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1892049 |
Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans
ITPR1 Deletion Causes Ataxia
Abstract
We observed a severe autosomal recessive movement disorder in mice used within |
32 KB |
2025-10-02 |
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12 |
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10,162 |
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| PMC |
1253828 |
Two major branches of anti-cadmium defense in the mouse: MTF-1/metallothioneins and glutathione
Abstract
Metal-responsive transcription factor 1 (MTF-1) regulates expression of its target genes in re |
48.1 KB |
2020-10-02 |
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11 |
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14,862 |
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| PMC |
340383 |
Molecular cloning and characterization of the mouse Acdp gene family
Abstract
Background
We have recently cloned and characterized a novel gene family named ancient conserved domain protein (ACDP) in |
23.2 KB |
2020-10-02 |
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10 |
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8,567 |
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| PMC |
1183529 |
Fog2 Is Required for Normal Diaphragm and Lung Development in Mice and Humans
Fog2 Required for Diaphragm and Lung Development
Abstract
Congenital diaphragmatic hernia and other congenital diaphragma |
33.3 KB |
2020-10-02 |
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10 |
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10,159 |
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| PMC |
1084331 |
A Developmental Switch in the Response of DRG Neurons to ETS Transcription Factor Signaling
ETS Transcription Factor Signaling in DRG Neurons
Abstract
Two ETS transcription factors of the Pea3 subfam |
51.5 KB |
2020-10-02 |
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10 |
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13,940 |
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| PMC |
1140370 |
DNA binding and helicase actions of mouse MCM4/6/7 helicase
Abstract
Helicases play central roles in initiation and elongation of DNA replication. We previously reported that helicase and ATPase acti |
37 KB |
2020-09-18 |
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10 |
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15,955 |
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| PMC |
194730 |
Function, expression and localization of annexin A7 in platelets and red blood cells: Insights derived from an annexin A7 mutant mouse
Abstract
Background
Annexin A7 is a Ca2+- and phospholipid-bindi |
35.7 KB |
2020-10-02 |
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10 |
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13,058 |
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| PMC |
1540739 |
RMCE-ASAP: a gene targeting method for ES and somatic cells to accelerate phenotype analyses
Abstract
In recent years, tremendous insight has been gained on p53 regulation by targeting mutations at t |
29.4 KB |
2020-10-02 |
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10 |
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8,308 |
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| PMC |
1064854 |
PGC-1α Deficiency Causes Multi-System Energy Metabolic Derangements: Muscle Dysfunction, Abnormal Weight Control and Hepatic Steatosis
Metabolic Derangements in PGC-1α Deficiency
Abstract
The gene en |
76.1 KB |
2020-09-18 |
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10 |
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25,145 |
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| PMC |
516044 |
Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model
Abstract
Background
Pendred syndrome, a common autosomal-recessive disorder char |
32.8 KB |
2020-10-02 |
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9 |
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12,847 |
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