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Supporting Lgbtqi Communities Impacted By Breast Cancer: Results And Translational Outcomes Of The Out With Cancer Study

Breast (Edinburgh), 2023-04, Vol.68, p.233-234

2023

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Identification of an IL-22-Dependent Gene Signature as a Pharmacodynamic Biomarker

International journal of molecular sciences, 2021-07, Vol.22 (15), p.8205

2021

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Adult drinking in Australian schools

Australian and New Zealand journal of public health, 2014-06, Vol.38 (3), p.205-208

2014

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Ischemic stroke injury is reduced in mice lacking a functional NADPH oxidase

Stroke (1970), 1997-11, Vol.28 (11), p.2252-2258

1997

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X-Linked Chronic Granulomatous Disease: Mutations in the CYBB Gene Encoding the gp91- phox Component of Respiratory-Burst Oxidase

American journal of human genetics, 1998-06, Vol.62 (6), p.1320-1331

1998

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Induction of gp91-phox, a Component of the Phagocyte NADPH Oxidase, in Microglial Cells during Central Nervous System Inflammation

Journal of cerebral blood flow and metabolism, 2001-04, Vol.21 (4), p.374-384

2001

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Efficacy, Safety, and Pharmacodynamic Effects of the Bruton’s Tyrosine Kinase Inhibitor Fenebrutinib (GDC‐0853) in Systemic Lupus Erythematosus: Results of a Phase II, Randomized, Double‐Blind, Placebo‐Controlled Trial

Arthritis & rheumatology (Hoboken, N.J.), 2021-10, Vol.73 (10), p.1835-1846

2021

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Evaluating a teen STD prevention Web site

Journal of adolescent health, 2005-09, Vol.37 (3), p.236-242

2005

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Focus on FOCIS: The continuing diagnostic challenge of autosomal recessive chronic granulomatous disease

Clinical immunology (Orlando, Fla.), 2008-08, Vol.128 (2), p.117-126

2008

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Family-based prevention programmes for alcohol use in young people

Cochrane database of systematic reviews, 2019-03, Vol.3 (3), p.CD012287-CD012287

2019

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Pre-clinical and translational pharmacology of a human interleukin-22 IgG fusion protein for potential treatment of infectious or inflammatory diseases

Biochemical pharmacology, 2018-06, Vol.152, p.224-235

2018

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Hematologically Important Mutations: X-Linked Chronic Granulomatous Disease (Second Update)

Blood cells, molecules, & diseases, 2001, Vol.27 (1), p.16-26

2001

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Disrupted identities, invisibility and precarious support: a mixed methods study of LGBTQI adolescents and young adults with cancer

BMC public health, 2023-09, Vol.23 (1), p.1-1837, Article 1837

2023

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100 Essays I Don’t Have Time to Write: On Umbrellas and Sword Fights, Parades and Dogs, Fire Alarms, Children, and Theater by Sarah Ruhl (review)

Theatre topics, 2015-06, Vol.25 (2), p.179-180

Mollenkamp, Julie Rae

2015

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Hematologically Important Mutations: The Autosomal Recessive Forms of Chronic Granulomatous Disease (First Update)

Blood cells, molecules, & diseases, 2000-10, Vol.26 (5), p.561-565

2000

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Sa1826 Identification of Gene Signatures in Human Intestinal Organoids for Biomarker Analyses

Gastroenterology (New York, N.Y. 1943), 2016-04, Vol.150 (4), p.S374-S374

2016

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High Resolution Mapping of the Binding Site on Human IgG1 for FcγRI, FcγRII, FcγRIII, and FcRn and Design of IgG1 Variants with Improved Binding to the FcγR

The Journal of biological chemistry, 2001-03, Vol.276 (9), p.6591-6604

2001

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A Variant X-linked Chronic Granulomatous Disease Patient (X91+) with Partially Functional Cytochrome b(∗)

The Journal of biological chemistry, 1995-04, Vol.270 (14), p.8194-8200

1995

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Nonclinical safety assessment of a human interleukin‐22FC IG fusion protein demonstrates in vitro to in vivo and cross‐species translatability

