Lista de obras - Jinsei Jung - Dominio Público Uruguay

A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction

scientific article published on 22 May 2018

A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators

artículo científico publicado en 2018

ANO9/TMEM16J promotes tumourigenesis via EGFR and is a novel therapeutic target for pancreatic cancer.

artículo científico publicado en 2017

Activation of KCNQ4 as a Therapeutic Strategy to Treat Hearing Loss

artículo científico publicado en 2021

Association Between Eustachian Tube Dysfunction Questionnaire-7 Scores and Eustachian Tube Function Test Results in Symptomatic Patients With a Normal Drum

artículo científico publicado en 2022

Audiologic Gain of Incus Short Process Vibroplasty With Conventional Incus Long Process Vibroplasty: A Retrospective Analysis of 36 Patients.

artículo científico

Audiologic limitations of Vibrant Soundbridge device: Is the contralateral hearing aid fitting indispensable?

artículo científico

Benefits of Bimodal Hearing With Cochlear and Middle Ear Implants: Preliminary Results in Four Patients.

artículo científico publicado en 2018

Benefits of active middle ear implants in mixed hearing loss: Stapes versus round window.

artículo científico

Cleaved Cochlin Sequesters Pseudomonas aeruginosa and Activates Innate Immunity in the Inner Ear

scientific article published on 21 March 2019

Clinical Characteristics of Bilateral Meniere's Disease in a Single Asian Ethnic Group

article

Clinical Experience of Vibroplasty With Direct Coupling to the Oval Window Without Use of a Coupler

scientific article published on 24 January 2020

Clinical presentation and management of jugular foramen paraganglioma.

scientific article published on 26 March 2009

Correlation between genotype and phenotype in patients with bi-allelic SLC26A4 mutations.

artículo científico publicado en 2013

Discrepancies between video head impulse and caloric tests in patients with enlarged vestibular aqueduct.

artículo científico publicado en 2016

Distinct roles of stereociliary links in the nonlinear sound processing and noise resistance of cochlear outer hair cells

scientific article published on 01 May 2020

Does calmodulin regulate the bicarbonate permeability of ANO1/TMEM16A or not?

artículo científico publicado en 2015

Dynamic modulation of ANO1/TMEM16A HCO3(-) permeability by Ca2+/calmodulin

artículo científico publicado en 2012

Effect of Specific Retinoic Acid Receptor Agonists on Noise-Induced Hearing Loss

scientific article published on 16 September 2019

Effects of Contralateral Routing of Signal Hearing Aids on Audiological and Academic Performance in School-Age Children With Unilateral Hearing Loss

artículo científico publicado en 2021

Effects of Saccular Function on Recovery of Subjective Dizziness After Vestibular Rehabilitation

artículo científico publicado en 2017

Effects of self-reported hearing or vision impairment on depressive symptoms: a population-based longitudinal study.

artículo científico publicado en 2018

Electrogenic transport and K(+) ion channel expression by the human endolymphatic sac epithelium.

artículo científico publicado en 2015

Evaluation of Maximal Speech Intelligibility With Vibrant Soundbridge in Patients With Sensorineural Hearing Loss.

artículo científico publicado en 2017

Extended-duration deafness is correlated with better subjective satisfaction in CROS-tBAHI recipients

scientific article published on 23 May 2019

Feasibility of Revision Cochlear Implant Surgery for Better Speech Comprehension

scientific article published on 13 March 2019

Feasiblity of transoral robotic hypopharyngectomy for early-stage hypopharyngeal carcinoma.

artículo científico publicado en 2010

Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

scientific article published on 23 September 2019

Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation

artículo científico publicado en 2020

Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population

artículo científico publicado en 2017

Genetic aspects and clinical characteristics of familial Meniere's disease in a South Korean population.

artículo científico publicado en 2015

Hearing Preservation During Cochlear Implantation and Electroacoustic Stimulation in Patients With SLC26A4 Mutations

artículo científico

Heterogeneity of MYO15A variants significantly determine the feasibility of acoustic stimulation with hearing aid and cochlear implant

artículo científico publicado en 2021

Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants

article

Identification of novel functional null allele of SLC26A4 associated with enlarged vestibular aqueduct and its possible implication

artículo científico publicado en 2014

Increased incidence of unilateral sudden sensorineural hearing loss in patients with hematological malignancies requiring hematopoietic stem cell transplantation

scientific article published in 2021

Inflammatory Monocytes Infiltrate the Spiral Ligament and Migrate to the Basilar Membrane After Noise Exposure

artículo científico publicado en 2022

Investigation of intact mouse cochleae using two-photon laser scanning microscopy

artículo científico publicado en 2020

Is Early Progression to Bilateral Involvement in Menière's Disease a Poor Prognostic Indicator?

