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ab25085 has been referenced in 14 publications.

  • Bannerman P  et al. Brain Nat8l Knockdown Suppresses Spongiform Leukodystrophy in an Aspartoacylase-Deficient Canavan Disease Mouse Model. Mol Ther 26:793-800 (2018). PubMed: 29456021
  • Noreldin AE  et al. Immunohistochemical localization of osteoblast activating peptide in the mouse kidney. Acta Histochem N/A:N/A (2018). PubMed: 29534834
  • Li J  et al. Effects of age on intestinal phosphate transport and biochemical values of broiler chickens. Asian-Australas J Anim Sci 30:221-228 (2017). Chicken . PubMed: 27703131
  • Furukawa S  et al. Databases for technical aspects of immunohistochemistry. J Toxicol Pathol 30:79-107 (2017). IHC ; Rat . PubMed: 28190929
  • Kang CM  et al. Genetic Comparison of Stemness of Human Umbilical Cord and Dental Pulp. Stem Cells Int 2016:3453890 (2016). PubMed: 27087814
  • Zhao YG  et al. The autophagy gene Wdr45/Wipi4 regulates learning and memory function and axonal homeostasis. Autophagy 11:881-90 (2015). PubMed: 26000824
  • Mizutani E  et al. Generation of cloned mice from adult neurons by direct nuclear transfer. Biol Reprod 92:81 (2015). PubMed: 25653280
  • Kim JH  et al. Distinctive genetic activity pattern of the human dental pulp between deciduous and permanent teeth. PLoS One 9:e102893 (2014). IHC-P ; Human . PubMed: 25047033
  • Anders C  et al. Ex vivo modeling of chemical synergy in prenatal kidney cystogenesis. PLoS One 8:e57797 (2013). IHC-P ; Mouse . PubMed: 23554868
  • Jacquet BV  et al. Specification of a Foxj1-Dependent Lineage in the Forebrain Is Required for Embryonic-to-Postnatal Transition of Neurogenesis in the Olfactory Bulb. J Neurosci 31:9368-82 (2011). PubMed: 21697387
  • Barone S  et al. Deletion of the Cl-/HCO3- exchanger pendrin downregulates calcium-absorbing proteins in the kidney and causes calcium wasting. Nephrol Dial Transplant : (2011). WB . PubMed: 21873623
  • Mehedint MG  et al. Choline deficiency alters global histone methylation and epigenetic marking at the Re1 site of the calbindin 1 gene. FASEB J 24:184-95 (2010). WB ; Mouse . PubMed: 19752176
  • Gröger N  et al. SLC4A11 prevents osmotic imbalance leading to corneal endothelial dystrophy, deafness, and polyuria. J Biol Chem 285:14467-74 (2010). PubMed: 20185830
  • Sugawara M  et al. Purkinje cell loss in the cerebellar flocculus in patients with ataxia with ocular motor apraxia type 1/early-onset ataxia with ocular motor apraxia and hypoalbuminemia. Eur Neurol 59:18-23 (2008). Human . PubMed: 17917453


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