Lista de obras -

A case of the rare variant of Klinefelter syndrome 47,XY,i(X)(q10)

artículo científico publicado en 2013

A de novo centric fission of chromosome 11 in a patient with recurrent miscarriages

artículo científico publicado en 2007

A healthy delivery of twins by assisted reproduction followed by preimplantation genetic screening in a woman with X-linked dominant incontinentia pigmenti

artículo científico publicado en 2014

A healthy live birth after successful preimplantation genetic diagnosis for carriers of complex chromosome rearrangements

scientific article published on 20 February 2008

A new approach of digital PCR system for non-invasive prenatal screening of trisomy 21.

artículo científico publicado en 2017

A sibship with duplication of Xq28 inherited from the mother; genomic characterization and clinical outcomes.

artículo científico publicado en 2017

A transport system based on a quantum dot-modified nanotracer is genetically and developmentally stable in pregnant mice

artículo científico publicado en 2020

Analysis of the cell-free amniotic fluid transcriptome expressed during the euploid mid-trimester of pregnancy

artículo científico publicado en 2016

Application of a target array comparative genomic hybridization to prenatal diagnosis

artículo científico publicado en 2010

Association between Polymorphisms in the Renin-Angiotensin System Genes and Prevalence of Spontaneously Aborted Fetuses ⬇️

artículo científico publicado el 11 de marzo de 2013

Association between kinase insert domain-containing receptor polymorphisms (-604T>C, 1192G>A, 1719A>T) and premature ovarian failure in Korean women.

artículo científico publicado en 2012

Association between vascular endothelial growth factor promoter polymorphisms and the risk of recurrent implantation failure

artículo científico publicado en 2017

Association of IL-18 genotype with impaired glucose regulation in Korean women with polycystic ovary syndrome ⬇️

artículo científico publicado el 5 de enero de 2012

Association of methylenetetrahydrofolate reductase (MTHFR 677C>T) and thymidylate synthase (TSER and TS 1494del6) polymorphisms with premature ovarian failure in Korean women

artículo científico publicado en 2012

Association of miR-146aC>G, miR-196a2T>C, and miR-499A>G Polymorphisms With Risk of Premature Ovarian Failure in Korean Women ⬇️

artículo científico publicado el 7 de agosto de 2012

Association of polymorphisms in microRNA machinery genes (DROSHA, DICER1, RAN, and XPO5) with risk of idiopathic primary ovarian insufficiency in Korean women ⬇️

artículo científico publicado el 1 de octubre de 2013

Association of the miR‐146aC>G, miR‐149T>C, miR‐196a2T>C, and miR‐499A>G Polymorphisms with Risk of Spontaneously Aborted Fetuses ⬇️

artículo científico publicado el 13 de agosto de 2012

Association study of dopamine receptor D2 TaqI A polymorphism and reward-related personality traits in healthy Korean young females

artículo científico publicado en 2007

Association study of microRNA polymorphisms with risk of idiopathic recurrent spontaneous abortion in Korean women ⬇️

artículo científico publicado el 28 de diciembre de 2011

CRBL cells: establishment, characterization and susceptibility to prion infection

artículo científico publicado en 2008

Chondrogenic potential of stem cells derived from amniotic fluid, adipose tissue, or bone marrow encapsulated in fibrin gels containing TGF-β3 ⬇️

artículo científico publicado el 15 de agosto de 2011

Chromatin structure of the LCR in the human β-globin locus transcribing the adult δ- and β-globin genes ⬇️

artículo científico publicado el 13 de diciembre de 2011

Chromosomal abnormalities in spontaneous abortion after assisted reproductive treatment ⬇️

artículo científico publicado el 3 de noviembre de 2010

Clinical and Genetic Characteristics Analysis of Korean Patients with Stargardt Disease Using Targeted Exome Sequencing

artículo científico publicado en 2018

Clinical and social characteristics of Korean men with Klinefelter syndrome ⬇️

artículo científico publicado el 9 de febrero de 2012

Clinical evaluation of noninvasive prenatal testing for sex chromosome aneuploidies in 9,176 Korean pregnant women: a single-center retrospective study

artículo científico publicado en 2024

Combined Model-Based Prediction for Non-Invasive Prenatal Screening

artículo científico publicado en 2022

Complex chromosomal rearrangements in infertile males: complexity of rearrangement affects spermatogenesis

artículo científico publicado en 2011

Correction of the name of author: Pre-implantation genetic diagnosis and pre-implantation genetic screening: two years experience at a single center

artículo científico publicado en 2020

De novo balanced reciprocal translocation t(2;3)(q31;q27) in a fetus conceived using PGD in a t(2;14)(q35;q32.1) balanced reciprocal translocation carrier mother.

