Cha KB, Karolyi IJ, Hunt A, Wenglikowski AM, Wilkinson JE, Dolan DF, Dootz G, Finnegan AA, Seasholtz AF, Hankenson KD, Siracusa LD, Camper SA. Skeletal dysplasia and male infertility locus on mouse chromosome 9. Genomics;83(6):951-60, 2004. [abstract]

Cha KB, Douglas KR, Potok MA, Liang H, Jones SN, Camper SA. WNT5A signaling affects pituitary gland shape. Mech Dev; 121(2):183-94, 2004. [abstract]

Camper SA. Sox3 and sexual dysfunction: it's in the head.  Nat Genet;36(3):217-9, 2004. [abstract]

Martin DM, Skidmore JM, Philips ST, Vieira C, Gage PJ, Condie BG, Raphael Y, Martinez S, Camper SA. PITX2 is required for normal development of neurons in the mouse subthalamic nucleus and midbrain. Dev Biol;267(1):93-108, 2004. [abstract]

Raetzman LT, Ross SA, Cook S, Dunwoodie SL, Camper SA, Thomas PQ. Developmental regulation of Notch signaling genes in the embryonic pituitary: Prop1 deficiency affects Notch2 expression. Dev Biol;265(2):329-40, 2004. [abstract] [cover]

Karolyi IJ, Probst FJ, Beyer L, Odeh H, Dootz G, Cha KB, Martin DM, Avraham KB, Kohrman D, Dolan DF, Raphael Y, Camper SA. Myo15 function is distinct from Myo6, Myo7a, and pirouette genes in development of cochlear stereocilia. Hum Mol Genet;12(21):2797-805, 2003[abstract] [cover]

Ben-Yosef T, Belyantseva IA, Saunders TL, Hughes ED, Kawamoto K, Van Itallie CM, Beyer LA, Halsey K, Gardner DJ, Wilcox ER,
Rasmussen J,Anderson JM, Dolan DF, Forge A, Raphael Y, Camper SA, Friedman TB. Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. Hum Mol Genet;12(16):2049-61, 2003. [abstract] [cover]

Brinkmeier ML, Potok MA, Cha KB, Gridley T, Stifani S, Meeldijk J, Clevers H, Camper SA. TCF4 and groucho-related genes influence pituitary growth and development. Mol Endocrinol;17(11):2152-61, 2003. [abstract]

Raetzman LT, Camper SA. Beyond big and small mice: applications of mouse molecular genetics in endocrinology. Trends Endocrinol Metab; 14:204-5,2003. [abstract]

Keegan CE, Camper SA. Mouse knockout solves endocrine puzzle and promotes new pituitary lineage model. Genes Dev; 15;17(6):677-82,2003. [abstract]

Suszko MI, Lo DJ, Suh H, Camper SA, Woodruff TK. Regulation of the rat follicle-stimulating hormone beta-subunit promoter by activin. Mol Endocrinol;17;318-32,2003.[abstract]

Marcil A, Dumontier E, Chamberland M, Camper SA, Drouin J. Pitx1 and Pitx2 are required for development of hindlimb buds. Development;130:45-55, 2003.[abstract]

Martin DM, Skidmore JM, Fox SE, Gage PJ, Camper SA. Pitx2 distinguishes subtypes of terminally differentiated neurons in the developing mouse neuroepithelium. Dev Biol ;252:84-99, 2002.[abstract]

Raetzman LT, Ward R, Camper SA. Lhx4 and Prop1 are required for cell survival and expansion of the pituitary primordia.
Development ;129:4229-39, 2002.[abstract]

Martin DM, Probst FJ, Fox SE, Schimmenti LA, Semina EV, Hefner MA, Belmont JW, Camper SA. Exclusion of PITX2 mutations as a major cause of CHARGE association. Am J Med Genet ;111:27-30, 2002.[abstract]

Kanzaki S, Ogawa K, Camper SA, Raphael Y. Transgene expression in neonatal mouse inner ear explants mediated by first and advanced generation adenovirus vectors. Hear Res;169:112-20, 2002.[abstract]

Suh H, Gage PJ, Drouin J, Camper SA. Pitx2 is required at multiple stages of pituitary organogenesis: pituitary primordium formation and cell specification. Development ;129:329-37, 2002.[abstract]

