David M. Kingsley, Ph.D.
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Publications on:
Genetics of Evolutionary Change in Vertebrates
Developmental and Medical Genetics in Mice and Humans
Genetics of Evolutionary Change in Vertebrates:

Arnegard, M.E., M.D. McGee, B. Matthews, K.B. Marchinko, G.L. Conte, S. Kabir, N. Bedford, S. Bergek, Y.F. Chan, F.C. Jones, D.M. Kingsley, C.L. Peichel, and D. Schluter (2014). Genetics of ecological divergence during speciation. Nature 511: 307-311.

 

Guenther, C. A., B. Tasic, L. Luo, M. A. Bedell and D. M. Kingsley (2014). A molecular basis for classic blond hair color in Europeans. Nature Genetics 46:748-752.

 

Miller, C.T., A.M. Glazer, B.R. Summers, B.K. Blackman, A.R. Norman, M.D. Shapiro, B.L. Cole, C.L. Peichel, D. Schulter, and D.M. Kingsley (2014). Modular skeletal evolution in sticklebacks is controlled by additive and clustered quantitative trait loci. Genetics 197:405-420.

 

Reno, PL, CY McLean, JE Hines, TD Capellini, G Bejerano, and DM Kingsley (2013). A penile spine/vibrissa enhancer sequence is missing in modern and extinct humans but is retained in multiple primates with penile spines and sensory vibrissae. PLOS One 8:e84258.

 

Deagle BE, Jones FC, Absher DM, Kingsley DM, Reimchen TE. (2013). Phylogeography and adaptation genetics of stickleback from the Haida Gwaii archipelago revealed using genome-wide single nucleotide polymorphism genotyping. Mol. Ecol. 22:1917-32.

 

Infante, CR, S. Park, A.G. Mihala, D.M. Kingsley, and D.B. Menke (2013). Pitx1 broadly associates with limb enhancers and is enriched on hindlimb cis-regulatory elements. Dev Biol 374: 234-244.

 

Hiller, M., B. T. Schaar, V. B. Indjeian, D. M. Kingsley, L. R. Hagey and G. Bejerano (2012). A "Forward genomics" approach links genotype to phenotype using independent phenotypic losses among related species. Cell Rep 2: 817-23.

 

Wark, A. R., M. G. Mills, L.-H. Dang, Y. F. Chan, F. C. Jones, S. D. Brady, D. M. Absher, J. Grimwood, J. Schmutz, R. M. Myers, D. M. Kingsley and C. L. Peichel (2012). Genetic architecture of variation in the lateral line sensory system of threespine sticklebacks. G3•Genes Genomes Genetics 2: 1047-56..

 

Jones, F. C., M. G. Grabherr, Y. F. Chan, P. Russell, E. Mauceli, J. Johnson, R. Swofford, M. Pirun, M. C. Zody, S. White, E. Birney, S. Searle, J. Schmutz, J. Grimwood, M. C. Dickson, R. M. Myers, C. T. Miller, B. R. Summers, A. K. Knecht, S. D. Brady, H. Zhang, A. A. Pollen, T. Howes, C. Amemiya, B. I. G. S. P. a. W. G. A. Team, E. S. Lander, F. Di Palma, K. Lindblad-Toh and D. M. Kingsley (2012). The genomic basis of adaptive evolution in threespine sticklebacks. Nature 484: 55-61.

View data from 21 stickleback genomes here: http://sticklebrowser.stanford.edu

 

Rogers, S. M., P. Tamkee, B. Summers, S. Balabhadra, M. Marks, D. M. Kingsley and D. Schluter (2012). Genetic signature of adaptive peak shift in threespine stickleback. Evolution 66: 2439-2450.

 

Deagle, B. E., F. C. Jones, Y. F. Chan, D. M. Absher, D. M. Kingsley and T. E. Reimchen (2012). "Population genomics of parallel phenotypic evolution in stickleback across stream-lake ecological transitions." Proc. R. Soc. B. 279: 1277-1286.

