S. Camper

S. Tilghman, S. Camper, I. Georgoff, 1992, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

Identification of pituitary thyrotrope signature genes and regulatory elements

Stephen C. J. Parker, S. Liebhaber, S. Camper, 2020, bioRxiv.

Deafness and Permanently Reduced Potassium Channel Gene Expression and Function in Hypothyroid Pit1dw Mutants

Y. Raphael, M. Mustapha, S. Camper, 2009, The Journal of Neuroscience.

Sequential expression and redundancy of Pitx2 and Pitx3 genes during muscle development.

Philip Gage, Alexandre Marcil, J. Drouin, 2007, Developmental biology.

Genetic Background of Prop1df Mutants Provides Remarkable Protection Against Hypothyroidism-Induced Hearing Impairment

M. Mustapha, S. Camper, D. Dolan, 2011, Journal of the Association for Research in Otolaryngology.

Altered anxiety and weight gain in corticotropin-releasing hormone-binding protein-deficient mice.

S. Camper, A. Seasholtz, I. Karolyi, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Pitx2 distinguishes subtypes of terminally differentiated neurons in the developing mouse neuroepithelium.

Donna M. Martin, S. Camper, P. Gage, 2002, Developmental biology.

Mouse Chromosome 11

S. Camper, M. Buckwalter, A. Buchberg, 2004, Mammalian Genome.

Aged PROP1 Deficient Dwarf Mice Maintain ACTH Production

F. Beuschlein, G. Hammer, S. Camper, 2011, PloS one.

Cloning and nucleotide sequencing of the bovine growth hormone gene.

S. Camper, R. Lyons, F. Rottman, 1982, Nucleic acids research.

raf regulates the postnatal repression of the mouse alpha-fetoprotein gene at the posttranscriptional level

J. Vacher, S. Tilghman, S. Camper, 1992 .

Cell proliferation and vascularization in mouse models of pituitary hormone deficiency.

S. Camper, L. Raetzman, R. Ward, 2006, Molecular endocrinology.

Targeted ablation of cells in the pituitary primordia of transgenic mice.

S. Camper, A. Seasholtz, H. L. Burrows, 1996, Molecular endocrinology.

Postnatal repression of the alpha-fetoprotein gene is enhancer independent.

S. Tilghman, S. Camper, 1989, Genes & development.

Morphologic effects of hGRH gene expression on the pituitary, liver, and pancreas of MT-hGRH transgenic mice. An in situ hybridization analysis.

B. Ross, L. Jin, R. Lloyd, 1992, The American journal of pathology.

Thyroid hormone-responsive pituitary hyperplasia independent of somatostatin receptor 2.

B. Ross, R. Lloyd, S. Camper, 2001, Molecular endocrinology.

Pit-1/ghf-1 transcription factor expression in rodent pituitaries

R. Lloyd, S. Camper, E. Kulig, 1993, Endocrine Pathology.

Mouse chromosome 11

J. Moskow, S. Camper, M. Buckwalter, 2004, Mammalian Genome.

SHORT COMMUNICATION The Pit4 Transcription Factor Gene Is a Candidate for the Murine Snell Dwarf Mutation

S. Camper, T. Saunders, R. W. Katz, 1990 .

Noggin regulates Bmp4 activity during pituitary induction.

S. Camper, S. Davis, 2007, Developmental biology.

Birthdating studies reshape models for pituitary gland cell specification.

S. Camper, A. Mortensen, S. Davis, 2011, Developmental biology.

Dishevelled-2 maps to human Chromosome 17 and distal to Wnt3a and vestigial tail (vt) on mouse Chromosome 11

S. Camper, D. Sussman, T. L. Greco, 1996, Mammalian Genome.

All Hormone-Producing Cell Types of the Pituitary Intermediate and Anterior Lobes Derive From Prop1-Expressing Progenitors.

