Biblio

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

A

Yu Y, Wang C, Ye S, Xu Z, Lin H, Texter K, Shukla V, Ghadiali S, Ma Q, Garg V, et al. Abnormal Progenitor Cell Differentiation and Cardiomyocyte Proliferation in Hypoplastic Right Heart Syndrome. Circulation. 2024;149(11):888-891.

Yang P, Dai A, Alexenko AP, Liu Y, Stephens AJ, Schulz LC, Schust DJ, R Roberts M, Ezashi T. Abnormal Oxidative Stress Responses in Fibroblasts from Preeclampsia Infants. PLoS One. 2014;9(7):e103110.

Salmon B, Bardet C, Coyac BR, Baroukh B, Naji J, Rowe PS, S Vital O, Linglart A, McKee MD, Chaussain C. Abnormal osteopontin and matrix extracellular phosphoglycoprotein localization, and odontoblast differentiation, in X-linked hypophosphatemic teeth. Connect Tissue Res. 2014;55(S1):79-82.

Ogawa Y, Sasanuma Y, Shitara S, Koshiduka A, Okada R, Sakuraba H, Oishi K. Abnormal organization during neurodevelopment in a mouse model of Sandhoff disease. Neurosci Res. 2019.

Ku T, Ren Z, Yang R, Liu QS, Sang N, Faiola F, Zhou Q, Jiang G. Abnormal neural differentiation in response to graphene quantum dots through histone modification interference. Environ Int. 2022;170:107572.

Latta L, Ludwig N, Krammes L, Stachon T, Fries FN, Mukwaya A, Szentmáry N, Seitz B, Wowra B, Kahraman M, et al. Abnormal neovascular and proliferative conjunctival phenotype in limbal stem cell deficiency is associated with altered microRNA and gene expression modulated by PAX6 mutational status in congenital aniridia. Ocul Surf. 2020.

Nie Z, Wang C, Chen J, Ji Y, Zhang H, Zhao F, Zhou X, Guan M-X. Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathy. Hum Mol Genet. 2022.

Lu L, Guo D, Chen X, Xiong W, Jie S, Li H. Abnormal miRNAs Targeting Chromosome Open Reading Frame Genes were Enriched in Microvesicles Derived from the Circulation of HCC. Biochem Genet. 2015.

Bannoehr J, Balmer P, Stoffel MH, Jagannathan V, Gaschen V, Kühni K, Sayar B, Drögemüller M, Howald D, Wiener DJ, et al. Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK). PLoS One. 2020;15(3):e0225901.

Quader S, Tanabe S, Cabral H. Abnormal Glycosylation in Cancer Cells and Cancer Stem Cells as a Therapeutic Target. Adv Exp Med Biol. 2022;1393:141-156.

Monsalve EM, García-Gutiérrez MS, Navarrete F, Giner S, Laborda J, Manzanares J. Abnormal Expression Pattern of Notch Receptors, Ligands, and Downstream Effectors in the Dorsolateral Prefrontal Cortex and Amygdala of Suicidal Victims. Mol Neurobiol. 2013.

Zhang Y, Xu F, Tan Y, Hu J, Wang H. [Abnormal expression of PEX10 gene may be related to epilepsy associated with 1p36 copy number variations.]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015;32(1):6-10.

Zhang J, Zhang C, Hu L, He Y, Shi Z, Tang S, Chen Y. Abnormal Expression of miR-21 and miR-95 in Cancer Stem-Like Cells is Associated with Radioresistance of Lung Cancer. Cancer Invest. 2015.

Xu P, Wang L, Liu Q, Gao P, Hu F, Xie X, Jiang L, Bi R, Ding F, Yang Q, et al. The abnormal expression of circ-ARAP2 promotes ESCC progression through regulating miR-761/FOXM1 axis-mediated stemness and the endothelial-mesenchymal transition. J Transl Med. 2022;20(1):318.

McCole RB, Fonseka CY, Koren A, Wu C-T. Abnormal Dosage of Ultraconserved Elements Is Highly Disfavored in Healthy Cells but Not Cancer Cells. PLoS Genet. 2014;10(10):e1004646.

Chan C-H, Lam Y-Y, Wong N, Geng L, Zhang J, Ahola V, Zare A, Li RAdolphus, Lanner F, Keung W, et al. Abnormal developmental trajectory and vulnerability to cardiac arrhythmias in tetralogy of Fallot with DiGeorge syndrome. Commun Biol. 2023;6(1):969.

Douvaras P, Dorà NJ, Mort RL, Lodge EJ, Hill RE, West JD. Abnormal corneal epithelial maintenance in heterozygous Mp/+ mutant mice. Exp Eye Res. 2016.

Liu P-P, Lu S-P, Li X, Bin Tang G-, Liu X, Dai S-K, Jiao L-F, Lin X-W, Li X-G, Hu B, et al. Abnormal chromatin remodeling caused by ARID1A deletion leads to malformation of the dentate gyrus. Cell Death Differ. 2023.

Hou C, Ding L, Zhang J, Jin Y, Sun C, Li Z, Sun X, Zhang T, Zhang A, Li H, et al. Abnormal cerebellar development and Purkinje cell Defects in Lgl1-Pax2 conditional knockout mice. Dev Biol. 2014.

Niu W, Deng L, Mojica-Perez SP, Tidball AM, Sudyk R, Stokes K, Parent JM. Abnormal cell sorting and altered early neurogenesis in a human cortical organoid model of Protocadherin-19 clustering epilepsy. Front Cell Neurosci. 2024;18:1339345.

Wang G, Zhang G, Li Z, Fawcett CH, Coble M, Sosa MX, Tsai T, Malesky K, Thibodeaux SJ, Zhu P, et al. Abnormal Behavior of Zebrafish Mutant in Dopamine Transporter Is Rescued by Clozapine. iScience. 2019;17:325-333.

Adachi M, Asakura Y, Muroya K, Goto H, Kigasawa H. Abnormal adipose tissue distribution with unfavorable metabolic profile in five children following hematopoietic stem cell transplantation: a new etiology for acquired partial lipodystrophy. Clin Pediatr Endocrinol. 2013;22(4):53-64.

Sabbah R, Saadi S, Shahar-Gabay T, Gerassy S, Yehudai-Resheff S, Zuckerman T. Abnormal adipogenic signaling in the bone marrow mesenchymal stem cells contributes to supportive microenvironment for leukemia development. Cell Commun Signal. 2023;21(1):277.

Volnitskiy A, Shtam T, Burdakov V, Kovalev R, Konev A, Filatov M. Abnormal activity of transcription factors gli in high-grade gliomas. PLoS One. 2019;14(2):e0211980.

Younis S, Jouneau A, Larsson M, Oudin J-F, Adenot P, Omar J, Brochard V, Andersson L. Ablation of ZC3H11A causes early embryonic lethality and dysregulation of metabolic processes. Proc Natl Acad Sci U S A. 2023;120(23):e2216799120.

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