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Sally Camper, Ph. D. - Publications

Affiliations: 
Human Genetics University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Pituitary developement
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141 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Cheung LYM, Menage L, Rizzoti K, Hamilton G, Dumontet T, Basham K, Daly AZ, Brinkmeier ML, Masser BE, Treier M, Cobb J, Delogu A, Lovell-Badge R, Hammer GD, Camper SA. Novel candidate regulators and developmental trajectory of pituitary thyrotropes. Endocrinology. PMID 37183548 DOI: 10.1210/endocr/bqad076  0.326
2023 Winningham AH, Camper SA. Pituitary Stem Cell Regulation by Zeb2 and BMP Signaling. Endocrinology. 164. PMID 36683433 DOI: 10.1210/endocr/bqad016  0.314
2022 Bando H, Brinkmeier ML, Castinetti F, Fang Q, Lee MS, Saveanu A, Albarel F, Dupuis C, Brue T, Camper SA. Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man. Human Molecular Genetics. PMID 35951005 DOI: 10.1093/hmg/ddac192  0.345
2020 Brinkmeier ML, Bando H, Camarano AC, Fujio S, Yoshimoto K, de Souza FSJ, Camper SA. Rathke's cleft-like cysts arise from Isl1 deletion in murine pituitary progenitors. The Journal of Clinical Investigation. PMID 32453714 DOI: 10.1172/JCI136745  0.314
2020 Bando H, Gergics P, Bohnsack BL, Toolan KP, Richter CE, Shavit JA, Camper SA. otx2b mutant zebrafish have pituitary, eye and mandible defects that model mammalian disease. Human Molecular Genetics. PMID 32277752 DOI: 10.1093/hmg/ddaa064  0.312
2020 Cheung L, Daly A, Brinkmeier M, Camper SA. OR16-05 Single-Cell Sequencing Identifies Novel Regulators of Thyrotrope Populations and POU1F1-Independent Thyroid-Stimulating Hormone Expression Journal of the Endocrine Society. 4. DOI: 10.1210/jendso/bvaa046.655  0.314
2020 Brinkmeier M, Camper SA. SAT-288 Pituitary Developmental Defects Caused by Haploinsufficiency for the Transcription Factor SIX3 Are Worsened by POU1F1 Deficiency Journal of the Endocrine Society. 4. DOI: 10.1210/jendso/bvaa046.634  0.384
2020 Dudley LA, Daley AZ, Mortensen AH, Sridhar R, Brinkmeier M, Cheung L, Camper SA. MON-715 How Heterogeneous Are Pituitary Thyrotropes? Journal of the Endocrine Society. 4. DOI: 10.1210/jendso/bvaa046.630  0.357
2020 Pereira Ferreira NGB, Madeira JLdO, Kertsz R, Gergics P, Benedetti AFF, Biscotto IP, Fang Q, Ma Q, Ozel BA, Li J, Camper SA, Jorge AAL, Mendonca BB, Arnhold IJ, Carvalho LRS. SAT-LB58 Molecular Investigation of Recessive Inheritance by Exome Sequencing of Patients With Congenital Hypopituitarism Journal of the Endocrine Society. 4. DOI: 10.1210/Jendso/Bvaa046.1986  0.306
2020 Vishnopolska SA, Braslavsky D, Keselman AC, Bergada I, Marino RM, Ramirez PC, Natalia PG, Ciaccio M, Palma MID, Belgorosky A, Miras M, Nicola JP, Mortensen AH, Martí MA, Camper SA, et al. MON-717 Novel GLI2 Mutations Identified in Pediatric Patients with Combined Pituitary Hormone Deficiency: One Gene, Various Genotypes Journal of the Endocrine Society. 4. DOI: 10.1210/Jendso/Bvaa046.1778  0.341
2020 Daly A, Cheung L, Brinkmeier M, Camper SA. MON-723 Identification of Thyrotrope Signature Genes and Regulatory Elements Journal of the Endocrine Society. 4. DOI: 10.1210/jendso/bvaa046.1660  0.315
2020 Bando H, Brinkmeier ML, Castinetti F, Gergics P, Mortensen AH, Ozel AB, Ma Q, Li JZ, Brue T, Camper SA. SAT-291 SIX3 Is Essential for Hypothalamic and Pituitary Development Journal of the Endocrine Society. 4. DOI: 10.1210/Jendso/Bvaa046.159  0.365
2020 Kertsz R, Ferreira N, Madeira JLom, Benedetti AFF, Azevedo B, Bissegatto DD, Camper S, Mendonca BB, Jorge A, Arnhold IJp, Carvalho LRS. SUN-723 CDH2 Gene Analysis in a Cohort of Patients with Congenital Hypopituitarism Journal of the Endocrine Society. 4. DOI: 10.1210/Jendso/Bvaa046.1223  0.35
2019 Sanguineti N, Scaglia P, Braslavsky D, Keselman A, Ballerini M, Ropelato M, Suco S, Kitzman J, Vishnopolska S, Marti M, Domene H, Rey R, Perez-Millan M, Camper S, Bergadá I. SUN-245 Heterozygous GH1 p.R209H Variant within a Large Pedigree May Mimic a Growth Hormone Insensitivity Pattern Journal of the Endocrine Society. 3. DOI: 10.1210/Js.2019-Sun-245  0.302