S. Camper, M. Pérez-Millán, S. Davis, 2016, Endocrinology.

Cre‐mediated recombination in pituitary somatotropes

S. Camper, I. Nasonkin, M. A. Potok, 2009, Genesis.

Regulation of pituitary stem cells by epithelial to mesenchymal transition events and signaling pathways

S. Camper, M. Brinkmeier, L. Cheung, 2017, Molecular and Cellular Endocrinology.

Transgenic mice expressing LHX3 transcription factor isoforms in the pituitary: Effects on the gonadotrope axis and sex‐specific reproductive disease

S. Rhodes, R. Mullen, S. C. Colvin, 2007, Journal of cellular physiology.

Localization of sequences related to the human RAD6 DNA repair gene on mouse Chromosomes 11 and 13

A. Hagemeijer, S. Camper, A. Lossie, 1995, Mammalian Genome.

Skeletal dysplasia and male infertility locus on mouse chromosome 9.

S. Camper, L. Siracusa, A. Seasholtz, 2004, Genomics.

Localization of the dopamine transporter gene, Dat1, on mouse Chromosome 13

G. Uhl, S. Camper, A. Lossie, 1994, Mammalian Genome.

Lysyl oxidase (Lox) maps between Grl-1 and Adrb-2 on mouse Chromosome 18

S. Camper, M. Buckwalter, A. Lossie, 2004, Mammalian Genome.

Localization of thyrotropin-releasing hormone receptor and thyrotroph embryonic factor on mouse Chromosome 15

S. Camper, A. Lossie, D. Gordon, 2004, Mammalian Genome.

Corticotropin-releasing hormone (Crh) maps to mouse Chromosome 3

S. Camper, C. Keegan, A. Seasholtz, 2004, Mammalian Genome.

Exclusion of PITX2 mutations as a major cause of CHARGE association.

Donna M. Martin, J. Belmont, S. Camper, 2002, American journal of medical genetics.

Contributors

Lily Q. Dong, Armando R. Tovar, S. Sealfon, 1988, International Journal of Technology Assessment in Health Care.

OR06-06 Pituitary Tumors and Immortalized Cell Lines Generated by Cre-Inducible Expression of SV40 T-Antigen

S. Camper, A. Mortensen, Alexandre Z. Daly, 2020, Endocrinology.

otx2b mutant zebrafish have pituitary, eye and mandible defects that model mammalian disease.

S. Camper, J. Shavit, Brenda L. Bohnsack, 2020, Human molecular genetics.

Characterisation and genetic mapping of a new X linked deafness syndrome

D. M. Martin, E. Petty, S. Camper, 2000, Journal of medical genetics.

Biology of Pituitary Stem Cells

S. Camper, M. Millán, L. Cheung, 2021 .

Remodeling of hyperplastic pituitaries in hypothyroid α-subunit knockout mice after thyroxine and 17β-estradiol treatment: Role of apoptosis

R. Lloyd, S. Camper, E. Kulig, 1998, Endocrine pathology.

Pituitary-specific Gata2 knockout: effects on gonadotrope and thyrotrope function.

S. Camper, K. Owens, W. Wood, 2006, Molecular endocrinology.

Hormonal regulation of the bovine prolactin promoter in rat pituitary tumor cells.

S. Camper, F. Rottman, Y. Yao, 1985, The Journal of biological chemistry.

Vitronectin is not essential for normal mammalian development and fertility.

S. Camper, D. Ginsburg, L. Samuelson, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Mouse models of altered CRH-binding protein expression

S. Camper, A. Seasholtz, I. Karolyi, 2001, Peptides.

ISL1 Is Necessary for Maximal Thyrotrope Response to Hypothyroidism.

S. Camper, A. Hollenberg, M. Brinkmeier, 2015, Molecular endocrinology.

Effect of undermethylation on mRNA cytoplasmic appearance and half-life

S. Camper, F. Rottman, J. Coward, 1984, Molecular and cellular biology.

The role of alkaline phosphatase in cartilage mineralization.

A. G. Taylor, S. Camper, I. Shapiro, 1992, Bone and mineral.

Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum

Jun Z. Li, S. Camper, L. Montenegro, 2021, Genes.

Comparative Exome Capture Methods to Investigate Genes Involved in Hypopituitarism in a Brazilian Population

Jun Z. Li, S. Camper, A. Tahira, 2021 .

A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2).

J. Lupski, T. Friedman, S. Camper, 1999, Genomics.

Persistent expression of Notch2 delays gonadotrope differentiation.

