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StemBond hydrogels control the mechanical microenvironment for pluripotent stem cells

Nature communications, 2021-10, Vol.12 (1), p.6132-6132, Article 6132

2021

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Embryonic stem cells become mechanoresponsive upon exit from ground state of pluripotency

Open biology, 2019-01, Vol.9 (1), p.180203-180203

2019

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Equally probable positive and negative Poisson's ratios in disordered planar systems

Soft matter, 2018, Vol.14 (31), p.6554-656

2018

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High Prevalence of Symptoms of Menière's Disease in three Families With a Mutation in the COCH Gene

Human molecular genetics, 1999-08, Vol.8 (8), p.1425-1429

1999

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Involvement of T-cell receptor-β alterations in the development of otosclerosis linked to OTSC2

Genes and immunity, 2010-04, Vol.11 (3), p.246-253

2010

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Otosclerosis: a genetically heterogeneous disease involving at least three different genes

Bone (New York, N.Y.), 2002-04, Vol.30 (4), p.624-630

2002

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Immunoassay of murine t-PA, u-PA and PAI-1 using monoclonal antibodies raised in gene-inactivated mice

Thrombosis and haemostasis, 1995-11, Vol.74 (5), p.1305-1309

1995

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The cancer survival gap between elderly and middle-aged patients in Europe is widening

European journal of cancer (1990), 2009-04, Vol.45 (6), p.1006-1016

2009

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Measurement of Plasminogen Activator Inhibitor 1 In Biologic Fluids With a Murine Monoclonal Antibody-Based Enzyme-Linked Immunosorbent Assay

Blood, 1988-01, Vol.71 (1), p.220-225

1988

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Multiple tumours in survival estimates

European journal of cancer (1990), 2009-04, Vol.45 (6), p.1080-1094

2009

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Survival for Ovarian Cancer in Europe: The across-country variation did not shrink in the past decade

Acta oncologica, 2012-04, Vol.51 (4), p.441-453

2012

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Enhancement of the otic capsule in active retrofenestral otosclerosis

Otology & neurotology, 2004-07, Vol.25 (4), p.633-634

2004

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Invasive extramammary Paget’s disease and the risk for secondary tumours in Europe

European journal of surgical oncology, 2012-03, Vol.38 (3), p.214-221

2012

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Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH gene

Otology & neurotology, 2001-11, Vol.22 (6), p.874

2001

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A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus

Journal of medical genetics, 1999-07, Vol.36 (7), p.532-536

1999

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Generation of Monoclonal Antibodies against Autologous Proteins in Gene-inactivated Mice

The Journal of biological chemistry, 1995-04, Vol.270 (15), p.8397-8400

1995

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Nonmyocardial Production of ST2 Protein in Human Hypertrophy and Failure Is Related to Diastolic Load

Journal of the American College of Cardiology, 2008-12, Vol.52 (25), p.2166-2174

2008

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Nonsyndromic hearing impairment is associated with a mutation in DFNA5

Nature genetics, 1998-10, Vol.20 (2), p.194-197

1998

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Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Nature genetics, 1998-05, Vol.19 (1), p.60-62

1998

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Hemodynamic Response to Acute Volume Load and Endomyocardial NO-synthase Gene Expression in Heart Transplant Recipients

Transplantation direct, 2022-06, Vol.8 (6), p.e1336-e1336

2022

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Myocardial Gene Expression in Heart Failure Patients Treated With Cardiac Resynchronization Therapy

Journal of the American College of Cardiology, 2008-01, Vol.51 (2), p.129-136

2008

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Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families

Human molecular genetics, 1999-07, Vol.8 (7), p.1321-1328

1999

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Functional outcome after repair of distal biceps tendon ruptures using the endobutton technique

Journal of shoulder and elbow surgery, 2009-03, Vol.18 (2), p.283-287

2009

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Screening Panels of Monoclonal Antibodies Using Phage-Displayed Antigen

Analytical biochemistry, 1997-06, Vol.248 (2), p.211-215

1997

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StemBond hydrogels control the mechanical microenvironment for pluripotent stem cells

Embryonic stem cells become mechanoresponsive upon exit from ground state of pluripotency

Equally probable positive and negative Poisson's ratios in disordered planar systems

High Prevalence of Symptoms of Menière's Disease in three Families With a Mutation in the COCH Gene

Involvement of T-cell receptor-β alterations in the development of otosclerosis linked to OTSC2

Otosclerosis: a genetically heterogeneous disease involving at least three different genes

Immunoassay of murine t-PA, u-PA and PAI-1 using monoclonal antibodies raised in gene-inactivated mice

The cancer survival gap between elderly and middle-aged patients in Europe is widening

Measurement of Plasminogen Activator Inhibitor 1 In Biologic Fluids With a Murine Monoclonal Antibody-Based Enzyme-Linked Immunosorbent Assay

Multiple tumours in survival estimates

Survival for Ovarian Cancer in Europe: The across-country variation did not shrink in the past decade

Enhancement of the otic capsule in active retrofenestral otosclerosis

Invasive extramammary Paget’s disease and the risk for secondary tumours in Europe

Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH gene

A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus

Generation of Monoclonal Antibodies against Autologous Proteins in Gene-inactivated Mice

Nonmyocardial Production of ST2 Protein in Human Hypertrophy and Failure Is Related to Diastolic Load

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Hemodynamic Response to Acute Volume Load and Endomyocardial NO-synthase Gene Expression in Heart Transplant Recipients

Myocardial Gene Expression in Heart Failure Patients Treated With Cardiac Resynchronization Therapy

Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families

Functional outcome after repair of distal biceps tendon ruptures using the endobutton technique

Screening Panels of Monoclonal Antibodies Using Phage-Displayed Antigen

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