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NDNF variants are rare in patients with congenital hypogonadotropic hypogonadism

Human genome variation, 2021-02, Vol.8 (1), p.5-5, Article 5

2021

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Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature

Endocrine Journal, 2017, Vol.64(10), pp.947-954

2017

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Germ cells are essential for sexual dimorphism in the medaka gonad

Proceedings of the National Academy of Sciences - PNAS, 2007-10, Vol.104 (43), p.16958-16963

2007

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Enhanced Self-Renewal of Hematopoietic Stem Cells Mediated by the Polycomb Gene Product Bmi-1

Immunity (Cambridge, Mass.), 2004-12, Vol.21 (6), p.843-851

2004

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Expression levels and DNA methylation profiles of the growth gene SHOX in cartilage tissues and chondrocytes

Scientific reports, 2024-04, Vol.14 (1), p.8069-8069, Article 8069

2024

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Intrauterine Hyponutrition Reduces Fetal Testosterone Production and Postnatal Sperm Count in the Mouse

Journal of the Endocrine Society, 2022-04, Vol.6 (4), p.bvac022-bvac022

2022

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Cbx2, a Polycomb Group Gene, Is Required for Sry Gene Expression in Mice

Endocrinology (Philadelphia), 2012-02, Vol.153 (2), p.913-924

2012

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Aristaless related homeobox gene, Arx, is implicated in mouse fetal Leydig cell differentiation possibly through expressing in the progenitor cells

PloS one, 2013-06, Vol.8 (6), p.e68050-e68050

2013

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A critical time window of Sry action in gonadal sex determination in mice

Development (Cambridge), 2009-01, Vol.136 (1), p.129-138

2009

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MYRF haploinsufficiency causes 46,XY and 46,XX disorders of sex development: bioinformatics consideration

Human molecular genetics, 2019-07, Vol.28 (14), p.2319-2329

2019

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Homozygous 6-bp deletion of IGFALS in a prepubertal boy with short stature

Human genome variation, 2024-07, Vol.11 (1), p.27-3, Article 27

2024

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A case of combined 21‐hydroxylase deficiency and CHARGE syndrome featuring micropenis and cryptorchidism

Molecular genetics & genomic medicine, 2019-06, Vol.7 (6), p.e730-n/a

2019

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WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome

European journal of medical genetics, 2020-01, Vol.63 (1), p.103626-103626, Article 103626

2020

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Frequency of Common Copy-Number Variations at 15q11.2q13 in Sperm of Healthy Men

Cytogenetic and genome research, 2019, Vol.159 (2), p.66-73

2019

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The mouse homolog of Drosophila Vasa is required for the development of male germ cells

Genes & development, 2000-04, Vol.14 (7), p.841-853

2000

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Quantification of Maternal Microchimeric Cells in the Liver of Children With Biliary Atresia

Journal of pediatric gastroenterology and nutrition, 2022-04, Vol.74 (4), p.e83-e86

2022

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Abnormal Epithelial Cell Polarity and Ectopic Epidermal Growth Factor Receptor (EGFR) Expression Induced in Emx2 KO Embryonic Gonads

Endocrinology (Philadelphia), 2010-12, Vol.151 (12), p.5893-5904

2010

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Role of Liquid–Liquid Separation in Endocrine and Living Cells

Journal of the Endocrine Society, 2021-10, Vol.5 (10), p.bvab126-bvab126

2021

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A single amino acid mutation in SNAP-25 induces anxiety-related behavior in mouse

PloS one, 2011-09, Vol.6 (9), p.e25158

2011

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A novel C-terminal truncating NR5A1 mutation in dizygotic twins

Human genome variation, 2017-03, Vol.4 (1), p.17008-17008, Article 17008

2017

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Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells

BMC medical genomics, 2019-05, Vol.12 (1), p.77-77, Article 77

2019

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Thymocyte Proliferation Induced by Pre-T Cell Receptor Signaling Is Maintained through Polycomb Gene Product Bmi-1-Mediated Cdkn2a Repression

Immunity (Cambridge, Mass.), 2008-02, Vol.28 (2), p.231-245

2008

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Mechanism of asymmetric ovarian development in chick embryos

Development (Cambridge), 2008-02, Vol.135 (4), p.677-685

2008

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Testicular dysgenesis/regression without campomelic dysplasia in patients carrying missense mutations and upstream deletion of SOX9

Molecular genetics & genomic medicine, 2015-11, Vol.3 (6), p.550-557

2015

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Importance of forkhead transcription factor Fkhl18 for development of testicular vasculature

Molecular reproduction and development, 2008-09, Vol.75 (9), p.1361-1371

2008

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NDNF variants are rare in patients with congenital hypogonadotropic hypogonadism

Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature

Germ cells are essential for sexual dimorphism in the medaka gonad

Enhanced Self-Renewal of Hematopoietic Stem Cells Mediated by the Polycomb Gene Product Bmi-1

Expression levels and DNA methylation profiles of the growth gene SHOX in cartilage tissues and chondrocytes

Intrauterine Hyponutrition Reduces Fetal Testosterone Production and Postnatal Sperm Count in the Mouse

Cbx2, a Polycomb Group Gene, Is Required for Sry Gene Expression in Mice

Aristaless related homeobox gene, Arx, is implicated in mouse fetal Leydig cell differentiation possibly through expressing in the progenitor cells

A critical time window of Sry action in gonadal sex determination in mice

MYRF haploinsufficiency causes 46,XY and 46,XX disorders of sex development: bioinformatics consideration

Homozygous 6-bp deletion of IGFALS in a prepubertal boy with short stature

A case of combined 21‐hydroxylase deficiency and CHARGE syndrome featuring micropenis and cryptorchidism

WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome

Frequency of Common Copy-Number Variations at 15q11.2q13 in Sperm of Healthy Men

The mouse homolog of Drosophila Vasa is required for the development of male germ cells

Quantification of Maternal Microchimeric Cells in the Liver of Children With Biliary Atresia

Abnormal Epithelial Cell Polarity and Ectopic Epidermal Growth Factor Receptor (EGFR) Expression Induced in Emx2 KO Embryonic Gonads

Role of Liquid–Liquid Separation in Endocrine and Living Cells

A single amino acid mutation in SNAP-25 induces anxiety-related behavior in mouse

A novel C-terminal truncating NR5A1 mutation in dizygotic twins

Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells

Thymocyte Proliferation Induced by Pre-T Cell Receptor Signaling Is Maintained through Polycomb Gene Product Bmi-1-Mediated Cdkn2a Repression

Mechanism of asymmetric ovarian development in chick embryos

Testicular dysgenesis/regression without campomelic dysplasia in patients carrying missense mutations and upstream deletion of SOX9

Importance of forkhead transcription factor Fkhl18 for development of testicular vasculature

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