Bayly S. Wheeler, S. Camper, S. Ross, 2006, Molecular endocrinology.

Ames dwarf mice exhibit somatotrope commitment but lack growth hormone-releasing factor response.

R. Lloyd, S. Camper, A. Lossie, 1995, Endocrinology.

Targeted ablation of pituitary gonadotropes in transgenic mice.

L. Jin, R. Lloyd, S. Camper, 1991, Molecular endocrinology.

Comprehensive identification of pathogenic gene variants in patients with neuroendocrine disorders.

J. Kitzman, S. Camper, I. Bergadá, 2021, The Journal of clinical endocrinology and metabolism.

Mechanisms underlying pituitary hypoplasia and failed cell specification in Lhx3-deficient mice.

B. Ellsworth, S. Camper, Darcy L. Butts, 2008, Developmental biology.

The Biology of Pituitary Stem Cells

S. Camper, M. Millán, 2014 .

Excess corticotropin releasing hormone-binding protein in the hypothalamic-pituitary-adrenal axis in transgenic mice.

S. Camper, A. Inui, A. Seasholtz, 1998, The Journal of clinical investigation.

p.R209H GH1 variant challenges short stature assessment.

S. Camper, R. Rey, I. Bergadá, 2019, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

19th International Mouse Genome Conference

S. Camper, J. Dackor, N. Solomon, 2006, Mammalian Genome.

PITX2 AND PITX1 regulate thyrotroph function and response to hypothyroidism.

S. Camper, A. Hollenberg, M. Brinkmeier, 2011, Molecular endocrinology.

The regulation of α-foetoprotein minigene expression in the germline of mice

R. Krumlauf, R. Hammer, S. Tilghman, 1986 .

Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development.

M M Newhouse, A. McMahon, S. Camper, 1996, Genes & development.

A missense mutation in the gene encoding the α1 subunit of the inhibitory glycine receptor in the spasmodic mouse

P. O'Connell, P. Schofield, R. Shiang, 1994, Nature Genetics.

A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death.

W. White, S. Camper, M. Davisson, 1994, Human molecular genetics.

Biotin-binding protein from egg yolk. A protein distinct from egg white avidin.

S. Camper, H. B. White, H. W. Meslar, 1978, The Journal of biological chemistry.

The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells.

Y. Raphael, D. W. Anderson, L. Beyer, 2000, Human molecular genetics.

The role of mouse mutants in the identification of human hereditary hearing loss genes

S. Camper, F. Probst, 1999, Hearing Research.

The Developmental Regulation of Albumin and α-Fetoprotein Gene Expression

R. Godbout, S. Tilghman, S. Camper, 1989 .

The α(1,3)Fucosyltransferase Fuc-TVII Controls Leukocyte Trafficking through an Essential Role in L-, E-, and P-selectin Ligand Biosynthesis

Petr Malý, Ole Hindsgaul, Sally A Camper, 1996, Cell.

Gene Expression in Mouse Thyrotrope Adenoma: Transcription Elongation Factor Stimulates Proliferation.

H. Christian, S. Camper, P. Gergics, 2016, Endocrinology.

Enhancer-mediated high level expression of mouse pituitary glycoprotein hormone alpha-subunit transgene in thyrotropes, gonadotropes, and developing pituitary gland.

D F Gordon, R. Lloyd, S. Camper, 1994, Molecular endocrinology.

Targeted disruption of the pituitary glycoprotein hormone alpha-subunit produces hypogonadal and hypothyroid mice.

R. Wood, S. Camper, L. Samuelson, 1995, Genes & development.

Gonadal defects and hormonal alterations in transgenic mice expressing a single chain human chorionic gonadotropin-lutropin receptor complex.

S. Camper, T. Meehan, D. Puett, 2005, Journal of molecular endocrinology.

Role of prophet of Pit1 (PROP1) in gonadotrope differentiation and puberty.

