alanine has been researched along with Autism in 9 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
| Excerpt | Relevance | Reference |
|---|---|---|
| "A random retrospective chart review was conducted to document serum carnitine levels on 100 children with autism." | 7.72 | Relative carnitine deficiency in autism. ( Cummings, C; Filipek, PA; Gargus, JJ; Juranek, J; Nguyen, MT, 2004) |
| " Patients with autism or Asperger syndrome and their siblings and parents all had raised glutamic acid, phenylalanine, asparagine, tyrosine, alanine, and lysine (p < ." | 3.72 | Plasma amino acid levels in children with autism and their families. ( Aldred, S; Fitzgerald, M; Moore, KM; Waring, RH, 2003) |
| "A random retrospective chart review was conducted to document serum carnitine levels on 100 children with autism." | 3.72 | Relative carnitine deficiency in autism. ( Cummings, C; Filipek, PA; Gargus, JJ; Juranek, J; Nguyen, MT, 2004) |
| "We screened autism, mental retardation (MR), and control populations for sequence variation within this region, and identified variation in approximately 1% of MR cases screened (N = 1,410)." | 1.34 | Sequence variants within exon 1 of MECP2 occur in females with mental retardation. ( Alfred, SE; Guo, R; Harvey, CG; Kennedy, JL; Menon, SD; Mensah, AK; Minassian, BA; Mnatzakanian, GN; Noor, A; Proctor, A; Roberts, W; Scherer, SW; Srivastava, AK; Srivistava, AK; Stachowiak, B; Vincent, JB, 2007) |
| "Autism is a developmental, cognitive disorder clinically characterized by impaired social interaction, communication and restricted behaviours." | 1.34 | Aberrant amino acid transport in fibroblasts from children with autism. ( Bjerkenstedt, L; Edman, G; Fernell, E; Karagiannakis, A; Venizelos, N; Wiesel, FA, 2007) |
| "Autism is a spectrum of neurodevelopmental disorders with a primarily genetic etiology exhibiting deficits in (1) development of language and (2) social relationships and (3) patterns of repetitive, restricted behaviors or interests and resistance to change." | 1.33 | Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors. ( Blakely, RD; Delahanty, RJ; Folstein, SE; Han, Q; Jiang, L; Li, C; McCauley, JL; Prasad, HC; Sutcliffe, JS, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (11.11) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 7 (77.78) | 29.6817 |
| 2010's | 1 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Rodríguez-Escudero, I | 1 |
| Oliver, MD | 1 |
| Andrés-Pons, A | 1 |
| Molina, M | 1 |
| Cid, VJ | 1 |
| Pulido, R | 1 |
| Aldred, S | 1 |
| Moore, KM | 1 |
| Fitzgerald, M | 1 |
| Waring, RH | 1 |
| VISAKORPI, JK | 1 |
| WASZ-HOECKERT, O | 1 |
| TOERMAE, T | 1 |
| Conciatori, M | 1 |
| Stodgell, CJ | 1 |
| Hyman, SL | 1 |
| O'Bara, M | 1 |
| Militerni, R | 1 |
| Bravaccio, C | 1 |
| Trillo, S | 1 |
| Montecchi, F | 1 |
| Schneider, C | 1 |
| Melmed, R | 1 |
| Elia, M | 1 |
| Crawford, L | 1 |
| Spence, SJ | 1 |
| Muscarella, L | 1 |
| Guarnieri, V | 1 |
| D'Agruma, L | 1 |
| Quattrone, A | 1 |
| Zelante, L | 1 |
| Rabinowitz, D | 1 |
| Pascucci, T | 1 |
| Puglisi-Allegra, S | 1 |
| Reichelt, KL | 1 |
| Rodier, PM | 1 |
| Persico, AM | 1 |
| Filipek, PA | 1 |
| Juranek, J | 1 |
| Nguyen, MT | 1 |
| Cummings, C | 1 |
| Gargus, JJ | 1 |
| Sutcliffe, JS | 1 |
| Delahanty, RJ | 1 |
| Prasad, HC | 1 |
| McCauley, JL | 1 |
| Han, Q | 1 |
| Jiang, L | 1 |
| Li, C | 1 |
| Folstein, SE | 1 |
| Blakely, RD | 1 |
| Harvey, CG | 1 |
| Menon, SD | 1 |
| Stachowiak, B | 1 |
| Noor, A | 1 |
| Proctor, A | 1 |
| Mensah, AK | 1 |
| Mnatzakanian, GN | 1 |
| Alfred, SE | 1 |
| Guo, R | 1 |
| Scherer, SW | 1 |
| Kennedy, JL | 1 |
| Roberts, W | 1 |
| Srivastava, AK | 1 |
| Srivistava, AK | 1 |
| Minassian, BA | 1 |
| Vincent, JB | 1 |
| Fernell, E | 1 |
| Karagiannakis, A | 1 |
| Edman, G | 1 |
| Bjerkenstedt, L | 1 |
| Wiesel, FA | 1 |
| Venizelos, N | 1 |
| Coutinho, AM | 1 |
| Oliveira, G | 1 |
| Katz, C | 1 |
| Feng, J | 1 |
| Yan, J | 1 |
| Yang, C | 1 |
| Marques, C | 1 |
| Ataíde, A | 1 |
| Miguel, TS | 1 |
| Borges, L | 1 |
| Almeida, J | 1 |
| Correia, C | 1 |
| Currais, A | 1 |
| Bento, C | 1 |
| Mota-Vieira, L | 1 |
| Temudo, T | 1 |
| Santos, M | 1 |
| Maciel, P | 1 |
| Sommer, SS | 1 |
| Vicente, AM | 1 |
9 other studies available for alanine and Autism
| Article | Year |
|---|---|
A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes.
Topics: Alanine; Amino Acid Sequence; Aspartic Acid; Autistic Disorder; Catalytic Domain; DNA Mutational Ana | 2011 |
Plasma amino acid levels in children with autism and their families.
Topics: Adolescent; Alanine; Amino Acids; Asparagine; Asperger Syndrome; Autistic Disorder; Brain Diseases, | 2003 |
THE AMINO ACIDS OF CEREBROSPINAL FLUID IN VARIOUS DISEASES AFFECTING THE CENTRAL NERVOUS SYSTEM.
Topics: Adolescent; Alanine; Amino Acids; Autistic Disorder; Brain Neoplasms; Cerebrospinal Fluid; Child; En | 1964 |
Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alanine; Americas; Asperger Syndrome; Autistic Disorder; | 2004 |
Relative carnitine deficiency in autism.
Topics: Adolescent; Alanine; Autistic Disorder; Carnitine; Child; Child, Preschool; Diagnostic and Statistic | 2004 |
Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.
Topics: Alanine; Alleles; Autistic Disorder; Blood Platelets; Chromosomes, Human, Pair 17; Compulsive Behavi | 2005 |
Sequence variants within exon 1 of MECP2 occur in females with mental retardation.
Topics: Adult; Alanine; Amino Acid Sequence; Autistic Disorder; Base Sequence; Case-Control Studies; DNA Mut | 2007 |
Aberrant amino acid transport in fibroblasts from children with autism.
Topics: Alanine; Autistic Disorder; Biological Transport; Biopsy; Child; Child, Preschool; Female; Fibroblas | 2007 |
MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.
Topics: 3' Untranslated Regions; Adolescent; Alanine; Autistic Disorder; Case-Control Studies; Child; Child, | 2007 |