Perkins B B - OmicsDI

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4x(2)H labeled dimethylated residue (1)

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Lab affiliation

Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, Barcelona 08003, Spain (5)
Charles Perkins Centre, School of Medical Sciences, University of Sydney, Sydney, Australia. (4)
Harry Perkins Institute of Medical Research and ARC Centre of Excellence in Synthetic Biology, QEII Medical Centre, Nedlands, Western Australia 6009, Australia (3)
Leader of the Molecular and Systems Oncology Team in the Division of Molecular Pathology at The Institute of Cancer Research, London, UK (3)
Charles Perkins Centre, The University of Sydney (2)
Charles Perkins Centre, University of Sydney (2)
Director, Centre for Proteome Research Department of Biochemistry & Systems Biology Institute of Systems, Molecular & Integrative Biology University of Liverpool Crown Street, Liverpool L69 7ZB +44 151 795 4424 (2)
School of Life and Environmental Sciences, Charles Perkins Centre, Faculty of Science, The University of Sydney, NSW, Australia. (2)
Waters Corporation (2)
-Harry Perkins Institute of Medical Research, Nedlands, Western Australia 6009, Australia -School of Pharmacy and Biomedical Sciences, Curtin University, Bentley, Western Australia 6102, Australia -Curtin Health Innovation Research Institute, Curtin University, Bentley, WA 6102, Australia (1)
-Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands, Western Australia 6009, Australia -Centre for Medical Research, The University of Western Australia, QEII Medical Centre, Nedlands, Western Australia 6009, Australia -School of Molecular Sciences, The University of Western Australia, Crawley, Western Australia 6009, Australia (1)
ARC Centre of Excellence in Plant Energy Biology, School of Molecular Sciences, The University of Western Australia, Australia and Harry Perkins Institute of Medical Research, Perth, Western Australia, Australia (1)
Aarhus University (1)
CRG, UPF (1)
CRG/UPF Proteomics Unit, Center for Genomics Regulation, Universitat Pompeu Fabra, 08003 Barcelona, Spain. (1)
Canada Research Chair in Proteomics and Systems Biology, Faculty of Dentistry, Department of Oral Biological and Medical Sciences, University of British Columbia (1)
Center for Genomic Regulation (1)
Center for Genomic Regulation, 08003 Barcelona, Spain (1)
Centre for Genomic Regulation (CRG), the Barcelona Institute of Science and Technology, Carrer Dr. Aiguader 88, Barcelona 08003, Spain. (1)
Centre for Heamato-Oncology / Barts Cancer Institute (1)
Centre for Proteome Research Institute of Integrative Biology University of Liverpool Biosciences Building Crown Street Liverpool L69 7ZB UK (1)
Centre for Proteome Research University of Liverpool Liverpool L69 7ZB (1)
Centre of Molecular and Environmental Biology (CBMA), Department of Biology, University of Minho, Braga, Portugal (1)
Charles Perkins Centre and School of Medical Sciences, University of Sydney, Australia (1)
Charles Perkins Centre and School of Medical Sciences, University of Sydney, Sydney, Australia. (1)
Charles Perkins Centre, School of Life and Environmental Sciences, The University of Sydney, Sydney, NSW, 2006, Australia. (1)
Charles Perkins Centre, School of Life and Environmental Sciences, University of Sydney, Sydney, Australia. (1)
Charles Perkins Centre, School of Medical Sciences, The University of Sydney, Sydney, NSW, Australia. (1)
Charles Perkins Centre, University of Sydney, Camperdown, NSW, Australia (1)
Department of Chemistry and Biomolecular Sciences, Macquarie University, Australia (1)

Tags

xref:PubMed:28725461 (2)
xref:PubMed:23115635 (1)
xref:PubMed:26912320 (1)
xref:PubMed:27203220 (1)
xref:PubMed:32487174 (1)

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Transcription profiling of mouse AM-14 B cells stimulated through the B cell receptor (BCR) and/or Toll-like receptors (TLR)

We have previously shown that rheumatoid factors (RF) produced by Fas-deficient autoimmune-prone mice typically bind autologous IgG2a with remarkably low affinity. Nevertheless, B cells representative of this RF population proliferate vigorously in response IgG2a/chromatin immune complexes through a...

ORGANISM(S): Mus musculus

2008-06-15 | E-GEOD-6674 | biostudies-arrayexpress

ONGOING CHROMOSOMAL INSTABILITY ACROSS ANEUPLOID SUBTYPES OF CHILDHOOD B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA ASSOCIATES WITH DISEASE PROGRESSION

Chromosomal instability (CIN), defined as an increased occurrence of chromosome segregation errors during cell division, is a prominent form of genomic instability (Bakhoum and Avi Landau, 2017). It is the major cause of aneuploidy, an imbalanced complement of whole chromosomes or chromosome arms, w...

ORGANISM(S): Homo sapiens (Human)

2023-09-15 | PXD042785 | Pride

The complete chloroplast genome sequence of Styrax duclouxii Perkins (Styracaceae).

Not available

S-EPMC7748768 | biostudies-literature

Dietary carbohydrate, particularly glucose, drives B cell lymphopoiesis and function.

Not available

S-EPMC8333167 | biostudies-literature

Positive and negative regulation of lymphomagenesis by the NF-kappaB subunit c-Rel

'The REL gene, encoding the NF-κB subunit c-Rel, is frequently amplified in B-cell lymphoma and functions as a tumour promoting transcription factor. Here we report the surprising result that c-rel -/- mice display significantly earlier lymphomagenesis in the c-Myc driven, Eμ-Myc model of B-cell lym...

ORGANISM(S): Mus musculus

2014-12-31 | E-MTAB-2774 | biostudies-arrayexpress

Circulating clonotypic B cells in classic Hodgkin lymphoma.

Not available

S-EPMC2700327 | biostudies-literature

New therapeutic opportunities from dissecting the pre-B leukemia bone marrow microenvironment.

Not available

S-EPMC6224400 | biostudies-literature

Cercopidae spittle-bugs (Hemiptera, Cicadomorpha) of Madagascar: a new species of Bourgoinrana and revision of the Locris species.

Not available

S-EPMC7969582 | biostudies-literature

Transcription profiling of human T-cell acute lymphoblastic leukemia, T-cell lymphoblastic lymphoma and B-precursor acute lymphoblastic leukemia samples

T-cell acute lymphoblastic leukemia (T-ALL) and T-cell lymphoblastic lymphoma (T-LL) and are often thought to represent a spectrum of a single disease. The malignant cells in T-ALL and T-LL are morphologically indistinguishable, and they share the expression of common cell surface antigens and cyto...

ORGANISM(S): Homo sapiens

2007-08-13 | E-GEOD-1577 | biostudies-arrayexpress

The NF-κB subunit c-Rel regulates Bach2 tumour suppressor expression in B-cell lymphoma.

Not available

S-EPMC4853301 | biostudies-literature

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