UB Paderborn / Katalog / Suche / in CDI

Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy

American journal of human genetics, 2012-02, Vol.90 (2), p.356-362

2012

Volltextzugriff (PDF)

FLT4/VEGFR3 and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update

Human mutation, 2013-01, Vol.34 (1), p.23-31

2013

Volltextzugriff (PDF)

Chemotherapy regimens induce inhibitory immune checkpoint protein expression on stem-like and senescent-like oesophageal adenocarcinoma cells

Translational oncology, 2021-06, Vol.14 (6), p.101062-101062, Article 101062

2021

Volltextzugriff (PDF)

PD-1 blockade attenuates surgery-mediated immunosuppression and boosts Th1 immunity perioperatively in oesophagogastric junctional adenocarcinoma

Frontiers in immunology, 2023-06, Vol.14, p.1150754-1150754

2023

Volltextzugriff (PDF)

Cooperation between chemotherapy and immune checkpoint blockade to enhance anti-tumour T cell immunity in oesophageal adenocarcinoma

Translational oncology, 2022-06, Vol.20, p.101406, Article 101406

2022

Volltextzugriff (PDF)

Clinical and molecular consequences of disease-associated de novo mutations in SATB2

Genetics in medicine, 2017-08, Vol.19 (8), p.900-908

2017

Volltextzugriff (PDF)

PD-1 and TIGIT blockade differentially affect tumour cell survival under hypoxia and glucose deprived conditions in oesophageal adenocarcinoma; implications for overcoming resistance to PD-1 blockade in hypoxic tumours

Translational oncology, 2022-05, Vol.19, p.101381-101381, Article 101381

2022

Volltextzugriff (PDF)

Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations

European journal of human genetics : EJHG, 2014-07, Vol.22 (7), p.881-887

2014

Volltextzugriff (PDF)

Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype

Journal of medical genetics, 2011-04, Vol.48 (4), p.251-255

2011

Volltextzugriff (PDF)

FLOT and CROSS chemotherapy regimens alter the frequency of CD27+ and CD69+ T cells in oesophagogastric adenocarcinomas: implications for combination with immunotherapy

Journal of cancer research and clinical oncology, 2023-07, Vol.149 (7), p.3753-3774

2023

Volltextzugriff (PDF)

776 A role for immune checkpoint blockade to enhance T cell-mediated responses in combination with chemotherapy in oesophageal adenocarcinoma

Journal for immunotherapy of cancer, 2020-11, Vol.8 (Suppl 3), p.A465-A467

2020

Volltextzugriff (PDF)

FLT 4 / VEGFR 3 and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update

Human mutation, 2013-01, Vol.34 (1), p.23-31

2013

Volltextzugriff (PDF)

Phenotypic Characterization of Primary Lymphedema

Annals of the New York Academy of Sciences, 2008-05, Vol.1131 (1), p.140-146

2008

Volltextzugriff (PDF)

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Nature communications, 2018-11, Vol.9 (1), p.4619-12, Article 4619

2018

Volltextzugriff (PDF)

Identification of Ligand-binding Site III on the Immunoglobulin-like Domain of the Granulocyte Colony-stimulating Factor Receptor

The Journal of biological chemistry, 2001-09, Vol.276 (39), p.36779-36787

2001

Volltextzugriff (PDF)

Visceral adipose tissue secretome from early and late-stage oesophageal cancer patients differentially affects effector and regulatory T cells

Journal of cancer research and clinical oncology, 2023-08, Vol.149 (9), p.6583-6599

2023

Volltextzugriff (PDF)

Clinical and molecular consequences of disease-associated de novo mutations in SATB2

Genetics in medicine, 2017-08, Vol.19 (8), p.900-908

2017

Volltextzugriff (PDF)

Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia

Human genetics, 2010-02, Vol.127 (2), p.231-241

2010

Volltextzugriff (PDF)

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Nature communications, 2019-05, Vol.10 (1), p.2079-2079, Article 2079

2019

Volltextzugriff (PDF)

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Nature communications, 2019-02, Vol.10 (1), p.883-4, Article 883

2019

Volltextzugriff (PDF)

Our evolving understanding of 22q.11 deletion syndrome

Developmental medicine and child neurology, 2005-12, Vol.47 (12), p.796-796

2005

Volltextzugriff (PDF)

Re: "conjunctival edema and distichiasis in association with congenital lymphedema of the lower legs"

Ophthalmic plastic and reconstructive surgery, 2010-05, Vol.26 (3), p.222

2010

Volltextzugriff (PDF)

Rapid identification of mutations in GJC2 in four limb primary lymphoedema using whole exome sequencing combined with linkage analysis

Journal of medical genetics, 2011-01, Vol.48 (4)

2011

Volltextzugriff (PDF)

Erratum to: Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia

Human genetics, 2010-02, Vol.127 (2), p.243-243

2010

Volltextzugriff (PDF)

Birmingham's condom distribution scheme--an opportunity to promote sexual health in a primary setting

British journal of general practice, 2001-02, Vol.51 (463), p.142-142

2001

Volltextzugriff (PDF)

Menü

Weitere Dienste

Einstellungen

Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy

FLT4/VEGFR3 and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update

Chemotherapy regimens induce inhibitory immune checkpoint protein expression on stem-like and senescent-like oesophageal adenocarcinoma cells

PD-1 blockade attenuates surgery-mediated immunosuppression and boosts Th1 immunity perioperatively in oesophagogastric junctional adenocarcinoma

Cooperation between chemotherapy and immune checkpoint blockade to enhance anti-tumour T cell immunity in oesophageal adenocarcinoma

Clinical and molecular consequences of disease-associated de novo mutations in SATB2

PD-1 and TIGIT blockade differentially affect tumour cell survival under hypoxia and glucose deprived conditions in oesophageal adenocarcinoma; implications for overcoming resistance to PD-1 blockade in hypoxic tumours

Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations

Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype

FLOT and CROSS chemotherapy regimens alter the frequency of CD27+ and CD69+ T cells in oesophagogastric adenocarcinomas: implications for combination with immunotherapy

776 A role for immune checkpoint blockade to enhance T cell-mediated responses in combination with chemotherapy in oesophageal adenocarcinoma

FLT 4 / VEGFR 3 and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update

Phenotypic Characterization of Primary Lymphedema

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Identification of Ligand-binding Site III on the Immunoglobulin-like Domain of the Granulocyte Colony-stimulating Factor Receptor

Visceral adipose tissue secretome from early and late-stage oesophageal cancer patients differentially affects effector and regulatory T cells

Clinical and molecular consequences of disease-associated de novo mutations in SATB2

Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Our evolving understanding of 22q.11 deletion syndrome

Re: "conjunctival edema and distichiasis in association with congenital lymphedema of the lower legs"

Rapid identification of mutations in GJC2 in four limb primary lymphoedema using whole exome sequencing combined with linkage analysis

Erratum to: Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia

Birmingham's condom distribution scheme--an opportunity to promote sexual health in a primary setting

Aktive Filter

Suchergebnisse filtern