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51

Heterochromatic deposition of centromeric histone H3-like proteins

Henikoff, S., Ahmad, K., Platero, J. S., van Steensel, B.

Journal:

Proceedings of the National Academy of Sciences

Year:

2000

Language:

english

File:

PDF, 690 KB

english, 2000

52

Implementation of an automatic 3D vision monitor for dairy cow locomotion in a commercial farm

Van Hertem, Tom, Schlageter Tello, Andrés, Viazzi, Stefano, Steensels, Machteld, Bahr, Claudia, Romanini, Carlos Eduardo Bites, Lokhorst, Kees, Maltz, Ephraim, Halachmi, Ilan, Berckmans, Daniel

Journal:

Biosystems Engineering

Year:

2017

Language:

english

File:

PDF, 1.31 MB

english, 2017

53

Easy quantification of template-directed CRISPR/Cas9 editing

Brinkman, Eva K, Kousholt, Arne N, Harmsen, Tim, Leemans, Christ, Chen, Tao, Jonkers, Jos, van Steensel, Bas

Journal:

Nucleic Acids Research

Year:

2018

Language:

english

File:

PDF, 687 KB

english, 2018

54

Risk factors for parental psychopathology: a study in families with children or adolescents with psychopathology

Wesseldijk, L. W., Dieleman, G. C., van Steensel, F. J. A., Bartels, M., Hudziak, J. J., Lindauer, R. J. L., Bögels, S. M., Middeldorp, C. M.

Journal:

European Child & Adolescent Psychiatry

Year:

2018

Language:

english

File:

PDF, 2.13 MB

english, 2018

55

Cost-effectiveness of Family Group Conferencing in child welfare: a controlled study

Dijkstra, Sharon, Creemers, Hanneke E., van Steensel, Francisca J. A., Deković, Maja, Stams, Geert Jan J. M., Asscher, Jessica J.

Journal:

BMC Public Health

Year:

2018

Language:

english

File:

PDF, 1.54 MB

english, 2018

56

Management of sepsis in out-of-hours primary care: a retrospective study of patients admitted to the intensive care unit

Loots, Feike J, Smits, Marleen, van Steensel, Carlijn, Giesen, Paul, Hopstaken, Rogier M, van Zanten, Arthur R H

Journal:

Year:

2018

Language:

english

File:

PDF, 359 KB

english, 2018

57

Framework nucleic acids as programmable carrier for transdermal drug delivery

Wiraja, Christian, Zhu, Ying, Lio, Daniel Chin Shiuan, Yeo, David C., Xie, Mo, Fang, Weina, Li, Qian, Zheng, Mengjia, Van Steensel, Maurice, Wang, Lihua, Fan, Chunhai, Xu, Chenjie

Journal:

Nature Communications

Year:

2019

Language:

english

File:

PDF, 6.21 MB

english, 2019

58

Laparotomy closure techniques: Do surgeons follow the latest guidelines? Results of a questionnaire

Bloemen, A., De Kleijn, R.J.C.M.F., Van Steensel, S., Aarts, F., Schreinemacher, M.H.F., Bouvy, N.D.

Journal:

International Journal of Surgery

Year:

2019

Language:

english

File:

PDF, 418 KB

english, 2019

59

Oto-spondylo-megaepiphyseal dysplasia (OSMED): Clinical description of three patients homozygous for a missense mutation in the COL11A2 gene

van Steensel, M. A. M., Buma, P., de Waal Malefijt, M. C., van den Hoogen, F. H. J., Brunner, H. G.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 3.44 MB

english, 1997

60

Hypomelanosis of Ito: A symptom, not a syndrome

van Steensel, M.A.M., Steijlen, P.M.