artículo científico publicado en 2017

Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.

artículo científico

Effects and pregnancy outcomes of L-carnitine supplementation in culture media for human embryo development from in vitro fertilization (IVF)

artículo científico publicado en 2018

Endothelial nitric oxide synthase gene polymorphisms (−786T>C, 4a4b, 894G>T) and haplotypes in Korean patients with recurrent spontaneous abortion ⬇️

artículo científico publicado el 17 de junio de 2010

Erectile dysfunction and extramarital sex induced by timed intercourse: a prospective study of 439 men

artículo científico publicado el 3 de mayo de 2012

Erratum: Correction of Acknowledgements

artículo científico publicado en 2018

Evaluation of 28 human embryonic stem cell lines for use as unrelated donors in stem cell therapy: implications of HLA and ABO genotypes

artículo científico publicado en 2010

Functional recapitulation of smooth muscle cells via induced pluripotent stem cells from human aortic smooth muscle cells

artículo científico publicado en 2009

Gene expression analysis of the microdissected trophoblast layer of human placenta after the spontaneous onset of labor

artículo científico publicado en 2013

Gene sequencing in neonates and infants with the long QT syndrome.

artículo científico publicado en 2005

Generation of FISH probes using laser microbeam microdissection and application to clinical molecular cytogenetics.

artículo científico publicado en 2007

Generation of a B2M homozygous knockout human somatic cell nuclear transfer-derived embryonic stem cell line using the CRISPR/Cas9 system

Generation of cancerous neural stem cells forming glial tumor by oncogenic stimulation.

artículo científico publicado en 2012

Genetic Variation of Methylenetetrahydrofolate Reductase (MTHFR) and Thymidylate Synthase (TS) Genes Is Associated with Idiopathic Recurrent Implantation Failure

artículo científico publicado en 2016

Genome stabilization by RAD51-stimulatory compound 1 enhances efficiency of somatic cell nuclear transfer-mediated reprogramming and full-term development of cloned mouse embryos

artículo científico publicado en 2021

Genome-wide screening of severe male factor infertile patients using BAC-array comparative genomic hybridization (CGH).

artículo científico publicado en 2012

Genomic aspects in reproductive medicine

artículo científico publicado en 2024

Global gene expression analysis of cell-free RNA in amniotic fluid from women destined to develop preeclampsia

article

Global gene expression changes of amniotic fluid cell free RNA according to fetal development

artículo científico publicado en 2017

Homozygous deletions at 3p22, 5p14, 6q15, and 9p21 result in aberrant expression of tumor suppressor genes in gastric cancer

artículo científico publicado en 2014

HomozygousCYP17A1mutation (H373L) identified in a 46,XX female with combined 17α-hydroxylase/17,20-lyase deficiency ⬇️

artículo científico publicado el 28 de marzo de 2012

Human chorionic-plate-derived mesenchymal stem cells and Wharton’s jelly-derived mesenchymal stem cells: a comparative analysis of their potential as placenta-derived stem cells ⬇️

artículo científico publicado el 11 de octubre de 2011

Human somatic cell nuclear transfer using adult cells.