 

Jones, F. C., Y. F. Chan, J. Schmutz, J. Grimwood, S. D. Brady, A. M. Southwick, D. M. Absher, R. M. Myers, T. E. Reimchen, B. E. Deagle, D. Schluter and D. M. Kingsley (2012). "A genome-wide SNP genotyping array reveals patterns of global and repeated species pair divergence in sticklebacks." Current Biology, 22(1):83-90.

 

Lowe, C. B., M. Kellis, A. C. Siepel, B. J. Raney, M. Clamp, S. R. Salama, D. M. Kingsley, K. Lindblad-Toh and D. Hausler (2011). "Three periods of regulatory innovation during vertebrate evolution." Science (Aug 19, 2011).

 

McLean, C. Y., P. L. Reno, A. A. Pollen, A. I. Bassan, T. D. Capellini, C. Guenther, V. B. Indjeian, X. Lim, D. B. Menke, B. T. Schaar, A. M. Wenger, G. Bejerano and D. M. Kingsley (2011). "Human-specific loss of regulatory DNA and the evolution of human-specific traits." Nature 471: 216–219.

 

Greenwood, A. K., F. C. Jones, Y. F. Cha, S. D. Brady, D. M. Absher, J. Grimwood, J. Schmutz, R. M. Myers, D. M. Kingsley and C. L. Peichel (2011). "The genetic basis of divergent pigment patterns in juvenile threespine sticklebacks." Heredity 107: 155-166.

 

Kingsley, D. (2010) Genetics, geology, and miracles. In P.R. Grant, B.R. Grant, eds. In search of the causes of evolution. From Field Observations to Mechanisms. Princeton University Press, Princeton NJ.

 

Chan, Y. F., M. E. Marks, F. C. Jones, G. Villarreal, M. D. Shapiro, S. D. Brady, A. M. Southwick, D. M. Absher, J. Grimwood, J. Schmutz, R. M. Myers, D. Petrov, B. Jonsson, D. Schluter, M. A. Bell and D. M. Kingsley (2010). "Adaptive evolution of pelvic reduction in sticklebacks by recurrent deletion of a Pitx1 enhancer."Science 327: 302-305 (full reprint here).

 

Kitano, J., J. A. Ross, S. Mori, M. Kume, F. C. Jones, Y. F. Chan, D. M. Absher, J. Grimwood, J. Schmutz, R. M. Myers, D. M. Kingsley and C. L. Peichel (2009). "A role for a neo-sex chromosome in stickleback speciation." Nature 461: 1079-1083.

 

Genome 10K Community of Scientists (2009). "Genome 10K: a proposal to obtain whole-genome sequence for 10,000 vertebrate species." J Hered. 2009 Nov-Dec;100(6):659-74. Epub 2009 Nov 5. PMID: 19892720

 

Shapiro, M. D., B. R. Summers, S. Balabhadra, J. T. Aldenhoven, A. L. Miller, C. B. Cunningham, M.A. Bell and D. M. Kingsley (2009). "The genetic architecture of skeletal convergence and sex determination in ninespine sticklebacks." Current Biology 19: 1140-1145.

 

Kingsley, David (2009). "From atoms to traits." Special 150th anniversary issue on The Evolution of Evolution. Scientific American  300: 52-9.

 
Albert, A. Y. K., S. Sawaya, T. H. Vines, A. K. Knecht, C. T. Miller, B. R. Summers, S. Balabhadra, D. M. Kingsley and D. Schluter (2008). "The genetics of adaptive shape shift in stickleback: pleiotropy and effect size." Evolution 62: 76-85.
 
Miller, C. T., S. Beleza, A. A. Pollen, D. Schluter, R. A. Kittles, M. D. Shriver and D. M. Kingsley (2007). "cis-Regulatory changes in Kit Ligand expression and parallel evolution of pigmentation in sticklebacks and humans." Cell 131: 1179-1189.
 
Knecht, A. K., K. E. Hosemann and D. M. Kingsley (2007). "Constraints on utilization of the EDA signaling pathway in threespine stickleback evolution." Evolution & Development 9:141-154.
 
Kingsley, D. M. and C. L. Peichel (2007). The molecular genetics of evolutionary change in sticklebacks. Biology of the three-spine stickleback. S. Ostlund-Nilsson, I. Mayer and F. A. Huntingford, CRC Press: 41-81.
 
