Schulz HL - Search Results

1

Genomic structure and assessment of the retinally expressed RFamide-related peptide gene in dominant cystoid macular dystrophy.

Schulz HL, Stoehr H, White K, van Driel MA, Hoyng CB, Cremers F, Weber BH. Schulz HL, et al. Mol Vis. 2002 Mar 19;8:67-71. Mol Vis. 2002. PMID: 11951088 Free article.

2

Identification of a novel retina-specific gene located in a subtelomeric region with polymorphic distribution among multiple human chromosomes.

Mah N, Stoehr H, Schulz HL, White K, Weber BH. Mah N, et al. Among authors: schulz hl. Biochim Biophys Acta. 2001 Dec 30;1522(3):167-74. doi: 10.1016/s0167-4781(01)00328-1. Biochim Biophys Acta. 2001. PMID: 11779631

3

Characterization of three novel isoforms of the metabotrobic glutamate receptor 7 (GRM7).

Schulz HL, Stohr H, Weber BH. Schulz HL, et al. Neurosci Lett. 2002 Jun 21;326(1):37-40. doi: 10.1016/s0304-3940(02)00306-3. Neurosci Lett. 2002. PMID: 12052533

4

Identifying differentially expressed genes in the mammalian retina and the retinal pigment epithelium by suppression subtractive hybridization.

Schulz HL, Rahman FA, Fadl El Moula FM, Stojic J, Gehrig A, Weber BH. Schulz HL, et al. Cytogenet Genome Res. 2004;106(1):74-81. doi: 10.1159/000078564. Cytogenet Genome Res. 2004. PMID: 15218245

5

EST mining of the UniGene dataset to identify retina-specific genes.

Stöhr H, Mah N, Schulz HL, Gehrig A, Fröhlich S, Weber BH. Stöhr H, et al. Among authors: schulz hl. Cytogenet Cell Genet. 2000;91(1-4):267-77. doi: 10.1159/000056856. Cytogenet Cell Genet. 2000. PMID: 11173868

6

The Retinome - defining a reference transcriptome of the adult mammalian retina/retinal pigment epithelium.

Schulz HL, Goetz T, Kaschkoetoe J, Weber BH. Schulz HL, et al. BMC Genomics. 2004 Jul 29;5(1):50. doi: 10.1186/1471-2164-5-50. BMC Genomics. 2004. PMID: 15283859 Free PMC article.

7

TMEM16B, a novel protein with calcium-dependent chloride channel activity, associates with a presynaptic protein complex in photoreceptor terminals.

Stöhr H, Heisig JB, Benz PM, Schöberl S, Milenkovic VM, Strauss O, Aartsen WM, Wijnholds J, Weber BH, Schulz HL. Stöhr H, et al. Among authors: schulz hl. J Neurosci. 2009 May 27;29(21):6809-18. doi: 10.1523/JNEUROSCI.5546-08.2009. J Neurosci. 2009. PMID: 19474308 Free PMC article.

8

Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular Lesions.

Brandl C, Schulz HL, Charbel Issa P, Birtel J, Bergholz R, Lange C, Dahlke C, Zobor D, Weber BHF, Stöhr H. Brandl C, et al. Among authors: schulz hl. Genes (Basel). 2017 Jun 23;8(7):170. doi: 10.3390/genes8070170. Genes (Basel). 2017. PMID: 28644393 Free PMC article.

9

Mutation-Dependent Pathomechanisms Determine the Phenotype in the Bestrophinopathies.

Nachtigal AL, Milenkovic A, Brandl C, Schulz HL, Duerr LMJ, Lang GE, Reiff C, Herrmann P, Kellner U, Weber BHF. Nachtigal AL, et al. Among authors: schulz hl. Int J Mol Sci. 2020 Feb 26;21(5):1597. doi: 10.3390/ijms21051597. Int J Mol Sci. 2020. PMID: 32111077 Free PMC article.

10

Meta-analysis of genome scans of age-related macular degeneration.

Fisher SA, Abecasis GR, Yashar BM, Zareparsi S, Swaroop A, Iyengar SK, Klein BE, Klein R, Lee KE, Majewski J, Schultz DW, Klein ML, Seddon JM, Santangelo SL, Weeks DE, Conley YP, Mah TS, Schmidt S, Haines JL, Pericak-Vance MA, Gorin MB, Schulz HL, Pardi F, Lewis CM, Weber BH. Fisher SA, et al. Among authors: schulz hl. Hum Mol Genet. 2005 Aug 1;14(15):2257-64. doi: 10.1093/hmg/ddi230. Epub 2005 Jun 29. Hum Mol Genet. 2005. PMID: 15987700

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