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 30 KB

english, 1998

61

Paradominant inheritance, a hypothesis explaining occasional familial occurrence of sporadic syndromes

Steijlen, Peter M., van Steensel, Maurice A.M.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 60 KB

english, 1999

62

PML-containing nuclear bodies: Their spatial distribution in relation to other nuclear components

Marjolein A. Grande, Ineke van der Kraan, Bas van Steensel, Wouter Schul, Hugues de Thé, Hans T.M. van der Voort, Luitzen de Jong, Roel van Driel

Journal:

Journal of Cellular Biochemistry

Year:

1996

Language:

english

File:

PDF, 1.23 MB

english, 1996

63

Poland anomaly: Not unilateral or bilateral but mosaic

Maurice A.M. van Steensel

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 30 KB

english, 2004

64

A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma

M.A.M. van Steensel, L. Spruijt, I. van der Burgt, R.S. Bladergroen, M. Vermeer, P.M. Steijlen, M. van Geel

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 163 KB

english, 2005

65

Some twin spots may not be twins

Maurice A.M. van Steensel

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 28 KB

english, 2005

66

Myhre syndrome in a female with previously undescribed symptoms: Further delineation of the phenotype

M.A.M. van Steensel, M. Vreeburg, P.M. Steijlen, C. de Die-Smulders

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 204 KB

english, 2005

67

Skin changes in oculo-dento-digital dysplasia are correlated with C-terminal truncations of connexin 43

M. Vreeburg, E.A. de Zwart-Storm, M.I. Schouten, R.G.L. Nellen, D. Marcus-Soekarman, M. Devies, M. van Geel, M.A.M. van Steensel

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 143 KB

english, 2007

68

Two Dutch brothers with Borrone dermato-cardio-skeletal syndrome

M.A.M. van Steensel, R.P.M. Ceulen, T. Delhaas, C. de Die-Smulders

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 178 KB

english, 2007

69

A case of Lelis syndrome with hystrix-like ichthyosis

M.A.M. van Steensel, V. Winnepenninckx, I.F. Nagtzaam, R. Janssens, R. De Vos, P.M. Steijlen

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 338 KB

english, 2008

70

Contiguous gene syndrome due to a maternally inherited 8.41 Mb distal deletion of chromosome band Xp22.3 in a boy with short stature, ichthyosis, epilepsy, mental retardation, cerebral cortical heterotopias and Dandy–Walker malformation

M.A.M. van Steensel, M. Vreeburg, J. Engelen, S. Ghesquiere, A.P.A. Stegmann, J. Herbergs, J. van Lent, B. Smeets, J.H. Vles

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 159 KB

english, 2008

71

The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron

M.A.M. van Steensel, A.P. Oranje, J.G. van der Schroeff, A. Wagner, M. van Geel

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 274 KB

english, 2009

72

A novel TP63 mutation in family with ADULT syndrome presenting with eczema and hypothelia

W.A.G. van Zelst-Stams, M.A.M. van Steensel

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 98 KB

english, 2009

73

Lelis Syndrome may be a manifestation of hypohidrotic ectodermal dysplasia

Maurice A.M. van Steensel, Annemarie H. van der Hout

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 88 KB

english, 2009

74

Adermatoglyphia, previously unrecognized manifestation in ADULT syndrome

Hiram Larangeira de Almeida Jr., Patrícia Caspary, Rodrigo Pereira Duquia, Rowdy Meijer, Maurice van Steensel

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 69 KB

english, 2010

75

A de novo p.Asp18Asn mutation in TREX1 in a patient with Aicardi–Goutières syndrome

Charlotte A. Haaxma, Yanick J. Crow, Maurice A.M. van Steensel, Martin M.Y. Lammens, Gillian I. Rice, Marcel M. Verbeek, Michèl A.A.P. Willemsen

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 324 KB

english, 2010

76

Molecular genetics of hereditary hair and nail disease

M.A.M. van Steensel, M. van Geel, P.M. Steijlen

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2004

Language:

english

File:

PDF, 208 KB

english, 2004

77

Gap junction diseases of the skin: Am J Med Genet 131C: 12–19

M.A.M. van Steensel

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2006

File:

PDF, 46 KB

2006

78

Lack of SSH1 mutations in Dutch patients with disseminated superficial actinic porokeratosis: is there really an association?

