Page last updated: 2024-10-18

glycine and Dwarfism

glycine has been researched along with Dwarfism in 8 studies

Dwarfism: A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height.

Research Excerpts

ExcerptRelevanceReference
"Isovaleric acidaemia was diagnosed in a 9-year-old girl with an unusual clinical presentation."5.26Isovaleric acidaemia presenting with dwarfism, cataract and congenital abnormalities. ( Batenburg-Plenter, AM; Bruinvis, L; Duran, M; Ketting, D; van Pelt, BC; Wadman, SK, 1982)
"A solution of 10% glycine (250 mg/kg of body weight) was injected in within 5-10 minutes in 22 healthy, sexually immature children who were previously tested for insulin-induced hypoglycemia."3.65Growth hormone release by glycine injected intravenously in 22 healthy sexually immature children. ( Florea, I; Popa, M, 1975)
"Isovaleric acidaemia was diagnosed in a 9-year-old girl with an unusual clinical presentation."1.26Isovaleric acidaemia presenting with dwarfism, cataract and congenital abnormalities. ( Batenburg-Plenter, AM; Bruinvis, L; Duran, M; Ketting, D; van Pelt, BC; Wadman, SK, 1982)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19905 (62.50)18.7374
1990's1 (12.50)18.2507
2000's0 (0.00)29.6817
2010's1 (12.50)24.3611
2020's1 (12.50)2.80

Authors

AuthorsStudies
Sterrett, MC1
Enyenihi, L1
Leung, SW1
Hess, L1
Strassler, SE1
Farchi, D1
Lee, RS1
Withers, ES1
Kremsky, I1
Baker, RE1
Basrai, MA1
van Hoof, A1
Fasken, MB1
Corbett, AH1
Chen, J1
Yang, J1
Zhao, S1
Ying, H1
Li, G1
Xu, C1
Duran, M1
Bruinvis, L1
Ketting, D1
Wadman, SK1
van Pelt, BC1
Batenburg-Plenter, AM1
Popa, M1
Florea, I1
Chen, WY1
Wight, DC1
Mehta, BV1
Wagner, TE1
Kopchick, JJ1
Vissing, H1
D'Alessio, M1
Lee, B1
Ramirez, F1
Godfrey, M1
Hollister, DW1
Richter, I1
Heine, W1
Plath, C1
Mix, M1
Wutzke, KD1
Töwe, J1
Minder, FC1
Dubach, UC1
Antener, I1

Other Studies

8 other studies available for glycine and Dwarfism

ArticleYear
A budding yeast model for human disease mutations in the
    RNA (New York, N.Y.), 2021, Volume: 27, Issue:9

    Topics: Amino Acid Sequence; Amino Acid Substitution; Aspartic Acid; Dwarfism; Exoribonucleases; Exosome Mul

2021
Identification of a novel mutation in the FGFR3 gene in a Chinese family with Hypochondroplasia.
    Gene, 2018, Jan-30, Volume: 641

    Topics: Adult; Asian People; Aspartic Acid; Bone and Bones; Child; Dwarfism; Exome; Glycine; Heterozygote; H

2018
Isovaleric acidaemia presenting with dwarfism, cataract and congenital abnormalities.
    Journal of inherited metabolic disease, 1982, Volume: 5, Issue:2

    Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Cataract; Child; Dwarfism; Female; Gl

1982
Growth hormone release by glycine injected intravenously in 22 healthy sexually immature children.
    Biomedicine / [publiee pour l'A.A.I.C.I.G.], 1975, Apr-30, Volume: 23, Issue:4

    Topics: Antibodies; Child; Dwarfism; Female; Glycine; Growth Hormone; Humans; Hypoglycemia; Insulin; Male; N

1975
Glycine 119 of bovine growth hormone is critical for growth-promoting activity.
    Molecular endocrinology (Baltimore, Md.), 1991, Volume: 5, Issue:12

    Topics: Alanine; Amino Acid Sequence; Animals; Base Sequence; Cell Membrane; Cells, Cultured; DNA; Dwarfism;

1991
Glycine to serine substitution in the triple helical domain of pro-alpha 1 (II) collagen results in a lethal perinatal form of short-limbed dwarfism.
    The Journal of biological chemistry, 1989, Nov-05, Volume: 264, Issue:31

    Topics: Amino Acid Sequence; Base Sequence; Cloning, Molecular; Codon; Dwarfism; Glycine; Humans; Molecular

1989
15N tracer techniques for the differential diagnosis of dwarfism and prediction of growth hormone action in children.
    The Journal of clinical endocrinology and metabolism, 1987, Volume: 65, Issue:1

    Topics: Adolescent; Child; Child, Preschool; Diagnosis, Differential; Dwarfism; Female; Glycine; Growth Horm

1987
[Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland)].
    Zeitschrift fur klinische Medizin, 1965, Dec-31, Volume: 158, Issue:7

    Topics: Adolescent; Adult; Aged; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Deafness; Dw

1965