2019 Camper S, Brinkmeier M, Bando H, Fujio S, Yashimoto K, Camarano A, de Souza F. SAT-042 Pituitary Expression Of Isl1 Prevents Ectopic, Foxa1 And Foxj1 Mediated Differentiation Of Progenitors Into Rathke’S Cleft Cysts Journal of the Endocrine Society. 3. DOI: 10.1210/Js.2019-Sat-042  0.336
2018 Cheung LYM, George AS, McGee SR, Daly AZ, Brinkmeier ML, Ellsworth BS, Camper SA. Single-cell RNA sequencing reveals novel markers of male pituitary stem cells and hormone-producing cell-types. Endocrinology. PMID 30335147 DOI: 10.1210/En.2018-00750  0.307
2017 Home P, Kumar RP, Ganguly A, Saha B, Milano-Foster J, Bhattacharya B, Ray S, Gunewardena S, Paul A, Camper SA, Fields PE, Paul S. Genetic redundancy of GATA factors in extraembryonic trophoblast lineage ensures progression of both pre and postimplantation mammalian development. Development (Cambridge, England). PMID 28232602 DOI: 10.1242/Dev.145318  0.309
2016 Rubel CA, Wu SP, Lin L, Wang T, Lanz RB, Li X, Kommagani R, Franco HL, Camper SA, Tong Q, Jeong JW, Lydon JP, DeMayo FJ. A Gata2-Dependent Transcription Network Regulates Uterine Progesterone Responsiveness and Endometrial Function. Cell Reports. 17: 1414-1425. PMID 27783953 DOI: 10.1016/j.celrep.2016.09.093  0.31
2016 Mortensen AH, Camper SA. Cocaine-and Amphetamine Regulated Transcript (CART) Peptide Is Expressed in Precursor Cells and Somatotropes of the Mouse Pituitary Gland. Plos One. 11: e0160068. PMID 27685990 DOI: 10.1371/journal.pone.0160068  0.309
2016 Cheung LY, Okano H, Camper SA. Sox21 deletion in mice causes postnatal growth deficiency without physiological disruption of hypothalamic-pituitary endocrine axes. Molecular and Cellular Endocrinology. PMID 27616671 DOI: 10.1016/J.Mce.2016.09.005  0.329
2016 Gergics P, Christian HC, Choo MS, Ajmal A, Camper SA. Gene Expression in Mouse Thyrotrope Adenoma: Transcription Elongation Factor Stimulates Proliferation. Endocrinology. 157: 3631-46. PMID 27580811 DOI: 10.1210/en.2016-1183  0.381
2016 Pérez Millán MI, Brinkmeier ML, Mortensen AH, Camper SA. PROP1 triggers epithelial-mesenchymal transition-like process in pituitary stem cells. Elife. 5. PMID 27351100 DOI: 10.7554/eLife.14470  0.333
2016 Davis SW, Keisler JL, Pérez-Millán MI, Schade V, Camper SA. All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from Prop1 expressing progenitors. Endocrinology. en20151862. PMID 26812162 DOI: 10.1210/en.2015-1862  0.409
2015 Brinkmeier ML, Geister KA, Jones M, Waqas M, Maillard I, Camper SA. The Histone Methyltransferase Gene Absent, Small, or Homeotic Discs-1 Like Is Required for Normal Hox Gene Expression and Fertility in Mice. Biology of Reproduction. PMID 26333994 DOI: 10.1095/Biolreprod.115.131516  0.313
2015 Castinetti F, Brinkmeier ML, Mortensen AH, Vella KR, Gergics P, Brue T, Hollenberg AN, Gan L, Camper SA. ISL1 Is Necessary for Maximal Thyrotrope Response to Hypothyroidism. Molecular Endocrinology (Baltimore, Md.). 29: 1510-21. PMID 26296153 DOI: 10.1210/me.2015-1192  0.319
2015 Gergics P, Brinkmeier ML, Camper SA. Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia. Molecular Endocrinology (Baltimore, Md.). 29: 597-612. PMID 25668206 DOI: 10.1210/me.2014-1380  0.316
2015 Mortensen AH, Schade V, Lamonerie T, Camper SA. Deletion of OTX2 in neural ectoderm delays anterior pituitary development. Human Molecular Genetics. 24: 939-53. PMID 25315894 DOI: 10.1093/hmg/ddu506  0.34
2014 Chase J, Jones M, Brinkmeier M, Friedman A, Camper S, Maillard I. The Trithorax group gene Ash1l regulates quiescence, self-renewal potential and niche occupancy in adult hematopoietic stem cells Experimental Hematology. 42: S28. DOI: 10.1016/J.Exphem.2014.07.100  0.309
2013 de Pater E, Kaimakis P, Vink CS, Yokomizo T, Yamada-Inagawa T, van der Linden R, Kartalaei PS, Camper SA, Speck N, Dzierzak E. Gata2 is required for HSC generation and survival. The Journal of Experimental Medicine. 210: 2843-50. PMID 24297996 DOI: 10.1084/Jem.20130751  0.333