artículo científico publicado en 2019

Is dehydration test using isosorbide useful in Meniere's disease?

artículo científico publicado en 2016

LCCL peptide cleavage after noise exposure exacerbates hearing loss and is associated with the monocyte infiltration in the cochlea

artículo científico publicado en 2021

Lessons From an Analysis of Newborn Hearing Screening Data for Children With Cochlear Implants

scientific article published on 01 October 2019

Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis

artículo científico publicado en 2014

Meta-analysis of Delayed Facial Palsy Following Middle Ear Surgery

artículo científico publicado en 2019

Non-syndromic hearing loss caused by the dominant cis mutation R75Q with the recessive mutation V37I of the GJB2 (Connexin 26) gene

artículo científico publicado en 2015

Novel COCH p.V123E Mutation, Causative of DFNA9 Sensorineural Hearing Loss and Vestibular Disorder, Shows Impaired Cochlin Post-Translational Cleavage and Secretion

artículo científico publicado en 2015

Outcomes and Predictive Factors of Electroacoustic Stimulation Rehabilitation in Children With Limited Low-Frequency Hearing

scientific article published on 01 October 2019

Overlooked KCNQ4 variants augment the risk of hearing loss

scientific article published in 2023

P2RX2 and P2RX4 receptors mediate cation absorption in transitional cells and supporting cells of the utricular macula

artículo científico publicado en 2019

Pore dilatation increases the bicarbonate permeability of CFTR, ANO1 and glycine receptor anion channels

artículo científico publicado en 2015

Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment

artículo científico publicado en 2019

Relationship between Hearing Loss and Dementia Differs According to the Underlying Mechanism

artículo científico publicado en 2021

Resistance to hypertension and high Cl- excretion in humans with SLC26A4 mutations.

artículo científico publicado en 2016

Role of calcium signaling in epithelial bicarbonate secretion

artículo científico

Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure

artículo científico publicado en 2015

Shank2 mutant mice display a hypersecretory response to cholera toxin.

artículo científico publicado en 2014

Statistical analysis of pure tone audiometry and caloric test in herpes zoster oticus

artículo científico publicado en 2008

Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency

article

The HSP70 co-chaperone DNAJC14 targets misfolded pendrin for unconventional protein secretion

artículo científico publicado en 2016

The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report

artículo científico publicado en 2019

The oncologic safety and functional preservation of supraglottic partial laryngectomy

artículo científico publicado en 2009

Ventilation tube insertion is not effective to the treatment of hearing impairment in pediatric patients with Cornelia de Lange syndrome.

artículo científico publicado en 2016

Vestibular function is associated with residual low-frequency hearing loss in patients with bi-allelic mutations in the SLC26A4 gene.

artículo científico publicado en 2016

Vibrant Soundbridge can improve the most comfortable listening level in sensorineural hearing loss: our experience of 61 patients.

artículo científico

Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report

artículo científico publicado en 2017

Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss

artículo científico publicado en 2018

β1- and β2-adrenergic stimulation-induced electrogenic transport by human endolymphatic sac epithelium and its clinical implications

artículo científico publicado en 2017

Lista de obras de Jinsei Jung

A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction

A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators

ANO9/TMEM16J promotes tumourigenesis via EGFR and is a novel therapeutic target for pancreatic cancer.

Activation of KCNQ4 as a Therapeutic Strategy to Treat Hearing Loss

Association Between Eustachian Tube Dysfunction Questionnaire-7 Scores and Eustachian Tube Function Test Results in Symptomatic Patients With a Normal Drum

Audiologic Gain of Incus Short Process Vibroplasty With Conventional Incus Long Process Vibroplasty: A Retrospective Analysis of 36 Patients.

Audiologic limitations of Vibrant Soundbridge device: Is the contralateral hearing aid fitting indispensable?

Benefits of Bimodal Hearing With Cochlear and Middle Ear Implants: Preliminary Results in Four Patients.

Benefits of active middle ear implants in mixed hearing loss: Stapes versus round window.

Cleaved Cochlin Sequesters Pseudomonas aeruginosa and Activates Innate Immunity in the Inner Ear

Clinical Characteristics of Bilateral Meniere's Disease in a Single Asian Ethnic Group

Clinical Experience of Vibroplasty With Direct Coupling to the Oval Window Without Use of a Coupler

Clinical presentation and management of jugular foramen paraganglioma.

