serine has been researched along with Amyloid Neuropathies in 9 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
Amyloid Neuropathies: Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 5 (55.56) | 18.2507 |
| 2000's | 2 (22.22) | 29.6817 |
| 2010's | 2 (22.22) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yang, NC | 1 |
| Lee, MJ | 1 |
| Chao, CC | 1 |
| Chuang, YT | 1 |
| Lin, WM | 1 |
| Chang, MF | 1 |
| Hsieh, PC | 1 |
| Kan, HW | 1 |
| Lin, YH | 1 |
| Yang, CC | 1 |
| Chiu, MJ | 1 |
| Liou, HH | 1 |
| Hsieh, ST | 2 |
| Yazaki, M | 1 |
| Liepnieks, JJ | 1 |
| Kincaid, JC | 1 |
| Benson, MD | 2 |
| Uemichi, T | 1 |
| Gertz, MA | 1 |
| Jacobson, DR | 1 |
| Buxbaum, JN | 1 |
| Wilce, JA | 1 |
| Salvatore, D | 1 |
| Wade, JD | 1 |
| Craik, DJ | 1 |
| Misrahi, AM | 1 |
| Plante, V | 1 |
| Lalu, T | 1 |
| Serre, L | 1 |
| Adams, D | 1 |
| Lacroix, DC | 1 |
| Saïd, G | 1 |
| Kishikawa, M | 1 |
| Nakanishi, T | 1 |
| Miyazaki, A | 1 |
| Hatanaka, M | 1 |
| Shimizu, A | 1 |
| Tamoto, S | 1 |
| Ohsawa, N | 1 |
| Hayashi, H | 1 |
| Kanai, M | 1 |
| Lachmann, HJ | 1 |
| Booth, DR | 1 |
| Bybee, A | 1 |
| Hawkins, PN | 1 |
1 review available for serine and Amyloid Neuropathies
| Article | Year |
|---|---|
Amyloid neuropathy with transthyretin mutations: overview and unique Ala97Ser in Taiwan.
Topics: Age of Onset; Alanine; Amyloid Neuropathies; Female; Genetic Predisposition to Disease; Humans; Male | 2011 |
8 other studies available for serine and Amyloid Neuropathies
| Article | Year |
|---|---|
Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser.
Topics: Aged; Alanine; Amino Acid Substitution; Amyloid Neuropathies; Amyloid Neuropathies, Familial; Female | 2010 |
Contribution of wild-type transthyretin to hereditary peripheral nerve amyloid.
Topics: Alanine; Amyloid; Amyloid Neuropathies; Blotting, Western; Dimerization; Electrophoresis, Polyacryla | 2003 |
A new transthyretin variant (Ser 24) associated with familial amyloid polyneuropathy.
Topics: Aged; Amyloid Neuropathies; Cardiomyopathies; Codon; Cytosine; DNA; Exons; Family Health; Female; Ge | 1995 |
A double-variant transthyretin allele (Ser 6, Ile 33) in the Israeli patient "SKO" with familial amyloidotic polyneuropathy.
Topics: Alleles; Amino Acid Sequence; Amyloid Neuropathies; Base Sequence; DNA; DNA Primers; Exons; Humans; | 1994 |
1H-NMR structural studies of a cystine-linked peptide containing residues 71-93 of transthyretin and effects of a Ser84 substitution implicated in familial amyloidotic polyneuropathy.
Topics: Amino Acid Sequence; Amino Acid Substitution; Amyloid Neuropathies; Cystine; Hydrogen Bonding; Magne | 1999 |
New transthyretin variants SER 91 and SER 116 associated with familial amyloidotic polyneuropathy. Mutations in brief no. 151. Online.
Topics: Aged; Alanine; Amyloid Neuropathies; Humans; Male; Mutation; Prealbumin; Protein Isoforms; Serine; T | 1998 |
A new nonamyloid transthyretin variant, G101S, detected by electrospray ionization/mass spectrometry. Mutations in brief no. 201. Online.
Topics: Aged; Amyloid Neuropathies; Glycine; Humans; Male; Mass Spectrometry; Point Mutation; Prealbumin; Pr | 1998 |
Transthyretin Ala97Ser is associated with familial amyloidotic polyneuropathy in a Chinese-Taiwanese family.
Topics: Alanine; Amino Acid Substitution; Amyloid Neuropathies; Codon, Nonsense; Humans; Male; Middle Aged; | 2000 |