Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene.

Appenzeller S, Schirmacher A, Halfter H, Bäumer S, Pendziwiat M, Timmerman V, De Jonghe P, Fekete K, Stögbauer F, Lüdemann P, Hund M, Quabius ES, Ringelstein EB, Kuhlenbäumer G (2010)
In: American Journal of Human Genetics, 86(1)
Type of Publication: Research article (journal)

Bex1 is involved in the regeneration of axons after injury.

Khazaei MR, Halfter H, Karimzadeh F, Koo JH, Margolis FL, Young P (2010)
In: Journal of Neurochemistry, 115(4)
Type of Publication: Research article (journal)

EXPRESSION AND ACTIVITY OF THE SODIUM-DEPENDENT VITAMIN C TRANSPORTER 2 (SVCT2) IS NECESSARY FOR ASCORBIC ACID UPTAKE INTO SCHWANN CELLS

Gess B, Halfter H, Young P (2009)
In: Journal of the Peripheral Nervous System, 14 Suppl.
Type of Publication: Research article (journal)

Inhibition of N-cadherin and beta-catenin function reduces axon-induced Schwann cell proliferation.

Gess B, Halfter H, Kleffner I, Monje P, Athauda G, Wood PM, Young P, Wanner IB (2008)
In: Journal of Neuroscience Research, 86(4)
Type of Publication: Research article (journal)

Mutations in SEPT9 cause hereditary neuralgic amyotrophy.

Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF (2005)
In: Nature Genetics, 37(10)
Type of Publication: Research article (journal)

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Altered dynamics in the circadian oscillation of clock genes in dermal fibroblasts of patients suffering from idiopathic hypersomnia Lippert JP, Halfter H, Heidbreder A, Roehr D, Gess B, Osada N, Young P (2012) In: Journal of Sleep Research, 21 1 Type of Publication: Research article (journal)
Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene. Appenzeller S, Schirmacher A, Halfter H, Bäumer S, Pendziwiat M, Timmerman V, De Jonghe P, Fekete K, Stögbauer F, Lüdemann P, Hund M, Quabius ES, Ringelstein EB, Kuhlenbäumer G (2010) In: American Journal of Human Genetics, 86(1) Type of Publication: Research article (journal)
Sodium-dependent vitamin C transporter 2 (SVCT2) is necessary for the uptake of L-ascorbic acid into Schwann cells. Gess B, Lohmann C, Halfter H, Young P (2010) In: Glia, 58(3) Type of Publication: Research article (journal)
Bex1 is involved in the regeneration of axons after injury. Khazaei MR, Halfter H, Karimzadeh F, Koo JH, Margolis FL, Young P (2010) In: Journal of Neurochemistry, 115(4) Type of Publication: Research article (journal)
Varying survival of motoneurons and activation of distinct molecular mechanism in response to altered peripheral myelin protein 22 gene dosage. Nattkämper H, Halfter H, Khazaei MR, Lohmann T, Gess B, Eisenacher M, Willscher E, Young P (2009) In: Journal of Neurochemistry, 110(3) Type of Publication: Research article (journal)
EXPRESSION AND ACTIVITY OF THE SODIUM-DEPENDENT VITAMIN C TRANSPORTER 2 (SVCT2) IS NECESSARY FOR ASCORBIC ACID UPTAKE INTO SCHWANN CELLS Gess B, Halfter H, Young P (2009) In: Journal of the Peripheral Nervous System, 14 Suppl. Type of Publication: Research article (journal)
THE MOLECULAR FUNCTION OF BEX-1 IN THE REGENERATION OF DEMYELINATED NEURONS IN THE PNS Khazaei MR, Halfter H, Young P (2009) In: Journal of the Peripheral Nervous System, 14 Suppl. Type of Publication: Research article (journal)
Inhibition of N-cadherin and beta-catenin function reduces axon-induced Schwann cell proliferation. Gess B, Halfter H, Kleffner I, Monje P, Athauda G, Wood PM, Young P, Wanner IB (2008) In: Journal of Neuroscience Research, 86(4) Type of Publication: Research article (journal)
Alterations of lymphoid enhancer factor-1 isoform expression in solid tumors and acute leukemias. Wang W, Ji P, Steffen B, Metzger R, Schneider PM, Halfter H, Schrader M, Berdel WE, Serve H, Müller-Tidow C (2005) In: Acta Biochimica et Biophysica Sinica, 37(3) Type of Publication: Research article (journal)
Mutations in SEPT9 cause hereditary neuralgic amyotrophy. Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF (2005) In: Nature Genetics, 37(10) Type of Publication: Research article (journal)