Correlation between genotype and phenotype in patients with bi-allelic SLC26A4 mutations.

Discrepancies between video head impulse and caloric tests in patients with enlarged vestibular aqueduct.

Distinct roles of stereociliary links in the nonlinear sound processing and noise resistance of cochlear outer hair cells

Does calmodulin regulate the bicarbonate permeability of ANO1/TMEM16A or not?

Dynamic modulation of ANO1/TMEM16A HCO3(-) permeability by Ca2+/calmodulin

Effect of Specific Retinoic Acid Receptor Agonists on Noise-Induced Hearing Loss

Effects of Contralateral Routing of Signal Hearing Aids on Audiological and Academic Performance in School-Age Children With Unilateral Hearing Loss

Effects of Saccular Function on Recovery of Subjective Dizziness After Vestibular Rehabilitation

Effects of self-reported hearing or vision impairment on depressive symptoms: a population-based longitudinal study.

Electrogenic transport and K(+) ion channel expression by the human endolymphatic sac epithelium.

Evaluation of Maximal Speech Intelligibility With Vibrant Soundbridge in Patients With Sensorineural Hearing Loss.

Extended-duration deafness is correlated with better subjective satisfaction in CROS-tBAHI recipients

Feasibility of Revision Cochlear Implant Surgery for Better Speech Comprehension

Feasiblity of transoral robotic hypopharyngectomy for early-stage hypopharyngeal carcinoma.

Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation

Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population

Genetic aspects and clinical characteristics of familial Meniere's disease in a South Korean population.

Hearing Preservation During Cochlear Implantation and Electroacoustic Stimulation in Patients With SLC26A4 Mutations

Heterogeneity of MYO15A variants significantly determine the feasibility of acoustic stimulation with hearing aid and cochlear implant

Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants

Identification of novel functional null allele of SLC26A4 associated with enlarged vestibular aqueduct and its possible implication

Increased incidence of unilateral sudden sensorineural hearing loss in patients with hematological malignancies requiring hematopoietic stem cell transplantation

Inflammatory Monocytes Infiltrate the Spiral Ligament and Migrate to the Basilar Membrane After Noise Exposure

Investigation of intact mouse cochleae using two-photon laser scanning microscopy

Is Early Progression to Bilateral Involvement in Menière's Disease a Poor Prognostic Indicator?

Is dehydration test using isosorbide useful in Meniere's disease?

LCCL peptide cleavage after noise exposure exacerbates hearing loss and is associated with the monocyte infiltration in the cochlea

Lessons From an Analysis of Newborn Hearing Screening Data for Children With Cochlear Implants

Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis

Meta-analysis of Delayed Facial Palsy Following Middle Ear Surgery

Non-syndromic hearing loss caused by the dominant cis mutation R75Q with the recessive mutation V37I of the GJB2 (Connexin 26) gene

Novel COCH p.V123E Mutation, Causative of DFNA9 Sensorineural Hearing Loss and Vestibular Disorder, Shows Impaired Cochlin Post-Translational Cleavage and Secretion

Outcomes and Predictive Factors of Electroacoustic Stimulation Rehabilitation in Children With Limited Low-Frequency Hearing

Overlooked KCNQ4 variants augment the risk of hearing loss

P2RX2 and P2RX4 receptors mediate cation absorption in transitional cells and supporting cells of the utricular macula

Pore dilatation increases the bicarbonate permeability of CFTR, ANO1 and glycine receptor anion channels

Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment

Relationship between Hearing Loss and Dementia Differs According to the Underlying Mechanism

Resistance to hypertension and high Cl- excretion in humans with SLC26A4 mutations.

Role of calcium signaling in epithelial bicarbonate secretion

Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure

Shank2 mutant mice display a hypersecretory response to cholera toxin.

Statistical analysis of pure tone audiometry and caloric test in herpes zoster oticus

Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency

The HSP70 co-chaperone DNAJC14 targets misfolded pendrin for unconventional protein secretion

The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report

The oncologic safety and functional preservation of supraglottic partial laryngectomy

Ventilation tube insertion is not effective to the treatment of hearing impairment in pediatric patients with Cornelia de Lange syndrome.

Vestibular function is associated with residual low-frequency hearing loss in patients with bi-allelic mutations in the SLC26A4 gene.

Vibrant Soundbridge can improve the most comfortable listening level in sensorineural hearing loss: our experience of 61 patients.

Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report

Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss

β1- and β2-adrenergic stimulation-induced electrogenic transport by human endolymphatic sac epithelium and its clinical implications