Jorge Frank, Maurice A.M. van Steensel, Michel van Geel

Journal:

Year:

2007

Language:

english

File:

PDF, 119 KB

english, 2007

79

Novel missense mutations in the FOXC2 gene alter transcriptional activity

M.A.M. van Steensel, R.J. Damstra, M. Heitink, R.S. Bladergroen, J. Veraart, Peter M. Steijlen, M. van Geel

Journal:

Year:

2009

Language:

english

File:

PDF, 174 KB

english, 2009

80

A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene

Derek H.K. Lim, Pauline K. Rehal, Michael S. Nahorski, Fiona Macdonald, Tijs Claessens, Michel Van Geel, Lieke Gijezen, Johan J.P. Gille, Sophie Giraud, Stephane Richard, Maurice van Steensel, Fred H.

Journal:

Year:

2010

Language:

english

File:

PDF, 285 KB

english, 2010

81

Domains of the human androgen receptor and glucocorticoid receptor involved in binding to the nuclear matrix

Bas van Steensel, Guido Jenster, Klaus Damm, Albert O. Brinkmann, Roel van Driel Dr.

Journal:

Journal of Cellular Biochemistry

Year:

1995

Language:

english

File:

PDF, 1.37 MB

english, 1995

82

A case of Rombo syndrome

M.A.M. Van Steensel, N.G.J. Jaspers, P.M. Steijlen

Journal:

British Journal of Dermatology

Year:

2001

Language:

english

File:

PDF, 503 KB

english, 2001

83

Woolly hair, premature loss of teeth, nail dystrophy, acral hyperkeratosis and facial abnormalities: possible new syndrome in a Dutch kindred

M.A.M. Van Steensel, M.I. Koedam, O.Q. Swinkels, F. Rietveld, P.M. Steijlen

Journal:

British Journal of Dermatology

Year:

2001

Language:

english

File:

PDF, 512 KB

english, 2001

84

New syndrome of hypotrichosis, striate palmoplantar keratoderma, acro-osteolysis and periodontitis not due to mutations in cathepsin C

M.A.M. Van Steensel, M. Van Geel, P.M. Steijlen

Journal:

British Journal of Dermatology

Year:

2002

Language:

english

File:

PDF, 324 KB

english, 2002

85

HID and KID syndromes are associated with the same connexin 26 mutation

M. Van Geel, M.A.M. Van Steensel, W. Küster, H.C. Hennies, R. Happle, P.M. Steijlen, A. König‡

Journal:

British Journal of Dermatology

Year:

2002

Language:

english

File:

PDF, 140 KB

english, 2002

86

Connexin 30.3 (GJB4) is not required for normal skin function in humans

M. Van Geel, M.A.M. Van Steensel, P.M. Steijlen

Journal:

British Journal of Dermatology

Year:

2002

Language:

english

File:

PDF, 555 KB

english, 2002

87

Endoscopic totally extraperitoneal repair of bilateral inguinal hernias

Dr M. T. T. Knook, W. F. Weidema, L. P. S. Stassen, R. U. Boelhouwer, C. J. van Steensel

Journal:

British Journal of Surgery

Year:

1999

Language:

english

File:

PDF, 68 KB

english, 1999

88

A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis-Ichthyosis-Deafness Syndrome

van Steensel, Maurice A. M., van Geel, Michel, Nahuys, Marc, Smitt, J. Henk Sillevis, Steijlen, Peter M.

Journal:

The Journal of Investigative Dermatology

Year:

2002

Language:

english

File:

PDF, 247 KB

english, 2002

89

Clouston Syndrome Can Mimic Pachyonychia Congenita

van Steensel, Maurice A.M., Jonkman, Marcel F., van Geel, Michel, Steijlen, Peter M., Irwin McLean, W.H., Smith, Frances J.D.

