K. Knapp

发表

SHP-1 inhibits LPS-mediated TNF and iNOS production in murine macrophages.

B. K. English, T. Yi, E. Meals, 2006, Biochemical and biophysical research communications.

Crystal structure of the human ecto-5'-nucleotidase (CD73): insights into the regulation of purinergic signaling.

C. Müller, N. Sträter, J. Pippel, 2012, Structure.

Crystallization and preliminary X-ray analysis of the open form of human ecto-5'-nucleotidase (CD73).

N. Sträter, M. Zebisch, K. Knapp, 2012, Acta crystallographica. Section F, Structural biology and crystallization communications.

Ceramide‐mediated stimulation of inducible nitric oxide synthase (iNOS) and tumor necrosis factor (TNF) accumulation in murine macrophages requires tyrosine kinase activity

B. K. English, K. Knapp, K. Knapp, 2000, Journal of leukocyte biology.

Biallelic variants in SLC35C1 as a cause of isolated short stature with intellectual disability

L. Bicknell, D. Lefeber, Fokje S M Zijlstra, 2020, Journal of Human Genetics.

Predictors of Viremia in Postpartum Women on Antiretroviral Therapy

J. Currier, K. R. Amico, E. Joao, 2019, Journal of acquired immune deficiency syndromes.

Role of vav1 in the Lipopolysaccharide-Mediated Upregulation of Inducible Nitric Oxide Synthase Production and Nuclear Factor for Interleukin-6 Expression Activity in Murine Macrophages

E. Meals, S. A. Godambe, K. Knapp, 2004, Clinical Diagnostic Laboratory Immunology.

Pathogenic variants causing ABL1 malformation syndrome cluster in a myristoyl-binding pocket and increase tyrosine kinase activity

S. Robertson, D. Baralle, R. Heller, 2020, European Journal of Human Genetics.

Expanding the phenotypic spectrum associated with DPF2: A new case report

L. Bicknell, G. Poke, D. Jenkins, 2019, American journal of medical genetics. Part A.

Histones: coming of age in Mendelian genetic disorders

L. Bicknell, G. van Haaften, K. Knapp, 2023, Journal of Medical Genetics.

A synonymous variant in a non-canonical exon of CDC45 disrupts splicing in two affected sibs with Meier-Gorlin syndrome with craniosynostosis.

A. Dalal, L. Bicknell, S. Aggarwal, 2021, European journal of medical genetics.

Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome

R. Pfundt, D. Baralle, I. Thiffault, 2022, American journal of human genetics.

Structures of Orf Virus Chemokine Binding Protein in Complex with Host Chemokines Reveal Clues to Broad Binding Specificity.

R. Couñago, L. Wise, A. Mercer, 2015, Structure.

MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency

E. Bongers, N. Pachter, J. Denecke, 2021, European Journal of Human Genetics.

Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome

C. Ferreira, A. Gezdirici, P. Arn, 2019, Journal of Medical Genetics.

Schizosaccharomyces pombe MutSα and MutLα Maintain Stability of Tetra-Nucleotide Repeats and Msh3 of Hepta-Nucleotide Repeats

O. Christensen, O. Fleck, D. Villahermosa, 2017, G3: Genes, Genomes, Genetics.

A mutated dph3 gene causes sensitivity of Schizosaccharomyces pombe cells to cytotoxic agents

O. Fleck, D. Villahermosa, K. Knapp, 2017, Current Genetics.

Successful pregnancies in an adult with Meier‐Gorlin syndrome harboring biallelic CDT1 variants

I. Temple, J. Murray, L. Bicknell, 2020, American journal of medical genetics. Part A.

Title 1 Pathogenic variants causing ABL 1 malformation syndrome cluster in a myristoyl-2 binding pocket and increase tyrosine kinase activity 3 4 Running title 5 ABL 1 pathogenic variants 6

S. Robertson, D. Baralle, R. Heller, 2020 .