CXCR4 nanobodies (VHH-based single variable domains) potently inhibit chemotaxis and HIV-1 replication and mobilize stem cells (Q34377450)

1 August 2017

title

CXCR4 nanobodies (VHH-based single variable domains) potently inhibit chemotaxis and HIV-1 replication and mobilize stem cells (English)

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1 August 2017

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Dominique Schols

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Sven Jähnichen

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1 August 2017

Christophe Blanchetot

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1 August 2017

David Maussang

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1 August 2017

Maria Gonzalez-Pajuelo

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1 August 2017

Ken Y Chow

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1 August 2017

Leontien Bosch

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1 August 2017

Sindi De Vrieze

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1 August 2017

Benedikte Serruys

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1 August 2017

Hans Ulrichts

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1 August 2017

Wesly Vandevelde

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1 August 2017

Michael Saunders

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1 August 2017

Hans J De Haard

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1 August 2017

Rob Leurs

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1 August 2017

Peter Vanlandschoot

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1 August 2017

Theo Verrips

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1 August 2017

Martine J Smit

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1 August 2017

language of work or name

English

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publication date

8 November 2010

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Proceedings of the National Academy of Sciences of the United States of America

1 August 2017

published in

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1 August 2017

volume

107

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1 August 2017

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1 August 2017

page(s)

20565-20570

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The development of nanobodies for therapeutic applications.

1 August 2017

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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Phase III prospective randomized double-blind placebo-controlled trial of plerixafor plus granulocyte colony-stimulating factor compared with placebo plus granulocyte colony-stimulating factor for autologous stem-cell mobilization and transplantatio

21 January 2018

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Plerixafor and G-CSF versus placebo and G-CSF to mobilize hematopoietic stem cells for autologous stem cell transplantation in patients with multiple myeloma

21 January 2018

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21 January 2018

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21 January 2018

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Formatted anti-tumor necrosis factor alpha VHH proteins derived from camelids show superior potency and targeting to inflamed joints in a murine model of collagen-induced arthritis

21 January 2018

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A point mutation that confers constitutive activity to CXCR4 reveals that T140 is an inverse agonist and that AMD3100 and ALX40-4C are weak partial agonists

21 January 2018

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Identifiers

DOI

10.1073/PNAS.1012865107

1 reference

1 August 2017

0 references

1 reference

1 August 2017

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