Page last updated: 2024-11-08

serine and Alagille Syndrome

serine has been researched along with Alagille Syndrome in 2 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.

Alagille Syndrome: A multisystem disorder that is characterized by aplasia of intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC), and malformations in the cardiovascular system, the eyes, the vertebral column, and the facies. Major clinical features include JAUNDICE, and congenital heart disease with peripheral PULMONARY STENOSIS. Alagille syndrome may result from heterogeneous gene mutations, including mutations in JAG1 on CHROMOSOME 20 (Type 1) and NOTCH2 on CHROMOSOME 1 (Type 2).

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Luca, VC1
Jude, KM1
Pierce, NW1
Nachury, MV1
Fischer, S1
Garcia, KC1
Morrissette, JD1
Colliton, RP1
Spinner, NB1

Other Studies

2 other studies available for serine and Alagille Syndrome

ArticleYear
Structural biology. Structural basis for Notch1 engagement of Delta-like 4.
    Science (New York, N.Y.), 2015, Feb-20, Volume: 347, Issue:6224

    Topics: Alagille Syndrome; Amino Acid Sequence; Amino Acid Substitution; Animals; Cell Line; Conserved Seque

2015
Defective intracellular transport and processing of JAG1 missense mutations in Alagille syndrome.
    Human molecular genetics, 2001, Feb-15, Volume: 10, Issue:4

    Topics: 3T3 Cells; Alagille Syndrome; Amino Acid Substitution; Animals; Arginine; Biological Transport, Acti

2001