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Misleading and reliable markers to differentiate between primate testis-derived multipotent stromal cells and spermatogonia in culture

Human reproduction (Oxford), 2012-06, Vol.27 (6), p.1754-1767

2012

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Novel genetic aspects of Klinefelter's syndrome

Molecular human reproduction, 2010-06, Vol.16 (6), p.386-395

2010

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A combined approach facilitates the reliable detection of human spermatogonia in vitro

Human reproduction (Oxford), 2013-11, Vol.28 (11), p.3012-3025

2013

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The pluripotency factor LIN28 in monkey and human testes: a marker for spermatogonial stem cells?

Molecular human reproduction, 2012-10, Vol.18 (9-10), p.477-488

2012

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Methylation Status of Imprinted Genes and Repetitive Elements in Sperm DNA from Infertile Males

Sexual development, 2011-01, Vol.5 (2), p.60-69

2011

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Ageing in men with normal spermatogenesis alters spermatogonial dynamics and nuclear morphology in Sertoli cells

Andrology (Oxford), 2019-11, Vol.7 (6), p.827-839

2019

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Developmental Expression of the Pluripotency Factor Sal-Like Protein 4 in the Monkey, Human and Mouse Testis: Restriction to Premeiotic Germ Cells

Cells, tissues, organs, 2012-01, Vol.196 (3), p.206-220

2012

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A Common Single Nucleotide Polymorphism in Exon 10 of the Human Follicle Stimulating Hormone Receptor Is a Major Determinant of Length and Hormonal Dynamics of the Menstrual Cycle

The journal of clinical endocrinology and metabolism, 2005-08, Vol.90 (8), p.4866-4872

2005

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Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1

International journal of andrology, 2010-08, Vol.33 (4), p.642-649

2010

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The Klinefelter syndrome: current management and research challenges

Andrology, 2016-05, Vol.4 (3), p.545-549

2016

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The RHOX homeobox gene cluster is selectively expressed in human oocytes and male germ cells

Human reproduction (Oxford), 2013-06, Vol.28 (6), p.1635-1646

2013

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Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses

Human molecular genetics, 2000-09, Vol.9 (15), p.2291-2296

2000

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Isoforms and single nucleotide polymorphisms of the FSH receptor gene: implications for human reproduction

Human reproduction update, 2002-09, Vol.8 (5), p.413-421

2002

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Role of the CAG repeat polymorphism of the androgen receptor gene in polycystic ovary syndrome (PCOS)

Experimental and clinical endocrinology & diabetes, 2012-02, Vol.120 (2), p.73

2012

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microRNA miR-513a-3p acts as a co-regulator of luteinizing hormone/chorionic gonadotropin receptor gene expression in human granulosa cells

Molecular and cellular endocrinology, 2014-06, Vol.390 (1-2), p.65-72

2014

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Partial deletions in the AZFc region of the Y chromosome occur in men with impaired as well as normal spermatogenesis

Human reproduction (Oxford), 2005-01, Vol.20 (1), p.191-197

2005

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Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background

Journal of medical genetics, 2009-01, Vol.46 (1), p.21-31

2009

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Male hypogonadism caused by homozygous deletion of exon 10 of the luteinizing hormone (LH) receptor : Differential action of human chorionic gonadotropin and LH

The journal of clinical endocrinology and metabolism, 2000-06, Vol.85 (6), p.2281-2286

2000

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DNA methylation in spermatozoa as a prospective marker in andrology

Andrology (Oxford), 2013-09, Vol.1 (5), p.731-740

2013

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FSHB ‐211G>T stratification for follicle‐stimulating hormone treatment of male infertility patients: making the case for a pharmacogenetic approach in genetic functional secondary hypogonadism

Andrology (Oxford), 2015-11, Vol.3 (6), p.1050-1053

2015

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The CAG repeat polymorphism in the androgen receptor gene modulates body fat mass and serum concentrations of leptin and insulin in men

Diabetologia, 2003, Vol.46 (1), p.31-39

2003

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Germ cell dynamics in the testis of the postnatal common marmoset monkey (Callithrix jacchus)

Reproduction (Cambridge, England), 2010-11, Vol.140 (5), p.733-742

2010

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An alternative interpretation of cellular ‘selfish spermatogonial selection’‐ clusters in the human testis indicates the need for 3‐D‐analyses

Andrology (Oxford), 2016-03, Vol.4 (2), p.213-217

2016

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Intratesticular testosterone is increased in men with Klinefelter syndrome and may not be released into the bloodstream owing to altered testicular vascularization – a preliminary report

Andrology (Oxford), 2014-03, Vol.2 (2), p.275-281

2014

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An activating mutation of the follicle-stimulating hormone receptor autonomously sustains spermatogenesis in a hypophysectomized man

The journal of clinical endocrinology and metabolism, 1996-04, Vol.81 (4), p.1367-1370

1996

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Misleading and reliable markers to differentiate between primate testis-derived multipotent stromal cells and spermatogonia in culture

Novel genetic aspects of Klinefelter's syndrome

A combined approach facilitates the reliable detection of human spermatogonia in vitro

The pluripotency factor LIN28 in monkey and human testes: a marker for spermatogonial stem cells?

Methylation Status of Imprinted Genes and Repetitive Elements in Sperm DNA from Infertile Males

Ageing in men with normal spermatogenesis alters spermatogonial dynamics and nuclear morphology in Sertoli cells

Developmental Expression of the Pluripotency Factor Sal-Like Protein 4 in the Monkey, Human and Mouse Testis: Restriction to Premeiotic Germ Cells

A Common Single Nucleotide Polymorphism in Exon 10 of the Human Follicle Stimulating Hormone Receptor Is a Major Determinant of Length and Hormonal Dynamics of the Menstrual Cycle

Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1

The Klinefelter syndrome: current management and research challenges

The RHOX homeobox gene cluster is selectively expressed in human oocytes and male germ cells

Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses

Isoforms and single nucleotide polymorphisms of the FSH receptor gene: implications for human reproduction

Role of the CAG repeat polymorphism of the androgen receptor gene in polycystic ovary syndrome (PCOS)

microRNA miR-513a-3p acts as a co-regulator of luteinizing hormone/chorionic gonadotropin receptor gene expression in human granulosa cells

Partial deletions in the AZFc region of the Y chromosome occur in men with impaired as well as normal spermatogenesis

Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background

Male hypogonadism caused by homozygous deletion of exon 10 of the luteinizing hormone (LH) receptor : Differential action of human chorionic gonadotropin and LH

DNA methylation in spermatozoa as a prospective marker in andrology

FSHB ‐211G>T stratification for follicle‐stimulating hormone treatment of male infertility patients: making the case for a pharmacogenetic approach in genetic functional secondary hypogonadism

The CAG repeat polymorphism in the androgen receptor gene modulates body fat mass and serum concentrations of leptin and insulin in men

Germ cell dynamics in the testis of the postnatal common marmoset monkey (Callithrix jacchus)

An alternative interpretation of cellular ‘selfish spermatogonial selection’‐ clusters in the human testis indicates the need for 3‐D‐analyses

Intratesticular testosterone is increased in men with Klinefelter syndrome and may not be released into the bloodstream owing to altered testicular vascularization – a preliminary report

An activating mutation of the follicle-stimulating hormone receptor autonomously sustains spermatogenesis in a hypophysectomized man

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