S. Camper, L. Raetzman, Amanda H. Vesper, 2006, Endocrinology.

raf regulates the postnatal repression of the mouse alpha-fetoprotein gene at the posttranscriptional level

R. Krumlauf, J. Vacher, S. Tilghman, 1992, Molecular and cellular biology.

Pitx2 deletion in pituitary gonadotropes is compatible with gonadal development, puberty, and fertility

S. Camper, A. Mortensen, M. A. Potok, 2008, Genesis.

Diversity of alpha-fetoprotein gene expression in mice is generated by a combination of separate enhancer elements.

R. Krumlauf, R. Hammer, S. Tilghman, 1987, Science.

Single-Cell RNA Sequencing Reveals Novel Markers of Male Pituitary Stem Cells and Hormone-Producing Cell Types

B. Ellsworth, S. Camper, M. Brinkmeier, 2018, Endocrinology.

Developmental regulation of Notch signaling genes in the embryonic pituitary: Prop1 deficiency affects Notch2 expression.

S. Dunwoodie, S. Camper, S. Ross, 2004, Developmental Biology.

Next generation sequencing panel based on single molecule molecular inversion probes for detecting genetic variants in children with hypopituitarism

Juan P. Bustamante, J. Kitzman, S. Camper, 2018, Molecular genetics & genomic medicine.

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

C. Morton, J. Touchman, T. Friedman, 1998, Science.

GATA2 controls lymphatic endothelial cell junctional integrity and lymphovenous valve morphogenesis through miR-126

J. D. Engel, S. Camper, B. Cha, 2019, Development.

Mouse Full-Length cDNA Encyclopedia Targeting a Complex Transcriptome: The Construction of the

M. Fagiolini, T. Hensch, W. Pavan, 2006 .

Pitx1 and Pitx2 are required for development of hindlimb buds

J. Drouin, S. Camper, Alexandre Marcil, 2003, Development.

Advances in Skeletal Dysplasia Genetics.

Sally A Camper, S. Camper, Krista A. Geister, 2015, Annual review of genomics and human genetics.

Rathke's cleft-like cysts arise from Isl1 deletion in murine pituitary progenitors.

S. Camper, K. Yoshimoto, M. Brinkmeier, 2020, The Journal of clinical investigation.

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

Y. Raphael, J. Touchman, T. Friedman, 1998, Science.

Dosage requirement of Pitx2 for development of multiple organs.

S. Camper, P. Gage, H. Suh, 1999, Development.

Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation.

S. Camper, P. Gage, 1997, Human molecular genetics.

SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice

U. Francke, P. Cohen, S. Camper, 2008, PloS one.

Pituitary stem cell update and potential implications for treating hypopituitarism.

S. Camper, T. Brue, F. Castinetti, 2011, Endocrine reviews.

Role of PROP1 in pituitary gland growth.

S. Camper, I. Nasonkin, H. Suh, 2005, Molecular endocrinology.

Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans

M. Dattani, I. Robinson, J. Blackburn, 2021, Nature Communications.

BRAF mutations disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mouse and humans 1

M. Dattani, I. Robinson, J. Blackburn, 2021 .

The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation.

S. Camper, R. Reeves, T. Saunders, 1990, Genomics.

Molecular basis of pituitary dysfunction in mouse and human

S. Camper, Sally A. Camper, Lisa J. Cushman, 2001, Mammalian Genome.

Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2.

W. Miller, D. W. Anderson, J. Touchman, 1999, Genomics.

Pituitary hypoplasia and respiratory distress syndrome in Prop1 knockout mice.

S. Camper, I. Nasonkin, A. Seasholtz, 2004, Human molecular genetics.

Mouse Chromosome 11

S. Camper, M. Buckwalter, A. Buchberg, 2004, Mammalian Genome.

Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5.

D. Watkins-Chow, S. Camper, M. Buckwalter, 1997, Genomics.

Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.

J. Lupski, T. Barber, T. Friedman, 1998, American journal of human genetics.

Construction of a 3-Mb contig and partial transcript map of the central region of mouse chromosome 11.

D. Watkins-Chow, S. Camper, M. Buckwalter, 1997, Genomics.

Encyclopedia of the mouse genome V. Mouse chromosome 11.

D. Watkins-Chow, S. Camper, A. Buchberg, 1996, Mammalian genome : official journal of the International Mammalian Genome Society.

Comparative mapping of the imprinted U2afbpL gene on mouse chromosome 11 and human chromosome 5.