2013 Davis SW, Ellsworth BS, Peréz Millan MI, Gergics P, Schade V, Foyouzi N, Brinkmeier ML, Mortensen AH, Camper SA. Pituitary gland development and disease: from stem cell to hormone production. Current Topics in Developmental Biology. 106: 1-47. PMID 24290346 DOI: 10.1016/B978-0-12-416021-7.00001-8  0.346
2013 Pérez-Millán MI, Zeidler MG, Saunders TL, Camper SA, Davis SW. Efficient, specific, developmentally appropriate cre-mediated recombination in anterior pituitary gonadotropes and thyrotropes. Genesis (New York, N.Y. : 2000). 51: 785-92. PMID 23996951 DOI: 10.1002/dvg.22425  0.36
2011 Nasonkin IO, Ward RD, Bavers DL, Beuschlein F, Mortensen AH, Keegan CE, Hammer GD, Camper SA. Aged PROP1 deficient dwarf mice maintain ACTH production. Plos One. 6: e28355. PMID 22145038 DOI: 10.1371/Journal.Pone.0028355  0.729
2011 Castinetti F, Brinkmeier ML, Gordon DF, Vella KR, Kerr JM, Mortensen AH, Hollenberg A, Brue T, Ridgway EC, Camper SA. PITX2 AND PITX1 regulate thyrotroph function and response to hypothyroidism. Molecular Endocrinology (Baltimore, Md.). 25: 1950-60. PMID 21964592 DOI: 10.1210/me.2010-0388  0.357
2011 Mortensen AH, MacDonald JW, Ghosh D, Camper SA. Candidate genes for panhypopituitarism identified by gene expression profiling. Physiological Genomics. 43: 1105-16. PMID 21828248 DOI: 10.1152/Physiolgenomics.00080.2011  0.393
2010 Carvalho LR, Brinkmeier ML, Castinetti F, Ellsworth BS, Camper SA. Corepressors TLE1 and TLE3 interact with HESX1 and PROP1. Molecular Endocrinology (Baltimore, Md.). 24: 754-65. PMID 20181723 DOI: 10.1210/Me.2008-0359  0.337
2010 Davis SW, Castinetti F, Carvalho LR, Ellsworth BS, Potok MA, Lyons RH, Brinkmeier ML, Raetzman LT, Carninci P, Mortensen AH, Hayashizaki Y, Arnhold IJ, Mendonça BB, Brue T, Camper SA. Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes. Molecular and Cellular Endocrinology. 323: 4-19. PMID 20025935 DOI: 10.1016/J.Mce.2009.12.012  0.316
2009 Davis SW, Potok MA, Brinkmeier ML, Carninci P, Lyons RH, MacDonald JW, Fleming MT, Mortensen AH, Egashira N, Ghosh D, Steel KP, Osamura RY, Hayashizaki Y, Camper SA. Genetics, gene expression and bioinformatics of the pituitary gland. Hormone Research. 71: 101-15. PMID 19407506 DOI: 10.1159/000192447  0.339
2009 Mustapha M, Fang Q, Gong TW, Dolan DF, Raphael Y, Camper SA, Duncan RK. Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 1212-23. PMID 19176829 DOI: 10.1523/Jneurosci.4957-08.2009  0.335
2009 Nasonkin IO, Potok MA, Camper SA. Cre-mediated recombination in pituitary somatotropes. Genesis (New York, N.Y. : 2000). 47: 55-60. PMID 19039787 DOI: 10.1002/Dvg.20462  0.754
2008 Charles MA, Mortensen AH, Potok MA, Camper SA. Pitx2 deletion in pituitary gonadotropes is compatible with gonadal development, puberty, and fertility. Genesis (New York, N.Y. : 2000). 46: 507-14. PMID 18802953 DOI: 10.1002/Dvg.20398  0.661
2008 Egashira N, Minematsu T, Miyai S, Takekoshi S, Camper SA, Osamura RY. Pituitary changes in Prop1 transgenic mice: hormone producing tumors and signet-ring type gonadotropes. Acta Histochemica Et Cytochemica. 41: 47-57. PMID 18636109 DOI: 10.1267/ahc.08007  0.331
2008 Potok MA, Cha KB, Hunt A, Brinkmeier ML, Leitges M, Kispert A, Camper SA. WNT signaling affects gene expression in the ventral diencephalon and pituitary gland growth. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 1006-20. PMID 18351662 DOI: 10.1002/dvdy.21511  0.737
2008 Ellsworth BS, Butts DL, Camper SA. Mechanisms underlying pituitary hypoplasia and failed cell specification in Lhx3-deficient mice. Developmental Biology. 313: 118-29. PMID 18037398 DOI: 10.1016/J.Ydbio.2007.10.006  0.329
2007 Karolyi IJ, Dootz GA, Halsey K, Beyer L, Probst FJ, Johnson KR, Parlow AF, Raphael Y, Dolan DF, Camper SA. Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 596-608. PMID 17899304 DOI: 10.1007/S00335-007-9038-0  0.67
2007 Hughes ED, Qu YY, Genik SJ, Lyons RH, Pacheco CD, Lieberman AP, Samuelson LC, Nasonkin IO, Camper SA, Van Keuren ML, Saunders TL. Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 549-58. PMID 17828574 DOI: 10.1007/S00335-007-9054-0  0.703
