Results 211 to 220 of about 488,818 (245)

Genomic copy-number variants drive apoptotic evasion underlying acquired resistance to immune checkpoint inhibitors. [PDF]

Immunity
Wu M, Yang S, Yang Z, Fan J, Lomeli SH, Dharanipragada P, Moriceau G, Damoiseaux R, Kelley MC, Prieto-Granada CN, Giubellino A, Nosrati M, Kashani-Sabet M, Kim KB, Johnson DB, Liu S, Lo RS.   +16 more
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A Novel N-Terminal <i>PRPF6</i> Variant in Autosomal Dominant Retinitis Pigmentosa. [PDF]

Clin Case Rep
Li N, Dang Y.
europepmc   +1 more source

Molecular and genomic insights into viral resistance in <i>Capsicum</i> spp.: pathogenesis, defense mechanisms, and breeding innovations. [PDF]

Front Plant Sci
Shilpha J, Kang WH.
europepmc   +1 more source

Expanding the clinical phenotype of DYNC1H1 -associated mutations: a Chinese family with autosomal dominant complex hereditary spastic paraplegia. [PDF]

BMC Med Genomics
Yuan X, Zhang S, Tang Y.
europepmc   +1 more source

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The Runx genes as dominant oncogenes

Blood Cells, Molecules, and Diseases, 2003
We have shown previously that Runx2 is a frequent target (approximately equal to 30%) for proviral insertion in murine leukemia virus (MLV) induced T cell tumors in CD2-MYC transgenic mice. Further investigation of a large panel of these tumors revealed that a small number also contain insertions at either Runx3 or Runx1.
Ewan R, Cameron, Karen, Blyth, Linda, Hanlon, Anna, Kilbey, Nancy, Mackay, Monica, Stewart, Anne, Terry, Francois, Vaillant, Sandy, Wotton, James C, Neil   +9 more
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TransgenicArabidopsis tester lines with dominant marker genes

Molecular and General Genetics MGG, 1996
The map positions of a set of eight T-DNA insertions in the Arabidopsis genome have been determined by using closely linked visible markers. The insertions are dispersed over four of the five chromosomes. Each T-DNA insert contains one or more of the chimeric marker genes neomycin phosphotransferase (neo), hygromycin phosphotransferase (hpt ...
van Lijsebettens, M., Wang, X., Cnops, G., Boerjan, Wout, Desnos, Thierry, Höfte, Herman, van Montagu, Marc   +6 more
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Genetic mechanisms for dominant VH gene expression. The VHB512 gene

The Journal of Immunology, 1992
Abstract A total of 37 mAb with reactivity for dextran B512 have been studied; 30 of them were products of independent rearrangements and 21 made use of the same VH gene, the VHB512 gene. These results unambiguously established that the immune response to dextran in the high responder mouse strain C57BL/6 was restricted.
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Gene-Based Therapies for Dominant Retinopathies

Current Gene Therapy, 2010
Over the past two decades, significant progress has been made in defining the molecular pathogenesis of hereditary retinal degenerations. Many of these are characterised by immense genetic heterogeneity. For example, in retinitis pigmentosa (RP), the most common form of this group of disorders, approximately 50 disease causing genes have been ...
G. Jane Farrar, Arpad Palfi, Paul F.Kenna, Mary O'Reilly   +3 more
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Severe Renal Dysgenesis Produced by a Dominant Gene

Archives of Pediatrics & Adolescent Medicine, 1976
A woman with the autosomal dominant syndrome of preauricular pits, cervical fistulae, and partial deafness gave birth to two children with preauricular pits and severe renal dysgenesis. The facies had some features of the Potter facies of renal agenesis. One child died soon after birth because of pneumothorax and immature development of the lungs.
N, Fitch, H, Srolovitz
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Gene Augmentation for Autosomal Dominant CRX-Associated Retinopathies

2023
The cone-rod homeobox (CRX) protein is a key transcription factor essential for photoreceptor function and survival. Mutations in human CRX gene are linked to a wide spectrum of blinding diseases ranging from mild macular dystrophy to severe Leber congenital amaurosis (LCA), cone-rod dystrophy (CRD), and retinitis pigmentosa (RP).
Chi, Sun, Shiming, Chen
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