Nadeau JH, Balling R, Barsh G, Beier D, Brown SD, Bucan M, Camper S, Carlson G, Copeland N, Eppig J, Fletcher C, Frankel WN, Ganten D, Goldowitz D, Goodnow C, Guenet JL, Hicks G, de Angelis MH, Jackson I, Jacob HJ, Jenkins N, Johnson D, Justice M, Kay S, Kingsley D, Lehrach H, Magnuson T, Meisler M, Poustka A, Rinchik EM, Rossant J, Russell LB, Schimenti J, Shiroishi T, Skarnes WC, Soriano P, Stanford W, Takahashi JS, Wurst W, Zimmer A. Sequence interpretation. Functional annotation of mouse genome sequences. Science 291:1251-5,2001.[abstract]

Brinkmeier ML, Stahl JH, Gordon DF, Ross BD, Sarapura VD, Dowding JM, Kendall SK, Lloyd RV, Ridgway EC, Camper SA. Thyroid hormone-responsive pituitary hyperplasia independent of somatostatin receptor 2. Mol Endocrinol 15:2129-36, 2001.[abstract]

Douglas KR, Brinkmeier ML, Kennell JA, Eswara P, Harrison TA, Patrianakos AI, Sprecher BS, Potok MA, Lyons RH Jr, MacDougald OA, Camper SA. Identification of members of the Wnt signaling pathway in the embryonic pituitary gland. Mamm Genome 12:843-51,2001.[abstract][cover]

Cushman LJ, Camper SA. Molecular basis of pituitary dysfunction in mouse and human. Mamm Genome 12:485-94,2001.[abstract]

Zhao L, Bakke M, Krimkevich Y, Cushman LJ, Parlow AF, Camper SA, Parker KL. Hypomorphic phenotype in mice with pituitary-specific knockout of steroidogenic factor 1. Genesis 30:65-9,2001.[abstract]

Cushman LJ, Watkins-Chow DE, Brinkmeier ML, Raetzman LT, Radak AL, Lloyd RV, Camper SA. Persistent Prop1 expression delays gonadotrope differentiation and enhances pituitary tumor susceptibility. Hum Mol Genet 10:1141-53, 2001.[abstract]

Seasholtz AF, Burrows HL, Karolyi IJ, Camper SA. Mouse models of altered CRH-binding protein expression. Peptides 22:743-51, 2001.[abstract]

Beyer LA, Odeh H, Probst FJ, Lambert EH, Dolan DF, Camper SA, Kohrman DC, Raphael Y. Hair cells in the inner ear of the pirouette and shaker 2 mutant mice. J Neurocytol 29:227-40,2000.[abstract][cover]

Douglas KR, Camper SA. Partial transcriptome of the developing pituitary gland. Genomics 70:335-46,2000.[abstract]

Zhao L, Bakke M, Krimkevich Y, Cushman LJ, Parlow AF, Camper SA, Parker KL. Steroidogenic factor 1 (SF1) is essential for pituitary gonadotrope function. Development 128:147-54,2001.[abstract]

Cushman LJ, Burrows HL, Seasholtz AF, Lewandoski M, Muzyczka N, Camper SA. Cre-mediated recombination in the pituitary gland. Genesis ;28:167-74,2000.[abstract]

Martin DM, Probst FJ, Camper SA, Petty EM. Characterisation and genetic mapping of a new X linked deafness syndrome. J Med Genet 37:836-41,2000.[abstract]

Anderson DW, Probst FJ, Belyantseva IA, Fridell RA, Beyer L, Martin DM, Wu D, Kachar B, Friedman TB, Raphael Y, Camper SA. The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells. Hum Mol Genet 9:1729-38,2000.[abstract][cover]

Brown NS, Smart A, Sharma V, Brinkmeier ML, Greenlee L, Camper SA, Jensen DR, Eckel RH, Krezel W, Chambon P, Haugen BR. Thyroid hormone resistance and increased metabolic rate in the RXR-gamma-deficient mouse. J Clin Invest 106:73-9,2000.[abstract]

Friedman TB, Hinnant JT, Fridell RA, Wilcox ER, Raphael Y, Camper SA. DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15. Adv Otorhinolaryngol 56:131-44,2000.[abstract]