2007 Ward RD, Davis SW, Cho M, Esposito C, Lyons RH, Cheng JF, Rubin EM, Rhodes SJ, Raetzman LT, Smith TP, Camper SA. Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 521-37. PMID 17557180 DOI: 10.1007/S00335-007-9008-6  0.311
2007 L'Honoré A, Coulon V, Marcil A, Lebel M, Lafrance-Vanasse J, Gage P, Camper S, Drouin J. Sequential expression and redundancy of Pitx2 and Pitx3 genes during muscle development. Developmental Biology. 307: 421-33. PMID 17540357 DOI: 10.1016/J.Ydbio.2007.04.034  0.3
2007 Hertzano R, Dror AA, Montcouquiol M, Ahmed ZM, Ellsworth B, Camper S, Friedman TB, Kelley MW, Avraham KB. Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system. The European Journal of Neuroscience. 25: 999-1005. PMID 17331196 DOI: 10.1111/J.1460-9568.2007.05332.X  0.341
2007 Savage JJ, Mullen RD, Sloop KW, Colvin SC, Camper SA, Franklin CL, Rhodes SJ. Transgenic mice expressing LHX3 transcription factor isoforms in the pituitary: effects on the gonadotrope axis and sex-specific reproductive disease. Journal of Cellular Physiology. 212: 105-17. PMID 17311285 DOI: 10.1002/Jcp.21010  0.346
2006 Ellsworth BS, Egashira N, Haller JL, Butts DL, Cocquet J, Clay CM, Osamura RY, Camper SA. FOXL2 in the pituitary: molecular, genetic, and developmental analysis. Molecular Endocrinology (Baltimore, Md.). 20: 2796-805. PMID 16840539 DOI: 10.1210/Me.2005-0303  0.385
2006 Gong TW, Karolyi IJ, Macdonald J, Beyer L, Raphael Y, Kohrman DC, Camper SA, Lomax MI. Age-related changes in cochlear gene expression in normal and shaker 2 mice. Journal of the Association For Research in Otolaryngology : Jaro. 7: 317-28. PMID 16794912 DOI: 10.1007/S10162-006-0046-7  0.322
2006 Kanzaki S, Beyer L, Karolyi IJ, Dolan DF, Fang Q, Probst FJ, Camper SA, Raphael Y. Transgene correction maintains normal cochlear structure and function in 6-month-old Myo15a mutant mice. Hearing Research. 214: 37-44. PMID 16580798 DOI: 10.1016/J.Heares.2006.01.017  0.704
2006 Ward RD, Stone BM, Raetzman LT, Camper SA. Cell proliferation and vascularization in mouse models of pituitary hormone deficiency. Molecular Endocrinology (Baltimore, Md.). 20: 1378-90. PMID 16556738 DOI: 10.1210/me.2005-0409  0.315
2006 Charles MA, Saunders TL, Wood WM, Owens K, Parlow AF, Camper SA, Ridgway EC, Gordon DF. Pituitary-specific Gata2 knockout: effects on gonadotrope and thyrotrope function. Molecular Endocrinology (Baltimore, Md.). 20: 1366-77. PMID 16543408 DOI: 10.1210/Me.2005-0378  0.636
2006 Vesper AH, Raetzman LT, Camper SA. Role of prophet of Pit1 (PROP1) in gonadotrope differentiation and puberty. Endocrinology. 147: 1654-63. PMID 16384867 DOI: 10.1210/en.2005-1080  0.387
2006 Potok MA, Cha KB, Hunt A, Brinkmeier ML, Kispert A, Camper SA. Wnt genes affect patterning of the ventral diencephalon and pituitary gland growth Developmental Biology. 295: 456. DOI: 10.1016/j.ydbio.2006.04.404  0.718
2006 Davis S, Camper S. Gonadotrope cell specification in the pituitary gland Developmental Biology. 295: 413. DOI: 10.1016/J.Ydbio.2006.04.269  0.374
2005 Charles MA, Suh H, Hjalt TA, Drouin J, Camper SA, Gage PJ. PITX genes are required for cell survival and Lhx3 activation. Molecular Endocrinology (Baltimore, Md.). 19: 1893-903. PMID 15761027 DOI: 10.1210/Me.2005-0052  0.754
2005 Ward RD, Raetzman LT, Suh H, Stone BM, Nasonkin IO, Camper SA. Role of PROP1 in pituitary gland growth. Molecular Endocrinology (Baltimore, Md.). 19: 698-710. PMID 15591534 DOI: 10.1210/Me.2004-0341  0.801
2004 Nasonkin IO, Ward RD, Raetzman LT, Seasholtz AF, Saunders TL, Gillespie PJ, Camper SA. Pituitary hypoplasia and respiratory distress syndrome in Prop1 knockout mice. Human Molecular Genetics. 13: 2727-35. PMID 15459176 DOI: 10.1093/Hmg/Ddh311  0.722
2004 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: 951-60. PMID 15177549 DOI: 10.1016/J.Ygeno.2003.12.020  0.743
