cysteine has been researched along with Symptom Cluster in 32 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (3.13) | 18.7374 |
| 1990's | 9 (28.13) | 18.2507 |
| 2000's | 16 (50.00) | 29.6817 |
| 2010's | 4 (12.50) | 24.3611 |
| 2020's | 2 (6.25) | 2.80 |
| Authors | Studies |
|---|---|
| Agamasu, C; Insinna, C; Morrison, DK; Ritt, DA; Spencer-Smith, R; Stauffer, J; Stephen, AG; Terrell, EM; Wagner, ME | 1 |
| Delon, J; El Masri, R | 1 |
| Boutati, E; Economopoulos, T; Hadjidakis, D; Kamakari, S; Panayiotides, IG; Peppa, M; Peros, G; Pikounis, V; Raptis, SA | 1 |
| Hogan, KJ; Vladutiu, GD | 1 |
| Bindoff, LA; Engelsen, BE; Ersland, L; Moen, G; Mørk, SJ; Neckelmann, G; Tzoulis, C; Viscomi, C; Zeviani, M | 1 |
| Ang, BU; Kirschner, RE; Nah, HD; Spivak, RM | 1 |
| Mese, G; Sánchez, HA; Srinivas, M; Verselis, VK; White, TW | 1 |
| Farooq, A; McDonald, CB; Sudol, M | 1 |
| Adamek-Guzik, T; Czerniawska-Mysik, G; Guzik, TJ; Korpanty, G; Mastalerz, L; Radwan, J; Szczeklik, A | 1 |
| Ignatius, J; Kääriäinen, H; Körkkö, J; Löppönen, T; Lundan, T; Seppänen, U | 1 |
| Furui, S; Hatanaka, Y; Kaminaga, T; Takeshita, T; Tatsumi, T | 1 |
| Biaggioni, I; Byrne, DW; Cascorbi, I; Garland, EM; Harris, PA; Jiang, L; Phillips, JA; Robertson, D; Rüdiger, H; Stanton, K; Williams, SM; Winker, R | 1 |
| Anderson, PJ; Cox, TC; David, DJ; Netherway, DJ; Roscioli, T | 1 |
| Hur, JW; Lee, CW; Yoo, DH | 1 |
| Allingham, RR; Challa, P; Freedman, SF; Hauser, MA; Luna, CC; McDonald, MT; Pericak-Vance, M; Yang, J | 1 |
| Dericioglu, N; Saygi, S | 1 |
| Liu, J; Wang, J; Zhang, Q | 1 |
| Araújo, D; Bianchin, MM; de Azevedo-Marques, PM; Fernandes, RM; Kato, M; Oliveira, LF; Sakamoto, AC; Santos, AC; Velasco, TR; Wichert-Ana, L | 1 |
| Fujioka, T; Konno, S; Kurihara, T; Murata, M; Nakazora, H; Nemoto, H; Nomoto, N; Sugimoto, H; Toda, T; Wakata, N; Yoshii, Y | 1 |
| Cosentino, V; Costa-Lima, MA; Fonseca, R; Orioli, IM | 1 |
| Ahn, BD; Kim, JW; Kim, YJ; Lee, SH; Lee, SJ; Lee, SK; Lee, ZH | 1 |
| Arai, K; Chrousos, GP; DiGeorge, AM; Latronico, AC; Rapaport, R; Tsigos, C | 1 |
| Diaz, GJ; Julian, RJ; Squires, EJ | 1 |
| Granholm, DE; Granholm, NH; Reese, RN | 1 |
| Blume-Peytavi, U; Föhles, J; Gollnick, H; Orfanos, CE; Schulz, R; Wortmann, G | 1 |
| Ayuso, C; Beneyto, M; Cuevas, JM; Espinós, C; García-Sandoval, B; Millán, JM; Nájera, C; Sánchez, F; Trujillo, MJ | 1 |
| Blaha, L; Eilles, C; Marienhagen, J; Poser, S; Weingärtner, U; Zerr, I | 1 |
| Goto, M; Kotani, M; Mukoyama, M; Nakagawa, M; Nakao, K; Ogawa, Y; Shimatsu, A; Sugawara, A; Tanaka, I; Tanaka, K; Yahata, K | 1 |
| Büsse, M; Collmann, H; Halliger-Keller, B; Kress, W; Mueller, CR | 1 |
| Plietz, J | 1 |
| Fritschi, T; Fröscher, W; Maier, V | 1 |
| Arimori, S; Ichikawa, Y; Shimizu, H | 1 |
4 review(s) available for cysteine and Symptom Cluster
| Article | Year |
|---|---|