artículo científico publicado en 2014

Impact of RFC1, MTHFR, and MTHFD1 polymorphism on unexplained pregnancy loss (UPL): comparative analysis of maternal and fetal components using mother-abortus paired samples

artículo científico publicado en 2018

Impaired Spermatogenesis and gr/gr Deletions Related to Y Chromosome Haplogroups in Korean Men ⬇️

artículo científico publicado el 23 de agosto de 2012

Inhibition of pluripotent stem cell-derived teratoma formation by small molecules ⬇️

artículo científico publicado el 5 de agosto de 2013

Isolation and Characterization of Novel, Highly Proliferative Human CD34/CD73-Double-Positive Testis-Derived Stem Cells for Cell Therapy ⬇️

artículo científico publicado el 3 de mayo de 2013

Long-term safety and tolerability of subretinal transplantation of embryonic stem cell-derived retinal pigment epithelium in Asian Stargardt disease patients

scientific article published on 29 July 2020

MEF2C-Related 5q14.3 Microdeletion Syndrome Detected by Array CGH: A Case Report

artículo científico publicado en 2015

Male Infertility Associated with a Supernumerary Marker Chromosome

artículo científico publicado en 2017

Molecular analysis of miscarriage products using multiplex ligation-dependent probe amplification (MLPA): alternative to conventional karyotype analysis.

artículo científico

Molecular cytogenetic analysis of the monoblastic cell line U937. karyotype clarification by G-banding, whole chromosome painting, microdissection and reverse painting, and comparative genomic hybridization

artículo científico

Molecular genetic and cytogenetic characterization of a partial Xp duplication and Xq deletion in a patient with premature ovarian failure

artículo científico publicado en 2013

Mutations in SOHLH1 gene associate with nonobstructive azoospermia

artículo científico publicado en 2010

Neurodegeneration in an adolescent with Sjogren-Larsson syndrome: a decade-long follow-up case report

artículo científico publicado en 2018

Neuronal properties, in vivo effects, and pathology of a Huntington's disease patient-derived induced pluripotent stem cells

artículo científico

Optimization Protocol of Fixation Method for Trophoblast Retrieval from the Cervix (TRIC): A Preliminary Study

artículo científico publicado en 2020

PLGA nanoparticles with multiple modes are a biologically safe nanocarrier for mammalian development and their offspring

scientific article published on 21 August 2018

Pre-implantation genetic diagnosis and pre-implantation genetic screening: two years experience at a single center.

artículo científico publicado en 2018

Precise prenatal diagnosis of tuberous sclerosis by sequencing the TSC2 gene

article

Preeclampsia leads to dysregulation of various signaling pathways in placenta

artículo científico publicado en 2011

Preimplantation genetic diagnosis for couples with a Robertsonian translocation: practical information for genetic counseling ⬇️

artículo científico publicado el 12 de noviembre de 2011

Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies

artículo científico publicado en 2019

Prenatal diagnosis of partial trisomy 3q resulting from t(3;14) in a fetus with multiple anomalies including vermian hypoplasia

artículo científico publicado en 2012

Prevention of chemotherapy-induced premature ovarian insufficiency in mice by scaffold-based local delivery of human embryonic stem cell-derived mesenchymal progenitor cells

artículo científico publicado en 2021

Rapid Production and Genetic Stability of Human Mesenchymal Progenitor Cells Derived from Human Somatic Cell Nuclear Transfer-Derived Pluripotent Stem Cells

artículo científico publicado en 2021

Recombinant human phospholipase C zeta 1 induces intracellular calcium oscillations and oocyte activation in mouse and human oocytes ⬇️

artículo científico publicado el 28 de marzo de 2012

Repurposing the Cord Blood Bank for Haplobanking of HLA-Homozygous iPSCs and Their Usefulness to Multiple Populations

scientific article published on 29 July 2018

RuvB-Like Protein 2 (Ruvbl2) Has a Role in Directing the Neuroectodermal Differentiation of Mouse Embryonic Stem Cells

artículo científico publicado en 2016

SRY-negative 46,XX infertile male with Leydig cell hyperplasia: clinical, cytogenetic, and molecular analysis and review of the literature

artículo científico publicado en 2010

Senescent growth arrest in mesenchymal stem cells is bypassed by Wip1-mediated downregulation of intrinsic stress signaling pathways

artículo científico

Sequence variations of the EGR4 gene in Korean men with spermatogenesis impairment

artículo científico publicado en 2017

Sexual dysfunctions induced by stress of timed intercourse and medical treatment

artículo científico publicado en 2012

Sexual function and stress level of male partners of infertile couples during the fertile period

artículo científico publicado en 2015

Siblings with opposite chromosome constitutions, dup(2q)/del(7q) and del(2q)/dup(7q).