2004 Cha KB, Douglas KR, Potok MA, Liang H, Jones SN, Camper SA. WNT5A signaling affects pituitary gland shape. Mechanisms of Development. 121: 183-94. PMID 15037319 DOI: 10.1016/J.Mod.2003.12.002  0.8
2004 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 Developmental Biology. 265: 329-340. PMID 14732396 DOI: 10.1016/j.ydbio.2003.09.033  0.35
2003 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. Human Molecular Genetics. 12: 2797-805. PMID 12966030 DOI: 10.1093/Hmg/Ddg308  0.808
2003 Brinkmeier ML, Potok MA, Cha KB, Gridley T, Stifani S, Meeldijk J, Clevers H, Camper SA. TCF and Groucho-related genes influence pituitary growth and development. Molecular Endocrinology (Baltimore, Md.). 17: 2152-61. PMID 12907761 DOI: 10.1210/Me.2003-0225  0.762
2003 Suszko MI, Lo DJ, Suh H, Camper SA, Woodruff TK. Regulation of the rat follicle-stimulating hormone beta-subunit promoter by activin. Molecular Endocrinology (Baltimore, Md.). 17: 318-32. PMID 12554780 DOI: 10.1210/Me.2002-0081  0.618
2002 Raetzman LT, Ward R, Camper SA. Lhx4 and Prop1 are required for cell survival and expansion of the pituitary primordia. Development (Cambridge, England). 129: 4229-39. PMID 12183375  0.351
2002 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. American Journal of Medical Genetics. 111: 27-30. PMID 12124729 DOI: 10.1002/Ajmg.10473  0.653
2002 Suh H, Gage PJ, Drouin J, Camper SA. Pitx2 is required at multiple stages of pituitary organogenesis: pituitary primordium formation and cell specification. Development (Cambridge, England). 129: 329-37. PMID 11807026  0.659
2001 Douglas KR, Brinkmeier ML, Kennell JA, Eswara P, Harrison TA, Patrianakos AI, Sprecher BS, Potok MA, Lyons RH, MacDougald OA, Camper SA. Identification of members of the Wnt signaling pathway in the embryonic pituitary gland. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 843-51. PMID 11845287 DOI: 10.1007/S00335-001-2076-0  0.779
2001 Cushman LJ, Camper SA. Molecular basis of pituitary dysfunction in mouse and human. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 485-94. PMID 11420609 DOI: 10.1007/S003350040002  0.809
2001 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 (New York, N.Y. : 2000). 30: 65-9. PMID 11416865 DOI: 10.1002/Gene.1034  0.795
2001 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. Human Molecular Genetics. 10: 1141-53. PMID 11371507 DOI: 10.1093/Hmg/10.11.1141  0.802
2001 Seasholtz AF, Burrows HL, Karolyi IJ, Camper SA. Mouse models of altered CRH-binding protein expression. Peptides. 22: 743-51. PMID 11337087 DOI: 10.1016/S0196-9781(01)00387-4  0.669
2001 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 (Cambridge, England). 128: 147-54. PMID 11124111  0.813
2000 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. Journal of Neurocytology. 29: 227-40. PMID 11276175 DOI: 10.1023/A:1026515619443  0.666
2000 Douglas KR, Camper SA. Partial transcriptome of the developing pituitary gland. Genomics. 70: 335-46. PMID 11161784 DOI: 10.1006/Geno.2000.6400  0.776
2000 Cushman LJ, Burrows HL, Seasholtz AF, Lewandoski M, Muzyczka N, Camper SA. Cre-mediated recombination in the pituitary gland. Genesis (New York, N.Y. : 2000). 28: 167-74. PMID 11105060 DOI: 10.1002/1526-968X(200011/12)28:3/4<167::Aid-Gene120>3.0.Co;2-N  0.814
2000 Cushman LJ, Burrows HL, Seasholtz AF, Lewandoski M, Muzyczka N, Camper SA. Mouse embryonic stem (ES) cell lines established from neuronal cell-derived cloned blastocysts Genesis. 28: 156-163. PMID 11105058 DOI: 10.1002/1526-968X(200011/12)28:3/4<156::Aid-Gene100>3.0.Co;2-T  0.765
2000 Martin DM, Probst FJ, Camper SA, Petty EM. Characterisation and genetic mapping of a new X linked deafness syndrome. Journal of Medical Genetics. 37: 836-41. PMID 11073537 DOI: 10.1136/Jmg.37.11.836  0.658
2000 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. Human Molecular Genetics. 9: 1729-38. PMID 10915760 DOI: 10.1093/Hmg/9.12.1729  0.696
1999 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, et al. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Genomics. 61: 243-58. PMID 10552926 DOI: 10.1006/Geno.1999.5976  0.717
