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J Mendell

Showing results (31-40 of 45) with videos related to

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Annals of Neurology|June 1, 1996
Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY GroupR Tawil, J Forrester, R C Griggs, et al.
Indoor Air|March 20, 2013
Association of classroom ventilation with reduced illness absence: a prospective study in California elementary schoolsM J Mendell, E A Eliseeva, M M Davies, et al.
Journal of Occupational and Environmental Hygiene|April 1, 2006
Indicators of moisture and ventilation system contamination in U.S. office buildings as risk factors for respiratory and mucous membrane symptoms: analyses of the EPA BASE dataMark J Mendell, Myrna Cozen, Quanhong Lei-Gomez, et al.
Indoor Air|August 22, 2014
Effects of ventilation rate per person and per floor area on perceived air quality, sick building syndrome symptoms, and decision-makingR Maddalena, M J Mendell, K Eliseeva, et al.
Environmental Science. Processes & Impacts|March 1, 2021
Associations of observed home dampness and mold with the fungal and bacterial dust microbiomesJennie Cox, Timothy Stone, Patrick Ryan, et al.
Indoor Air|June 3, 2014
Next-generation DNA sequencing reveals that low fungal diversity in house dust is associated with childhood asthma developmentK C Dannemiller, M J Mendell, J M Macher, et al.
Indoor Air|December 15, 2015
Higher measured moisture in California homes with qualitative evidence of dampnessJ M Macher, M J Mendell, K Kumagai, et al.
Indoor Air|May 10, 2014
Evaluation of the indoor air quality minimum ventilation rate procedure for use in California retail buildingsS M Dutton, M J Mendell, W R Chan, et al.
American Journal of Human Genetics|August 1, 1992
Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35B Weiffenbach, R Bagley, K Falls, et al.
Clinical Genetics|April 13, 2011
Maternal uniparental disomy of chromosome 4 in a patient with limb-girdle muscular dystrophy 2E confirmed by SNP array technologyC E Cottrell, J Mendell, M Hart-Kothari, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Annals of Neurology|June 1, 1996
Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY GroupR Tawil, J Forrester, R C Griggs, et al.
Indoor Air|March 20, 2013
Association of classroom ventilation with reduced illness absence: a prospective study in California elementary schoolsM J Mendell, E A Eliseeva, M M Davies, et al.
Journal of Occupational and Environmental Hygiene|April 1, 2006
Indicators of moisture and ventilation system contamination in U.S. office buildings as risk factors for respiratory and mucous membrane symptoms: analyses of the EPA BASE dataMark J Mendell, Myrna Cozen, Quanhong Lei-Gomez, et al.
Indoor Air|August 22, 2014
Effects of ventilation rate per person and per floor area on perceived air quality, sick building syndrome symptoms, and decision-makingR Maddalena, M J Mendell, K Eliseeva, et al.
Environmental Science. Processes & Impacts|March 1, 2021
Associations of observed home dampness and mold with the fungal and bacterial dust microbiomesJennie Cox, Timothy Stone, Patrick Ryan, et al.
Indoor Air|June 3, 2014
Next-generation DNA sequencing reveals that low fungal diversity in house dust is associated with childhood asthma developmentK C Dannemiller, M J Mendell, J M Macher, et al.
Indoor Air|December 15, 2015
Higher measured moisture in California homes with qualitative evidence of dampnessJ M Macher, M J Mendell, K Kumagai, et al.
Indoor Air|May 10, 2014
Evaluation of the indoor air quality minimum ventilation rate procedure for use in California retail buildingsS M Dutton, M J Mendell, W R Chan, et al.
American Journal of Human Genetics|August 1, 1992
Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35B Weiffenbach, R Bagley, K Falls, et al.
Clinical Genetics|April 13, 2011
Maternal uniparental disomy of chromosome 4 in a patient with limb-girdle muscular dystrophy 2E confirmed by SNP array technologyC E Cottrell, J Mendell, M Hart-Kothari, et al.
Pageof 5