Page last updated: 2024-08-17

histidine and Decreased Muscle Tone

histidine has been researched along with Decreased Muscle Tone in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	1 (33.33)	24.3611
2020's	1 (33.33)	2.80

Authors

Authors	Studies
Astudillo, MF; Bacino, CA; Burrage, LC; Chao, HT; Dai, H; Gibson, JB; Lalani, SR; Lee, BH; Lewis, RA; Lin, Y; Magyar, CL; Murdock, DR; Rosenfeld, JA; Tran, AA	1
Groeneweg, S; Lima de Souza, EC; Meima, ME; Peeters, RP; Visser, TJ; Visser, WE	1
Bax, R; Freisinger, P; Horn, N; Horváth, R; Jaksch, M; Mayr, JA; Merl, T; Moller, LB; Müller-Höcker, J; Pongratz, D; Rubio, R	1

Reviews

1 review(s) available for histidine and Decreased Muscle Tone

Article	Year
PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literature. American journal of medical genetics. Part A, 2022, Volume: 188, Issue:6 Topics: Child; Exons; Histidine; Humans; Male; Microcephaly; Muscle Hypotonia; Pedigree; Phosphoric Monoester Hydrolases	2022

Other Studies

2 other study(ies) available for histidine and Decreased Muscle Tone

Article	Year
Outward-Open Model of Thyroid Hormone Transporter Monocarboxylate Transporter 8 Provides Novel Structural and Functional Insights. Endocrinology, 2017, 10-01, Volume: 158, Issue:10 Topics: Animals; Arginine; Binding Sites; Biological Transport; Cell Line; Chlorocebus aethiops; COS Cells; Histidine; Humans; Mental Retardation, X-Linked; Models, Molecular; Molecular Structure; Monocarboxylic Acid Transporters; Muscle Hypotonia; Muscular Atrophy; Mutagenesis, Site-Directed; Mutation; Protein Conformation; Symporters; Thyroid Hormones; Transfection; Triiodothyronine	2017
Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolism. Journal of inherited metabolic disease, 2005, Volume: 28, Issue:4 Topics: Adenosine Triphosphatases; Blotting, Southern; Brain; Cataract; Cation Transport Proteins; Copper; Copper-Transporting ATPases; Cytochrome-c Oxidase Deficiency; Developmental Disabilities; DNA Mutational Analysis; Electrophysiology; Exons; Fibroblasts; Hearing Loss, Sensorineural; Histidine; Humans; Immunoblotting; Immunohistochemistry; Infant; Magnetic Resonance Imaging; Male; Mitochondria; Muscle Hypotonia; Muscle, Skeletal; Muscles; Mutation; Myoblasts; Recombinant Fusion Proteins; Superoxide Dismutase	2005

Article

Year

Outward-Open Model of Thyroid Hormone Transporter Monocarboxylate Transporter 8 Provides Novel Structural and Functional Insights.

Endocrinology, 2017, 10-01, Volume: 158, Issue:10

Topics: Animals; Arginine; Binding Sites; Biological Transport; Cell Line; Chlorocebus aethiops; COS Cells; Histidine; Humans; Mental Retardation, X-Linked; Models, Molecular; Molecular Structure; Monocarboxylic Acid Transporters; Muscle Hypotonia; Muscular Atrophy; Mutagenesis, Site-Directed; Mutation; Protein Conformation; Symporters; Thyroid Hormones; Transfection; Triiodothyronine

2017

Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolism.

Journal of inherited metabolic disease, 2005, Volume: 28, Issue:4

Topics: Adenosine Triphosphatases; Blotting, Southern; Brain; Cataract; Cation Transport Proteins; Copper; Copper-Transporting ATPases; Cytochrome-c Oxidase Deficiency; Developmental Disabilities; DNA Mutational Analysis; Electrophysiology; Exons; Fibroblasts; Hearing Loss, Sensorineural; Histidine; Humans; Immunoblotting; Immunohistochemistry; Infant; Magnetic Resonance Imaging; Male; Mitochondria; Muscle Hypotonia; Muscle, Skeletal; Muscles; Mutation; Myoblasts; Recombinant Fusion Proteins; Superoxide Dismutase

2005