proline and Down Syndrome

proline has been researched along with Down Syndrome in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19901 (11.11)18.7374
1990's3 (33.33)18.2507
2000's3 (33.33)29.6817
2010's1 (11.11)24.3611
2020's1 (11.11)2.80

Authors

AuthorsStudies
Barg, E; Bodetko, A; Hetman, M; Mielko, K; Młynarz, P; Placzkowska, S1
Almeida, LM; Almeida, Mdo C; Barros, AS; Carreira, IM; Domingues, MR; Duarte, D; Galhano, E; Gil, AM; Martins, AS; Pinto, J; Pita, C1
Han, SW; Henrique-Silva, F; Machado-Santelli, GM; Pfister, SC1
Chen-Hwang, MC; Hwang, YW; Lu, RC; Murakami, N; Wieraszko, A; Xie, W1
Bosch, A; Estivill, X; Ferrer, I; Fuentes, JJ; Planas, AM; Pritchard, MA1
Arrigo, P; Egeo, A; Giglio, S; Mazzocco, M; Oliva, R; Pirola, B; Rasore-Quartino, A; Scartezzini, P; Vidal-Taboada, JM1
Badmajew, E; Dowjat, WK; Kuchna, I; Kulczycki, J; Popovitch, E; Tarnawski, M; Wegiel, J; Wisniewski, HM; Wisniewski, T1
Brown, EJ; Malkin, D; Zipursky, A1
Komrower, GM1

Other Studies

9 other study(ies) available for proline and Down Syndrome

ArticleYear
Predisposition to atherosclerosis in children and adults with trisomy 21: biochemical and metabolomic studies.
    Pediatric endocrinology, diabetes, and metabolism, 2023, Volume: 29, Issue:3

    Topics: Acetates; Adolescent; Adult; Apolipoprotein A-I; Apolipoproteins B; Atherosclerosis; Cardiovascular Diseases; Child; Creatinine; Down Syndrome; Formates; Glutamine; Humans; Lysine; Proline; Pyrrolidonecarboxylic Acid; Risk Factors; Xanthines

2023
Impact of fetal chromosomal disorders on maternal blood metabolome: toward new biomarkers?
    American journal of obstetrics and gynecology, 2015, Volume: 213, Issue:6

    Topics: Acetates; Adult; Biomarkers; Blood Glucose; Case-Control Studies; Chromosome Disorders; Citric Acid; Creatinine; Down Syndrome; Fatty Acids; Female; Humans; Ketone Bodies; Lipid Metabolism; Lipoproteins, HDL; Lipoproteins, VLDL; Magnetic Resonance Spectroscopy; Metabolome; Methanol; Pregnancy; Pregnancy Trimester, First; Pregnancy Trimester, Second; Proline; Pyruvic Acid; Serum Albumin; Urea; Young Adult

2015
Mutational analyses of the signals involved in the subcellular location of DSCR1.
    BMC cell biology, 2002, Sep-11, Volume: 3

    Topics: Amino Acid Motifs; Animals; Calcineurin; Calcineurin Inhibitors; Cell Line; Chlorocebus aethiops; CHO Cells; COS Cells; Cricetinae; Cyclosporine; DNA-Binding Proteins; Down Syndrome; Humans; Intracellular Signaling Peptides and Proteins; Ionomycin; Kidney; Muscle Proteins; Mutagenesis, Site-Directed; Nuclear Proteins; Point Mutation; Proline; Protein Isoforms; Protein Sorting Signals; Serine; src Homology Domains; Tetradecanoylphorbol Acetate; Threonine

2002
Phosphorylation of amphiphysin I by minibrain kinase/dual-specificity tyrosine phosphorylation-regulated kinase, a kinase implicated in Down syndrome.
    The Journal of biological chemistry, 2006, Aug-18, Volume: 281, Issue:33

    Topics: Adaptor Proteins, Signal Transducing; Amino Acid Substitution; Animals; Binding Sites, Antibody; CHO Cells; Cricetinae; Down Syndrome; Dyrk Kinases; Electrophysiology; Endocytosis; Hippocampus; Humans; Mice; Nerve Tissue Proteins; NIH 3T3 Cells; Organ Culture Techniques; Phosphorylation; Proline; Protein Binding; Protein Serine-Threonine Kinases; Protein Structure, Tertiary; Protein-Tyrosine Kinases; Rats; Recombinant Fusion Proteins; Serine

2006
A new human gene from the Down syndrome critical region encodes a proline-rich protein highly expressed in fetal brain and heart.
    Human molecular genetics, 1995, Volume: 4, Issue:10

    Topics: Aging; Amino Acid Sequence; Animals; Base Sequence; Brain; Chromosome Mapping; Chromosomes, Artificial, Yeast; Chromosomes, Human, Pair 21; Cloning, Molecular; DNA Primers; DNA-Binding Proteins; Down Syndrome; Exons; Gene Expression; Gene Expression Regulation; Genetic Markers; Heart; Heart Defects, Congenital; Humans; Intellectual Disability; Intracellular Signaling Peptides and Proteins; Molecular Sequence Data; Muscle Proteins; Myocardium; Polymerase Chain Reaction; Proline; Protein Biosynthesis; Proteins; Rats; Restriction Mapping; Sequence Homology, Amino Acid; Signal Transduction; Transcription, Genetic

1995
Identification and characterization of a new human gene encoding a small protein with high homology to the proline-rich region of the SH3BGR gene.
    Biochemical and biophysical research communications, 1998, Jun-18, Volume: 247, Issue:2

    Topics: Amino Acid Sequence; Animals; Base Sequence; Chromosome Mapping; Cloning, Molecular; Conserved Sequence; DNA, Complementary; Down Syndrome; Humans; In Situ Hybridization, Fluorescence; Mice; Molecular Sequence Data; Muscle Proteins; Proline; Proteins; RNA, Messenger; Sequence Homology, Amino Acid; src Homology Domains; Tissue Distribution; X Chromosome

1998
Cell-type-specific enhancement of amyloid-beta deposition in a novel presenilin-1 mutation (P117L).
    Journal of neuropathology and experimental neurology, 1998, Volume: 57, Issue:9

    Topics: Adult; Age of Onset; Aged; Alzheimer Disease; Amyloid beta-Peptides; Brain; Cerebellum; Dentate Gyrus; Down Syndrome; Entorhinal Cortex; Female; Hippocampus; Humans; Leucine; Male; Membrane Proteins; Middle Aged; Point Mutation; Poland; Presenilin-1; Proline

1998
The role of p53 in megakaryocyte differentiation and the megakaryocytic leukemias of Down syndrome.
    Cancer genetics and cytogenetics, 2000, Jan-01, Volume: 116, Issue:1

    Topics: Amino Acid Sequence; Arginine; Base Sequence; Cell Differentiation; Child; Child, Preschool; Down Syndrome; Female; Genes, p53; Glycine; Humans; Leukemia, Megakaryoblastic, Acute; Male; Megakaryocytes; Mutation; Proline; Sequence Analysis, DNA; Tumor Suppressor Protein p53; Valine

2000
The philosophy and practice of screening for inherited diseases.
    Pediatrics, 1974, Volume: 53, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Amniocentesis; Child; Child, Preschool; Chromatography, Paper; Chromosome Aberrations; Clinical Enzyme Tests; Costs and Cost Analysis; Down Syndrome; Female; Genetic Counseling; Genetic Diseases, Inborn; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Karyotyping; Male; Mass Screening; Phenylketonurias; Philosophy, Medical; Pregnancy; Prenatal Diagnosis; Proline; Sex Determination Analysis

1974