Multiple endocrine neoplasia type 2A in two families with the familial medullary thyroid carcinoma associated G533C mutation of the RET proto-oncogene.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Carcinoma, Medullary; Cysteine; Female; Glycine; Humans; Male; Middle Aged; Multiple Endocrine Neoplasia Type 2a; Pedigree; Phenotype; Point Mutation; Proto-Oncogene Mas; Proto-Oncogene Proteins c-ret; Syndrome; Thyroid Neoplasms; Young Adult | 2008 |
Molecular insights into the WW domain of the Golabi-Ito-Hall syndrome protein PQBP1.
Topics: Amino Acid Sequence; Carrier Proteins; Cysteine; Disulfides; DNA-Binding Proteins; Humans; Intellectual Disability; Ligands; Molecular Sequence Data; Mutation; Nuclear Proteins; Oxygen; Protein Binding; Protein Conformation; Protein Structure, Tertiary; RNA, Messenger; Sequence Homology, Amino Acid; Syndrome | 2012 |
Childhood-onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75-Cys mutation in procollagen type II gene (COL2A1).
Topics: Adult; Arginine; Arthritis, Juvenile; Body Height; Collagen Type II; Cysteine; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Lumbar Vertebrae; Middle Aged; Mutation; Osteoarthritis; Scoliosis; Syndrome | 2004 |
"Yellow nail syndrome" and rheumatoid arthritis.
Topics: Anti-Inflammatory Agents, Non-Steroidal; Arthritis, Rheumatoid; Cysteine; Female; Humans; Male; Middle Aged; Nail Diseases; Nails; Penicillamine; Syndrome | 1991 |
1 trial(s) available for cysteine and Symptom Cluster
| Article | Year |
|---|---|
[The treatment of bronchitic syndrome using Transbronchin in the practice].
Topics: Adolescent; Adult; Aged; Bronchitis; Carbocysteine; Clinical Trials as Topic; Cysteine; Female; Humans; Male; Middle Aged; Syndrome | 1976 |
27 other study(ies) available for cysteine and Symptom Cluster
| Article | Year |
|---|---|
RASopathy mutations provide functional insight into the BRAF cysteine-rich domain and reveal the importance of autoinhibition in BRAF regulation.
Topics: Cysteine; Humans; Mutation; Protein Domains; Proto-Oncogene Proteins B-raf; Syndrome | 2022 |
[An abnormal palmitoylation arising from a mutation of CDC42 results in a severe autoinflammatory syndrome].
Topics: Amino Acid Substitution; Arginine; Autoimmune Diseases; cdc42 GTP-Binding Protein; Cysteine; Humans; Inflammation; Lipoylation; Mutation, Missense; Palmitic Acid; Syndrome | 2020 |
Malignant hyperthermia-like syndrome and carnitine palmitoyltransferase II deficiency with heterozygous R503C mutation.
Topics: Amino Acid Substitution; Anesthetics, Inhalation; Arginine; Carnitine O-Palmitoyltransferase; Child, Preschool; Cysteine; Female; Genetic Predisposition to Disease; Halothane; Heterozygote; Humans; Malignant Hyperthermia; Metabolism, Inborn Errors; Mutation; Neuromuscular Depolarizing Agents; Risk Factors; Succinylcholine; Syndrome | 2009 |
Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes.