Journal:

The Journal of Investigative Dermatology

Year:

2003

Language:

english

File:

PDF, 922 KB

english, 2003

90

Monocyte, macrophage and mast cell-derived PDGF control inflammation, tissue remodelling and autoimmunity in the pathophysiology of Graves’ ophthalmpathy

Leendert van Steensel, Dion Paridaens, P Martin van Hagen, Robert WAM Kuijpers, Willem A van den Bosch, Hemmo A Drexhage, Herbert Hooijkaas, Willem A Dik

Journal:

Journal of Translational Medicine

Year:

2011

Language:

english

File:

PDF, 72 KB

english, 2011

91

High-resolution mapping of heterochromatin redistribution in aDrosophilaposition-effect variegation model

Maartje J Vogel, Ludo Pagie, Wendy Talhout, Marja Nieuwland, Ron M Kerkhoven, Bas van Steensel

Journal:

Epigenetics & Chromatin

Year:

2009

Language:

english

File:

PDF, 2.03 MB

english, 2009

92

Bronchial carcinoid tumor in a 12-year-old child

Dr. H. A. van Steensel-Moll, R. de Groot, H. J. Neijens, J. C. den Hollander, M. Meradji

Journal:

Pediatric Pulmonology

Year:

1986

Language:

english

File:

PDF, 458 KB

english, 1986

93

A predictive model to estimate the risk of serious bacterial infections in febrile infants

R. M. F. Berger, M. Y. Berger, H. A. van Steensel-Moll, G. Dzoljic-Danilovic, G. Derksen-Lubsen

Journal:

European Journal of Pediatrics

Year:

1996

Language:

english

File:

PDF, 666 KB

english, 1996

94

Risk factors for mechanical ventilation in respiratory syncytial virus infection

W. J. E. Tissing, H. A. van Steensel-Moll, M. Offringa

Journal:

European Journal of Pediatrics

Year:

1993

Language:

english

File:

PDF, 317 KB

english, 1993

95

Chromatin domains in higher eukaryotes: insights from genome-wide mapping studies

Elzo de Wit, Bas van Steensel

Journal:

Year:

2009

Language:

english

File:

PDF, 422 KB

english, 2009

96

Reorganization of the nuclear lamina and cytoskeleton in adipogenesis

Valerie L. R. M. Verstraeten, Johan Renes, Frans C. S. Ramaekers, Miriam Kamps, Helma J. Kuijpers, Fons Verheyen, Martin Wabitsch, Peter M. Steijlen, Maurice A. M. van Steensel, Jos L. V. Broers

Journal:

Histochemistry and Cell Biology

Year:

2011

Language:

english

File:

PDF, 1.70 MB

english, 2011

97

Laparoscopic repair of recurrent inguinal hernias after endoscopic herniorrhaphy

M. T. T. Knook, W. F. Weidema, L. P. S. Stassen, C. J. van Steensel

Journal:

Surgical Endoscopy

Year:

1999

Language:

english

File:

PDF, 31 KB

english, 1999

98

Long-term results after modified Gallie technique for incisional hernia repair: Results in 19 patients

J. Heisterkamp, P. T. den Hoed, J. Kluin, W. F. Weidema, C. J. van Steensel

Journal:

Year:

2005

Language:

english

File:

PDF, 300 KB

english, 2005

99

Cryptic Splicing at a Non-Consensus Splice-Donor in a Patient with a Novel Mutation in the Plakophilin-1 Gene

Steijlen, Peter M., van Steensel, Maurice A. M., Jansen, Bastiaan J. H., Blokx, Willeke, van de Kerkhof, Peter C. M., Happle, Rudolf, van Geel, Michel

Journal:

The Journal of Investigative Dermatology

Year:

2004

Language:

english

File:

PDF, 1.89 MB

english, 2004

100

A Phenotype Resembling the Clouston Syndrome with Deafness Is Associated with a Novel Missense GJB2 Mutation

van Steensel, Maurice A.M., Steijlen, Peter M., Bladergroen, Reno S., Hoefsloot, Elisabeth H., van Ravenswaaij-Arts, Connie M., van Geel, Michel

Journal:

The Journal of Investigative Dermatology

Year:

2004

Language:

english

File:

PDF, 1.18 MB

english, 2004