Liang Y, Wang A, Belyantseva IA, Anderson DW, Probst FJ, Barber TD, Miller W, Touchman JW, Jin L, Sullivan SL, Sellers JR, Camper SA, Lloyd RV, Kachar B, Friedman TB, Fridell RA. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Genomics 61:243-58,1999.[abstract[cover]

Burrows HL, Douglas KR, Seasholtz AF, Camper SA. Genealogy of the Anterior Pituitary Gland: Tracing a Family Tree. Trends Endocrinol Metab 10:343-352,1999.[abstract][cover]

Karolyi IJ, Burrows HL, Ramesh TM, Nakajima M, Lesh JS, Seong E, Camper SA, Seasholtz AF. Altered anxiety and weight gain in corticotropin-releasing hormone-binding protein-deficient mice. Proc Natl Acad Sci U S A 96:11595-600,1999.[abstract]

Gage PJ, Suh H, Camper SA. Dosage requirement of Pitx2 for development of multiple organs. Development 126:4643-51,1999.[abstract]

Probst FJ, Camper SA. The role of mouse mutants in the identification of human hereditary hearing loss genes. Hear Res 130:1-6,1999.[abstract]

Stahl JH, Kendall SK, Brinkmeier ML, Greco TL, Watkins-Chow DE, Campos-Barros A, Lloyd RV, Camper SA. Thyroid hormone is essential for pituitary somatotropes and lactotropes. Endocrinology 140:1884-92,1999.[abstract]

Probst FJ, Chen KS, Zhao Q, Wang A, Friedman TB, Lupski JR, Camper SA. A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2). Genomics 55:348-52,1999.[abstract]

Gage PJ, Suh H, Camper SA. The bicoid-related Pitx gene family in development. Mamm Genome10:197-200,1999.[abstract][cover]

Yu RN, Ito M, Saunders TL, Camper SA, Jameson JL. Role of Ahch in gonadal development and gametogenesis. Nat Genet 20:353-7,1998.[abstract]

Watkins-Chow DE, Camper SA. How many homeobox genes does it take to make a pituitary gland? Trends Genet 14:284-90,1998.[abstract]

Wang A, Liang Y, Fridell RA, Probst FJ, Wilcox ER, Touchman JW, Morton CC, Morell RJ, Noben-Trauth K, Camper SA, Friedman TB. Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. Science 280:1447-51,1998.[abstract]

Probst FJ, Fridell RA, Raphael Y, Saunders TL, Wang A, Liang Y, Morell RJ, Touchman JW, Lyons RH, Noben-Trauth K, Friedman TB, Camper SA. Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. Science 280:1444-7,1998.[abstract]

Liang Y, Wang A, Probst FJ, Arhya IN, Barber TD, Chen KS, Deshmukh D, Dolan DF, Hinnant JT, Carter LE, Jain PK, Lalwani AK, Li XC, Lupski JR, Moeljopawiro S, Morell R, Negrini C, Wilcox ER, Winata S, Camper SA, Friedman TB.
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2. Am J Hum Genet 62:904-915,1998. [abstract]

Watkins-Chow DE, Douglas KR, Buckwalter MS, Probst FJ, Camper SA. Construction of a 3 Mb contig and transcript map of the central region of Mouse Chromosome 11. Genomics 45:147-157,1997. [abstract]

Brinkmeier ML, Camper SA. Localization of somatostatin receptor genes on mouse chromosomes 2, 11, 12, 15 and 17; correlation with growth QTLs. Genomics 43: 9-14, 1997. [abstract]

Gage PJ, Camper SA. Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation. Hum Mol Genet 6:457-64, 1997. [abstract]

Watkins-Chow DE, Buckwalter MS, Newhouse MM, Lossie AC, Brinkmeier ML, Camper SA. Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation and human chromosome 5. Genomics 40:114-22, 1997. [abstract]

Watkins-Chow D, Roller M, Newhouse MM, Buchberg AM, Camper SA. Mouse Chromosome 11. Mamm Genome 6 Spec No:S201-S220, 1996. [abstract]

Gage PJ, Brinkmeier ML, Scarlett LM, Knapp LT, Camper SA Mahon KA. The Ames dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage specific cell proliferation. Mol Endocrinol 10:1570-81, 1996. [abstract]

Burrows HL, Birkmeier TS, Seasholtz AF, Camper SA. Targeted ablation of cells in the pituitary primordia of transgenic mice. Mol Endocrinol 10:1467-77, 1996. [abstract][cover]