Topics: Arginine; Brain; Brain Diseases; Cerebellum; Cysteine; Diffuse Cerebral Sclerosis of Schilder; Diffusion Magnetic Resonance Imaging; Disease Progression; DNA Polymerase gamma; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Electroencephalography; Energy Metabolism; Epilepsy; Glycine; Humans; Magnetic Resonance Angiography; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mitochondrial Diseases; Mutation; Neocortex; Sensitivity and Specificity; Spinocerebellar Ataxias; Stroke; Syndrome; Thalamus; Tomography, X-Ray Computed | 2010 |
Dura in the pathogenesis of syndromic craniosynostosis: fibroblast growth factor receptor 2 mutations in dural cells promote osteogenic proliferation and differentiation of osteoblasts.
Topics: Acrocephalosyndactylia; Adenoviridae; Alkaline Phosphatase; Animals; Arginine; Biomarkers; Cell Differentiation; Cell Proliferation; Cells, Cultured; Coculture Techniques; Coloring Agents; Core Binding Factor Alpha 1 Subunit; Craniofacial Dysostosis; Craniosynostoses; Cysteine; Dura Mater; Genetic Vectors; Mice; Osteoblasts; Osteogenesis; Osteopontin; Phenylalanine; Point Mutation; Receptor, Fibroblast Growth Factor, Type 2; Syndrome; Tetrazolium Salts; Thiazoles | 2010 |
Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome.
Topics: Amino Acid Substitution; Animals; Barium; Calcium; Cell Line, Tumor; Chelating Agents; Chloride Channels; Connexin 26; Connexins; Cysteine; Deafness; Electrophysiological Phenomena; Ethylenediamines; Gap Junctions; Humans; Ion Channel Gating; Keratitis; Membrane Potentials; Mesylates; Mice; Mutation, Missense; Oocytes; Permeability; RNA, Messenger; Streptomyces; Sulfhydryl Reagents; Syndrome; Transfection; Xenopus laevis | 2010 |
Urinary leukotriene levels are increased during exacerbation of atopic eczema/dermatitis syndrome. Relation to clinical status.
Topics: Adolescent; Adult; Cysteine; Dermatitis; Eczema; Eosinophils; Female; Humans; Hypersensitivity; Immunoglobulin E; Leukocyte Count; Leukotrienes; Male; Middle Aged; Remission Induction; Severity of Illness Index; Syndrome | 2002 |
Regional cerebral blood flow in a patient with Nasu-Hakola disease.
Topics: Adult; Brain; Cerebrovascular Circulation; Chromosome Disorders; Cysteine; Dementia, Vascular; Female; Humans; Lipodystrophy; Memory Disorders; Organotechnetium Compounds; Osteochondrodysplasias; Radionuclide Imaging; Radiopharmaceuticals; Syndrome | 2005 |
Endothelial NO synthase polymorphisms and postural tachycardia syndrome.
Topics: Adolescent; Adult; Alleles; Aspartic Acid; Case-Control Studies; Cysteine; Female; Genotype; Glutamic Acid; Heart Rate; Homozygote; Humans; Male; Middle Aged; Nitric Oxide Synthase Type III; Norepinephrine; Polymorphism, Genetic; Posture; Severity of Illness Index; Syndrome; Tachycardia; Threonine | 2005 |
Do Craniosynostosis syndrome phenotypes with both FGFR2 and TWIST mutations have a worse clinical outcome?
Topics: Acrocephalosyndactylia; Adenine; Adolescent; Arginine; Child, Preschool; Craniofacial Dysostosis; Craniosynostoses; Cysteine; Cytosine; DNA Transposable Elements; Female; Follow-Up Studies; Guanine; Humans; Male; Mutation; Receptor, Fibroblast Growth Factor, Type 2; Sequence Deletion; Serine; Syndrome; Thymine; Treatment Outcome; Tryptophan; Twist-Related Protein 1 | 2006 |
Bucillamine-induced pemphigus vulgaris in a patient with rheumatoid arthritis and polymyositis overlap syndrome.