1999 Burrows HL, Douglas KR, Seasholtz AF, Camper SA. Genealogy of the Anterior Pituitary Gland: Tracing a Family Tree. Trends in Endocrinology and Metabolism: Tem. 10: 343-352. PMID 10511693 DOI: 10.1016/S1043-2760(99)00189-7  0.79
1999 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. Proceedings of the National Academy of Sciences of the United States of America. 96: 11595-600. PMID 10500222 DOI: 10.1073/Pnas.96.20.11595  0.693
1999 Gage PJ, Suh H, Camper SA. Dosage requirement of Pitx2 for development of multiple organs Development. 126: 4643-4651. PMID 10498698  0.559
1999 Probst FJ, Camper SA. The role of mouse mutants in the identification of human hereditary hearing loss genes. Hearing Research. 130: 1-6. PMID 10320095 DOI: 10.1016/S0378-5955(98)00231-7  0.689
1999 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. PMID 10049592 DOI: 10.1006/Geno.1998.5669  0.69
1999 Gage PJ, Suh H, Camper SA. The bicoid-related Pitx gene family in development Mammalian Genome. 10: 197-200. PMID 9922405 DOI: 10.1007/S003359900970  0.585
1998 Kulig E, Camper SA, Kuecker S, Jin L, Lloyd RV. Remodeling of Hyperplastic Pituitaries in Hypothyroid us-Subunit Knockout Mice After Thyroxine and 1713-Estradiol Treatment: Role of Apoptosis. Endocrine Pathology. 9: 261-274. PMID 12114718  0.304
1998 Watkins-Chow DE, Camper SA. How many homeobox genes does it take to make a pituitary gland? Trends in Genetics. 14: 284-289. PMID 9676531 DOI: 10.1016/S0168-9525(98)01476-0  0.354
1998 Brinkmeier ML, Gordon DF, Dowding JM, Saunders TL, Kendall SK, Sarapura VD, Wood WM, Ridgway EC, Camper SA. Cell-specific expression of the mouse glycoprotein hormone α-subunit gene requires multiple interacting DNA elements in transgenic mice and cultured cells Molecular Endocrinology. 12: 622-633. PMID 9605925  0.345
1998 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 (New York, N.Y.). 280: 1447-51. PMID 9603736 DOI: 10.1126/Science.280.5368.1447  0.684
1998 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 (New York, N.Y.). 280: 1444-7. PMID 9603735 DOI: 10.1126/Science.280.5368.1444  0.706
1998 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, ... ... Camper SA, et al. Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2. American Journal of Human Genetics. 62: 904-15. PMID 9529344 DOI: 10.1086/301786  0.69
1998 Burrows HL, Nakajima M, Lesh JS, Goosens KA, Samuelson LC, Inui A, Camper SA, Seasholtz AF. Excess corticotropin releasing hormone-binding protein in the hypothalamic-pituitary-adrenal axis in transgenic mice. The Journal of Clinical Investigation. 101: 1439-47. PMID 9525987 DOI: 10.1172/Jci1963  0.702
1997 Lesh JS, Burrows HL, Seasholtz AF, Camper SA. Mapping of the mouse corticotropin-releasing hormone receptor 2 gene (Crhr2) to chromosome 6. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 944-5. PMID 9383293 DOI: 10.1007/S003359900644  0.71
1997 Watkins-Chow DE, Douglas KR, Buckwalter MS, Probst FJ, Camper SA. Construction of a 3-Mb contig and partial transcript map of the central region of mouse chromosome 11. Genomics. 45: 147-57. PMID 9339371 DOI: 10.1006/Geno.1997.4931  0.792
1997 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. PMID 9226367 DOI: 10.1006/geno.1997.4781  0.336
1997 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 Human Molecular Genetics. 6: 457-464. PMID 9147650 DOI: 10.1093/Hmg/6.3.457  0.375
1997 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 with human chromosome 5. Genomics. 40: 114-22. PMID 9070927 DOI: 10.1006/Geno.1996.4532  0.792
1996 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. Molecular Endocrinology (Baltimore, Md.). 10: 1570-81. PMID 8961267 DOI: 10.1210/Mend.10.12.8961267  0.399
1996 Burrows HL, Birkmeier TS, Seasholtz AF, Camper SA. Targeted ablation of cells in the pituitary primordia of transgenic mice. Molecular Endocrinology (Baltimore, Md.). 10: 1467-77. PMID 8923471 DOI: 10.1210/Mend.10.11.8923471  0.712
1995 Sorenson RC, Primo-Parmo SL, Camper SA, La Du BN. The genetic mapping and gene structure of mouse paraoxonase/arylesterase. Genomics. 30: 431-8. PMID 8825627 DOI: 10.1006/geno.1995.1261  0.312
