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Natural orifice versus conventional mini-laparotomy for specimen extraction after reduced-port laparoscopic surgery for colorectal cancer: propensity score-matched comparative study

Surgical endoscopy, 2022, Vol.36 (1), p.155-166

2022

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Elevated miR‐200a and miR‐141 inhibit endocrine gland‐derived vascular endothelial growth factor expression and ciliogenesis in preeclampsia

The Journal of physiology, 2019-06, Vol.597 (12), p.3069-3083

2019

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Primary Cilium‐Regulated EG‐VEGF Signaling Facilitates Trophoblast Invasion

Journal of cellular physiology, 2017-06, Vol.232 (6), p.1467-1477

2017

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miR‐346 and miR‐582‐3p‐regulated EG‐VEGF expression and trophoblast invasion via matrix metalloproteinases 2 and 9

BioFactors (Oxford), 2017-03, Vol.43 (2), p.210-219

2017

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Transplacental passage of nirmatrelvir in pregnant women with COVID‐19

International journal of gynecology and obstetrics, 2024-01, Vol.164 (1), p.351-353

2024

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Differential miR-346 and miR-582-3p Expression in Association with Selected Maternal and Fetal Complications

International journal of molecular sciences, 2017-07, Vol.18 (7), p.1570

2017

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Setting up a specialized maternity unit in a tertiary hospital: An oasis for pregnant women with COVID-19 during the pandemic

Taiwanese journal of obstetrics & gynecology, 2023-11, Vol.62 (6), p.823-829

2023

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Gene-gene interactions and risk of recurrent miscarriages in carriers of endocrine gland–derived vascular endothelial growth factor and prokineticin receptor polymorphisms

Fertility and sterility, 2014-10, Vol.102 (4), p.1071-1077.e3

2014

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Association of sex hormone receptor gene polymorphisms with recurrent pregnancy loss: a systematic review and meta-analysis

Fertility and sterility, 2011-12, Vol.96 (6), p.1435-1444.e1

2011

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Genetic association studies of ACE and PAI-1 genes in women with recurrent pregnancy loss: a systematic review and meta-analysis

Thrombosis and haemostasis, 2013-01, Vol.109 (1), p.8

2013

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The E3 ubiquitin ligase Rnf8 stabilizes Tpp1 to promote telomere end protection

Nature structural & molecular biology, 2011-12, Vol.18 (12), p.1400

2011

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Association of polymorphisms/haplotypes of the genes encoding vascular endothelial growth factor and its KDR receptor with recurrent pregnancy loss

Human reproduction (Oxford), 2011-04, Vol.26 (4), p.758-764

2011

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A Common Variant of PROK1 (V67I) Acts as a Genetic Modifier in Early Human Pregnancy through Down-Regulation of Gene Expression

International journal of molecular sciences, 2016-01, Vol.17 (2), p.162-162

2016

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Gene-gene interactions and gene polymorphisms of VEGFA and EG-VEGF gene systems in recurrent pregnancy loss

Journal of assisted reproduction and genetics, 2014-06, Vol.31 (6), p.699-705

2014

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Two Y chromosomes with duplication of the distal long arm including the entire AZFc region

Gene, 2014-02, Vol.536 (2), p.444-448

2014

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Association of progesterone receptor polymorphism with idiopathic recurrent pregnancy loss in Taiwanese Han population

Journal of assisted reproduction and genetics, 2011-03, Vol.28 (3), p.239-243

2011

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Polymorphisms of endocrine gland-derived vascular endothelial growth factor gene and its receptor genes are associated with recurrent pregnancy loss

Human reproduction (Oxford), 2010-11, Vol.25 (11), p.2923-2930

2010

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Euchromatic variants of 8q21.2 in twins

Taiwanese journal of obstetrics & gynecology, 2017-04, Vol.56 (2), p.227-229

2017

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Critical Roles of Ring Finger Protein RNF8 in Replication Stress Responses