Topics: Antioxidants; Arthritis; Arthritis, Rheumatoid; Biopsy; Cysteine; Female; Humans; Middle Aged; Pemphigus; Polymyositis; Skin; Syndrome | 2006 |
Juvenile bilateral lens dislocation and glaucoma associated with a novel mutation in the fibrillin 1 gene.
Topics: Adult; Aged; Amino Acid Substitution; Child; Child, Preschool; Corneal Diseases; Cysteine; Exons; Female; Fibrillin-1; Fibrillins; Genetic Linkage; Glaucoma; Humans; Lens Subluxation; Lod Score; Male; Microfilament Proteins; Middle Aged; Mutation, Missense; Pedigree; Serine; Syndrome | 2006 |
Intractable cryptogenic frontal lobe epilepsy in a patient with MURCS association.
Topics: Adult; Cysteine; Drug Resistance; Epilepsy, Frontal Lobe; Female; Humans; Kidney Diseases; Magnetic Resonance Imaging; Mullerian Ducts; Organotechnetium Compounds; Radiography; Radiopharmaceuticals; Stellate Ganglion; Syndrome; Tomography, Emission-Computed, Single-Photon | 2006 |
FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
Topics: Asian People; Blepharophimosis; Blepharoptosis; Cysteine; Cytosine; Eye Abnormalities; Eyelids; Forkhead Box Protein L2; Forkhead Transcription Factors; Guanine; Heterozygote; Histidine; Humans; Mutation; Mutation, Missense; Polymorphism, Single-Stranded Conformational; Serine; Syndrome; Thymine; Tyrosine | 2007 |
Ictal technetium-99 m ethyl cysteinate dimer single-photon emission tomographic findings in epileptic patients with polymicrogyria syndromes: a subtraction of ictal-interictal SPECT coregistered to MRI study.
Topics: Adolescent; Brain; Child; Cysteine; Epilepsy; Female; Humans; Magnetic Resonance Imaging; Male; Malformations of Cortical Development; Organotechnetium Compounds; Radiopharmaceuticals; Subtraction Technique; Syndrome; Tomography, Emission-Computed, Single-Photon | 2008 |
Familial Creutzfeldt-Jakob Disease with a codon 200 mutation presenting as thalamic syndrome: diagnosis by single photon emission computed tomography using (99m)Tc-ethyl cysteinate dimer.
Topics: Codon; Creutzfeldt-Jakob Syndrome; Cysteine; Female; Humans; Middle Aged; Mutation; Radiopharmaceuticals; Syndrome; Technetium; Thalamic Diseases; Tomography, Emission-Computed, Single-Photon | 2008 |
Second case of Beare-Stevenson syndrome with an FGFR2 Ser372Cys mutation.
Topics: Abnormalities, Multiple; Amino Acid Substitution; Base Sequence; Craniosynostoses; Cysteine; Humans; Infant; Male; Molecular Sequence Data; Point Mutation; Receptor, Fibroblast Growth Factor, Type 2; Serine; Skin Abnormalities; Skull; Syndrome | 2008 |
DLX3 mutation in a new family and its phenotypic variations.
Topics: Amelogenesis Imperfecta; Child; Codon; Cysteine; Dental Enamel Hypoplasia; Dental Pulp Cavity; Frameshift Mutation; Hair; Homeodomain Proteins; Humans; Male; Nails, Malformed; Pedigree; Phenotype; Sequence Deletion; Syndrome; Threonine; Transcription Factors | 2008 |
A novel mutation of the adrenocorticotropin receptor (ACTH-R) gene in a family with the syndrome of isolated glucocorticoid deficiency, but no ACTH-R abnormalities in two families with the triple A syndrome.