1995 Zheng X, Saunders TL, Camper SA, Samuelson LC, Ginsburg D. Vitronectin is not essential for normal mammalian development and fertility Proceedings of the National Academy of Sciences of the United States of America. 92: 12426-12430. PMID 8618914 DOI: 10.1073/Pnas.92.26.12426  0.304
1995 Gage PJ, Lossie AC, Scarlett LM, Lloyd RV, Camper SA. Ames dwarf mice exhibit somatotrope commitment but lack growth hormone-releasing factor response Endocrinology. 136: 1161-1167. PMID 7867569 DOI: 10.1210/Endo.136.3.7867569  0.709
1995 Lossie AC, Haugen BR, Wood WM, Camper SA, Gordon DF. Chromosomal localization of the large subunit of mouse replication factor C in the mouse and human Mammalian Genome. 6: 58-59. PMID 7719032 DOI: 10.1007/Bf00350900  0.671
1995 Burrows HL, Seasholtz AF, Camper SA. Localization of the corticotropin-releasing hormone receptor gene on mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 55-6. PMID 7719029 DOI: 10.1007/Bf00350896  0.707
1995 Camper SA, Saunders TL, Kendall SK, Keri RA, Seasholtz AF, Gordon DF, Birkmeier TS, Keegan CE, Karolyi IJ, Roller ML, Burrows HL, Samuelson LC. Implementing transgenic and embryonic stem cell technology to study gene expression, cell-cell interactions and gene function Biology of Reproduction. 52: 246-257. PMID 7711194 DOI: 10.1095/Biolreprod52.2.246  0.733
1995 Roller ML, Camper SA. Localization of the thyrotropin-releasing hormone gene, Trh, on mouse Chromosome 6 Mammalian Genome. 6: 443-444. PMID 7647472 DOI: 10.1007/BF00355651  0.314
1995 Roller ML, Lossie AC, Koken MHM, Smit EME, Hagemeijer A, Camper SA. Localization of sequences related to the human RAD6 DNA repair gene on mouse Chromosomes 11 and 13 Mammalian Genome. 6: 305-306. PMID 7613042 DOI: 10.1007/Bf00352425  0.679
1994 Lossie AC, Vandenbergh DJ, Uhl GR, Camper SA. Localization of the dopamine transporter gene, Dat1, on mouse chromosome 13. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: 117-8. PMID 8180472 DOI: 10.1007/Bf00292340  0.661
1994 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 alpha 1 subunit of the inhibitory glycine receptor in the spasmodic mouse. Nature Genetics. 7: 131-5. PMID 7920629 DOI: 10.1038/Ng0694-131  0.642
1994 Zhu W, Lossie AC, Camper SA, Gumucio DL. Chromosomal localization of the transcription factor YY1 in the mouse and human Mammalian Genome. 5: 234-236. PMID 7912122 DOI: 10.1007/Bf00360552  0.626
1994 Buckwalter MS, Cook SA, Davisson MT, White WF, Camper SA. A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death. Human Molecular Genetics. 3: 2025-30. PMID 7874121 DOI: 10.1093/Hmg/3.11.2025  0.619
1994 Lossie AC, Eipper BA, Hand TA, Camper SA. Localization of the peptidylglycine alpha-amidating monooxygenase gene (Pam) introduces a region of homology between human chromosome 5q and mouse chromosome 1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: 738-9. PMID 7873888 DOI: 10.1007/Bf00426085  0.684
1994 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. Molecular and Cellular Neurosciences. 5: 505-14. PMID 7704423 DOI: 10.1006/Mcne.1994.1062  0.313
1994 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 α-subunit transgene in thyrotropes, gonadotropes, and developing pituitary gland Molecular Endocrinology. 8: 1420-1433. PMID 7531821 DOI: 10.1210/me.8.10.1420  0.344
1993 Gay D, Saunders T, Camper S, Weigert M. Receptor editing: an approach by autoreactive B cells to escape tolerance. The Journal of Experimental Medicine. 177: 999-1008. PMID 8459227 DOI: 10.1084/Jem.177.4.999  0.308
1993 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: 279-86. PMID 8406478 DOI: 10.1006/geno.1993.1322  0.677
1993 Lossie AC, Buckwalter MS, Camper SA. Lysyl oxidase (Lox) maps between Grl-1 and Adrb-2 on mouse chromosome 18. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 177-8. PMID 8094989 DOI: 10.1007/Bf00352234  0.762
1993 Lossie AC, Gordon DF, Camper SA. Localization of thyrotropin-releasing hormone receptor and thyrotroph embryonic factor on mouse Chromosome 15 Mammalian Genome. 4: 621-623. PMID 7903570 DOI: 10.1007/Bf00361398  0.707
