Page last updated: 2024-10-18

glycine and Xeroderma

glycine has been researched along with Xeroderma in 10 studies

Research Excerpts

ExcerptRelevanceReference
"Glycine is an amino acid with unique properties because its side chain is composed of a single hydrogen atom."2.72The Complex and Critical Role of Glycine 12 (G12) in Beta-Connexins of Human Skin. ( Bailey, RA; Beahm, DL; Skerrett, IM, 2021)

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19902 (20.00)18.7374
1990's3 (30.00)18.2507
2000's1 (10.00)29.6817
2010's2 (20.00)24.3611
2020's2 (20.00)2.80

Authors

AuthorsStudies
Pan, Y1
Feng, C1
Wang, H1
Lee, M1
Tang, Z1
Lin, Z1
Bailey, RA1
Beahm, DL1
Skerrett, IM1
Jaszczuk, I1
Schlotawa, L1
Dierks, T1
Ohlenbusch, A1
Koppenhöfer, D1
Babicz, M1
Lejman, M1
Radhakrishnan, K1
Ługowska, A1
Zhang, Y1
Hao, H1
Désilets, A1
Béliveau, F1
Vandal, G1
McDuff, FO1
Lavigne, P1
Leduc, R1
Huber, M1
Yee, VC1
Burri, N1
Vikerfors, E1
Lavrijsen, AP1
Paller, AS1
Hohl, D1
de Koning, TJ1
Poll-The, BT1
Jaeken, J1
Lee, LD1
Baden, HP1
Jacobson, TM1
Yüksel, KU1
Geesin, JC1
Gordon, JS1
Lane, AT1
Gracy, RW1
Ionasescu, V1
Stegink, L1
Mueller, S1
Weinstein, M1

Reviews

3 reviews available for glycine and Xeroderma

ArticleYear
The Complex and Critical Role of Glycine 12 (G12) in Beta-Connexins of Human Skin.
    International journal of molecular sciences, 2021, Mar-05, Volume: 22, Issue:5

    Topics: Amino Acid Substitution; Connexins; Epidermis; Erythrokeratodermia Variabilis; Gap Junctions; Glycin

2021
Continuing education in neurometabolic disorders--serine deficiency disorders.
    Neuropediatrics, 1999, Volume: 30, Issue:1

    Topics: Adolescent; Amino Acids; Child; Deficiency Diseases; Female; Glycine; Humans; Ichthyosis; Male; Meta

1999
Chemistry and composition of the keratins.
    International journal of dermatology, 1975, Volume: 14, Issue:3

    Topics: Amino Acids; Animals; Chemical Phenomena; Chemistry; Collagen; Feathers; Glycine; Guinea Pigs; Hair;

1975

Other Studies

7 other studies available for glycine and Xeroderma

ArticleYear
Ichthyosis with confetti caused by new and recurrent mutations in KRT10 associated with varying degrees of keratin 10 mis-localization.
    Journal of dermatological science, 2020, Volume: 98, Issue:1

    Topics: Adolescent; Amino Acid Sequence; Arginine; Biopsy; Cell Nucleus; Child, Preschool; DNA Mutational An

2020
Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease.
    Molecular genetics and metabolism, 2017, Volume: 121, Issue:3

    Topics: Cells, Cultured; Child, Preschool; Computer Simulation; Enzymes; Glycine; Humans; Ichthyosis; Male;

2017
Conserved glycine at position 45 of major cochlear connexins constitutes a vital component of the Ca²⁺ sensor for gating of gap junction hemichannels.
    Biochemical and biophysical research communications, 2013, Jul-05, Volume: 436, Issue:3

    Topics: Amino Acid Substitution; Calcium; Calcium Channels; Cell Death; Cell Membrane; Cell Membrane Permeab

2013
Mutation G827R in matriptase causing autosomal recessive ichthyosis with hypotrichosis yields an inactive protease.
    The Journal of biological chemistry, 2008, Apr-18, Volume: 283, Issue:16

    Topics: Arginine; Cell Membrane; DNA Mutational Analysis; Genes, Recessive; Glycine; Humans; Hypotrichosis;

2008
Consequences of seven novel mutations on the expression and structure of keratinocyte transglutaminase.
    The Journal of biological chemistry, 1997, Aug-22, Volume: 272, Issue:34

    Topics: Arginine; Binding Sites; Factor XIII; Female; Genes, Recessive; Glycine; Humans; Ichthyosis; Keratin

1997
Effects of aging and xerosis on the amino acid composition of human skin.
    The Journal of investigative dermatology, 1990, Volume: 95, Issue:3

    Topics: Aging; Amino Acids; Female; Filaggrin Proteins; Glycine; Humans; Ichthyosis; Leucine; Phenylalanine;

1990
Amino acid abnormality in Sjögren-Larsson syndrome.
    Archives of neurology, 1973, Volume: 28, Issue:3

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Dental Enamel Hypoplasia; Epilepsy; Ethylamines; G

1973
chemdatabank.com