Shapiro, M. D., M. A. Bell and D. M. Kingsley (2006). "Parallel genetic origins of pelvic reduction in vertebrates." Proc Natl Acad Sci U S A 103: 13753-13758.
 
Colosimo, P. F., K. E. Hosemann, S. Balabhadra, G. Villareal , M. Dickson, J. Grimwood, J. Schmutz, R. Myers, D. Schluter and D. M. Kingsley (2005). "Widespread parallel evolution in sticklebacks by repeated fixation of ectodysplasin alleles." Science 307: 1928-1933.
 
Shapiro, M. D., M. E. Marks, C. L. Peichel, B. K. Blackman, K. S. Nereng, D. Schluter, B. Jonsson and D. M. Kingsley (2004). "Genetic and developmental basis of evolutionary pelvic reduction in threespine sticklebacks." Nature 428: 717-723.
 
Peichel, C. L., J. A. Ross, C. K. Matson, M. Dickson, J. Grimwood, J. Schmutz, R. M. Myers, S. Mori, D. Schluter and D. M. Kingsley (2004). "The master sex-determination locus in threespine sticklebacks is on a nascent Y chromosome." Curr Biol 14(16): 1416-1424.
 
McKinnon, J. S., S. Mori, B. K. Blackman, L. David, D. M. Kingsley, L. Jamieson, J. Chou and D. Schluter (2004). "Evidence for ecology's role in speciation." Nature 429(6989): 294-298.
 
Kingsley, D. M., B. Zhu, K. Osoegawa, P. J. de Jong, J. Schein, M. Marra, C. L. Peichel, C. Amemiya, D. Schluter, S. Balabhadra, B. Friedlander, Y. M. Cha, M. Dickson, J. Grimwood, J. Schmutz, W. S. Talbot and R. M. Myers (2004). "New genomic tools for molecular studies of evolutionary change in sticklebacks." Behaviour 141: 1331-1344.
 
Hosemann, K. E., P. F. Colosimo, B. R. Summers and D. M. Kingsley (2004). "A simple and efficient microinjection protocol for making transgenic sticklebacks." Behaviour 141: 1345-1355.
 
Colosimo, P. F., C. L. Peichel, K. S. Nereng, B. K. Blackman, M. D. Shapiro, D. Schluter and D. M. Kingsley (2004). "The genetic architecture of parallel armor plate reduction in threespine sticklebacks." PLoS Biology 2: 635-641.
 
Kingsley, D. M. (2003). Sequencing the genome of threespine sticklebacks (Gasterosteus aculeatus). National Human Genome Research Institute White Paper.
 
Peichel, C. L., K. S. Nereng, K. A. Ohgi, B. L. Cole, P. F. Colosimo, C. A. Buerkle, D. Schluter and D. M. Kingsley (2001). "The genetic architecture of divergence between threespine stickleback species." Nature 414(6866): 901-905.
Developmental and Medical Genetics in Mice and Humans:

Guenther, C. A., B. Tasic, L. Luo, M. A. Bedell and D. M. Kingsley (2014). A molecular basis for classic blond hair color in Europeans. Nature Genetics 46:748-752.

 

Reno, PL, CY McLean, JE Hines, TD Capellini, G Bejerano, and DM Kingsley (2013). A penile spine/vibrissa enhancer sequence is missing in modern and extinct humans but is retained in multiple primates with penile spines and sensory vibrissae. PLOS One 8:e84258.

 

Infante, CR, S. Park, A.G. Mihala, D.M. Kingsley, and D.B. Menke (2013). Pitx1 broadly associates with limb enhancers and is enriched on hindlimb cis-regulatory elements. Dev Biol 374: 234-244.

 

Foster, B. L., K. J. Nagatomo, S. O. Bamashmous, K. A. Tompkins, H. Fong, D. Dund, E. Y. Chu, C. Guenther, D. M. Kingsley, R. B. Rutherford and M. J. Somerman (2011). "The progressive ankylosis protein (ANK) regulates cementum apposition and extracellular matrix composition." Cells Tissues Organs (DOI: 10.1159/000323457).