The Journal of biological chemistry, 2011-06, Vol.286 (25), p.22355-22361

2011

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A non-mosaic isodicentric Y chromosome resulting from breakage and fusion at the Yq pseudo-autosomal region in a fetus

Journal of assisted reproduction and genetics, 2013-12, Vol.30 (12), p.1559-1562

2013

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Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells

Taiwanese journal of obstetrics & gynecology, 2014-12, Vol.53 (4), p.598-601

2014

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A family with Xq22.3q25 interstitial deletion and normal ovarian function

Fertility and sterility, 2011-07, Vol.96 (1), p.e29-e34

2011

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A dicentric Y chromosome resulting from pericentric inversion between the centromere and Yq heterochromatin

Taiwanese journal of obstetrics & gynecology, 2013-09, Vol.52 (3), p.443-445

2013

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Non-mosaic uniparental trisomy 16 presenting with asplenia syndrome and placental abruption: A case report and literature review

European journal of medical genetics, 2013-04, Vol.56 (4), p.197-201

2013

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Constitutional complex chromosomal rearrangements in azoospermic men—case report and literature review

Urology (Ridgewood, N.J.), 2006-12, Vol.68 (6), p.1343.e5-1343.e8

2006

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Natural orifice versus conventional mini-laparotomy for specimen extraction after reduced-port laparoscopic surgery for colorectal cancer: propensity score-matched comparative study

Elevated miR‐200a and miR‐141 inhibit endocrine gland‐derived vascular endothelial growth factor expression and ciliogenesis in preeclampsia

Primary Cilium‐Regulated EG‐VEGF Signaling Facilitates Trophoblast Invasion

miR‐346 and miR‐582‐3p‐regulated EG‐VEGF expression and trophoblast invasion via matrix metalloproteinases 2 and 9

Transplacental passage of nirmatrelvir in pregnant women with COVID‐19

Differential miR-346 and miR-582-3p Expression in Association with Selected Maternal and Fetal Complications

Setting up a specialized maternity unit in a tertiary hospital: An oasis for pregnant women with COVID-19 during the pandemic

Gene-gene interactions and risk of recurrent miscarriages in carriers of endocrine gland–derived vascular endothelial growth factor and prokineticin receptor polymorphisms

Association of sex hormone receptor gene polymorphisms with recurrent pregnancy loss: a systematic review and meta-analysis

Genetic association studies of ACE and PAI-1 genes in women with recurrent pregnancy loss: a systematic review and meta-analysis

The E3 ubiquitin ligase Rnf8 stabilizes Tpp1 to promote telomere end protection

Association of polymorphisms/haplotypes of the genes encoding vascular endothelial growth factor and its KDR receptor with recurrent pregnancy loss

A Common Variant of PROK1 (V67I) Acts as a Genetic Modifier in Early Human Pregnancy through Down-Regulation of Gene Expression

Gene-gene interactions and gene polymorphisms of VEGFA and EG-VEGF gene systems in recurrent pregnancy loss

Two Y chromosomes with duplication of the distal long arm including the entire AZFc region

Association of progesterone receptor polymorphism with idiopathic recurrent pregnancy loss in Taiwanese Han population

Polymorphisms of endocrine gland-derived vascular endothelial growth factor gene and its receptor genes are associated with recurrent pregnancy loss

Euchromatic variants of 8q21.2 in twins

Critical Roles of Ring Finger Protein RNF8 in Replication Stress Responses

A non-mosaic isodicentric Y chromosome resulting from breakage and fusion at the Yq pseudo-autosomal region in a fetus

Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells

A family with Xq22.3q25 interstitial deletion and normal ovarian function

A dicentric Y chromosome resulting from pericentric inversion between the centromere and Yq heterochromatin

Non-mosaic uniparental trisomy 16 presenting with asplenia syndrome and placental abruption: A case report and literature review

Constitutional complex chromosomal rearrangements in azoospermic men—case report and literature review

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