These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

135 related items for PubMed ID: 24456035

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. High proportion of transient neonatal zinc deficiency causing alleles in the general population.
    Golan Y, Lehvy A, Horev G, Assaraf YG.
    J Cell Mol Med; 2019 Feb; 23(2):828-840. PubMed ID: 30450693
    [Abstract] [Full Text] [Related]

  • 9. Symptomatic zinc deficiency in a full-term breast-fed infant.
    Murthy SC, Udagani MM, Badakali AV, Yelameli BC.
    Dermatol Online J; 2010 Jun 15; 16(6):3. PubMed ID: 20579458
    [Abstract] [Full Text] [Related]

  • 10. Transient Neonatal Zinc Deficiency Caused by a Novel Mutation in the SLC30A2 Gene.
    Liew HM, Tan CW, Ho CK, Chee JN, Koh MJ.
    Pediatr Dermatol; 2017 Mar 15; 34(2):e104-e105. PubMed ID: 28111782
    [Abstract] [Full Text] [Related]

  • 11. A dominant negative heterozygous G87R mutation in the zinc transporter, ZnT-2 (SLC30A2), results in transient neonatal zinc deficiency.
    Lasry I, Seo YA, Ityel H, Shalva N, Pode-Shakked B, Glaser F, Berman B, Berezovsky I, Goncearenco A, Klar A, Levy J, Anikster Y, Kelleher SL, Assaraf YG.
    J Biol Chem; 2012 Aug 24; 287(35):29348-61. PubMed ID: 22733820
    [Abstract] [Full Text] [Related]

  • 12. Identification of a mutation in SLC30A2 (ZnT-2) in women with low milk zinc concentration that results in transient neonatal zinc deficiency.
    Chowanadisai W, Lönnerdal B, Kelleher SL.
    J Biol Chem; 2006 Dec 22; 281(51):39699-707. PubMed ID: 17065149
    [Abstract] [Full Text] [Related]

  • 13. Overview of Inherited Zinc Deficiency in Infants and Children.
    Kambe T, Fukue K, Ishida R, Miyazaki S.
    J Nutr Sci Vitaminol (Tokyo); 2015 Dec 22; 61 Suppl():S44-6. PubMed ID: 26598882
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Novel SLC30A2 mutations in the pathogenesis of transient neonatal zinc deficiency.
    Muto T, Kawase Y, Aiba K, Okuma M, Itsumura N, Luo S, Ogawa N, Tsuji T, Kambe T.
    Pediatr Investig; 2023 Mar 22; 7(1):6-12. PubMed ID: 36967740
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Exome Sequencing of SLC30A2 Identifies Novel Loss- and Gain-of-Function Variants Associated with Breast Cell Dysfunction.
    Alam S, Hennigar SR, Gallagher C, Soybel DI, Kelleher SL.
    J Mammary Gland Biol Neoplasia; 2015 Dec 22; 20(3-4):159-72. PubMed ID: 26293594
    [Abstract] [Full Text] [Related]

  • 18. [Acrodermatitis enteropathica in a breast-fed infant].
    Gutiérrez-González E, Alvarez-Pérez A, Loureiro M, Sánchez-Aguilar D, Toribio J.
    Actas Dermosifiliogr; 2012 Mar 22; 103(2):170-2. PubMed ID: 21925631
    [No Abstract] [Full Text] [Related]

  • 19. Transient symptomatic zinc deficiency in a breast-fed infant: relevance of a genetic study.
    El Fékih N, Monia K, Schmitt S, Dorbani I, Küry S, Kamoun MR.
    Nutrition; 2011 Oct 22; 27(10):1087-9. PubMed ID: 21907902
    [Abstract] [Full Text] [Related]

  • 20. Acrodermatitis enteropathica: a novel SLC39A4 gene mutation found in a patient with an early-onset.
    Santiago F, Matos J, Moreno A, Schmitt S, Bézieau S, Tellechea O.
    Pediatr Dermatol; 2011 Oct 22; 28(6):735-736. PubMed ID: 21906148
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.