artículo científico publicado en 2013

Single cell-derived clonally expanded mesenchymal progenitor cells from somatic cell nuclear transfer-derived pluripotent stem cells ameliorate the endometrial function in the uterus of a murine model with Asherman's syndrome

artículo científico publicado en 2019

Solute Carrier Family 19, member 1 (SLC19A1) polymorphisms (-43T>C, 80G>A, and 696C>T), and haplotypes in idiopathic recurrent spontaneous abortion in a Korean population

artículo científico publicado en 2012

Spontaneous ovarian hyperstimulation syndrome following a thawed embryo transfer cycle

artículo científico publicado en 2014

Study of circulating hepcidin in association with iron excess, metabolic syndrome, and BMP-6 expression in granulosa cells in women with polycystic ovary syndrome

artículo científico publicado en 2014

Sunflower-type nanogels carrying a quantum dot nanoprobe for both superior gene delivery efficacy and tracing of human mesenchymal stem cells

artículo científico publicado en 2015

Survival of Transplanted Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells in a Human Recipient for 22 Months

artículo científico publicado en 2017

The ELK3-GATA3 axis orchestrates invasion and metastasis of breast cancer cells in vitro and in vivo

artículo científico publicado en 2016

The association of stromal antigen 3 (STAG3) sequence variations with spermatogenic impairment in the male Korean population

artículo científico publicado en 2020

The expansion of human ES and iPS cells on porous membranes and proliferating human adipose-derived feeder cells ⬇️

artículo científico publicado el 31 de julio de 2010

Treatment of macular degeneration using embryonic stem cell-derived retinal pigment epithelium: preliminary results in Asian patients

artículo científico publicado en 2015

Tumor necrosis factor-α gene polymorphisms in Korean patients with recurrent spontaneous abortion

artículo científico publicado en 2012

Usage and perceptions of phosphodiesterase type 5 inhibitors among the male partners of infertile couples

artículo científico publicado en 2016

Vascular Endothelial Growth Factor Gene Polymorphisms in Spontaneously Aborted Fetuses ⬇️

artículo científico publicado el 8 de septiembre de 2011

Vascular endothelial growth factor gene polymorphisms in Korean patients with premature ovarian failure

artículo científico publicado en 2011

Verification of Long-Term Genetic Stability of hMSCs during Subculture after Internalization of Sunflower-Type Nanoparticles (SF-NPs)

artículo científico publicado en 2018

[Down-Turner syndrome (45,X/47,XY,+21): case report and review]

artículo científico publicado en 2010

hESC Expansion and Stemness Are Independent of Connexin Forty-Three-Mediated Intercellular Communication between hESCs and hASC Feeder Cells ⬇️

artículo científico publicado el 26 de julio de 2013

Lista de obras de

A case of the rare variant of Klinefelter syndrome 47,XY,i(X)(q10)

A de novo centric fission of chromosome 11 in a patient with recurrent miscarriages

A healthy delivery of twins by assisted reproduction followed by preimplantation genetic screening in a woman with X-linked dominant incontinentia pigmenti

A healthy live birth after successful preimplantation genetic diagnosis for carriers of complex chromosome rearrangements

A new approach of digital PCR system for non-invasive prenatal screening of trisomy 21.

A sibship with duplication of Xq28 inherited from the mother; genomic characterization and clinical outcomes.

A transport system based on a quantum dot-modified nanotracer is genetically and developmentally stable in pregnant mice

Analysis of the cell-free amniotic fluid transcriptome expressed during the euploid mid-trimester of pregnancy

Application of a target array comparative genomic hybridization to prenatal diagnosis

Association between Polymorphisms in the Renin-Angiotensin System Genes and Prevalence of Spontaneously Aborted Fetuses ⬇️

Association between kinase insert domain-containing receptor polymorphisms (-604T>C, 1192G>A, 1719A>T) and premature ovarian failure in Korean women.