D. Watkins-Chow, C. Plass, I. Kalcheva, 1995, Cytogenetics and cell genetics.

Genetic mapping and evaluation of candidate genes for spasmodic, a neurological mouse mutation with abnormal startle response.

J. Noebels, S. Camper, M. Buckwalter, 1993, Genomics.

Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backcross.

S. Camper, M. Buckwalter, R. W. Katz, 1991, Genomics.

PROP1-Dependent Retinoic Acid Signaling Regulates Developmental Pituitary Morphogenesis and Hormone Expression.

S. Camper, L. Cheung, 2020, Endocrinology.

A Transient Transgenic RNAi Strategy for Rapid Characterization of Gene Function during Embryonic Development

S. Orkin, B. Bjork, D. Beier, 2010, PloS one.

A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type.

M. Conti, S. Camper, M. Hsieh, 2013, Human molecular genetics.

Thyroid hormone resistance and increased metabolic rate in the RXR-γ–deficient mouse

R. Eckel, P. Chambon, B. Haugen, 2000 .

Regulation of the Rat Follicle-Stimulating Hormone β-Subunit Promoter by Activin

S. Camper, T. Woodruff, H. Suh, 2003 .

Discovery of transcriptional regulators and signaling pathways in the developing pituitary gland by bioinformatic and genomic approaches.

D. Ghosh, J. Kawai, Piero Carninci, 2009, Genomics.

Pitx2 is required at multiple stages of pituitary organogenesis: pituitary primordium formation and cell specification.

Sally A Camper, J. Drouin, S. Camper, 2002, Development.

Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia.

S. Camper, M. Brinkmeier, P. Gergics, 2015, Molecular endocrinology.

The site and stage of anti-DNA B-cell deletion

R. Hardy, M. Radic, S. Camper, 1995, Nature.

INDUCED EXPRESSION OF A BOVINE GROWTH HORMONE CONSTRUCT IN TRANSGENIC PIGS

M. Surani, S. Barton, S. Camper, 1989 .

Linkage mapping of murine homolog of the yeast SPT6 gene to MMU11B1

A. Ashworth, D. Watkins-Chow, P. Baldacci, 2009, Mammalian Genome.

Multi-omic profiling of pituitary thyrotropic cells and progenitors

Stephen C. J. Parker, S. Liebhaber, S. Camper, 2021, BMC biology.

Thyroid hormone resistance and increased metabolic rate in the RXR-gamma-deficient mouse.

R. Eckel, P. Chambon, B. Haugen, 2000, The Journal of clinical investigation.

Expression of anti-DNA immunoglobulin transgenes in non-autoimmune mice

R. Hardy, M. Radic, S. Camper, 1991, Nature.

The Histone Methyltransferase Gene Absent, Small, or Homeotic Discs-1 Like Is Required for Normal Hox Gene Expression and Fertility in Mice1

S. Camper, M. Brinkmeier, I. Maillard, 2015, Biology of reproduction.

Gonadotrope-specific Deletion of Dicer Results in Severely Suppressed Gonadotropins and Fertility Defects*

S. Camper, P. Conn, M. Brinkmeier, 2014, The Journal of Biological Chemistry.

Molecular basis for pituitary dysfunction: Comparison of Prop1 and Pit1 mutant mice

S. Camper, M. Brinkmeier, M. A. Potok, 2006 .

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.

Yehoash Raphael, Andrew Forge, Sally A Camper, 2003, Human molecular genetics.

Mouse knockout solves endocrine puzzle and promotes new pituitary lineage model.

S. Camper, C. Keegan, 2003, Genes & development.

Chapter 2 Etiologies of Primary Ovarian Insufficiency

S. Camper, L. Green, N. Foyouzi, 2017 .

Etiologies of Primary Ovarian Insufficiency

S. Camper, L. Green, N. Foyouzi, 2016 .

Genetic variation in thyroid folliculogenesis influences susceptibility to hypothyroidism-induced hearing impairment

Thomas J. Jones, S. Camper, K. Johnson, 2019, Mammalian Genome.

Report of the second international workshop on human chromosome 5 mapping.

