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p53-mediated apoptosis of CLL cells: evidence for a transcription-independent mechanism

Blood, 2008-11, Vol.112 (9), p.3827-3834

2008

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Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization

Clinical endocrinology (Oxford), 2001-08, Vol.55 (2), p.163-174

2001

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Frequency of JAK2 Exon 12 Mutations in JAK2 Exon 14 V617F-Negative Patients: High Frequency in ET Patients

Blood, 2007-11, Vol.110 (11), p.2539-2539

2007

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The neuroradiology of Kallmann's syndrome : A genotypic and phenotypic analysis

The journal of clinical endocrinology and metabolism, 1996-08, Vol.81 (8), p.3010-3017

1996

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P53-mediated apoptosis of CLL cells : evidence for a transcription-independent mechanism. Commentary

Blood, 2008, Vol.112 (9)

2008

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High Prevalence of B-Cell Clonality in Patients with Gaucher's Disease

Blood, 2004-11, Vol.104 (11), p.2391-2391

2004

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Conserved Amino Acid Sequences Occur in a Limited Group of CLL Patients with Predominantly Mutated IGH Rearrangements

Blood, 2004-11, Vol.104 (11), p.2000-2000

2004

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MLL-AF4 Positive Adult ALL Patients: VH6 Immunoglobulin Gene Rearrangements Predominate While FLT3 Mutations Are Rare

Blood, 2004-11, Vol.104 (11), p.1089-1089

2004

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KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human development

Molecular and cellular endocrinology, 1995-04, Vol.110 (1), p.73-79

1995

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Idiopathic gonadotrophin deficiency: Genetic questions addressed through phentopic characterization

Clinical endocrinology (Oxford), 2001-08, Vol.55 (2), p.163

2001

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V(H) gene usage differs in germline and mutated B-cell chronic lymphocytic leukemia

Haematologica (Roma), 2003-11, Vol.88 (11), p.1259

2003

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Kallmann's syndrome

Current opinion in obstetrics & gynecology, 1994-06, Vol.6 (3), p.301

1994

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Contrasting Expression ofKALin Cell-Free Systems: 5′ UTR and Coding Region Structural Effects on Translation

Protein expression and purification, 1998-07, Vol.13 (2), p.235-242

1998

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Contrasting expression of KAL in cell-free systems: 5' UTR and coding region structural effects on translation

Protein expression and purification, 1998-07, Vol.13 (2), p.235-242

1998

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Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error

American journal of human genetics, 2013-08, Vol.93 (2), p.264-277

2013

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Prognostic Implications of NOTCH1 and FBXW7 Mutations in Adults With T-Cell Acute Lymphoblastic Leukemia Treated on the MRC UKALLXII/ECOG E2993 Protocol

Journal of clinical oncology, 2009-09, Vol.27 (26), p.4352-4356

2009

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When nature needs a helping hand: Different levels of human intervention for mangrove (re-)establishment

Frontiers in Forests and Global Change, 2022-08, Vol.5

2022

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Minimal residual disease is a significant predictor of treatment failure in non T‐lineage adult acute lymphoblastic leukaemia: final results of the international trial UKALL XII/ECOG2993

British journal of haematology, 2010-01, Vol.148 (1), p.80-89

2010

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Deletion of 6q16-q21 in human lymphoid malignancies: a mapping and deletion analysis

Cancer research (Chicago, Ill.), 2000-06, Vol.60 (11), p.2775-2779

2000

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Unlike Paediatric T-ALL, Notch-1 and FBXW7 Mutations Do Not Seem to Predict a Better Outcome in Adult Patients: Data from the UKALLXII/ECOG2993 Protocol

Blood, 2008-11, Vol.112 (11), p.2548-2548

2008

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Proteinuria, hypertension and chronic renal failure in X-linked Kallmann's syndrome, a defined genetic cause of solitary functioning kidney

Nephrology, dialysis, transplantation, 1998-08, Vol.13 (8), p.1998-2003

1998

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Kallmann Syndrome - Genetics
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Leukemias. Malignant Lymphomas. Malignant Reticulosis. Myelofibrosis
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p53-mediated apoptosis of CLL cells: evidence for a transcription-independent mechanism

Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization

Frequency of JAK2 Exon 12 Mutations in JAK2 Exon 14 V617F-Negative Patients: High Frequency in ET Patients

The neuroradiology of Kallmann's syndrome : A genotypic and phenotypic analysis

P53-mediated apoptosis of CLL cells : evidence for a transcription-independent mechanism. Commentary

High Prevalence of B-Cell Clonality in Patients with Gaucher's Disease

Conserved Amino Acid Sequences Occur in a Limited Group of CLL Patients with Predominantly Mutated IGH Rearrangements

MLL-AF4 Positive Adult ALL Patients: VH6 Immunoglobulin Gene Rearrangements Predominate While FLT3 Mutations Are Rare

KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human development

Idiopathic gonadotrophin deficiency: Genetic questions addressed through phentopic characterization

V(H) gene usage differs in germline and mutated B-cell chronic lymphocytic leukemia

Kallmann's syndrome

Contrasting Expression ofKALin Cell-Free Systems: 5′ UTR and Coding Region Structural Effects on Translation

Contrasting expression of KAL in cell-free systems: 5' UTR and coding region structural effects on translation

Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error

Prognostic Implications of NOTCH1 and FBXW7 Mutations in Adults With T-Cell Acute Lymphoblastic Leukemia Treated on the MRC UKALLXII/ECOG E2993 Protocol

Introducing the Mangrove Microbiome Initiative: Identifying Microbial Research Priorities and Approaches To Better Understand, Protect, and Rehabilitate Mangrove Ecosystems

When nature needs a helping hand: Different levels of human intervention for mangrove (re-)establishment

Minimal residual disease is a significant predictor of treatment failure in non T‐lineage adult acute lymphoblastic leukaemia: final results of the international trial UKALL XII/ECOG2993

Chromosomally unstable mouse tumours have genomic alterations similar to diverse human cancers

Deletion of 6q16-q21 in human lymphoid malignancies: a mapping and deletion analysis

Unlike Paediatric T-ALL, Notch-1 and FBXW7 Mutations Do Not Seem to Predict a Better Outcome in Adult Patients: Data from the UKALLXII/ECOG2993 Protocol

Proteinuria, hypertension and chronic renal failure in X-linked Kallmann's syndrome, a defined genetic cause of solitary functioning kidney

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