Maly P, Thall AD, Petryniak B, Rogers CE, Smith PL, Marks RM, Kelly RJ, Gersten KM, Cheng G, Saunders TL, Camper SA, Camphousen RT, Sullivan FX, Isogai Y, Hindsgaul O, von Andrian UH, Lowe JB. The Fuc-TVII a(1,3)fucosyltransferase locus controls lymphocyte homing and blood leukocyte emigration through an essential role in L-, E-, and P-selectin ligand expression. Cell 86: 643-53, 1996. [abstract]

Greco TL, Sussman DJ, Camper SA. Dishevelled-2 maps to human Chromosome 17 and distal to Wnt3a and vestigial tail (vt) on mouse Chromosome 11. Mamm Genome 7:475-476, 1996. [abstract]

Chiang PW, Baldacci PA, Babinet C, Camper SA, Watkins-Chow D, Baker DD, Tsai CH, Ramamoorthy S, King E, Slack AC, Fogel E, Morahan G, Ashworth A, Blackburn CC, Kurnit DM. Linkage mapping of murine homologue of the yeast SPT6 gene to MMU11B1. Mamm Genome 7:459-60, 1996. [abstract]

Greco TL, Takada S, Newhouse MM, McMahon JA, McMahon AP, Camper SA. Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development. Genes Dev 10: 313-324, 1996. [abstract]

Gage PJ, Roller ML, Saunders TL, Scarlett LM, Camper SA. Anterior pituitary cells defective in the cell-autonomous factor, df, undergo cell lineage specification but not expansion. Development 122: 151-160, 1996. [abstract]

Camper SA, Saunders TL, Kendall SK, Keri RA, Seasholtz AF, Gordon DF, Birkmeier TS, Keegan CE, Karolyi IJ, Roller ML, Burrows HL and Samuelson LC. Implementing transgenic and embryonic stem cell technology to study gene expression, cell-cell interactions and gene function. Biol Reprod 52: 246-257, 1995. [abstract]

Sorenson RC, Primo-Parmo SL, Camper SA, La Du BN. The genetic mapping and gene structure of mouse paraoxonase/arylesterase.Genomics 30: 431-438, 1995. [abstract]

Zheng X, Saunders TL, Camper SA, Samuelson LC, Ginsburg D. Vitronectin is not essential for normal mammalian development and fertility. Proc Natl Acad Sci USA 92: 12426-12430, 1995. [abstract]

Spicer AP, Roller ML, Camper SA, McPherson JC, Wasmuth JJ, Hakim SH, Wang C, Turley EA, McDonald JA. The human and mouse receptors for hyaluronan-mediated motility, RHAMM, genes (HMMR) map to human chromosome 5q33.2-qter and mouse chromosome 11. Genomics 30: 115-117, 1995. [abstract]

Kendall SK, Samuelson LC, Saunders TL, Wood RI, Camper SA. Targeted disruption of the pituitary glycoprotein hormone a-subunit produces hypogonadal and hypothyroid mice. Genes Dev 9: 2007-2019, 1995. [abstract]

Radic MZ, Ibrahim SM, Rauch J, Camper SA, Weigert M. Constitutive secretion of transgene-encoded IgG2b autoantibodies leads to symptoms of autoimmune disease. J Immunol 155:3213-3222, 1995. [abstract]

Roller ML, Camper SA. Localization of the thyrotropin-releasing hormone gene Trh, on mouse Chromosome 6. Mamm Genome 6: 443-444, 1995. [abstract]

Gage PJ, Lossie AC, Scarlett LM, Lloyd RV and Camper SA. Ames dwarf mice exhibit somatotrope commitment but lack growth hormone-releasing factor response. Endocrinology 136: 1161-1167, 1995. [abstract]

Roller ML, Lossie AC, Koken MHM, Smit EME, Hagemeijer A and Camper SA. Localization of sequences related to the human RAD6 DNA repair gene on mouse Chromosomes 11 and 13. Mamm Genome 6: 305, 1995. [abstract]

Roller ML and Camper SA. Chromosomal localization of the zinc finger protein 15, Zfp15, on mouse chromosome 4. Mamm Genome 6: 305, 1995. [abstract]

