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	101.	Patterns of hematopoietic chimerism following bone marrow transplantation for childhood acute lymphoblastic leukemia from volunteer unrelated donors. [electronic resource] by Molloy, K Goulden, N Lawler, M Cornish, J Oakhill, A Pamphilon, D Potter, M Steward, C Langlands, K Humphries, P McCann, S R Producer: 19960718 In: Blood vol. 87 Availability: No items available. Save to lists Add to cart (remove)
	102.	Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7q. [electronic resource] by Bowne, S J Sullivan, L S Ding, L Traer, E Prescott, S M Birch, D G Kennan, A Humphries, P Daiger, S P Producer: 20000316 In: Molecular vision vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	103.	Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin. [electronic resource] by Farrar, G J Kenna, P Redmond, R Shiels, D McWilliam, P Humphries, M M Sharp, E M Jordan, S Kumar-Singh, R Humphries, P Producer: 19920313 In: Genomics vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	104.	Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locus. [electronic resource] by Bradley, D G Farrar, G J Sharp, E M Kenna, P Humphries, M M McConnell, D J Daiger, S P McWilliam, P Humphries, P Producer: 19890503 In: American journal of human genetics vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	105.	Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene. [electronic resource] by McNally, N Kenna, P Humphries, M M Hobson, A H Khan, N W Bush, R A Sieving, P A Humphries, P Farrar, G J Producer: 19990816 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	106.	Apoptotic photoreceptor death in the rhodopsin knockout mouse in the presence and absence of c-fos. [electronic resource] by Hobson, A H Donovan, M Humphries, M M Tuohy, G McNally, N Carmody, R Cotter, T Farrar, G J Kenna, P F Humphries, P Producer: 20001018 In: Experimental eye research vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex. [electronic resource] by Humphries, M M Sheils, D M Farrar, G J Kumar-Singh, R Kenna, P F Mansergh, F C Jordan, S A Young, M Humphries, P Producer: 19930521 In: Human mutation vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	108.	Transfusion-associated graft-versus-host disease, monoclonal gammopathy and PCR. [electronic resource] by Blundell, E L Pamphilon, D H Anderson, N A Slade, R R Burton, P A Martin, A Ray, T Bradley, B A Lawler, M Humphries, P Producer: 19930219 In: British journal of haematology vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population. [electronic resource] by van Soest, S van den Born, L I Gal, A Farrar, G J Bleeker-Wagemakers, L M Westerveld, A Humphries, P Sandkuijl, L A Bergen, A A Producer: 19950120 In: Genomics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa. [electronic resource] by Bleeker-Wagemakers, L M Gal, A Kumar-Singh, R van den Born, L I Li, Y Schwinger, E Sandkuijl, L A Bergen, A A Kenna, P Humphries, P Producer: 19921217 In: Genomics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	Comparative structural and functional analysis of photoreceptor neurons of Rho-/- mice reveal increased survival on C57BL/6J in comparison to 129Sv genetic background. [electronic resource] by Humphries, M M Kiang, S McNally, N Donovan, M A Sieving, P A Bush, R A Machida, S Cotter, T Hobson, A Farrar, J Humphries, P Kenna, P Producer: 20011226 In: Visual neuroscience vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	112.	Strategems in vitro for gene therapies directed to dominant mutations. [electronic resource] by Millington-Ward, S O'Neill, B Tuohy, G Al-Jandal, N Kiang, A S Kenna, P F Palfi, A Hayden, P Mansergh, F Kennan, A Humphries, P Farrar, G J Producer: 19980202 In: Human molecular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland. [electronic resource] by Humphries, M M Mansergh, F C Kiang, A S Jordan, S A Sheils, D M Martin, M J Farrar, G J Kenna, P F Young, M M Humphries, P Producer: 19961120 In: Human mutation vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	114.	New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis. [electronic resource] by Seeliger, M W Grimm, C Ståhlberg, F Friedburg, C Jaissle, G Zrenner, E Guo, H Remé, C E Humphries, P Hofmann, F Biel, M Fariss, R N Redmond, T M Wenzel, A Producer: 20010927 In: Nature genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	115.	Bone spicule pigment formation in retinitis pigmentosa: insights from a mouse model. [electronic resource] by Jaissle, Gesine B May, Christian Albrecht van de Pavert, Serge A Wenzel, Andreas Claes-May, Ellen Giessl, Andreas Szurman, Peter Wolfrum, Uwe Wijnholds, Jan Fischer, M D Fisher, M D Humphries, P Seeliger, M W Producer: 20100830 In: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie vol. 248 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	Retinopathy induced in mice by targeted disruption of the rhodopsin gene. [electronic resource] by Humphries, M M Rancourt, D Farrar, G J Kenna, P Hazel, M Bush, R A Sieving, P A Sheils, D M McNally, N Creighton, P Erven, A Boros, A Gulya, K Capecchi, M R Humphries, P Producer: 19970310 In: Nature genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	117.	Dose-dependent expression of claudin-5 is a modifying factor in schizophrenia. [electronic resource] by Greene, C Kealy, J Humphries, M M Gong, Y Hou, J Hudson, N Cassidy, L M Martiniano, R Shashi, V Hooper, S R Grant, G A Kenna, P F Norris, K Callaghan, C K Islam, M dN O'Mara, S M Najda, Z Campbell, S G Pachter, J S Thomas, J Williams, N M Humphries, P Murphy, K C Campbell, M Producer: 20190731 In: Molecular psychiatry vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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