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Items: 19

1.

Genome-wide analysis of PDX1 target genes in human pancreatic progenitors.

Wang X, Sterr M, Burtscher I, Chen S, Hieronimus A, Machicao F, Staiger H, Häring HU, Lederer G, Meitinger T, Cernilogar FM, Schotta G, Irmler M, Beckers J, Hrabě de Angelis M, Ray M, Wright CVE, Bakhti M, Lickert H.

Mol Metab. 2018 Mar;9:57-68. doi: 10.1016/j.molmet.2018.01.011. Epub 2018 Jan 31.

2.

Generation of a human induced pluripotent stem cell (iPSC) line from a patient with family history of diabetes carrying a C18R mutation in the PDX1 gene.

Wang X, Chen S, Burtscher I, Sterr M, Hieronimus A, Machicao F, Staiger H, Häring HU, Lederer G, Meitinger T, Lickert H.

Stem Cell Res. 2016 Sep;17(2):292-295. doi: 10.1016/j.scr.2016.08.005. Epub 2016 Aug 6.

3.

Generation of a human induced pluripotent stem cell (iPSC) line from a patient carrying a P33T mutation in the PDX1 gene.

Wang X, Chen S, Burtscher I, Sterr M, Hieronimus A, Machicao F, Staiger H, Häring HU, Lederer G, Meitinger T, Lickert H.

Stem Cell Res. 2016 Sep;17(2):273-276. doi: 10.1016/j.scr.2016.08.004. Epub 2016 Aug 5.

4.

Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndrome.

Bonfig W, Salem NJ, Heiliger K, Hempel M, Lederer G, Bornkamm M, Wieland K, Lohse P, Burdach S, Oexle K.

J Pediatr Endocrinol Metab. 2012;25(9-10):991-5. doi: 10.1515/jpem-2012-0103.

PMID:
23426831
5.

Microdeletion syndrome 16p11.2-p12.2: clinical and molecular characterization.

Hempel M, Rivera Brugués N, Wagenstaller J, Lederer G, Weitensteiner A, Seidel H, Meitinger T, Strom TM.

Am J Med Genet A. 2009 Oct;149A(10):2106-12. doi: 10.1002/ajmg.a.33042.

PMID:
19676056
6.

Delineation of a 2q deletion in a girl with dysmorphic features and epilepsy.

Langer S, Geigl JB, Wagenstaller J, Lederer G, Hempel M, Daumer-Haas C, Leifheit HJ, Speicher MR.

Am J Med Genet A. 2006 Apr 1;140(7):764-8.

PMID:
16523518
7.

Analysis of gene expression patterns and chromosomal changes associated with aging.

Geigl JB, Langer S, Barwisch S, Pfleghaar K, Lederer G, Speicher MR.

Cancer Res. 2004 Dec 1;64(23):8550-7.

8.

Order of genetic events is critical determinant of aberrations in chromosome count and structure.

Fauth C, O'Hare MJ, Lederer G, Jat PS, Speicher MR.

Genes Chromosomes Cancer. 2004 Aug;40(4):298-306.

PMID:
15188452
9.

Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy in a case of a small supernumerary marker chromosome detected at prenatal diagnosis.

von Eggeling F, Langer S, Hoppe C, Liehr T, Weise A, Lederer G, Kotzot D.

Clin Genet. 2003 Aug;64(2):168-71. No abstract available.

PMID:
12859416
10.

A familial unbalanced subtelomeric translocation resulting in monosomy 6q27-->qter.

Kraus J, Lederer G, Keri C, Seidel H, Rost I, Wirtz A, Fauth C, Speicher MR.

J Med Genet. 2003 Apr;40(4):e48. No abstract available.

11.

Multicolor FISH in two and three dimensions for clastogenic analyses.

Maierhofer C, Jentsch I, Lederer G, Fauth C, Speicher MR.

Mutagenesis. 2002 Nov;17(6):523-7. Review.

PMID:
12435849
12.

A new strategy for the detection of subtelomeric rearrangements.

Fauth C, Zhang H, Harabacz S, Brown J, Saracoglu K, Lederer G, Rittinger O, Rost I, Eils R, Kearney L, Speicher MR.

Hum Genet. 2001 Dec;109(6):576-83. Epub 2001 Nov 9.

PMID:
11810269
13.

Carcinogen-specific induction of genetic instability.

Bardelli A, Cahill DP, Lederer G, Speicher MR, Kinzler KW, Vogelstein B, Lengauer C.

Proc Natl Acad Sci U S A. 2001 May 8;98(10):5770-5. Epub 2001 Apr 10.

14.

Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetry.

Schmidt H, Uhrig S, Lederer G, Murken J, Speicher MR, Schuffenhauer S.

J Med Genet. 2000 Oct;37(10):804-7. No abstract available.

15.

A heritable folate-sensitive fragile site on chromosome 2p 11.2 (FRA2L).

Schuffenhauer S, Lederer G, Murken J.

Chromosome Res. 1996 Apr;4(3):252-4. No abstract available.

PMID:
8793213
16.

De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boy.

Schuffenhauer S, Callen DF, Seidel H, Shen Y, Lederer G, Murken J.

Clin Genet. 1992 Nov;42(5):246-50.

PMID:
1486702
17.

Persistent Schistosoma mansoni infection in Yemeni immigrants to Israel.

Hornstein L, Lederer G, Schechter J, Greenberg Z, Boem R, Bilguray B, Giladi L, Hamburger J.

Isr J Med Sci. 1990 Jul;26(7):386-9.

PMID:
2117600
18.

[Trends in rehabilitation of cervical cord injuries].

Lederer G.

Osterr Krankenpflegez. 1980;33(10):285-6. German. No abstract available.

PMID:
6904941
19.

[Training in planned orthotic care for restoration of prehensile ability in lesions of the cervical medulla].

Stöger M, Lederer G.

Z Orthop Ihre Grenzgeb. 1971 May;109(2):239-43. German. No abstract available.

PMID:
4254053

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