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M Rautenbach

Showing results (21-30 of 30) with videos related to

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South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 15, 1983
Albinism in blacks--aberrant circadian plasma immunoreactive melatonin levelsJ M Oosthuizen, J J Theron, A C Meyer, et al.
Zeitschrift Fur Arztliche Fortbildung|May 15, 1973
[The intrauterine retarded newborn infant. Review and recommendations of the Society for Perinatal Medicine of the DDR. II. Etiology, pathogenesis, prenatal diagnosis, prenatal and postnatal therapy and prognosis]K Beyreibb, W Hoepffner, J Holtorff, et al.
BMC Microbiology|June 15, 2019
Xenorhabdus khoisanae SB10 produces Lys-rich PAX lipopeptides and a Xenocoumacin in its antimicrobial complexJ Dreyer, M Rautenbach, E Booysen, et al.
Molecular Vision|May 10, 2011
Myocilin mutations in black South Africans with POAGBenjamin T Whigham, Susan E I Williams, Yutao Liu, et al.
Molecular Vision|January 5, 2013
The role of lysyl oxidase-like 1 DNA copy number variants in exfoliation glaucomaYutao Liu, Benjamin T Whigham, Joshua Wheeler, et al.
Human Molecular Genetics|April 16, 2019
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndromeDaniel Berner, Ursula Hoja, Matthias Zenkel, et al.
Human Molecular Genetics|August 27, 2015
Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locusMichael A Hauser, Inas F Aboobakar, Yutao Liu, et al.
Nature Genetics|May 29, 2015
Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndromeTin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.
Nature Genetics|February 24, 2015
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndromeTin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.
Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 15, 1983
Albinism in blacks--aberrant circadian plasma immunoreactive melatonin levelsJ M Oosthuizen, J J Theron, A C Meyer, et al.
Zeitschrift Fur Arztliche Fortbildung|May 15, 1973
[The intrauterine retarded newborn infant. Review and recommendations of the Society for Perinatal Medicine of the DDR. II. Etiology, pathogenesis, prenatal diagnosis, prenatal and postnatal therapy and prognosis]K Beyreibb, W Hoepffner, J Holtorff, et al.
BMC Microbiology|June 15, 2019
Xenorhabdus khoisanae SB10 produces Lys-rich PAX lipopeptides and a Xenocoumacin in its antimicrobial complexJ Dreyer, M Rautenbach, E Booysen, et al.
Molecular Vision|May 10, 2011
Myocilin mutations in black South Africans with POAGBenjamin T Whigham, Susan E I Williams, Yutao Liu, et al.
Molecular Vision|January 5, 2013
The role of lysyl oxidase-like 1 DNA copy number variants in exfoliation glaucomaYutao Liu, Benjamin T Whigham, Joshua Wheeler, et al.
Human Molecular Genetics|April 16, 2019
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndromeDaniel Berner, Ursula Hoja, Matthias Zenkel, et al.
Human Molecular Genetics|August 27, 2015
Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locusMichael A Hauser, Inas F Aboobakar, Yutao Liu, et al.
Nature Genetics|May 29, 2015
Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndromeTin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.
Nature Genetics|February 24, 2015
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndromeTin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.
Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.
Pageof 3