 

McLean, C. Y., P. L. Reno, A. A. Pollen, A. I. Bassan, T. D. Capellini, C. Guenther, V. B. Indjeian, X. Lim, D. B. Menke, B. T. Schaar, A. M. Wenger, G. Bejerano and D. M. Kingsley (2011). "Human-specific loss of regulatory DNA and the evolution of human-specific traits." Nature 471: 216–219.

 

Dy, P. , P. Smits, A. Silvester, A. Penzo-Méndez, B. Dumitriu, Y. Han, C. A. de la Motte, D. M. Kingsley, and V. Lefebvre (2010)."Synovial joint morphogenesis requires the chondrogenic action of Sox5 and Sox6 in growth plate and articular cartilage." Developmental Biology 34:346-59.

 

Kahn, J., Y. Shwartz, E. Blitz, S. Krief, A. Sharir, D.A. Breitel, R. Rattenbach, F. Relaix, P. Maire, R.B. Rountree, D.M. Kingsley, and E. Zelzer (2009). "Muscle Contraction Is Necessary to Maintain Joint Progenitor Cell Fate." Developmental Cell 16 (5): 734-743.

 

Guenther, C., L. Pantalena-Filho, and D.M. Kingsley (2008). "Shaping skeletal growth by modular regulatory elements in the Bmp5 gene." PLoS Genetics 4(12): e1000308 doi:10.1371/journal.pgen.1000308

 
Menke, D.B., C. Guenther, and D.M. Kingsley (2008). "Dual hindlimb control elements in the Tbx4 gene and region-specific control of bone size in vertebrate limbs." Development 135(15):2543-2553.
 
Ho, A. M., P. C. Marker, H. Peng, A. J. Quintero, D. M. Kingsley and J. Huard (2008). "Dominant negative Bmp5 mutation reveals key role of BMPs in skeletal response to mechanical stimulation." BMC Dev Biol 8: 35.
 
Koyama, E., Y. Shibukawa, M. Nagayama, H. Sugito, B. Young, T. Yuasa, T. Okabe, T. Ochiai, N. Kamiya, R. B. Rountree, D. M. Kingsley, M. Iwamoto, M. Enomoto-Iwamoto and M. Pacifici (2008). "A distinct cohort of progenitor cells participates in synovial joint and articular cartilage formation during mouse limb skeletogenesis." Dev Biol 316: 62-73.
 
Koyama, E., T. Ochiai, R.B. Rountree, D.M. Kingsley, M. Enomoto-Iwamoto, M. Iwamoto, M. Pacifici (2007). "Synovial Joint Formation during Mouse Limb Skeletogenesis." Roles of Indian Hedgehog Signaling. Ann. N.Y. Acad. Sci. 1116, 100–112.
 
Miller, C. T., S. Beleza, A. A. Pollen, D. Schluter, R. A. Kittles, M. D. Shriver and D. M. Kingsley (2007). "cis-Regulatory changes in Kit Ligand expression and parallel evolution of pigmentation in sticklebacks and humans." Cell 131: 1179-1189.
 
Feldman, G. J., R. V. Patel, P. Billings, R. J. Caron, C. Guenther, D. M. Kingsley, F. S. Kaplan and E. M. Shore (2007). "Over-expression of Bmp4 and Bmp5 in a child with axial skeletal abnormalities and heterotopic ossification: a new syndrome." Am J Med Genet: 143A: 699-706.
 
Gurley, K. A., R. J. Reimer and D. M. Kingsley (2006). "Biochemical and genetic analysis of ANK in arthritis and bone disease." Am. J. Hum. Genet. 79: 1017-1029.
 
Gurley, K., H. Chen, C. Guenther, E. Nguyen, R. B. Rountree, M. Schoor and D. M. Kingsley (2006). "Mineral formation in joints caused by complete or joint-specific loss of ANK function." J Bone Miner Res 21: 1238-1247.
 
Portnoy, M. E., K. J. McDermott, A. Antonellis, E. H. Marguiles, A. B. Prasad, N. C. S. Program, D. M. Kingsley, E. D. Green and D. P. Mortlock (2005). "Detection of potential Gdf6 regulatory elements by multi-species sequence comparisons and identification of a skeletal joint enhancer." Genomics 86: 295-305.
 