Association between vascular endothelial growth factor promoter polymorphisms and the risk of recurrent implantation failure

Association of IL-18 genotype with impaired glucose regulation in Korean women with polycystic ovary syndrome ⬇️

Association of methylenetetrahydrofolate reductase (MTHFR 677C>T) and thymidylate synthase (TSER and TS 1494del6) polymorphisms with premature ovarian failure in Korean women

Association of miR-146aC&gt;G, miR-196a2T&gt;C, and miR-499A&gt;G Polymorphisms With Risk of Premature Ovarian Failure in Korean Women ⬇️

Association of polymorphisms in microRNA machinery genes (DROSHA, DICER1, RAN, and XPO5) with risk of idiopathic primary ovarian insufficiency in Korean women ⬇️

Association of the miR‐146aC&gt;G, miR‐149T&gt;C, miR‐196a2T&gt;C, and miR‐499A&gt;G Polymorphisms with Risk of Spontaneously Aborted Fetuses ⬇️

Association study of dopamine receptor D2 TaqI A polymorphism and reward-related personality traits in healthy Korean young females

Association study of microRNA polymorphisms with risk of idiopathic recurrent spontaneous abortion in Korean women ⬇️

CRBL cells: establishment, characterization and susceptibility to prion infection

Chondrogenic potential of stem cells derived from amniotic fluid, adipose tissue, or bone marrow encapsulated in fibrin gels containing TGF-β3 ⬇️

Chromatin structure of the LCR in the human β-globin locus transcribing the adult δ- and β-globin genes ⬇️

Chromosomal abnormalities in spontaneous abortion after assisted reproductive treatment ⬇️

Clinical and Genetic Characteristics Analysis of Korean Patients with Stargardt Disease Using Targeted Exome Sequencing

Clinical and social characteristics of Korean men with Klinefelter syndrome ⬇️

Clinical evaluation of noninvasive prenatal testing for sex chromosome aneuploidies in 9,176 Korean pregnant women: a single-center retrospective study

Combined Model-Based Prediction for Non-Invasive Prenatal Screening

Complex chromosomal rearrangements in infertile males: complexity of rearrangement affects spermatogenesis

Correction of the name of author: Pre-implantation genetic diagnosis and pre-implantation genetic screening: two years experience at a single center

De novo balanced reciprocal translocation t(2;3)(q31;q27) in a fetus conceived using PGD in a t(2;14)(q35;q32.1) balanced reciprocal translocation carrier mother.

Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.

Effects and pregnancy outcomes of L-carnitine supplementation in culture media for human embryo development from in vitro fertilization (IVF)

Endothelial nitric oxide synthase gene polymorphisms (−786T&gt;C, 4a4b, 894G&gt;T) and haplotypes in Korean patients with recurrent spontaneous abortion ⬇️

Erectile dysfunction and extramarital sex induced by timed intercourse: a prospective study of 439 men

Erratum: Correction of Acknowledgements

Evaluation of 28 human embryonic stem cell lines for use as unrelated donors in stem cell therapy: implications of HLA and ABO genotypes

Functional recapitulation of smooth muscle cells via induced pluripotent stem cells from human aortic smooth muscle cells

Gene expression analysis of the microdissected trophoblast layer of human placenta after the spontaneous onset of labor

Gene sequencing in neonates and infants with the long QT syndrome.

Generation of FISH probes using laser microbeam microdissection and application to clinical molecular cytogenetics.

Generation of a B2M homozygous knockout human somatic cell nuclear transfer-derived embryonic stem cell line using the CRISPR/Cas9 system

Generation of cancerous neural stem cells forming glial tumor by oncogenic stimulation.

Genetic Variation of Methylenetetrahydrofolate Reductase (MTHFR) and Thymidylate Synthase (TS) Genes Is Associated with Idiopathic Recurrent Implantation Failure

Genome stabilization by RAD51-stimulatory compound 1 enhances efficiency of somatic cell nuclear transfer-mediated reprogramming and full-term development of cloned mouse embryos

Genome-wide screening of severe male factor infertile patients using BAC-array comparative genomic hybridization (CGH).