Chen C, Nagy Z, Radic MZ, Hardy RR, Huszar D, Camper SA, Weigert M. The site and stage of anti-DNA B-cell deletion. Nature 373: 252-255, 1995. [abstract]

Lossie AC, Haugen BR, Wood WM, Camper SA and Gordon DF. Chromosomal localization of the large subunit of mouse replication factor C in the mouse and human. Mamm Genome 6: 58-59, 1995. [abstract]

Burrows HL, Seasholtz AF and Camper SA. Localization of the corticotropin-releasing hormone receptor gene on mouse Chromosome 11. Mamm Genome 6: 55-56, 1995.[abstract]
 

Kalcheva I, Plass C, Sait S, Eddy R, Shows T, Watkins-Chow D, Camper S, Shibata H, Ueda T, Takagi N, Hayashizaki Y and Chapman V. Comparative mapping of the imprinted U2afbprs gene on mouse chromosome 11 and human chromosome 5. Cytogenet Cell Genet 68:19-24, 1995.[abstract]

Lossie AC, MacPhee M, Buchberg AM and Camper SA. Mouse chromosome 11. Mamm Genome 5 Spec No:S164-S180, 1994.[abstract]

Buckwalter MS, Cook SA, Davisson MT, White WF, Camper SA. A frameshift mutation in the mouse a1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death. Hum Mol Genet 3:2025-2030, 1994. [abstract][cover]

Keegan CA, Karolyi IJ, Burrows HL, Camper SA, Seasholtz AF. Homologous recombination in fertilized mouse eggs and assessment of heterologous locus control region function. Transgenics 1:439-449, 1994.

Zhu W, Lossie AC, Camper SA, Gumucio DL. Chromosomal localization of the transcription factor Yyl in the mouse and the human. Mamm Genome 5:234-236, 1994 [abstract]

Keri RA, Wolfe MW, Saunders TL, Anderson I, Kendall SK, Wagner T, Yeung J, Gorski J, Nett TM, Camper SA, Nilson JH. The proximal promoter of the bovine luteinizing hormone b-subunit gene confers gonadotrope-specific expression and regulation by gonadotropin-releasing hormone, testosterone, and 17b-estradiol in transgenic mice. Mol Endocrinol 8:1807-1816, 1994.[abstract]

Kendall SK, Gordon DF, Birkmeier TS, Petrey D, Sarapura VD, O'Shea KS, Wood WM, Lloyd RV, Ridgway EC, Camper SA. Enhancer-mediated high level expression of mouse pituitary glycoprotein hormone alpha-subunit transgene in thyrotropes, gonadotropes, and developing pituitary gland. Mol Endocrinol 8:1420-1433, 1994. [abstract]

Lossie AC, Eipper BA, Hand TA, Camper SA. Localization of the peptidylgycine a-amidating monooxygenase gene (Pam) introduces a region of homology between human chromosome 5q and mouse chromosome 1. Mamm Genome 5:738-739, 1994. [abstract]

Keegan CE, Karolyi IJ, Knapp LT, Bourbonais FJ, Camper SA, Seasholtz AF. Expression of corticotropin-releasing hormone transgenes in neurons of adult and developing mice. Mol Cell Neurosci 5:505-514, 1994. [abstract]

Chen C, Radic MZ, Erikson J, Camper SA, Litwin S, Hardy RR, Weigert M. Deletion and editing of B cells that express antibodies to DNA. J Immunol 152:1970-1982, 1994. [abstract]

Ryan SG, Buckwalter MS, Lynch JW, Handford CA, Segura L, Shiang R, Wasmuth JJ, Camper SA, Schofield P, O'Connell P. A missense mutation in the gene encoding the a1 subunit of the inhibitory glycine receptor in the spasmodic mouse. Nat Genet 7:131-135, 1994. [abstract][cover]

Keegan CE, Herman JP, Karolyi IJ, O'Shea KS, Camper SA, Seasholtz AF. Differential expression of corticotropin-releasing hormone in developing mouse embryos and adult brain. Endocrinology 134:2547-2555, 1994. [abstract]

Lossie AC, Vandenberg DJ, Uhl GR, Camper SA. Localization of the dopamine transporter gene, Dat1, on mouse chromosome 13. Mamm Genome 5:117-118, 1994. [abstract]