Rountree, R. B., M. Schoor, H. Chen, M. E. Marks, V. Harley, Y. Mishina and D. M. Kingsley (2004). "BMP receptor signaling is required for postnatal maintenance of articular cartilage." PLOS Biology 2: e355.
 
Settle, S. H., R. B. Rountree, A. Sinha, A. Thacker, K. Higgins and D. M. Kingsley (2003). "Multiple joint and skeletal patterning defects caused by single and double mutations in the mouse Gdf6 and Gdf5 genes." Dev Biol 254: 116-130.
 
Mortlock, D. P., C. Guenther and D. M. Kingsley (2003). "A general approach for identifying distant regulatory elements applied to the Gdf6 gene." Genome Res 13: 2069-2081.
 
Pendleton, A., M. D. Johnson, A. Hughes, K. A. Gurley, A. M. Ho, M. Doherty, J. Dixey, P. Gillet, D. Loeuille, R. McGrath, A. Reginato, R. Shiang, G. Wright, P. Netter, C. Williams and D. M. Kingsley (2002). "Mutations in ANKH cause chondrocalcinosis." Am J Hum Genet 71(4): 933-940.
 
Nociti, F. H., Jr., J. E. Berry, B. L. Foster, K. A. Gurley, D. M. Kingsley, T. Takata, M. Miyauchi and M. J. Somerman (2002). "Cementum: a phosphate-sensitive tissue." J Dent Res 81(12): 817-821.
 
Thut, C. J., R. B. Rountree, M. Hwa and D. M. Kingsley (2001). "A large-scale in situ screen provides molecular evidence for the induction of eye anterior segment structures by the developing lens." Dev Biol 231(1): 63-76.
 
Settle, S., P. Marker, K. Gurley, A. Sinha, A. Thacker, Y. Wang, K. Higgins, G. Cunha and D. M. Kingsley (2001). "The BMP family member Gdf7 is required for seminal vesicle growth, branching morphogenesis, and cytodifferentiation." Dev Biol 234(1): 138-150.
 
Kingsley, D. M. (2001). "Genetic control of bone and joint formation." Novartis Found Symp 232: 213-222; discussion 222-234, 272-282.
 
Clark, R. M., P. C. Marker, E. Roessler, A. Dutra, J. C. Schimenti, M. Muenke and D. M. Kingsley (2001). "Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting lmbr1." Genetics 159(2): 715-726.
 
Ho, A., M. Johnson and D. M. Kingsley (2000). "Role of the mouse ank gene in tissue calcification and arthritis." Science 289: 265-270.
 
DiLeone, R. J., G. A. Marcus, M. D. Johnson and D. M. Kingsley (2000). "Efficient studies of long-distance Bmp5 gene regulation using bacterial artificial chromosomes." Proc. Natl. Acad. Sci. (USA) 97: 1612-1617.
 
Clark, R. M., P. C. Marker and D. M. Kingsley (2000). "A novel candidate for mouse and human preaxial polydactyly with altered expression in limbs of Hemimelic extra toes mice." Genomics 67: 19-27.
 
Storm, E. E. and D. M. Kingsley (1999). "GDF5 coordinates bone and joint formation during digit development." Dev. Biol. 209: 11-27.
 
Kingsley, D. M. (1998). Bone morphogenetic proteins in the formation and repair of cartilage, bone, and joints. Skeletal growth and development: clinical issues and basic science advances. J. A. Buckwalter, M. G. Ehrlich, L. J. Sandell and S. B. Trippel. Rosemont, IL, American Academy of Orthopaedic Surgeons: 87-98.
 
DiLeone, R. J., L. B. Russell and D. M. Kingsley (1998). "An extensive 3' regulatory region controls expression of Bmp5 in specific anatomical structures of the mouse embryo." Genetics 148: 401-408.
 
Marker, P. C., K. Seung, A. E. Bland, L. B. Russell and D. M. Kingsley (1997). "Spectrum of Bmp5 mutations from germline mutagenesis experiments in mice." Genetics 145: 435-443.
 
