Nöthen MM - Search Results

1

The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function.

Brockschmidt FF, Nöthen MM, Hillmer AM. Brockschmidt FF, et al. Among authors: nothen mm. J Mol Endocrinol. 2007 Jul;39(1):1-8. doi: 10.1677/JME-06-0072. J Mol Endocrinol. 2007. PMID: 17601880

2

The human serotonin 7 (5-HT7) receptor gene: genomic organization and systematic mutation screening in schizophrenia and bipolar affective disorder.

Erdmann J, Nöthen MM, Shimron-Abarbanell D, Rietschel M, Albus M, Borrmann M, Maier W, Franzek E, Körner J, Weigelt B, Fimmers R, Propping P. Erdmann J, et al. Among authors: nothen mm. Mol Psychiatry. 1996 Nov;1(5):392-7. Mol Psychiatry. 1996. PMID: 9154233

3

Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.

Cichon S, Anker M, Vogt IR, Rohleder H, Pützstück M, Hillmer A, Farooq SA, Al-Dhafri KS, Ahmad M, Haque S, Rietschel M, Propping P, Kruse R, Nöthen MM. Cichon S, et al. Among authors: nothen mm. Hum Mol Genet. 1998 Oct;7(11):1671-9. doi: 10.1093/hmg/7.11.1671. Hum Mol Genet. 1998. PMID: 9736769

4

Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia.

Kruse R, Cichon S, Anker M, Hillmer AM, Barros-Núñez P, Cantú JM, Leal E, Weinlich G, Schmuth M, Fritsch P, Ruzicka T, Propping P, Nöthen MM. Kruse R, et al. Among authors: nothen mm. J Invest Dermatol. 1999 Dec;113(6):954-9. doi: 10.1046/j.1523-1747.1999.00790.x. J Invest Dermatol. 1999. PMID: 10594736 Free article.

5

Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1).

Grünhage F, Schulze TG, Müller DJ, Lanczik M, Franzek E, Albus M, Borrmann-Hassenbach M, Knapp M, Cichon S, Maier W, Rietschel M, Propping P, Nöthen MM. Grünhage F, et al. Among authors: nothen mm. Mol Psychiatry. 2000 May;5(3):275-82. doi: 10.1038/sj.mp.4000711. Mol Psychiatry. 2000. PMID: 10889530

6

A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.

Cichon S, Kruse R, Hillmer AM, Kukuk G, Anker M, Altland K, Knapp M, Propping P, Nöthen MM. Cichon S, et al. Among authors: nothen mm. Br J Dermatol. 2000 Oct;143(4):811-4. doi: 10.1046/j.1365-2133.2000.03781.x. Br J Dermatol. 2000. PMID: 11069461

7

Variant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopecia.

Hillmer AM, Kruse R, Betz RC, Schumacher J, Heyn U, Propping P, Nöthen MM, Cichon S. Hillmer AM, et al. Among authors: nothen mm. Am J Hum Genet. 2001 Jul;69(1):235-7. doi: 10.1086/321273. Am J Hum Genet. 2001. PMID: 11410842 Free PMC article. No abstract available.

8

The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach.

Hillmer AM, Kruse R, Macciardi F, Heyn U, Betz RC, Ruzicka T, Propping P, Nöthen MM, Cichon S. Hillmer AM, et al. Among authors: nothen mm. Br J Dermatol. 2002 Apr;146(4):601-8. doi: 10.1046/j.1365-2133.2002.04766.x. Br J Dermatol. 2002. PMID: 11966690

9

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.

Levy-Nissenbaum E, Betz RC, Frydman M, Simon M, Lahat H, Bakhan T, Goldman B, Bygum A, Pierick M, Hillmer AM, Jonca N, Toribio J, Kruse R, Dewald G, Cichon S, Kubisch C, Guerrin M, Serre G, Nöthen MM, Pras E. Levy-Nissenbaum E, et al. Among authors: nothen mm. Nat Genet. 2003 Jun;34(2):151-3. doi: 10.1038/ng1163. Nat Genet. 2003. PMID: 12754508

10

A family-based and case-control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder.

Abou Jamra R, Sircar I, Becker T, Freudenberg-Hua Y, Ohlraun S, Freudenberg J, Brockschmidt F, Schulze TG, Gross M, Spira F, Deschner M, Schmäl C, Maier W, Propping P, Rietschel M, Cichon S, Nöthen MM, Schumacher J. Abou Jamra R, et al. Among authors: nothen mm. Mol Psychiatry. 2005 Jul;10(7):618-20. doi: 10.1038/sj.mp.4001665. Mol Psychiatry. 2005. PMID: 15852064 No abstract available.

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