Buchberg AM, Camper SA. Mouse chromosome 11. Mamm Genome 4 Spec No:S164-175, 1993. [abstract]

Shlomchik MJ, Zharhary D, Saunders T, Camper SA, Weigert MG. A rheumatoid factor transgenic mouse model of autoantibody regulation. Int Immunol 5:1329-1341, 1993. [abstract]

Buckwalter MS, Testa CM, Noebels JL, Camper SA. Genetic mapping and evaluation of candidate genes for spasmodic, a neurological mouse mutation with abnormal startle response. Genomics 17:279-286, 1993. [abstract]

Knapp LT, Keegan CE, Seasholtz AF, Camper SA. Corticotropin-releasing hormone (Crh) maps to mouse chromosome 3. Mamm Genome 4:615-617, 1993. [abstract]

Lossie AC, Gordon DF, Camper SA. Localization of thyrotropin-releasing hormone receptor and thyrotroph embryonic factor on mouse chromosome 15. Mamm Genome 4:621-623, 1993. [abstract]

Lloyd RV, Jin L, Kulig E, Thiny MT, Fields K, Landefeld TD, Camper SA. Pit-1/GHF-1 transcription factor expression in normal, hyperplastic and neoplastic rodent pituitaries. Endocr Pathol 4:146-154, 1993.

Gay D, Saunders T, Camper S, Weigert M. Receptor editing: an approach by autoreactive B cells to escape tolerance. J Exp Med 177:999-1008, 1993. [abstract]

Lossie AC, Buckwalter MS, Camper SA. Lysyl oxidase (Lox) maps between Grl-1 and Adrb-2 on mouse chromosome 18. Mamm Genome 4:177-178, 1993. [abstract]

Westbrook C, Neuman W, Wasmuth J, Camper S, Platke R, Weber J, Wood S, Williamson R. Report from the Second International Workshop on Human Chromosome 5. Cytogenet Cell Genet 61:225-242, 1992. [abstract]

Buchberg AM, Buckwalter MS, Camper SA. Mouse Chromosome 11. Mamm Genome 3:S162-S181, 1992. [abstract]

Lloyd RV, Jin L, Chang A, Kulig E, Camper SA, Ross BD, Downs TR, Frohman LA. Morphologic effects of hGRH gene expression on the pituitary, liver and pancreas of MT-hGRH transgenic mice. Am J Pathol 141:895-906, 1992. [abstract]

Hu JM, Camper SA, Tilghman SM, Miller T, Georgoff I, Serra R, Isom HC. Functional analyses of albumin expression in a series of hepatocyte cell lines and in primary hepatocytes. Cell Growth Differ 3:577-588, 1992. [abstract]

Buckwalter MS, Lossie AC, Scarlett LM, Camper SA. Localization of the human chromosome 5q genes Gabra-1, Gabrg-2, Il-4, Il-5 and Irf-1 on mouse chromosome 11. Mamm Genome 3:604-607, 1992. [abstract]

Vacher J, Camper SA, Krumlauf R, Compton RS, Tilghman SM. Raf regulates the postnatal repression of the mouse -fetoprotein gene at the post-transcriptional level. Mol Cell Biol 12:856-864, 1992. [abstract]

Karolyi IJ, Guenet J-L, Rey-Campos, J, Camper SA. The gene coding for variant hepatic nuclear factor 1 (Tcf-2) maps between the Edp-1 and Erba genes on mouse chromosome 11. Mamm Genome 3:184-185, 1992. [abstract]

Buchberg AM, Moskow J, Buckwalter MS, Camper SA. Mouse Chromosome 11. Mamm Genome 1 Spec No:S158-191, 1991. [abstract]

Kendall SK, Saunders TL, Jin L, Lloyd RV, Glode LM, Nett TM, Keri RA, Nilson JH and Camper SA. Targeted ablation of pituitary gonadotropes in transgenic mice. Mol Endocrinol 5:2025-2036, 1991. [abstract][cover]

Seasholtz AF, Bourbonais FJ, Harnden CE, Camper SA. Nucleotide sequence and expression of the mouse corticotropin-releasing hormone gene. Mol Cell Neurosci 2:266-273, 1991

Carmack CE, Camper SA, Mackle JJ, Gerhard WU, Weigert MG. Influence of a Vk8 light chain transgene on endogenous gene rearrangements and the immune response to the Ha(SB) determinant on influenza virus. J Immunol 147:2024-2033, 1991. [abstract]

