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    AK1 adenylate kinase 1 [ Homo sapiens (human) ]

    Gene ID: 203, updated on 5-May-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    High expression of AK1 predicts inferior prognosis in acute myeloid leukemia patients undergoing chemotherapy.

    High expression of AK1 predicts inferior prognosis in acute myeloid leukemia patients undergoing chemotherapy.
    Qin T, Zhao H, Shao Y, Hu N, Shi J, Fu L, Zhang Y., Free PMC Article

    03/27/2021
    A co-expressed gene status of adenylate kinase 1/4 reveals prognostic gene signature associated with prognosis and sensitivity to EGFR targeted therapy in lung adenocarcinoma.

    A co-expressed gene status of adenylate kinase 1/4 reveals prognostic gene signature associated with prognosis and sensitivity to EGFR targeted therapy in lung adenocarcinoma.
    Jan YH, Lai TC, Yang CJ, Huang MS, Hsiao M., Free PMC Article

    10/24/2020
    Specific DNA methylation signatures for aggressive choroid plexus carcinoma (CPC) revealed AK1, PER2, and PLSCR4 as potential biomarkers for CPC that can be used to improve molecular stratification for diagnosis and treatment.

    DNA methylation signature is prognostic of choroid plexus tumor aggressiveness.
    Pienkowska M, Choufani S, Turinsky AL, Guha T, Merino DM, Novokmet A, Brudno M, Weksberg R, Shlien A, Hawkins C, Bouffet E, Tabori U, Gilbertson RJ, Finlay JL, Jabado N, Thomas C, Sill M, Capper D, Hasselblatt M, Malkin D., Free PMC Article

    06/20/2020
    The mRNA and protein expressions of AK1, AK6 and AK7 are significantly down-regulated in the sperm of asthenospermia patients, which may be closely related with reduced sperm motility.

    [Expressions of the adenylate kinase family in asthenospermia].
    Wang HS, Zhu Y, Sun F.

    05/23/2020
    Case Reports: first case of adenylate kinase deficiency in Indian population due to novel AK1 mutations (c.71A>G and c.413G>A) associated with nonspherocytic haemolytic anaemia without psychomotor impairment.

    Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A).
    Dongerdiye R, Kamat P, Jain P, Warang P, Devendra R, Wasekar N, Sharma R, Mhaskar K, Madkaikar MR, Manglani MV, Kedar PS.

    06/1/2019
    Studies indicate that the preferred substrate and phosphate donor of all adenylate kinases are AMP and ATP respectively.

    The many isoforms of human adenylate kinases.
    Panayiotou C, Solaroli N, Karlsson A.

    11/22/2014
    Dysregulation of AMPK is both a pathogenic factor for these disorders in humans and a target for their prevention and therapy. [Review]

    AMPK, insulin resistance, and the metabolic syndrome.
    Ruderman NB, Carling D, Prentki M, Cacicedo JM., Free PMC Article

    10/19/2013
    Ak(1)2-1 phenotype is more frequent in males conceived in the summer-autumn period than in those conceived in winter-spring, and this association depends on maternal Ak(1) phenotype.

    Ak(1) genetic polymorphism and season of conception.
    Gloria-Bottini F, Neri A, Pietropolli A, Bottini E, Magrini A.

    08/10/2013
    identified hitherto unrecognized soluble forms of AK1 and NTPDase1/CD39 that contribute in the active cycling between the principal platelet-recruiting agent ADP and other circulating nucleotides

    Metabolism of circulating ADP in the bloodstream is mediated via integrated actions of soluble adenylate kinase-1 and NTPDase1/CD39 activities.
    Yegutkin GG, Wieringa B, Robson SC, Jalkanen S., Free PMC Article

    12/29/2012
    Data indicate that the neuronal adenylate kinase-1 (AK1) is induced by Abeta(42) to increase abnormal tau phosphorylation via AMPK-GSK3beta and contributes to tau-mediated neurodegeneration.

