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J Gromoll

Showing results (61-70 of 84) with videos related to

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Human Molecular Genetics|September 26, 2000
Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 provirusesC Sun, H Skaletsky, S Rozen, et al.
The Journal of Clinical Endocrinology and Metabolism|May 12, 2005
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 cycleR R Greb, K Grieshaber, J Gromoll, et al.
Human Reproduction (Oxford, England)|August 31, 2002
Manifestation of Y-chromosomal deletions in the human testis: a morphometrical and immunohistochemical evaluationC M Luetjens, J Gromoll, M Engelhardt, et al.
The Journal of Clinical Endocrinology and Metabolism|October 16, 2001
The CAG repeat polymorphism in the AR gene affects high density lipoprotein cholesterol and arterial vasoreactivityM Zitzmann, M Brune, B Kornmann, et al.
Human Reproduction (Oxford, England)|September 5, 2013
A combined approach facilitates the reliable detection of human spermatogonia in vitroN Kossack, N Terwort, J Wistuba, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 5, 2011
Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile malesN El Hajj, U Zechner, E Schneider, et al.
Human Molecular Genetics|September 15, 1999
The Old World monkey DAZ (Deleted in AZoospermia) gene yields insights into the evolution of the DAZ gene cluster on the human Y chromosomeJ Gromoll, G F Weinbauer, H Skaletsky, et al.
The Journal of Clinical Endocrinology and Metabolism|February 19, 1998
A mutation in the first transmembrane domain of the lutropin receptor causes male precocious pubertyJ Gromoll, C J Partsch, M Simoni, et al.
Molecular Human Reproduction|April 13, 2011
Reduced expression of DNMT3B in the germ cells of patients with bilateral spermatogenic arrest does not lead to changes in the global methylation statusS K Adiga, J Ehmcke, S Schlatt, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|November 10, 2011
Role of the CAG repeat polymorphism of the androgen receptor gene in polycystic ovary syndrome (PCOS)A N Schüring, A Welp, J Gromoll, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|September 26, 2000
Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 provirusesC Sun, H Skaletsky, S Rozen, et al.
The Journal of Clinical Endocrinology and Metabolism|May 12, 2005
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 cycleR R Greb, K Grieshaber, J Gromoll, et al.
Human Reproduction (Oxford, England)|August 31, 2002
Manifestation of Y-chromosomal deletions in the human testis: a morphometrical and immunohistochemical evaluationC M Luetjens, J Gromoll, M Engelhardt, et al.
The Journal of Clinical Endocrinology and Metabolism|October 16, 2001
The CAG repeat polymorphism in the AR gene affects high density lipoprotein cholesterol and arterial vasoreactivityM Zitzmann, M Brune, B Kornmann, et al.
Human Reproduction (Oxford, England)|September 5, 2013
A combined approach facilitates the reliable detection of human spermatogonia in vitroN Kossack, N Terwort, J Wistuba, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 5, 2011
Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile malesN El Hajj, U Zechner, E Schneider, et al.
Human Molecular Genetics|September 15, 1999
The Old World monkey DAZ (Deleted in AZoospermia) gene yields insights into the evolution of the DAZ gene cluster on the human Y chromosomeJ Gromoll, G F Weinbauer, H Skaletsky, et al.
The Journal of Clinical Endocrinology and Metabolism|February 19, 1998
A mutation in the first transmembrane domain of the lutropin receptor causes male precocious pubertyJ Gromoll, C J Partsch, M Simoni, et al.
Molecular Human Reproduction|April 13, 2011
Reduced expression of DNMT3B in the germ cells of patients with bilateral spermatogenic arrest does not lead to changes in the global methylation statusS K Adiga, J Ehmcke, S Schlatt, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|November 10, 2011
Role of the CAG repeat polymorphism of the androgen receptor gene in polycystic ovary syndrome (PCOS)A N Schüring, A Welp, J Gromoll, et al.
Pageof 9