3,7,12-trihydroxycholestan-26-oic acid and Decreased Muscle Tone

3,7,12-trihydroxycholestan-26-oic acid has been researched along with Decreased Muscle Tone in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Christensen, E; Ferdinandusse, S; Gootjes, J; Skovby, F; Wanders, RJ	1
Fujiki, Y; Lazarow, PB; Moser, H; Small, GM; Watkins, P	1

Other Studies

2 other study(ies) available for 3,7,12-trihydroxycholestan-26-oic acid and Decreased Muscle Tone

Article	Year
Reinvestigation of trihydroxycholestanoic acidemia reveals a peroxisome biogenesis disorder. Neurology, 2004, Jun-08, Volume: 62, Issue:11 Topics: Amino Acid Sequence; Animals; Ataxia; Catalase; Child, Preschool; Cholestanols; Consensus Sequence; Diagnostic Errors; DNA Mutational Analysis; Dysarthria; Erythrocytes; Female; Fibroblasts; Fungi; Humans; Intellectual Disability; Mammals; Membrane Proteins; Molecular Sequence Data; Muscle Hypotonia; Oxidation-Reduction; Oxidoreductases; Peroxisomes; Phytanic Acid; Sequence Alignment; Sequence Homology, Amino Acid	2004
Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome). Proceedings of the National Academy of Sciences of the United States of America, 1986, Volume: 83, Issue:23 Topics: Catalase; Cell Compartmentation; Cholestanols; Facial Bones; Fatty Acids; Female; Humans; Immunosorbent Techniques; Intracellular Membranes; Liver; Membrane Proteins; Microbodies; Molecular Weight; Muscle Hypotonia; Pipecolic Acids; Syndrome	1986

Article

Year

Reinvestigation of trihydroxycholestanoic acidemia reveals a peroxisome biogenesis disorder.

Neurology, 2004, Jun-08, Volume: 62, Issue:11

Topics: Amino Acid Sequence; Animals; Ataxia; Catalase; Child, Preschool; Cholestanols; Consensus Sequence; Diagnostic Errors; DNA Mutational Analysis; Dysarthria; Erythrocytes; Female; Fibroblasts; Fungi; Humans; Intellectual Disability; Mammals; Membrane Proteins; Molecular Sequence Data; Muscle Hypotonia; Oxidation-Reduction; Oxidoreductases; Peroxisomes; Phytanic Acid; Sequence Alignment; Sequence Homology, Amino Acid

2004

Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome).

Proceedings of the National Academy of Sciences of the United States of America, 1986, Volume: 83, Issue:23

Topics: Catalase; Cell Compartmentation; Cholestanols; Facial Bones; Fatty Acids; Female; Humans; Immunosorbent Techniques; Intracellular Membranes; Liver; Membrane Proteins; Microbodies; Molecular Weight; Muscle Hypotonia; Pipecolic Acids; Syndrome

1986