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Prevalence and patterns of cognitive impairment in sporadic ALS

Neurology, 2005-08, Vol.65 (4), p.586

2005

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Aging effects and population splitting in single-particle trajectory averages

Physical review letters, 2013-01, Vol.110 (2), p.020602-020602, Article 020602

2013

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Impairment of human terminal erythroid differentiation by histone deacetylase 5 deficiency

Blood, 2021-10, Vol.138 (17), p.1615-1627

2021

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Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis

Blood, 2017-10, Vol.130 (16), p.1845-1856

2017

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Localized multiphoton emission of femtosecond electron pulses from metal nanotips

Physical review letters, 2007-01, Vol.98 (4), p.043907-043907, Article 043907

2007

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BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly

Proceedings of the National Academy of Sciences - PNAS, 2010-01, Vol.107 (4), p.1488-1493

2010

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Distinct roles for TET family proteins in regulating human erythropoiesis

Blood, 2017-04, Vol.129 (14), p.2002-2012

2017

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Human Extrafollicular CD4 + Th Cells Help Memory B Cells Produce Igs

The Journal of immunology (1950), 2018-09, Vol.201 (5), p.1359-1372

2018

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Altered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitment

Proceedings of the National Academy of Sciences - PNAS, 2012-05, Vol.109 (19), p.7362-7367

2012

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Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiation

Nucleic acids research, 2016-09, Vol.44 (15), p.7173

2016

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Neuronal mechanism for acute mechanosensitivity in tactile-foraging waterfowl

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (41), p.14941-14946

2014

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Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus

Haematologica (Roma), 2014-09, Vol.99 (9), p.e168

2014

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Identification of Biologically Relevant Enhancers in Human Erythroid Cells

The Journal of biological chemistry, 2013-03, Vol.288 (12), p.8433-8444

2013

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Sequencing-independent delocalization in a DNA-like double chain with base pairing

Physical review letters, 2005-09, Vol.95 (12), p.126601.1-126601.4, Article 126601

2005

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Global transcriptome analyses of human and murine terminal erythroid differentiation

Blood, 2014-05, Vol.123 (22), p.3466-3477

2014

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MKL1 and MKL2 play redundant and crucial roles in megakaryocyte maturation and platelet formation

Blood, 2012-09, Vol.120 (11), p.2317-2329

2012

Volltextzugriff (PDF)

Saccharomyces Rrm3p, a 5' to 3' DNA helicase that promotes replication fork progression through telomeric and subtelomeric DNA

Genes & development, 2002-06, Vol.16 (11), p.1383-1396

2002

Volltextzugriff (PDF)

EBNA1 Regulates Cellular Gene Expression by Binding Cellular Promoters

Proceedings of the National Academy of Sciences - PNAS, 2009-12, Vol.106 (52), p.22421-22426

2009

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Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis

Blood, 2015-09, Vol.126 (11), p.1281-1284

2015

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Pif1p Helicase, a Catalytic Inhibitor of Telomerase in Yeast

Science (American Association for the Advancement of Science), 2000-08, Vol.289 (5480), p.771-774

2000

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Isomerisation of 1,4-dichlorobenzene using highly acidic alkali chloroaluminate melts

Chemical communications (Cambridge, England), 2014-10, Vol.50 (79), p.11705-11708

2014

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Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis

Blood, 2012-08, Vol.120 (9), p.1908-1915

2012

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Functional genomic screen of human stem cell differentiation reveals pathways involved in neurodevelopment and neurodegeneration

Proceedings of the National Academy of Sciences - PNAS, 2013-07, Vol.110 (30), p.12361-12366

2013

Volltextzugriff (PDF)

Response Inhibition in Adolescents Diagnosed With Attention Deficit Hyperactivity Disorder During Childhood: An Event-Related fMRI Study

The American journal of psychiatry, 2004-09, Vol.161 (9), p.1650-1657

2004

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Patterns of Histone H3 Lysine 27 Monomethylation and Erythroid Cell Type-specific Gene Expression

The Journal of biological chemistry, 2011-11, Vol.286 (45), p.39457-39465

2011

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Prevalence and patterns of cognitive impairment in sporadic ALS

Aging effects and population splitting in single-particle trajectory averages

Impairment of human terminal erythroid differentiation by histone deacetylase 5 deficiency

Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis

Localized multiphoton emission of femtosecond electron pulses from metal nanotips

BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly

Distinct roles for TET family proteins in regulating human erythropoiesis

Human Extrafollicular CD4 + Th Cells Help Memory B Cells Produce Igs

Altered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitment

Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiation

Neuronal mechanism for acute mechanosensitivity in tactile-foraging waterfowl

Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus

Identification of Biologically Relevant Enhancers in Human Erythroid Cells

Sequencing-independent delocalization in a DNA-like double chain with base pairing

Global transcriptome analyses of human and murine terminal erythroid differentiation

MKL1 and MKL2 play redundant and crucial roles in megakaryocyte maturation and platelet formation

Saccharomyces Rrm3p, a 5' to 3' DNA helicase that promotes replication fork progression through telomeric and subtelomeric DNA

EBNA1 Regulates Cellular Gene Expression by Binding Cellular Promoters

Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis

Pif1p Helicase, a Catalytic Inhibitor of Telomerase in Yeast

Isomerisation of 1,4-dichlorobenzene using highly acidic alkali chloroaluminate melts

Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis

Functional genomic screen of human stem cell differentiation reveals pathways involved in neurodevelopment and neurodegeneration

Response Inhibition in Adolescents Diagnosed With Attention Deficit Hyperactivity Disorder During Childhood: An Event-Related fMRI Study

Patterns of Histone H3 Lysine 27 Monomethylation and Erythroid Cell Type-specific Gene Expression

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