DiLeone, R. J., J. A. King, E. E. Storm, N. G. Copeland, N. A. Jenkins and D. M. Kingsley (1997). "The Bmp8 gene is expressed in developing skeletal tissue and maps near the achondroplasia locus on mouse chromosome 4." Genomics 40: 196-198.
 
Storm, E. E. and D. M. Kingsley (1996). "Joint patterning defects caused by single and double mutations in members of the bone morphogenetic protein (BMP) family." Development 122: 3969-3979.
 
Mikic, B., M. C. H. van der Meulen, D. M. Kingsley and D. R. Carter (1996). "Mechanical and geometric changes in the growing femora of BMP-5 deficient mice." Bone 18: 601-607.
 
King, J. A., E. E. Storm, P. C. Marker, R. DiLeone and D. M. Kingsley (1996). "The role of BMPs and GDFs in development of region-specific skeletal structures." Annals New York Acad Sci 785: 70-79.
 
Mikic, B., M. C. H. van der Meulen, D. M. Kingsley and D. R. Carter (1995). "Long bone geometry and strength in adult BMP-5 deficient mice." Bone 16: 445-454.
 
Marker, P. C., J. A. King, N. G. Copeland, N. A. Jenkins and D. M. Kingsley (1995). "Chromosomal localization, embryonic expression, and imprinting tests for Bmp7 on distal mouse chromosome 2." Genomics 28: 576-580.
 
Avraham, K. B., T. Hasson, K. P. Steel, D. M. Kingsley, L. B. Russell, M. S. Mooseker, N. G. Copeland and N. A. Jenkins (1995). "The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells." Nat Genet 11(4): 369-375.
 
Storm, E. E., T. V. Huynh, N. G. Copeland, N. A. Jenkins, D. M. Kingsley and S.-L. Lee (1994). "Limb alterations in brachypodism mice due to mutations in a new member of the TGF-beta superfamily." Nature 368: 639-643.
 
Kingsley, D. M. (1994). "The TGF-beta superfamily: new members, new receptors, and new genetic tests of function in different organisms." Genes and Development 8: 133-146.
 
Kingsley, D. M. (1994). "What do BMPs do in mammals? Clues from the mouse short ear mutation." Trends Genet. 10: 16-21.
 
King, J. A., P. C. Marker, K. J. Seung and D. M. Kingsley (1994). "BMP5 and the molecular, skeletal, and soft-tissue alterations in short ear mice." Dev. Biol. 166: 112-122.
 
Imai, K. and D. M. Kingsley (1994). "Mouse chromosome 9." Mammalian Genome 5: S139-S153.
 
Kingsley, D. M. (1993). "Encylopedia of the mouse genome III: Mouse chromosome 9." Mammal Genome 4: S136-S153.
 
Kingsley, D. M., A. E. Bland, J. M. Grubber, P. C. Marker, L. B. Russell, N. G. Copeland and N. A. Jenkins (1992). "The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGF-? superfamily." Cell 71: 399-410.
 
Kingsley, D. M. (1992). "Mouse Chromosome 9." Mammalian Genome 3: S136-S152.
 
Kingsley, D. M. (1991). "Mouse Chromosome 9." Mammalian Genome 1: S127-S145.
 
Copeland, N. G., C. M. Silan, D. M. Kingsley, N. A. Jenkins, L. A. Cannizzaro, C. M. Croce, K. Huebner and J. E. Sims (1991). "Chromosomal location of murine and human IL-1 receptor genes." Genomics 9(1): 44-50.
 
Kingsley, D. M., E. M. Rinchik, L. B. Russell, H. P. Ottiger, J. G. Sutcliffe, N. G. Copeland and N. A. Jenkins (1990). "Genetic ablation of a mouse gene expressed specifically in brain." EMBO J 9(395): 395-399.
 
Freeman, M., J. Ashkenas, D. J. G. Rees, D. M. Kingsley, N. G. Copeland, N. A. Jenkins and M. Krieger (1990). "An ancient, highly conserved family of cysteine-rich protein domains revealed by cloning the type I and type II murine macrophage scavenger receptors." Proc. Natl. Acad. Sci. USA 87: 8810-8814.
 