Topics: Adenine; Adolescent; Adult; Amino Acid Sequence; Base Sequence; Cell Membrane; Cysteine; DNA; DNA Primers; Female; Genes, Recessive; Genetic Carrier Screening; Genetic Diseases, Inborn; Glucocorticoids; Guanine; Homozygote; Humans; Male; Middle Aged; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction; Protein Structure, Secondary; Receptors, Corticotropin; Syndrome; Tyrosine | 1995 |
Effect of selected dietary antioxidants on fatty liver-haemorrhagic syndrome in laying hens.
Topics: Animals; Antioxidants; Ascorbic Acid; Chickens; Cysteine; Fatty Liver; Female; Food, Fortified; Glutathione; Hemorrhage; Liver; Oviposition; Poultry Diseases; Syndrome; Vitamin E | 1994 |
Agouti alleles alter cysteine and glutathione concentrations in hair follicles and serum of mice (A y/a, A wJ/A wJ, and a/a).
Topics: Agouti Signaling Protein; Alleles; Animals; Cysteine; Female; Genes, Lethal; Genotype; Glutathione; Hair Color; Hair Follicle; Intercellular Signaling Peptides and Proteins; Mice; Mice, Mutant Strains; Phenotype; Proteins; Syndrome | 1996 |
Hypotrichosis, hair structure defects, hypercysteine hair and glucosuria: a new genetic syndrome?
Topics: Amino Acids; Cysteine; Electrophoresis, Polyacrylamide Gel; Female; Glycosuria; Hair; Humans; Hypotrichosis; Infant; Male; Microscopy, Electron, Scanning; Nuclear Family; Syndrome | 1996 |
Detection of a novel Cys628STOP mutation of the myosin VIIA gene in Usher syndrome type Ib.
Topics: Codon, Terminator; Cysteine; Deafness; DNA; DNA Mutational Analysis; Dyneins; Exons; Female; Genes, Recessive; Humans; Male; Middle Aged; Mutation; Myosin VIIa; Myosins; Pedigree; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Retinitis Pigmentosa; Syndrome | 1998 |
[Brain SPECT using Tc-99m-bicisate (ECD) in rapidly progressive dementia syndrome].
Topics: Brain; Cysteine; Dementia; Diagnosis, Differential; Disease Progression; Humans; Male; Middle Aged; Mutism; Organotechnetium Compounds; Radiopharmaceuticals; Syndrome; Tomography, Emission-Computed, Single-Photon | 1999 |
Identification of a novel R642C mutation in Na/Cl cotransporter with Gitelman's syndrome.
Topics: Adult; Arginine; Bartter Syndrome; Carrier Proteins; Chromosome Aberrations; Chromosome Disorders; Codon; Cysteine; DNA Mutational Analysis; Electrolytes; Exons; Female; Genes, Recessive; Humans; Kidney Function Tests; Male; Mutation, Missense; Pedigree; Sodium Chloride Symporters; Symporters; Syndrome | 1999 |
Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses).
Topics: Acrocephalosyndactylia; Amino Acid Sequence; Cohort Studies; Craniofacial Dysostosis; Cysteine; DNA Mutational Analysis; Female; Genetic Testing; Humans; Male; Molecular Sequence Data; Mutagenesis; Mutation; Nuclear Proteins; Pedigree; Phenotype; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 2; Receptors, Fibroblast Growth Factor; Syndrome; Transcription Factors; Twist-Related Protein 1 | 2000 |
Periodic hypersomnia: case report with biochemical and EEG findings.
Topics: Adult; Arousal; Cerebral Cortex; Circadian Rhythm; Cysteine; Depressive Disorder; Diagnosis, Differential; Disorders of Excessive Somnolence; Electroencephalography; Enkephalin, Leucine; Follow-Up Studies; Humans; Male; Neurologic Examination; Periodicity; Sleep Stages; Syndrome; Wakefulness | 1991 |