Novel genetic aspects of Klinefelter's syndrome : Klinefelter's syndrome: basic science to clinicTÜTTELMANN, F; GROMOLL, J.Molecular human reproduction. 2010, Vol 16, Num 5-6, pp 386-395, issn 1360-9947, 10 p.Article

Monitoring the transfection efficiency of the human follicle-stimulating hormone receptor cDNA in COS-7 cells : evaluation of the growth hormone transient gene expression assay systemSIMONI, M; GROMOLL, J.Journal of endocrinological investigation (Testo stampato). 1996, Vol 19, Num 6, pp 359-364, issn 0391-4097Article

Natural transmission of a partial AZFb deletion of the Y chromosome over three generationsROLF, C; GROMOLL, J; SIMONI, M et al.Human reproduction (Oxford. Print). 2002, Vol 17, Num 9, pp 2267-2271, issn 0268-1161Article

Male hypogonadism caused by homozygous deletion of exon 10 of the luteinizing hormone (LH) receptor : Differential action of human chorionic gonadotropin and LHGROMOLL, J; EIHOLZER, U; NIESCHLAG, E et al.The Journal of clinical endocrinology and metabolism. 2000, Vol 85, Num 6, pp 2281-2286, issn 0021-972XArticle

Cloning and sequence analysis of cDNA for precursor of a crustacean hyperglucemic hormoneWEIDEMANN, W; GROMOLL, J; KELLER, R et al.FEBS letters. 1989, Vol 257, Num 1, pp 31-34, issn 0014-5793, 4 p.Article

Une mutation activatrice du récepteur de la FSH induit la spermatogenèse chez un homme hypophysectomisé = An activating mutation of the FSH receptor induces spermatogenesis in an hypophysectomized manGROMOLL, J; SIMONI, M; NIESCHLAG, E et al.Références en gynécologie obstétrique. 1996, Vol 4, Num 2, issn 1244-8168, p.173Article

An activating mutation of the follicle-stimulating hormone receptor autonomously sustains spermatogenesis in a hypophysectomized manGROMOLL, J; SIMONI, M; NIESCHLAG, E et al.The Journal of clinical endocrinology and metabolism. 1996, Vol 81, Num 4, pp 1367-1370, issn 0021-972XArticle

Molecular cloning of a truncated isoform of the human follicle stimulating hormone receptorGROMOLL, J; GUDERMANN, T; NIESCHLAG, E et al.Biochemical and biophysical research communications (Print). 1992, Vol 188, Num 3, pp 1077-1083, issn 0006-291XArticle

The pluripotency factor LIN28 in monkey and human testes: a marker for spermatogonial stem cells?AECKERLE, N; EILDERMANN, K; BEHR, R et al.Molecular human reproduction. 2012, Vol 18, Num 9-10, pp 477-488, issn 1360-9947, 12 p.Article

No Correlation between Androgen Receptor CAG and GGN Repeat Length and the Degree of Genital Virilization in Females with 21-Hydroxylase DeficiencyWELZEL, M; SCHWARZ, H.-P; KRONE, N et al.The Journal of clinical endocrinology and metabolism. 2010, Vol 95, Num 5, pp 2443-2450, issn 0021-972X, 8 p.Article

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 cycleGREB, R. R; GRIESHABER, K; GROMOLL, J et al.The Journal of clinical endocrinology and metabolism. 2005, Vol 90, Num 8, pp 4866-4872, issn 0021-972X, 7 p.Article

The carboxyterminal peptide of chorionic gonadotropin facilitates activation of the marmoset LH receptorMÜLLER, T; GROMOLL, J; SIMULA, A. P et al.Experimental and clinical endocrinology & diabetes. 2004, Vol 112, Num 10, pp 574-579, issn 0947-7349, 6 p.Article

Identification of allelic variants in the follicle-stimulating hormone receptor genes of females with or without hypergonadotropic amenorrheaLIU, J. Y; GROMOLL, J; CEDARS, M. I et al.Fertility and sterility. 1998, Vol 70, Num 2, pp 326-331, issn 0015-0282Conference Paper

The follicle-stimulating hormone receptor : Biochemistry, molecular biology, physiology, and pathophysiologySIMONI, M; GROMOLL, J; NIESCHLAG, E et al.Endocrine reviews. 1997, Vol 18, Num 6, pp 739-773, issn 0163-769XArticle

The structure and organization of the human follicle-stimulating hormone receptor (FSHR) geneGROMOLL, J; PEKEL, E; NIESCHLAG, D et al.Genomics (San Diego, Calif.). 1996, Vol 35, Num 2, pp 308-311, issn 0888-7543Article

Mutation analysis of the X-chromosome linked, testis-specific TAF7L gene in spermatogenic failureAKINLOYE, O; GROMOLL, J; CALLIES, C et al.Andrologia. 2007, Vol 39, Num 5, pp 190-195, issn 0303-4569, 6 p.Article

The distribution of FSH receptor isoforms is related to basal FSH levels in subfertile women with normal menstrual cyclesDE KONING, C. H; BENJAMINS, T; HARMS, P et al.Human reproduction (Oxford. Print). 2006, Vol 21, Num 2, pp 443-446, issn 0268-1161, 4 p.Article

Mutation screening and isoform prevalence of the follicle stimulating hormone receptor gene in women with premature ovarian failure, resistant ovary syndrome and polycystic ovary syndromeCONWAY, G. S; CONWAY, E; WALKER, C et al.Clinical endocrinology (Oxford. Print). 1999, Vol 51, Num 1, pp 97-99, issn 0300-0664Article

Role of FSH in male gonadal functionSIMONI, M; WEINBAUER, G. F; GROMOLL, J et al.Annales d'endocrinologie. 1999, Vol 60, Num 2, pp 102-106, issn 0003-4266Conference Paper

Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1POPLINSKI, A; TÜTTELMANN, F; KANBER, D et al.International journal of andrology (Print). 2010, Vol 33, Num 4, pp 642-649, issn 0105-6263, 8 p.Article

The relationship between Y chromosome DNA haplotypes and Y chromosome deletions leading to male infertilityQUINTANA-MURCI, L; KRAUSZ, C; LEE, A. C et al.Human genetics. 2001, Vol 108, Num 1, pp 55-58, issn 0340-6717Article

Dazl protein expression in adult rat testis is up-regulated at meiosis and not hormonally regulatedROCCHIETTI-MARCH, M; WEINBAUER, G. F; PAGE, D. C et al.International journal of andrology (Print). 2000, Vol 23, Num 1, pp 51-56, issn 0105-6263Article

The Old World monkey DAZ (deleted in AZoospermia) gene yields insights into the evolution of the DAZ gene cluster on the human Y chromosomeGROMOLL, J; WEINBAUER, G. F; SKALETSKY, H et al.Human molecular genetics (Print). 1999, Vol 8, Num 11, pp 2017-2024, issn 0964-6906Article

Molecular pathophysiology and clinical manifestations of gonadotropin receptor defectsSIMONI, M; GROMOLL, J; NIESCHLAG, E et al.Steroids. 1998, Vol 63, Num 5-6, pp 288-293, issn 0039-128XConference Paper

Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermiaSIMONI, M; GROMOLL, J; NIESCHLAG, E et al.Fertility and sterility. 1997, Vol 67, Num 3, pp 542-547, issn 0015-0282Article