Dickinson, M. E., M. S. Kobrin, C. M. Silan, D. M. Kingsley, M. J. Justice, D. A. Miller, J. D. Ceci, L. F. Lock, A. Lee, A. M. Buchberg, L. D. Siracusa, K. M. Lyons, R. Derynck, B. L. M. Hogan, N. G. Copeland and N. A. Jenkins (1990). "Chromosomal location of seven members of the murine TGF-? superfamily suggests close linkage to several morphogenetic mutant loci." Genomics 6: 505-520.
 
Ceci, J. D., D. M. Kingsley, C. M. Silan, N. G. Copeland and N. A. Jenkins (1990). "An interspecific backcross linkage map of the proximal half of mouse chromosome 14." Genomics 6(4): 673-678.
 
Regnier, D. C., C. A. Kozak, D. M. Kingsley, N. A. Jenkins, N. G. Copeland, W. Y. Langdon and H. C. Morse (1989). "Identification of two murine loci homologous to the v-cbl oncogene." J Virol 63: 3678-3682.
 
Krieger, M., P. Reddy, K. Kozarsky, D. Kingsley, L. Hobbie and M. Penman (1989). "Analysis of the synthesis, intracellular sorting, and function of glycoproteins using a mammalian cell mutant with reversible glycosylation defects." Methods Cell Biol 32(57): 57-84.
 
Kingsley, D. M., N. A. Jenkins and N. G. Copeland (1989). "A molecular genetic linkage map of mouse chromosome 9 with regional localizations for the Gsta, T3g, Ets-1, and Ldlr loci." Genetics 123(165): 165-172.
 
Jenkins, N. A., M. C. Storbel, P. K. Seperack, D. M. Kingsley, K. J. Moore, J. A. Mercer, L. B. Russell and N. G. Copeland (1989). "A retroviral insertion in the dilute (d) locus provides molecular access to this region of mouse Chromosome 9." Progr Nucl Acid Res Mol Biol 36(207): 207-220.
 
Kozarsky, K., D. Kingsley and M. Krieger (1988). "Use of a mutant cell line to study the kinetics and function of O-linked glycosylation of low density lipoprotein receptors." Proc Natl Acad Sci U S A 85(12): 4335-4339.
 
Hobbie, L., D. M. Kingsley, K. F. Kozarsky, R. W. Jackman and M. Krieger (1987). "Restoration of LDL receptor activity in mutant cells by intercellular junctional communication." Science 235(4784): 69-73.
 
Kingsley, D. M., R. D. Sege, K. F. Kozarsky and M. Krieger (1986). "DNA-mediated transfer of a human gene required for low-density lipoprotein receptor expression and for multiple Golgi processing pathways." Mol Cell Biol 6(7): 2734-2737.
 
Kingsley, D. M., M. Krieger and J. B. Holton (1986). "Structure and function of low-density-lipoprotein receptors in epimerase-deficient galactosemia [letter]." N Engl J Med 314(19): 1257-1258.
 
Kingsley, D. M., K. F. Kozarsky, M. Segal and M. Krieger (1986). "Three types of low density lipoprotein receptor-deficient mutant have pleiotropic defects in the synthesis of N-linked, O-linked, and lipid-linked carbohydrate chains." J Cell Biol 102(5): 1576-1585.
 
Kingsley, D. M., K. F. Kozarsky, L. Hobbie and M. Krieger (1986). "Reversible defects in O-linked glycosylation and LDL receptor expression in a UDP-Gal/UDP-GalNAc 4-epimerase deficient mutant." Cell 44(5): 749-759.
 
Kingsley, D. M. and M. Krieger (1984). "Receptor-mediated endocytosis of low density lipoprotein: somatic cell mutants define multiple genes required for expression of surface-receptor activity." Proc Natl Acad Sci U S A 81(17): 5454-5458.
 
Krieger, M., J. Martin, M. Segal and D. Kingsley (1983). "Amphotericin B selection of mutant Chinese hamster cells with defects in the receptor-mediated endocytosis of low density lipoprotein and cholesterol biosynthesis." Proc Natl Acad Sci U S A 80(18): 5607-5611.
Stanford University School of Medicine,  Department of Developmental Biology,  279 Capus Drive,  Beckman Center B300,  Stanford, CA,  94305-5329