Buckwalter MS, Katz RW, Camper SA. Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backcross. Genomics 10:515-526, 1991. [abstract]

Camper SA, Tilghman SM. Activation and silencing of gene transcription in the liver. Biotechnology 16:81-87, 1991. [abstract]

Erikson J, Radic MZ, Camper SA, Hardy RR, Carmack C, Weigert M. Expression of anti-DNA immunoglobulin transgenes in non-autoimmune mice. Nature 8:331-334, 1991. [abstract]

Camper SA, Tilghman SM. Activation and silencing of gene transcription in the liver. IN: Transgenic Animals (First NL, Haseltine FP, eds.), Butterworth-Heinemann, Boston, 1990.

Camper SA, Saunders T, Katz RW, Reeves R. The Pit-1 transcription factor is a candidate gene for the Snell dwarf mutation. Genomics 8:586-590, 1990. [abstract]

Camper SA, Godbout R, Tilghman SM. The developmental regulation of albumin and a-fetoprotein gene expression. Prog Nucleic Acid Res 36:131-143, 1989. [abstract]

Camper SA, Tilghman SM. Postnatal repression of a-fetoprotein is enhancer-independent. Genes Dev 3:547-558, 1989. [abstract]

Camper SA, Krumlauf F, Compton RA, Hammer RE, Brinster R, Tilghman SM. Expression of the alpha-fetoprotein gene in transgenic mice. IN: Gene Transfer Vectors for Mammalian Cells. Banbury Report: Current Communications in Molecular Biology, CSH press, 1987.

Camper SA. Research applications of transgenic mice. Biotechniques 5:638-650, 1987.

Hammer RE, Krumlauf R, Camper SA, Brinster R, Tilghman SM. Diversity of a-fetoprotein gene expression in mice is generated by a combination of enhancer elements. Science 235:53-58, 1987. [abstract]

Rottman F, Narayan P, Goodwin R, Camper S, Yao Y, Horowitz A, Albers R, Ayers D, Maroney P, Nilsen T. Distribution of m6A in mRNA and its possible biological role. IN: Biological Methylation and Drug Design (Borchardt RT, Creveling CR and Ueland PM, eds.), Humana Press, 1986.

Hammer RE, Krumlauf R, Camper S, Brinster RL, Tilghman SM. The regulation of alpha-fetoprotein minigene expression in the germline of mice. J Embryol Exp Morpol 97:257-262, 1986. [abstract]

Rottman F, Camper S, Goodwin E, Hampson R, Lyons R, Sakai D, Woychik R, Yao Y. Structure and regulated expression of bovine prolactin and bovine growth hormone genes. Adv Exp Med Biol 205:281-99, 1986. [abstract]

Camper SA, Yao Y, Rottman FM. Hormonal regulation of the bovine prolactin promoter in rat pituitary tumor cells. J Biol Chem 260:12246-12251, 1985. [abstract]

Rottman FM, Camper SA, Woychik RP. Role of posttranscriptional RNA modification in the maintenance of eucaryotic mRNA levels. IN: Gene Expression: The Translational Step and its Control (Clark, BFC, ed.) Munksgaard Int. Publ. Ltd., Denmark, 1984.

Camper SA, Luck DN, Yao Y, Woychik R, Goodwin R, Lyons R, Rottman FM. Characterization of the bovine prolactin gene. DNA 3:237-249, 1984. [abstract]

Camper SA, Albers RJ, Coward JK, Rottman FM. Effect of undermethylation of mRNA cytoplasmic appearance and half-life. Mol Cell Biol 4:538-543, 1984. [abstract]

Nilson JH, Fink PA, Virgin JB, Cserbak M, Camper SA, Rottman FM. Developmental expression of growth hormone and prolactin genes in the bovine pituitary. J Biol Chem 258:4565-4570, 1983. [abstract]

Woychik RP, Camper SA, Lyons, Jr., RH, Horowitz S, Goodwin EC, Rottman FM. Cloning and nucleotide sequence of the bovine growth hormone gene. Nucleic Acids Res 10:7197-7210, 1982. [abstract]

Meslar HW, Camper SA, White III, HB. Biotin binding protein from egg yolk. J Biol Chem 253:6979-6982, 1978.[abstract]