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Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 03/2017, Volume 19, Issue 3, p. 350
Sodium taurocholate cotransporting polypeptide (NTCP) deficiency is caused by SLC10A1 mutations impairing the NTCP function to uptake plasma bile salts into... 
Jaundice, Obstructive - etiology | Organic Anion Transporters, Sodium-Dependent - deficiency | Symporters - blood | Humans | Symporters - genetics | Symporters - deficiency | Infant | Male | Organic Anion Transporters, Sodium-Dependent - blood | Organic Anion Transporters, Sodium-Dependent - genetics
Journal Article
Genome Biology, ISSN 1474-7596, 05/2018, Volume 19, Issue 1, pp. 59 - 59
Nucleotide base editors in plants have been limited to conversion of cytosine to thymine. Here, we describe a new plant adenine base editor based on an evolved... 
SgRNA forms | Herbicide resistance | Wheat | Cas9-adenosine deaminase | Rice | sgRNA forms | CRISPR | RESISTANT | ENDONUCLEASE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | GENOMIC DNA | Flow cytometry | Adenosine | tRNA | Base pairs | Thymine | Protoplasts | Adenine | Genomes | Adenosine deaminase | Conversion | Efficiency | Point mutation | Cytosine | Mutation | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 08/2016, Volume 18, Issue 8, p. 751
Progressive familial intrahepatic cholestasis type I (PFIC1) is an autosomal recessive disorder caused by biallelic mutations of ATP8B1 gene, with progressive... 
Cholestasis, Intrahepatic - genetics | DNA Mutational Analysis | Humans | Infant | Male | Adenosine Triphosphatases - genetics | Mutation | Sequence Analysis, DNA
Journal Article
Nature Biotechnology, ISSN 1087-0156, 11/2018, Volume 36, Issue 10, pp. 950 - 950
Base editors (BEs) have been used to create C-to-T substitutions in various organisms. However, editing with rat APOBEC1-based BE3 is limited to a 5-nt... 
FUTURE | MAIZE | WHEAT | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | DNA | Analysis | Plant genetics | Research | Proteins | Potatoes | Editors | Editing | Thymidine | Fusion protein | Wheat
Journal Article
IEEE Access, ISSN 2169-3536, 2019, Volume 7, pp. 12177 - 12191
To explore human emotions, in this paper, we design and build a multi-modal physiological emotion database, which collects four modal physiological signals,... 
Emotion recognition | LSTM | physiological signals | affective computing | EEG | Discrete emotion recognition | Electroencephalography | machine learning | Support vector machines | video-induced emotion | Databases | Brain modeling | Feature extraction | Physiology
Journal Article
Chinese Journal of Contemporary Pediatrics, ISSN 1008-8830, 11/2014, Volume 16, Issue 11, pp. 1188 - 1192
Journal Article
American Journal of Physiology, ISSN 0193-1857, 05/2014, Volume 306, Issue 9, p. G788
  Communication between neurons and glia in the dorsal root ganglia (DRG) and the central nervous system is critical for nociception. Both glial activation and... 
Cytokines | Microscopy | Neurons | Gene expression | Cells
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 01/2019, Volume 21, Issue 1, pp. 71 - 76
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 01/2019, Volume 21, Issue 1, pp. 64 - 70
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 01/2019, Volume 21, Issue 1, p. 71
GM1 gangliosidosis is an autosomal recessive disorder caused by galactosidase beta1 (GLB1) gene variants which affect the activity of β-galactosidase (GLB).... 
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 01/2019, Volume 21, Issue 1, p. 64
Dubin-Johnson syndrome (DJS) is an autosomal recessive disorder resulting from biallelic mutations of ABCC2 gene, with long-term or intermittent conjugated... 
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 10/2018, Volume 20, Issue 10, p. 857
Journal Article
Chinese Journal of Contemporary Pediatrics, ISSN 1008-8830, 09/2018, Volume 20, Issue 9, pp. 758 - 764
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 09/2018, Volume 20, Issue 9, p. 758
Progressive familial intrahepatic cholestasis type II (PFIC-2) is an autosomal recessive disorder caused by biallelic variants of ABCB11 gene. This paper... 
Jaundice | Infant | Cholestasis, Intrahepatic | ATP Binding Cassette Transporter, Subfamily B, Member 11 | Bile Acids and Salts | Humans
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 10/2017, Volume 19, Issue 10, pp. 1098 - 1103
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 10/2017, Volume 19, Issue 10, p. 1077
Arthrogryposis, renal dysfunction, and cholestasis (ARC) syndrome is an autosomal recessive disorder caused by mutations in the VPS33B or VIPAS39 gene. The aim... 
Cholestasis - blood | Cholestasis - genetics | Renal Insufficiency - genetics | Bilirubin - blood | Arthrogryposis - blood | Bile Acids and Salts - blood | Humans | Vesicular Transport Proteins - genetics | Arthrogryposis - genetics | Mutation | Renal Insufficiency - blood
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 10/2017, Volume 19, Issue 10, p. 1098
Alagille syndrome (ALGS) is an autosomal dominant disease affecting multiple systems including the liver, heart, skeleton, eyes, kidneys and face. This paper... 
Chromosome Deletion | Alagille Syndrome - genetics | Bile Acids and Salts - blood | gamma-Glutamyltransferase - blood | Humans | Child, Preschool | Male | Jagged-1 Protein - genetics
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 09/2017, Volume 19, Issue 9, p. 968
Microvillus inclusion disease (MVID) is an autosomal recessive disorder caused by biallelic mutations in the MYO5B or STX3 gene. Refractory diarrhea and... 
Microvilli - pathology | Malabsorption Syndromes - diagnosis | Microvilli - genetics | Myosin Type V - genetics | Humans | Myosin Heavy Chains - genetics | Female | Mucolipidoses - genetics | Mutation | Mucolipidoses - diagnosis | Infant, Newborn | Malabsorption Syndromes - genetics
Journal Article
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