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Experimental Dermatology|April 20, 2000
A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesionsV M Aita, W Ahmad, A A Panteleyev, et al.European Journal of Human Genetics : EJHG|June 15, 2000
Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardationS Ranta, Y Zhang, B Ross, et al.Arthritis and Rheumatism|April 9, 2005
Fibroblast expression of the coactivator p300 governs the intensity of profibrotic response to transforming growth factor betaSwati Bhattacharyya, Asish K Ghosh, Jaspreet Pannu, et al.Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 1, 1995
Genetic alterations of microsatellites on chromosome 18 in human breast carcinomaT H Huang, P L Yeh, M B Martin, et al.Human Pathology|June 27, 2003
Cutaneous lymphoid hyperplasia: a lymphoproliferative continuum with lymphomatous potentialMinakshi Nihal, Debra Mikkola, Nancy Horvath, et al.Cell|November 27, 2012
Three-dimensional architecture of the rod sensory cilium and its disruption in retinal neurodegenerationJared C Gilliam, Juan T Chang, Ivette M Sandoval, et al.Archives of Dermatology|March 18, 2009
Isolated benign primary cutaneous plasmacytosis in children: two illustrative casesAnita C Gilliam, Renata H Mullen, Gina Oviedo, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1988
Chromosome jumping from D4S10 (G8) toward the Huntington disease geneJ E Richards, T C Gilliam, J L Cole, et al.Neurology|September 1, 1991
Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locusP W Kleyn, L M Brzustowicz, K C Wilhelmsen, et al.Experimental Dermatology|December 21, 2005
Transduced monocyte/macrophages targeted to murine skin by UV lightAlexandra Y Zhang, Caiyun Wu, Lixin Zhou, et al.Pageof 18