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Introducing exceptional growth mining-Analyzing the impact of soil characteristics on on-farm crop growth and yield variability

PloS one, 2024-01, Vol.19 (1), p.e0296684-e0296684

2024

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Unconditioned unrelated donor bone marrow transplantation for IL7Rα- and Artemis-deficient SCID

Bone marrow transplantation (Basingstoke), 2017-07, Vol.52 (7), p.1036-1038

2017

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Hyper-IgE Syndrome with Recurrent Infections — An Autosomal Dominant Multisystem Disorder

The New England journal of medicine, 1999-03, Vol.340 (9), p.692-702

1999

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Human severe combined immunodeficiency: Genetic, phenotypic, and functional diversity in one hundred eight infants

The Journal of pediatrics, 1997-03, Vol.130 (3), p.378-387

1997

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An inherited disorder of lymphocyte apoptosis: the autoimmune lymphoproliferative syndrome

Annals of internal medicine, 1999-04, Vol.130 (7), p.591

1999

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Extreme drought and rainfall had a large impact on potato production in the Netherlands between 2015 and 2020

Communications earth & environment, 2024-09, Vol.5 (1), p.496-9, Article 496

2024

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Pathological Findings in Human Autoimmune Lymphoproliferative Syndrome

The American journal of pathology, 1998-11, Vol.153 (5), p.1541-1550

1998

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Autoimmune Lymphoproliferative Syndrome with Defective Fas: Genotype Influences Penetrance

American journal of human genetics, 1999-04, Vol.64 (4), p.1002-1014

1999

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Treatment of X-Linked Severe Combined Immunodeficiency by in Utero Transplantation of Paternal Bone Marrow

The New England journal of medicine, 1996-12, Vol.335 (24), p.1806-1810

1996

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The clinical spectrum in a large kindred with autoimmune lymphoproliferative syndrome caused by a Fas mutation that impairs lymphocyte apoptosis

The Journal of pediatrics, 1998-11, Vol.133 (5), p.629-633

1998

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Novel intraoral phenotypes in hyperimmunoglobulin-E syndrome

Oral diseases, 2008-01, Vol.14 (1), p.73-81

2008

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Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency

Nature genetics, 1996-07, Vol.13 (3), p.290-295

1996

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Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency

Blood, 1997-03, Vol.89 (6), p.1968-1977

1997

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The interleukin-2 receptor γ chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1

Human molecular genetics, 1993-08, Vol.2 (8), p.1099-1104

1993

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Inherited Human Caspase 10 Mutations Underlie Defective Lymphocyte and Dendritic Cell Apoptosis in Autoimmune Lymphoproliferative Syndrome Type II

Cell, 1999-07, Vol.98 (1), p.47-58

1999

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Retroviral-Mediated Gene Correction for X-Linked Severe Combined Immunodeficiency

Blood, 1996-04, Vol.87 (8), p.3097-3102

1996

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Dominant interfering fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome

Cell, 1995-06, Vol.81 (6), p.935-946

1995

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X Inactivation in Females with X-Linked Disease

The New England journal of medicine, 1998-01, Vol.338 (6), p.325-328

1998

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The Timing of Twinning: More Insights from X Inactivation

American journal of human genetics, 1998-08, Vol.63 (2), p.327-328

Puck, Jennifer M.

1998

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Immunophenotypic profiles in families with autoimmune lymphoproliferative syndrome

Blood, 2001-10, Vol.98 (8), p.2466-2473

2001

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Genetic Linkage of Hyper-IgE Syndrome to Chromosome 4

American journal of human genetics, 1999-09, Vol.65 (3), p.735-744

1999

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Interleukin‐4‐specific signal transduction events are driven by homotypic interactions of the interleukin‐4 receptor alpha subunit

The EMBO journal, 1996-09, Vol.15 (17), p.4506-4514

1996

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Carrier and prenatal diagnosis of X-linked severe combined immunodeficiency : mutation detection methods and utilization

Human genetics, 1997-05, Vol.99 (5), p.628-633

1997

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Introducing exceptional growth mining-Analyzing the impact of soil characteristics on on-farm crop growth and yield variability

Unconditioned unrelated donor bone marrow transplantation for IL7Rα- and Artemis-deficient SCID

Hypomorphic RAG deficiency: impact of disease burden on survival and thymic recovery argues for early diagnosis and HSCT

Hyper-IgE Syndrome with Recurrent Infections — An Autosomal Dominant Multisystem Disorder

Human severe combined immunodeficiency: Genetic, phenotypic, and functional diversity in one hundred eight infants

An inherited disorder of lymphocyte apoptosis: the autoimmune lymphoproliferative syndrome

Extreme drought and rainfall had a large impact on potato production in the Netherlands between 2015 and 2020

Pathological Findings in Human Autoimmune Lymphoproliferative Syndrome

Autoimmune Lymphoproliferative Syndrome with Defective Fas: Genotype Influences Penetrance

Treatment of X-Linked Severe Combined Immunodeficiency by in Utero Transplantation of Paternal Bone Marrow

The clinical spectrum in a large kindred with autoimmune lymphoproliferative syndrome caused by a Fas mutation that impairs lymphocyte apoptosis

Novel intraoral phenotypes in hyperimmunoglobulin-E syndrome

Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency

Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency

The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis

The interleukin-2 receptor γ chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1

Inherited Human Caspase 10 Mutations Underlie Defective Lymphocyte and Dendritic Cell Apoptosis in Autoimmune Lymphoproliferative Syndrome Type II

Retroviral-Mediated Gene Correction for X-Linked Severe Combined Immunodeficiency

Dominant interfering fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome

X Inactivation in Females with X-Linked Disease

The Timing of Twinning: More Insights from X Inactivation

Immunophenotypic profiles in families with autoimmune lymphoproliferative syndrome

Genetic Linkage of Hyper-IgE Syndrome to Chromosome 4

Interleukin‐4‐specific signal transduction events are driven by homotypic interactions of the interleukin‐4 receptor alpha subunit

Carrier and prenatal diagnosis of X-linked severe combined immunodeficiency : mutation detection methods and utilization

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