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| 1 | Diffuse and segmental variants of cutaneous leiomyomatosis: novel mutations in the fumarate hydratase gene and review of the literature 显示文摘 | Badeloe S van Geel M van Steensel MA | 2006 | Exp Dermatol2006，15，： | 1 |
| 2 | A missense mutation in the type Ⅱ hair keratin hHb3 is associated with monilethrix显示文摘 | VAN STEENSEL M A M STEIJLEN P M BLADERGROEN R S | 2005 | J Med Genet2005，42，3： | 1 |
| 3 | Prime boost vaccination with a fowl pox vector and an inactivated avian influenza vaccine is highly immunogenic in Pekin ducks challenged with Asian H5N1 HPAI 显示文摘 | STEENSELS M BUBLOT M VAN BORM S | 2009 | Vaccine2009，27，5： | 1 |
| 4 | The gene for hypertrichosis of Marie Unna maps between D8S258 and D8S298: Exclusion of the hr gene by cDNA and genomic sequencing 显示文摘 | van Steensel M Smith FJ Steijlen PM | 1999 | Am J Hum Genet1999，65，2： | 1 |
| 5 | Orbit-infiltrating mast cells, monocytes, and macrophages produce PDGF isoforms that orchestrate orbital fibroblast activation in Graves'ophthalmopathy显示文摘 | van Steensel L Paridaens D van Meurs M | | 0，，03： | 1 |
| 6 | Granulomatous rosacea and Crohn' s disease in a patient homozygous for the Crohn-associated NOD2/CARDl5 polymorphism R702W 显示文摘 | Van Steensel M Badeloe S Winnepenninckx V | 2008 | Expert Dermatol2008，17，12： | 1 |
| 7 | The effect of routine hoof trimming on locomotion score, ruminating time, activity, and milk yield of dairy cows显示文摘 | Hertem T V Parmet Y Steensels M | 2014 | Journal of Dairy Science2014，97，8： | 1 |
| 8 | Failure of PCR Based IS6110 analysis to detect vertebral spinndylodiscitis caused by Mycobacterium bovis显示文摘 | Steensels D Fauvilleqaux M Boie J | 2013 | J Clin Microbiol2013，51，1： | 1 |
| 9 | Genome-Wide Profiling of DNA Methylation Reveals Transposon Targets of CHROMOMETHYLASE3显示文摘 | Rachel Tompa Claire M McCallum Jeffrey Delrow Jorja G Henikoff Bas van Steensel Steven Henikoff | 2002 | Current Biology2002，，1： | 1 |
| 10 | A universal avian endogenous real-time reverse transcriptase-polymerase chain reaction control and its application to avian influenza diagnosis and quantification显示文摘 | Van BORM S V STEENSELS M FERREIRA H L | 2007 | Avian Dis2007，51，1： | 1 |
| 11 | Mutation S233L in the 1B domain of keratin 1 causes epidermolytie palmoplantar keratoderma with ' tonotubular' keratin显示文摘 | Terron-Kwiatkowski A van Steensel M A van Geel M | 2006 | J Invest Dermatol2006，126，3： | 1 |
| 12 | The gene for hypertrichosis of Marie Unna maps between D8S258 and D8S298 :exclusion of the hr gene by cDNA and genomic sequencing显示文摘 | Van Steensel M Smith FJD Steijlen PM | 1999 | Am J Hum Genet1999，65，： | 1 |
| 13 | A novel connexin 26 mutation in a patient diagnosed with keratosis-ichthyosis-deafness syndrome 显示文摘 | VAN STEENSEL M A VAN GEEL M NAHUYS M | 2002 | J Invest Dermatol2002，118，4： | 1 |
| 14 | A novel connexin 26 mutation in a patient diagnosed with keratitisichthyosis-deafness syndrome显示文摘 | van Steensel MA van Geel M Nahuys M | 2002 | J Invest Dermatol2002，118，4： | 1 |
| 15 | Orbit-infil-trating mast cells, monocytes, and macrophages produce PDGF isoforms that orchestrate orbital fibroblast activation in graves' ophthalmopathy 显示文摘 | van Steensel L Paridaens D van Meurs M | 2012 | J Clin Endocrinol Metab2012，97，： | 1 |
| 16 | The effect of routine hoof trimming on locomotion score,ruminating time,activity,and milk yield of dairy cows显示文摘 | VAN HERTEM T PARMET Y STEENSELS M | 2014 | J Dairy Sci2014，97，8： | 1 |
| 17 | A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis- deafness syndrome显示文摘 | van Steensel MA van Geel M Nahuys M | 2002 | J Invest Dermatol2002，118，4： | 1 |
| 18 | Prime-boost vac- cination with a fowlpox vector and an inactivated avian influ- enza vaccine is highly immunogenic in Pekin ducks challenged withAsian H5N1 HPAI显示文摘 | Steensels M Bublot M Van B S | 2009 | Vaccine2009，27，5： | 1 |
| 19 | Pharmacological and functional chraracterization of human mineralocorticoid and glucocorticoid receptor ligands显示文摘 | RUPPRECHT R REUL J M VAN STEENSEL B | 1993 | EurJ Pharmacol1993，247，： | 1 |
| 20 | HID and KID syndromes are associated with the same connexin 26 mutation 显示文摘 | van Geel M van Steensel MA Ktister W ct al | 2002 | Br J Demlatol2002，146，6： | 1 |
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