    Neuropathogenic role of adenylate kinase-1 in Aβ-mediated tau phosphorylation via AMPK and GSK3β.
    Park H, Kam TI, Kim Y, Choi H, Gwon Y, Kim C, Koh JY, Jung YK.

    10/13/2012
    AK1 phenotypic activity is associated with birth weight and placental weight; these associations are greater in infants born at gestational age greater than 38 weeks.

    Adenylate kinase locus 1 polymorphism and feto-placental development.
    Fulvia GB, Antonio P, Anna N, Patrizia S, Ada A, Egidio B, Andrea M.

    04/28/2012
    Our findings suggest a reduced reproductive efficiency of women carrying the Ak(1)2-1 phenotype: this could have practical importance in predicting the probability of reproductive success in couples with RSA

    Adenylate kinase genetic polymorphism and spontaneous abortion.
    Gloria-Bottini F, Nicotra M, Amante A, Pietropolli A, Neri A, Bottini E, Magrini A.

    04/14/2012
    The adipokine zinc-alpha2-glycoprotein activates AMP kinase in human primary skeletal muscle cells.

    The adipokine zinc-α2-glycoprotein activates AMP kinase in human primary skeletal muscle cells.
    Eckardt K, Schober A, Platzbecker B, Mracek T, Bing C, Trayhurn P, Eckel J.

    08/13/2011
    the correlation between blood glucose and glycated Hb in relation to AK1 and ACP1 polymorphism was studied.

    The effect of genetic variability on the correlation between blood glucose and glycated hemoglobin levels.
    Gloria-Bottini F, Antonacci E, Cozzoli E, De Acetis C, Bottini E.

    03/5/2011
    The data suggest that zygotes carrying AK1*2 allele are relatively protected from the damaging effects of smoking

    Smoking and human reproduction: the effect of adenylate kinase genetic polymorphism.
    Gloria-Bottini F, Magrini A, Pietropolli A, Bergamaschi A, Bottini E, Gloria-Bottini F, Magrini A, Pietropolli A, Bergamaschi A, Bottini E.

    01/21/2010
    Using shotgun mass spectrometry, we found this protein differentially expressed in the dorsolateral prefrontal cortex from patients with schizophrenia.

    Prefrontal cortex shotgun proteome analysis reveals altered calcium homeostasis and immune system imbalance in schizophrenia.
    Martins-de-Souza D, Gattaz WF, Schmitt A, Rewerts C, Maccarrone G, Dias-Neto E, Turck CW.

    01/28/2009
    Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator)

    Smoking and human reproduction: the effect of adenylate kinase genetic polymorphism.
    Gloria-Bottini F, Magrini A, Pietropolli A, Bergamaschi A, Bottini E, Gloria-Bottini F, Magrini A, Pietropolli A, Bergamaschi A, Bottini E.

    11/2/2008
    The alpha-borano or alpha-H on PMEA and PMPA were detrimental to the activity of recombinant human AMP kinases 1

    Acyclic phosphonate nucleotides and human adenylate kinases: impact of a borano group on alpha-P position.
    Topalis D, Alvarez K, Barral K, Munier-Lehmann H, Schneider B, Véron M, Guerreiro C, Mulard L, El-Amri C, Canard B, Deville-Bonne D.

    01/21/2010
    how mutations found in 2 patients may affect enzyme structure and function; a compound heterozygote for 2 different missense mutations 118G>A(Gly40Arg) and 190G>A(Gly64Arg); a homozygote for either aspartic acid (Asp) 140 or 141

    Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemia.
    Corrons JL, Garcia E, Tusell JJ, Varughese KI, West C, Beutler E.

    01/21/2010
    analysis of vascular endothelial ectoadenylate kinase and plasma membrane ATP synthase

    Ectoadenylate kinase and plasma membrane ATP synthase activities of human vascular endothelial cells.
    Quillen EE, Haslam GC, Samra HS, Amani-Taleshi D, Knight JA, Wyatt DE, Bishop SC, Colvert KK, Richter ML, Kitos PA.

    01/21/2010
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