title: Retroviral insertions in Evi12, a novel common virus integration site upstream of Tra1/Grp94, frequently coincide with insertions in the gene encoding the peripheral cannabinoid receptor Cnr2.
Volume: 73
Issue: 5
Pages: 3595-602
Publication
First Author: Peters LL
Year: 1995
Journal: J Cell Biol
Title: Ank3 (epithelial ankyrin), a widely distributed new member of the ankyrin gene family and the major ankyrin in kidney, is expressed in alternatively spliced forms, including forms that lack the repeat domain.
Volume: 130
Issue: 2
Pages: 313-30
Publication
First Author: Walter L
Year: 1995
Journal: Genomics
Title: Identification of a novel conserved human gene, TEGT.
Volume: 28
Issue: 2
Pages: 301-4
Publication
First Author: Taketo M
Year: 1992
Journal: Mamm Genome
Title: Mapping of recombinant retrovirus integration sites that cause expression of the viral genome in murine embryonal carcinoma cells.
Volume: 2
Issue: 4
Pages: 240-5
Publication
First Author: Taketo M
Year: 1994
Journal: Genomics
Title: Mapping of the genes encoding mouse thromboxane A2 receptor and prostaglandin E receptor subtypes EP2 and EP3.
Volume: 19
Issue: 3
Pages: 585-8
Publication
First Author: Kapfhamer D
Year: 1994
Journal: Genomics
Title: Genetic map of the region around grizzled (gr) and mocha (mh) on mouse chromosome 10, homologous to human 19p13.3.
Volume: 23
Issue: 3
Pages: 635-42
Publication
First Author: Mitchell M
Year: 1989
Journal: Genetics
Title: Localization of murine X and autosomal sequences homologous to the human Y located testis-determining region.
Volume: 121
Issue: 4
Pages: 803-9
Publication
First Author: King TR
Year: 1991
Journal: Genomics
Title: Mapping anti-müllerian hormone (Amh) and related sequences in the mouse: identification of a new region of homology between MMU10 and HSA19p.
Volume: 11
Issue: 2
Pages: 273-83
Publication
First Author: Yao J
Year: 2017
Journal: J Cell Biol
Title: Vascular endothelium plays a key role in directing pulmonary epithelial cell differentiation.
Volume: 216
Issue: 10
Pages: 3369-3385
Publication
First Author: Justice MJ
Year: 1990
Journal: Genetics
Title: A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross.
Volume: 125
Issue: 4
Pages: 855-66
Publication
First Author: Tomizawa M
Year: 2008
Journal: Cell Tissue Res
Title: Hepatoblast-like cells enriched from mouse embryonic stem cells in medium without glucose, pyruvate, arginine, and tyrosine.
Volume: 333
Issue: 1
Pages: 17-27