Gromoll J - Search Results

1

The human RHOX gene cluster: target genes and functional analysis of gene variants in infertile men.

Borgmann J, Tüttelmann F, Dworniczak B, Röpke A, Song HW, Kliesch S, Wilkinson MF, Laurentino S, Gromoll J. Borgmann J, et al. Among authors: gromoll j. Hum Mol Genet. 2016 Nov 15;25(22):4898-4910. doi: 10.1093/hmg/ddw313. Hum Mol Genet. 2016. PMID: 28171660 Free PMC article.

2

FSH receptor mRNA is expressed stage-dependently during rat spermatogenesis.

Kliesch S, Penttilä TL, Gromoll J, Saunders PT, Nieschlag E, Parvinen M. Kliesch S, et al. Among authors: gromoll j. Mol Cell Endocrinol. 1992 Apr;84(3):R45-9. doi: 10.1016/0303-7207(92)90039-9. Mol Cell Endocrinol. 1992. PMID: 1587387

3

Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia.

Simoni M, Gromoll J, Dworniczak B, Rolf C, Abshagen K, Kamischke A, Carani C, Meschede D, Behre HM, Horst J, Nieschlag E. Simoni M, et al. Among authors: gromoll j. Fertil Steril. 1997 Mar;67(3):542-7. doi: 10.1016/s0015-0282(97)80083-0. Fertil Steril. 1997. PMID: 9091344 Free article.

4

The Old World monkey DAZ (Deleted in AZoospermia) gene yields insights into the evolution of the DAZ gene cluster on the human Y chromosome.

Gromoll J, Weinbauer GF, Skaletsky H, Schlatt S, Rocchietti-March M, Page DC, Nieschlag E. Gromoll J, et al. Hum Mol Genet. 1999 Oct;8(11):2017-24. doi: 10.1093/hmg/8.11.2017. Hum Mol Genet. 1999. PMID: 10484770

5

Minutes of the 14th European workshop on molecular and cellular endocrinology of the testis.

Gromoll J, Michel C, Kostova E, Tüttelmann F, Wistuba J, Yeung CH, Henke A, Stukenborg JB, Akinloye O, Nieschlag E. Gromoll J, et al. Mol Cell Endocrinol. 2006 Sep 26;257-258:1-5. doi: 10.1016/j.mce.2006.06.001. Epub 2006 Jul 21. Mol Cell Endocrinol. 2006. PMID: 16859825 No abstract available.

6

Association of three isoforms of the meiotic BOULE gene with spermatogenic failure in infertile men.

Kostova E, Yeung CH, Luetjens CM, Brune M, Nieschlag E, Gromoll J. Kostova E, et al. Among authors: gromoll j. Mol Hum Reprod. 2007 Feb;13(2):85-93. doi: 10.1093/molehr/gal101. Epub 2006 Nov 17. Mol Hum Reprod. 2007. PMID: 17114206

7

Clinical consequences of microdeletions of the Y chromosome: the extended Münster experience.

Simoni M, Tüttelmann F, Gromoll J, Nieschlag E. Simoni M, et al. Among authors: gromoll j. Reprod Biomed Online. 2008 Feb;16(2):289-303. doi: 10.1016/s1472-6483(10)60588-3. Reprod Biomed Online. 2008. PMID: 18284889

8

Polymorphisms of the luteinizing hormone/chorionic gonadotropin receptor gene: association with maldescended testes and male infertility.

Simoni M, Tüttelmann F, Michel C, Böckenfeld Y, Nieschlag E, Gromoll J. Simoni M, et al. Among authors: gromoll j. Pharmacogenet Genomics. 2008 Mar;18(3):193-200. doi: 10.1097/FPC.0b013e3282f4e98c. Pharmacogenet Genomics. 2008. PMID: 18300940

9

[Genetics of male infertility].

Tüttelmann F, Gromoll J, Kliesch S. Tüttelmann F, et al. Among authors: gromoll j. Urologe A. 2008 Dec;47(12):1561-2, 1564-7. doi: 10.1007/s00120-008-1804-4. Urologe A. 2008. PMID: 18953522 Review. German.

10

Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome.

Poplinski A, Wieacker P, Kliesch S, Gromoll J. Poplinski A, et al. Among authors: gromoll j. Eur J Endocrinol. 2010 Jan;162(1):169-75. doi: 10.1530/EJE-09-0768. Epub 2009 Oct 7. Eur J Endocrinol. 2010. PMID: 19812237

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