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High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression

Leukemia, 2007-06, Vol.21 (6), p.1258-1266

2007

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How Central Is Too Central? Organizing Interorganizational Collaboration Networks for Breakthrough Innovation

The Journal of product innovation management, 2017-07, Vol.34 (4), p.526-542

2017

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A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism

The journal of clinical endocrinology and metabolism, 2016-03, Vol.101 (3), p.847-851

2016

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Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines

Oncogene, 2006-03, Vol.25 (10), p.1571-1583

2006

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Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland

Clinical endocrinology (Oxford), 2017-03, Vol.86 (3), p.410-418

2017

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Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

Leukemia, 2010-01, Vol.24 (1), p.242-246

2010

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Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

Journal of medical genetics, 2008-02, Vol.45 (2), p.81-86

2008

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Ligand-induced conformational changes in prolyl oligopeptidase: a kinetic approach

Protein engineering, design and selection, 2017-03, Vol.30 (3), p.219-226

2017

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Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2009-01, Vol.150B (1), p.140-147

2009

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Wild-type but not mutant huntingtin modulates the transcriptional activity of liver X receptors

Journal of medical genetics, 2009-07, Vol.46 (7), p.438-446

2009

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Constitutional DNA copy number changes in ICSI children

Human reproduction (Oxford), 2009-01, Vol.24 (1), p.233-240

2009

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Recurrent rearrangements in the high mobility group protein gene, HMGI-C , in benign mesenchymal tumours

Nature genetics, 1995-08, Vol.10 (4), p.436-444

1995

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The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly

Journal of medical genetics, 2002-02, Vol.39 (2), p.98-104

2002

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Selective DNA binding by the androgen receptor as a mechanism for hormone-specific gene regulation

Journal of steroid biochemistry and molecular biology, 2001-01, Vol.76 (1), p.23-30

2001

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Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes

Clinical genetics, 2008-12, Vol.74 (6), p.531-538

2008

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High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation

Journal of medical genetics, 2004-06, Vol.41 (6), p.425-432

2004

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Identification of truncated RUNX1 and RUNX1-PRDM16 fusion transcripts in a case of t(1;21)(p36;q22)-positive therapy-related AML

Leukemia, 2006-06, Vol.20 (6), p.1187-1189

2006

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Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas

Cytogenetic and genome research, 2007-01, Vol.118 (2-4), p.157-165

2007

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Allelic knockout of novel splice variants of human recombination repair gene RAD51B in t(12;14) uterine leiomyomas

Cancer research (Chicago, Ill.), 1999, Vol.59 (1), p.19-23

1999

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Identification of NFIB as recurrent translocation partner gene of HMGIC in pleomorphic adenomas

Oncogene, 1998-02, Vol.16 (7), p.865-872

1998

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LPP, the preferred fusion partner gene of HMGIC in lipomas, is a novel member of the LIM protein gene family

Genomics (San Diego, Calif.), 1996-08, Vol.36 (1), p.118-129

1996

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Integrated Profiling of Basal and Luminal Breast Cancers

Cancer research (Chicago, Ill.), 2007-12, Vol.67 (24), p.11565-11575

2007

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Expression of reciprocal hybrid transcripts of HMGIC and FHIT in a pleomorphic adenoma of the parotid gland

Cancer research (Chicago, Ill.), 1997, Vol.57 (1), p.13-17

1997

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ACCREDITATION IN THE EU: A FIRST STEP IN BENCHMARKING GERONTOLOGY PROGRAMS

Innovation in aging, 2017-07, Vol.1 (suppl_1), p.1078-1078

2017

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WHAT I FEEL AND DO WHEN I FEEL LONELY: A QUALITATIVE STUDY ON OLDER ADULTS’ COPING WITH LONELINESS

Innovation in aging, 2017-07, Vol.1 (suppl_1), p.1030-1030

2017

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High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression

How Central Is Too Central? Organizing Interorganizational Collaboration Networks for Breakthrough Innovation

A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism

Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines

Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland

Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

Ligand-induced conformational changes in prolyl oligopeptidase: a kinetic approach

Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion

Wild-type but not mutant huntingtin modulates the transcriptional activity of liver X receptors

Constitutional DNA copy number changes in ICSI children

Recurrent rearrangements in the high mobility group protein gene, HMGI-C , in benign mesenchymal tumours

The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly

Selective DNA binding by the androgen receptor as a mechanism for hormone-specific gene regulation

Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes

High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation

Identification of truncated RUNX1 and RUNX1-PRDM16 fusion transcripts in a case of t(1;21)(p36;q22)-positive therapy-related AML

Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas

Allelic knockout of novel splice variants of human recombination repair gene RAD51B in t(12;14) uterine leiomyomas

Identification of NFIB as recurrent translocation partner gene of HMGIC in pleomorphic adenomas

LPP, the preferred fusion partner gene of HMGIC in lipomas, is a novel member of the LIM protein gene family

Integrated Profiling of Basal and Luminal Breast Cancers

Expression of reciprocal hybrid transcripts of HMGIC and FHIT in a pleomorphic adenoma of the parotid gland

ACCREDITATION IN THE EU: A FIRST STEP IN BENCHMARKING GERONTOLOGY PROGRAMS

WHAT I FEEL AND DO WHEN I FEEL LONELY: A QUALITATIVE STUDY ON OLDER ADULTS’ COPING WITH LONELINESS

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