Results 81 to 90 of about 32,098 (126)

Genetic-epigenetic interactions (meQTLs) in orofacial clefts etiology. [PDF]

Mol Genet Genomics
Petrin AL, Machado-Paula LA, Keen HL, Hovey L, Doolittle B, Dunlay L, Awotoye W, Xie XJ, Zeng E, Butali A, Marazita ML, Murray JC, Moreno-Uribe LM.   +12 more
europepmc   +1 more source

Manipulating primordial germ cells from chicken and other bird species. [PDF]

J Reprod Dev
Blank MH, Ichikawa K, McGrew MJ.
europepmc   +1 more source

Genetic and epigenetic insights into perioperative neurocognitive disorders: a narrative review. [PDF]

Br J Anaesth
Thedim M, Li H, Formanek A, Wiener-Kronish J, Saxena R, Vacas S.   +5 more
europepmc   +1 more source

The role of <i>trans</i>-acting factors in the pathogenesis of common psychiatric disorders. [PDF]

Epigenetics
Peedicayil J, Grayson DR.
europepmc   +1 more source

Epigenetic variation in light of population genetic practice. [PDF]

Nat Commun
Mueller SA, Merondun J, Lečić S, Wolf JBW.   +3 more
europepmc   +1 more source

Phenotypic Heterogeny of Hereditary Angioedema Within a Single Family. [PDF]

Kans J Med
Fails JM, Gierer SA.
europepmc   +1 more source

Epigenetic disruption meets immune deficiency: a case report of ICF syndrome linked to DNMT3B mutation. [PDF]

Front Immunol
Ali ZA, Al-Ali KF, Al-Ali KF, Bader F, Alhalabiya N, Sous D, Abulehia A.   +6 more
europepmc   +1 more source

DNA Methylation Stochasticity Is Linked to Transcriptional Variability and Convergent Epigenetic Disruption across Genetic Subtypes of Acute Myeloid Leukemia. [PDF]

Cancer Res
Hilgart E, Zhou W, Martinez-Montes E, Tryggvadottir R, Gondek LP, Majeti R, Ji H, Koldobskiy MA, Feinberg AP.   +8 more
europepmc   +1 more source

Transcriptome- and Epigenome-Wide Association Studies of Tic Spectrum Disorder in Discordant Monozygotic Twins. [PDF]

Genes (Basel)
Dalsberg J, Jespersgaard C, Levy AM, Asplund AM, Bagger FO, Debes NM, Tan Q, Tümer Z, Hildonen M.   +8 more
europepmc   +1 more source

Variants in the CxxC domain of the epigenetic regulator KDM2B support its role in developmental eye anomalies. [PDF]

Eur J Hum Genet
Ceroni F, Reis LM, Watkins F, Bax DA, Fischer MC, Jeganathan K, Jewell R, Martin JS, Salt A, Seese SE, Thomson J, Semina EV, Ragge NK.   +12 more
europepmc   +1 more source