Pharmacology research & perspectives, 2018-12, Vol.6 (6), p.e00434-n/a

2018

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BARE

Theatre Journal, 2009-12, Vol.61 (4), p.643-645

MOLLENKAMP, JULIE RAE

2009

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Nonclinical safety assessment of a human interleukin‐22 FC IG fusion protein demonstrates in vitro to in vivo and cross‐species translatability

Pharmacology research & perspectives, 2018-12, Vol.6 (6)

2018

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Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease

The Journal of clinical investigation, 1998-12, Vol.102 (12), p.2146-2155

1998

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Cytochrome b−245 of the Neutrophil Superoxide-generating System Contains Two Nonidentical Hemes

The Journal of biological chemistry, 1995-07, Vol.270 (29), p.17075-17077

1995

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Chronic granulomatous disease caused by a deficiency in p47(phox) mimicking Crohn's disease

Clinical gastroenterology and hepatology, 2004-08, Vol.2 (8), p.690-695

2004

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The LDL receptor-related protein 1 (LRP1) regulates the PDGF signaling pathway by binding the protein phosphatase SHP-2 and modulating SHP-2- mediated PDGF signaling events

Craig, Julie Rae

2013

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Supporting Lgbtqi Communities Impacted By Breast Cancer: Results And Translational Outcomes Of The Out With Cancer Study

Identification of an IL-22-Dependent Gene Signature as a Pharmacodynamic Biomarker

Adult drinking in Australian schools

Ischemic stroke injury is reduced in mice lacking a functional NADPH oxidase

X-Linked Chronic Granulomatous Disease: Mutations in the CYBB Gene Encoding the gp91- phox Component of Respiratory-Burst Oxidase

Induction of gp91-phox, a Component of the Phagocyte NADPH Oxidase, in Microglial Cells during Central Nervous System Inflammation

Efficacy, Safety, and Pharmacodynamic Effects of the Bruton’s Tyrosine Kinase Inhibitor Fenebrutinib (GDC‐0853) in Systemic Lupus Erythematosus: Results of a Phase II, Randomized, Double‐Blind, Placebo‐Controlled Trial

Evaluating a teen STD prevention Web site

Focus on FOCIS: The continuing diagnostic challenge of autosomal recessive chronic granulomatous disease

Family-based prevention programmes for alcohol use in young people

Pre-clinical and translational pharmacology of a human interleukin-22 IgG fusion protein for potential treatment of infectious or inflammatory diseases

Hematologically Important Mutations: X-Linked Chronic Granulomatous Disease (Second Update)

Disrupted identities, invisibility and precarious support: a mixed methods study of LGBTQI adolescents and young adults with cancer

100 Essays I Don’t Have Time to Write: On Umbrellas and Sword Fights, Parades and Dogs, Fire Alarms, Children, and Theater by Sarah Ruhl (review)

Hematologically Important Mutations: The Autosomal Recessive Forms of Chronic Granulomatous Disease (First Update)

Sa1826 Identification of Gene Signatures in Human Intestinal Organoids for Biomarker Analyses

High Resolution Mapping of the Binding Site on Human IgG1 for FcγRI, FcγRII, FcγRIII, and FcRn and Design of IgG1 Variants with Improved Binding to the FcγR

A Variant X-linked Chronic Granulomatous Disease Patient (X91+) with Partially Functional Cytochrome b(∗)

Nonclinical safety assessment of a human interleukin‐22FC IG fusion protein demonstrates in vitro to in vivo and cross‐species translatability

BARE

Nonclinical safety assessment of a human interleukin‐22 FC IG fusion protein demonstrates in vitro to in vivo and cross‐species translatability

Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease

Cytochrome b−245 of the Neutrophil Superoxide-generating System Contains Two Nonidentical Hemes

Chronic granulomatous disease caused by a deficiency in p47(phox) mimicking Crohn's disease

The LDL receptor-related protein 1 (LRP1) regulates the PDGF signaling pathway by binding the protein phosphatase SHP-2 and modulating SHP-2- mediated PDGF signaling events

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