1992 Buchberg AM, Buckwalter MS, Camper SA. Mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 3: S162-81. PMID 1498430 DOI: 10.1007/BF00648429  0.626
1992 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 & Differentiation : the Molecular Biology Journal of the American Association For Cancer Research. 3: 577-588. PMID 1419909  0.583
1992 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: An in situ hybridization analysis American Journal of Pathology. 141: 895-906. PMID 1415483  0.306
1992 Vacher J, Camper SA, Krumlauf R, Compton RS, Tilghman SM. raf regulates the postnatal repression of the mouse α-fetoprotein gene at the posttranscriptional level Molecular and Cellular Biology. 12: 856-864. PMID 1370712  0.752
1992 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. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 3: 604-7. PMID 1358285 DOI: 10.1007/Bf00350629  0.754
1991 Buckwalter MS, Katz RW, Camper SA. Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backcross. Genomics. 10: 515-26. PMID 1889803 DOI: 10.1016/0888-7543(91)90430-M  0.683
1991 Buchberg AM, Moskow JJ, Buckwalter MS, Camper SA. Mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 1: S158-91. PMID 1799798 DOI: 10.1007/BF00656492  0.623
1991 Camper SA, Tilghman SM. The activation and silencing of gene transcription in the liver Biotechnology (Reading, Mass.). 16: 81-87. PMID 1706634  0.52
1991 Kendall SK, Saunders TL, Jin L, Lloyd RV, Glode LM, Nett TM, Keri RA, Nilson JH, Camper SA. Targeted ablation of pituitary gonadotropes in transgenic mice. Molecular Endocrinology (Baltimore, Md.). 5: 2025-36. PMID 1665205 DOI: 10.1210/Mend-5-12-2025  0.372
1990 Camper SA, Saunders TL, Katz RW, Reeves RH. The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation Genomics. 8: 586-590. PMID 1981057 DOI: 10.1016/0888-7543(90)90050-5  0.421
1989 Camper SA, Godbout R, Tilghman SM. The developmental regulation of albumin and alpha-fetoprotein gene expression. Progress in Nucleic Acid Research and Molecular Biology. 36: 131-43. PMID 2471987 DOI: 10.1016/S0079-6603(08)60167-1  0.618
1989 Camper SA, Tilghman SM. Postnatal repression of the alpha-fetoprotein gene is enhancer independent Genes & Development. 3: 537-546. PMID 2470646  0.589
1987 Hammer RE, Krumlauf R, Camper SA, Brinster RL, Tilghman SM. Diversity of Alpha-Fetoprotein gene expression in mice is generated by a combination of separate enhancer elements Science. 235: 53-58. PMID 2432657 DOI: 10.1126/Science.2432657  0.584
1986 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 Advances in Experimental Medicine and Biology. 205: 281-299. PMID 3466513 DOI: 10.1007/978-1-4684-5209-9_13  0.64
1986 Hammer RE, Krumlauf R, Camper S, Brinster RL, Tilghman SM. The regulation of α-foetoprotein minigene expression in the germline of mice Journal of Embryology and Experimental Morphology. 97: 257-262. PMID 2442281  0.541
1985 Camper SA, Yao YAS, Rottman FM. Hormonal regulation of the bovine prolactin promoter in rat pituitary tumor cell Journal of Biological Chemistry. 260: 12246-12251. PMID 2995368  0.636
1984 Camper SA, Albers RJ, Coward JK, Rottman FM. Effect of undermethylation on mRNA cytoplasmic appearance and half-life. Molecular and Cellular Biology. 4: 538-43. PMID 6201720  0.52
1984 Camper SA, Luck DN, Yao Y, Woychik RP, Goodwin RG, Lyons RH, Rottman FM. Characterization of the bovine prolactin gene Dna. 3: 237-249. PMID 6086257  0.592
1983 Nilson JH, Fink PA, Virgin JB, Cserbak MT, Camper SA, Rottman FM. Developmental expression of growth hormone and prolactin genes in the bovine pituitary. The Journal of Biological Chemistry. 258: 4565-70. PMID 6687594  0.586
1982 Woychik RP, Camper SA, Lyons RH, Horowitz S, Goodwin EC, Rottman FM. Cloning and nucleotide sequencing of the bovine growth hormone gene Nucleic Acids Research. 10: 7197-7210. PMID 6296767 DOI: 10.1093/nar/10.22.7197  0.602
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