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Novel synthetic kojic acid-methimazole derivatives inhibit mushroom tyrosinase and melanogenesis

Journal of bioscience and bioengineering, 2016-12, Vol.122 (6), p.666-672

2016

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The correlation with abnormal fetal outcome and a high level of amniotic fluid alpha-fetoprotein in mid-trimester

Taiwanese journal of obstetrics & gynecology, 2023-11, Vol.62 (6), p.863-868

2023

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Inhibitory effects of novel synthetic methimazole derivatives on mushroom tyrosinase and melanogenesis

Bioorganic & medicinal chemistry, 2014-05, Vol.22 (9), p.2809-2815

2014

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Prenatal diagnosis of persistent left superior vena cava, polyhydramnios and a small gastric bubble in a fetus with VACTERL association

Taiwanese journal of obstetrics & gynecology, 2021-03, Vol.60 (2), p.355-358

2021

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Monozygotic twins discordant for low-level mosaic trisomy 17 at amniocentesis in a pregnancy with a favorable outcome and a literature review of heterokaryotypic monozygotic twins at amniocentesis

Taiwanese journal of obstetrics & gynecology, 2020-03, Vol.59 (2), p.306-313

2020

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Kinetics of Mushroom Tyrosinase and Melanogenesis Inhibition by N-Acetyl-pentapeptides

TheScientificWorld, 2014-01, Vol.2014, p.409783-9

2014

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Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism

Taiwanese journal of obstetrics & gynecology, 2017-10, Vol.56 (5), p.691-693

2017

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Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound

Taiwanese journal of obstetrics & gynecology, 2018-10, Vol.57 (5), p.730-733

2018

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A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows

Taiwanese journal of obstetrics & gynecology, 2018-08, Vol.57 (4), p.583-587

2018

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Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus

Taiwanese journal of obstetrics & gynecology, 2018-02, Vol.57 (1), p.123-127

2018

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Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome

Taiwanese journal of obstetrics & gynecology, 2017-12, Vol.56 (6), p.840-842

2017

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Late-onset fetal bilateral pleural effusions associated with Down syndrome

Taiwanese journal of obstetrics & gynecology, 2018-02, Vol.57 (1), p.133-136

2018

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Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability

Taiwanese journal of obstetrics & gynecology, 2018-08, Vol.57 (4), p.578-582

2018

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Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome

Taiwanese journal of obstetrics & gynecology, 2017-12, Vol.56 (6), p.836-839

2017

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Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound

Taiwanese journal of obstetrics & gynecology, 2018-10, Vol.57 (5), p.734-738

2018

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Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect

Taiwanese journal of obstetrics & gynecology, 2017-08, Vol.56 (4), p.550-553

2017

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Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound

Taiwanese journal of obstetrics & gynecology, 2018-10, Vol.57 (5), p.739-744

2018

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Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome

Taiwanese journal of obstetrics & gynecology, 2017-08, Vol.56 (4), p.569-570

2017

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Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia

Taiwanese journal of obstetrics & gynecology, 2018-02, Vol.57 (1), p.119-122

2018

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Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia

Taiwanese journal of obstetrics & gynecology, 2017-06, Vol.56 (3), p.412-414

2017

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16

Taiwanese journal of obstetrics & gynecology, 2017-08, Vol.56 (4), p.545-549

2017

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Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9

Taiwanese journal of obstetrics & gynecology, 2017-08, Vol.56 (4), p.527-533

2017

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Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities

Taiwanese journal of obstetrics & gynecology, 2018-02, Vol.57 (1), p.128-132

2018

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Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13 , ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency

Taiwanese journal of obstetrics & gynecology, 2017-06, Vol.56 (3), p.398-401

2017

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Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1

Taiwanese journal of obstetrics & gynecology, 2017-06, Vol.56 (3), p.385-389

2017

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Novel synthetic kojic acid-methimazole derivatives inhibit mushroom tyrosinase and melanogenesis

The correlation with abnormal fetal outcome and a high level of amniotic fluid alpha-fetoprotein in mid-trimester

Inhibitory effects of novel synthetic methimazole derivatives on mushroom tyrosinase and melanogenesis

Prenatal diagnosis of persistent left superior vena cava, polyhydramnios and a small gastric bubble in a fetus with VACTERL association

Monozygotic twins discordant for low-level mosaic trisomy 17 at amniocentesis in a pregnancy with a favorable outcome and a literature review of heterokaryotypic monozygotic twins at amniocentesis

Kinetics of Mushroom Tyrosinase and Melanogenesis Inhibition by N-Acetyl-pentapeptides

Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism

Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound

A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows

Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus

Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome

Late-onset fetal bilateral pleural effusions associated with Down syndrome

Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome

Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound

Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect

Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound

Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome

Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia

Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16

Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9

Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities

Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13 , ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency

Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1

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