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Oncotarget
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November 9, 2017
Subclinical involvement of the liver is associated with prognosis in treatment naïve cancer patients
Noemi Pavo, Markus Raderer, Georg Goliasch, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 9, 2025
Biallelic BRF2 mutations disrupt redox homeostasis as etiological factors in syndromic immunodeficiency and developmental disorders
Seobin Yoon, Seungbok Lee, Haeyoon Kwon, et al.
Kidney Research and Clinical Practice
|
February 9, 2025
Clinical guidelines for the diagnosis, evaluation, and management of hypertension for Korean children and adolescents: the Korean Working Group of Pediatric Hypertension
Se Jin Park, Hyo Soon An, Sung Hye Kim, et al.
Biorxiv : the Preprint Server for Biology
|
June 22, 2026
Distinct fibroblast and perivascular senotypes define spatial niches that regulate fibrosis
Alexandra N Rindone, Sushma Nagaraj, Anna Cho, et al.
Clinical Genetics
|
February 24, 2026
Exploring the Impact of RNU4-2 Defects on Neurodevelopmental Disorders in a Korean Population
Juhyeon Hong, Seungbok Lee, Soo Yeon Kim, et al.
Frontiers in Genetics
|
October 10, 2022
Systematic analysis of inheritance pattern determination in genes that cause rare neurodevelopmental diseases
Soojin Park, Se Song Jang, Seungbok Lee, et al.
Scientific Reports
|
January 31, 2020
Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population
Youngha Lee, Soojin Park, Jin Sook Lee, et al.
Genome Medicine
|
August 7, 2025
Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disorders
Jihoon G Yoon, Hyunsoo Jang, Seungbok Lee, et al.
Muscle & Nerve
|
September 6, 2016
Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center
Anna Cho, Moon-Woo Seong, Byung Chan Lim, et al.
Orphanet Journal of Rare Diseases
|
March 22, 2019
The Korean undiagnosed diseases program: lessons from a one-year pilot project
Soo Yeon Kim, Byung Chan Lim, Jin Sook Lee, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 111) with videos related to
Sort By:
Page
of 12
Oncotarget
|
November 9, 2017
Subclinical involvement of the liver is associated with prognosis in treatment naïve cancer patients
Noemi Pavo, Markus Raderer, Georg Goliasch, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 9, 2025
Biallelic BRF2 mutations disrupt redox homeostasis as etiological factors in syndromic immunodeficiency and developmental disorders
Seobin Yoon, Seungbok Lee, Haeyoon Kwon, et al.
Kidney Research and Clinical Practice
|
February 9, 2025
Clinical guidelines for the diagnosis, evaluation, and management of hypertension for Korean children and adolescents: the Korean Working Group of Pediatric Hypertension
Se Jin Park, Hyo Soon An, Sung Hye Kim, et al.
Biorxiv : the Preprint Server for Biology
|
June 22, 2026
Distinct fibroblast and perivascular senotypes define spatial niches that regulate fibrosis
Alexandra N Rindone, Sushma Nagaraj, Anna Cho, et al.
Clinical Genetics
|
February 24, 2026
Exploring the Impact of RNU4-2 Defects on Neurodevelopmental Disorders in a Korean Population
Juhyeon Hong, Seungbok Lee, Soo Yeon Kim, et al.
Frontiers in Genetics
|
October 10, 2022
Systematic analysis of inheritance pattern determination in genes that cause rare neurodevelopmental diseases
Soojin Park, Se Song Jang, Seungbok Lee, et al.
Scientific Reports
|
January 31, 2020
Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population
Youngha Lee, Soojin Park, Jin Sook Lee, et al.
Genome Medicine
|
August 7, 2025
Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disorders
Jihoon G Yoon, Hyunsoo Jang, Seungbok Lee, et al.
Muscle & Nerve
|
September 6, 2016
Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center
Anna Cho, Moon-Woo Seong, Byung Chan Lim, et al.
Orphanet Journal of Rare Diseases
|
March 22, 2019
The Korean undiagnosed diseases program: lessons from a one-year pilot project
Soo Yeon Kim, Byung Chan Lim, Jin Sook Lee, et al.
Page
of 12