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Lorida Llaci

Showing results (1-10 of 19) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|February 10, 2018
Methods for CpG Methylation Array Profiling Via Bisulfite ConversionFatjon Leti, Lorida Llaci, Ivana Malenica, et al.
Experimental Eye Research|May 8, 2020
Transcriptomics analysis of pericytes from retinas of diabetic animals reveals novel genes and molecular pathways relevant to blood-retinal barrier alterations in diabetic retinopathySampathkumar Rangasamy, Finny Monickaraj, Christophe Legendre, et al.
Clinical Epigenetics|July 15, 2018
Differentially methylated loci in NAFLD cirrhosis are associated with key signaling pathwaysGlenn S Gerhard, Ivana Malenica, Lorida Llaci, et al.
The Journal of Clinical Investigation|July 1, 2024
Epigenetic developmental mechanisms underlying sex differences in cancerJoshua B Rubin, Tamara Abou-Antoun, Joseph E Ippolito, et al.
Neurology. Genetics|May 24, 2017
Compound heterozygous mutations in <i>MASP1</i> in a deaf child with absent cochlear nervesElina Kari, Isabelle Schrauwen, Lorida Llaci, et al.
Molecular Genetics & Genomic Medicine|October 10, 2019
A de novo SIX1 variant in a patient with a rare nonsyndromic cochleovestibular nerve abnormality, cochlear hypoplasia, and bilateral sensorineural hearing lossElina Kari, Lorida Llaci, John L Go, et al.
Iscience|February 20, 2026
NF-κB and STAT3 signaling uniquely stratify survival in female glioblastoma patientsJason P Wong, Lorida Llaci, Lloyd Tripp, et al.
Ear and Hearing|January 28, 2020
Genes Implicated in Rare Congenital Inner Ear and Cochleovestibular Nerve MalformationsElina Kari, Lorida Llaci, John L Go, et al.
Nature Communications|March 22, 2021
Loss of Quaking RNA binding protein disrupts the expression of genes associated with astrocyte maturation in mouse brainKristina Sakers, Yating Liu, Lorida Llaci, et al.
Human Genetics|June 30, 2018
De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafnessIsabelle Schrauwen, Elina Kari, Jacob Mattox, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|February 10, 2018
Methods for CpG Methylation Array Profiling Via Bisulfite ConversionFatjon Leti, Lorida Llaci, Ivana Malenica, et al.
Experimental Eye Research|May 8, 2020
Transcriptomics analysis of pericytes from retinas of diabetic animals reveals novel genes and molecular pathways relevant to blood-retinal barrier alterations in diabetic retinopathySampathkumar Rangasamy, Finny Monickaraj, Christophe Legendre, et al.
Clinical Epigenetics|July 15, 2018
Differentially methylated loci in NAFLD cirrhosis are associated with key signaling pathwaysGlenn S Gerhard, Ivana Malenica, Lorida Llaci, et al.
The Journal of Clinical Investigation|July 1, 2024
Epigenetic developmental mechanisms underlying sex differences in cancerJoshua B Rubin, Tamara Abou-Antoun, Joseph E Ippolito, et al.
Neurology. Genetics|May 24, 2017
Compound heterozygous mutations in <i>MASP1</i> in a deaf child with absent cochlear nervesElina Kari, Isabelle Schrauwen, Lorida Llaci, et al.
Molecular Genetics & Genomic Medicine|October 10, 2019
A de novo SIX1 variant in a patient with a rare nonsyndromic cochleovestibular nerve abnormality, cochlear hypoplasia, and bilateral sensorineural hearing lossElina Kari, Lorida Llaci, John L Go, et al.
Iscience|February 20, 2026
NF-κB and STAT3 signaling uniquely stratify survival in female glioblastoma patientsJason P Wong, Lorida Llaci, Lloyd Tripp, et al.
Ear and Hearing|January 28, 2020
Genes Implicated in Rare Congenital Inner Ear and Cochleovestibular Nerve MalformationsElina Kari, Lorida Llaci, John L Go, et al.
Nature Communications|March 22, 2021
Loss of Quaking RNA binding protein disrupts the expression of genes associated with astrocyte maturation in mouse brainKristina Sakers, Yating Liu, Lorida Llaci, et al.
Human Genetics|June 30, 2018
De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafnessIsabelle Schrauwen, Elina Kari, Jacob Mattox, et al.
Pageof 2