Genomic aspects in reproductive medicine

Global gene expression analysis of cell-free RNA in amniotic fluid from women destined to develop preeclampsia

Global gene expression changes of amniotic fluid cell free RNA according to fetal development

Homozygous deletions at 3p22, 5p14, 6q15, and 9p21 result in aberrant expression of tumor suppressor genes in gastric cancer

HomozygousCYP17A1mutation (H373L) identified in a 46,XX female with combined 17α-hydroxylase/17,20-lyase deficiency ⬇️

Human chorionic-plate-derived mesenchymal stem cells and Wharton’s jelly-derived mesenchymal stem cells: a comparative analysis of their potential as placenta-derived stem cells ⬇️

Human somatic cell nuclear transfer using adult cells.

Impact of RFC1, MTHFR, and MTHFD1 polymorphism on unexplained pregnancy loss (UPL): comparative analysis of maternal and fetal components using mother-abortus paired samples

Impaired Spermatogenesis and gr/gr Deletions Related to Y Chromosome Haplogroups in Korean Men ⬇️

Inhibition of pluripotent stem cell-derived teratoma formation by small molecules ⬇️

Isolation and Characterization of Novel, Highly Proliferative Human CD34/CD73-Double-Positive Testis-Derived Stem Cells for Cell Therapy ⬇️

Long-term safety and tolerability of subretinal transplantation of embryonic stem cell-derived retinal pigment epithelium in Asian Stargardt disease patients

MEF2C-Related 5q14.3 Microdeletion Syndrome Detected by Array CGH: A Case Report

Male Infertility Associated with a Supernumerary Marker Chromosome

Molecular analysis of miscarriage products using multiplex ligation-dependent probe amplification (MLPA): alternative to conventional karyotype analysis.

Molecular cytogenetic analysis of the monoblastic cell line U937. karyotype clarification by G-banding, whole chromosome painting, microdissection and reverse painting, and comparative genomic hybridization

Molecular genetic and cytogenetic characterization of a partial Xp duplication and Xq deletion in a patient with premature ovarian failure

Mutations in SOHLH1 gene associate with nonobstructive azoospermia

Neurodegeneration in an adolescent with Sjogren-Larsson syndrome: a decade-long follow-up case report

Neuronal properties, in vivo effects, and pathology of a Huntington's disease patient-derived induced pluripotent stem cells

Optimization Protocol of Fixation Method for Trophoblast Retrieval from the Cervix (TRIC): A Preliminary Study

PLGA nanoparticles with multiple modes are a biologically safe nanocarrier for mammalian development and their offspring

Pre-implantation genetic diagnosis and pre-implantation genetic screening: two years experience at a single center.

Precise prenatal diagnosis of tuberous sclerosis by sequencing the TSC2 gene

Preeclampsia leads to dysregulation of various signaling pathways in placenta

Preimplantation genetic diagnosis for couples with a Robertsonian translocation: practical information for genetic counseling ⬇️

Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies

Prenatal diagnosis of partial trisomy 3q resulting from t(3;14) in a fetus with multiple anomalies including vermian hypoplasia

Prevention of chemotherapy-induced premature ovarian insufficiency in mice by scaffold-based local delivery of human embryonic stem cell-derived mesenchymal progenitor cells

Rapid Production and Genetic Stability of Human Mesenchymal Progenitor Cells Derived from Human Somatic Cell Nuclear Transfer-Derived Pluripotent Stem Cells

Recombinant human phospholipase C zeta 1 induces intracellular calcium oscillations and oocyte activation in mouse and human oocytes ⬇️

Repurposing the Cord Blood Bank for Haplobanking of HLA-Homozygous iPSCs and Their Usefulness to Multiple Populations

RuvB-Like Protein 2 (Ruvbl2) Has a Role in Directing the Neuroectodermal Differentiation of Mouse Embryonic Stem Cells

SRY-negative 46,XX infertile male with Leydig cell hyperplasia: clinical, cytogenetic, and molecular analysis and review of the literature

Association of miR-146aC>G, miR-196a2T>C, and miR-499A>G Polymorphisms With Risk of Premature Ovarian Failure in Korean Women ⬇️

Association of the miR‐146aC>G, miR‐149T>C, miR‐196a2T>C, and miR‐499A>G Polymorphisms with Risk of Spontaneously Aborted Fetuses ⬇️

Endothelial nitric oxide synthase gene polymorphisms (−786T>C, 4a4b, 894G>T) and haplotypes in Korean patients with recurrent spontaneous abortion ⬇️