W. Neuman, S. Camper, C. Westbrook, 1992, Cytogenetics and cell genetics.

Pituitary Development and Organogenesis: Transcription Factors in Development and Disease

S. Camper, Alexandre Z. Daly, 2020 .

PITX genes are required for cell survival and Lhx3 activation.

J. Drouin, S. Camper, P. Gage, 2005, Molecular endocrinology.

Role of PITX2 in the Pituitary Gland

Donna M. Martin, S. Camper, I. Nasonkin, 2005 .

PITX2 is required for normal development of neurons in the mouse subthalamic nucleus and midbrain.

Donna M. Martin, Y. Raphael, S. Camper, 2004, Developmental biology.

20 – Pituitary Gland Development

Donna M. Martin, S. Camper, I. Nasonkin, 2002 .

Genealogy of the Anterior Pituitary Gland: Tracing a Family Tree

S. Camper, A. Seasholtz, H. L. Burrows, 1999, Trends in Endocrinology & Metabolism.

S. Camper, P. Gage, H. Suh, 1999, Mammalian Genome.

How many homeobox genes does it take to make a pituitary gland?

D. Watkins-Chow, S. Camper, 1998, Trends in genetics : TIG.

High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency

Michael H. Guo, J. Kitzman, Jun Z. Li, 2021, medRxiv.

Genetics, Gene Expression and Bioinformatics of the Pituitary Gland

K. Steel, D. Ghosh, Piero Carninci, 2009, Hormone Research in Paediatrics.

A Gata2-Dependent Transcription Network Regulates Uterine Progesterone Responsiveness and Endometrial Function.

R. Lanz, S. Camper, Q. Tong, 2016, Cell reports.

Pituitary stem cell regulation by Zeb2 and BMP signaling.

S. Camper, Amanda H Winningham, 2023, Endocrinology.

TCF4 deficiency expands ventral diencephalon signaling and increases induction of pituitary progenitors.

S. Camper, M. Brinkmeier, S. Davis, 2007, Developmental biology.

Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene

Jan-Fang Cheng, Edward M. Rubin, Timothy P. L. Smith, 2007, Mammalian Genome.

WNT5A signaling affects pituitary gland shape

S. Camper, Huiling Liang, M. A. Potok, 2004, Mechanisms of Development.

Cell-Specific Expression of the Mouse Glycoprotein Hormone α-Subunit Gene Requires Multiple Interacting DNA Elements in Transgenic Mice and Cultured Cells

S. Camper, V. Sarapura, M. Brinkmeier, 1998 .

Implementing transgenic and embryonic stem cell technology to study gene expression, cell-cell interactions and gene function.

S. Camper, R. Keri, C. Keegan, 1995, Biology of reproduction.

Deletion and editing of B cells that express antibodies to DNA.

R. Hardy, M. Radic, S. Litwin, 1994, Journal of immunology.

FOXL2 in the pituitary: molecular, genetic, and developmental analysis.

Jodi L. Haller, B. Ellsworth, S. Camper, 2006, Molecular endocrinology.

Localization of somatostatin receptor genes on mouse chromosomes 2, 11, 12, 15, and 17: correlation with growth QTLs.

S. Camper, M. Brinkmeier, 1997, Genomics.

Genetic Regulation of Forebrain and Pituitary Development

D. M. Martin, S. Camper, 2001 .

A rheumatoid factor transgenic mouse model of autoantibody regulation.

M. Shlomchik, S. Camper, M. Weigert, 1993, International immunology.

The activation and silencing of gene transcription in the liver.

S. Tilghman, S. Camper, 1991, Biotechnology.

The developmental regulation of albumin and alpha-fetoprotein gene expression.

R. Godbout, S. Tilghman, S. Camper, 1989, Progress in nucleic acid research and molecular biology.

Partial transcriptome of the developing pituitary gland.

S. Camper, K R Douglas, S A Camper, 2000, Genomics.

β-catenin is required in the neural crest and mesencephalon for pituitary gland organogenesis

K. Yamamura, S. Camper, Amanda L. Zacharias, 2016, BMC Developmental Biology.

Transgene correction maintains normal cochlear structure and function in 6-month-old Myo15a mutant mice

Y. Raphael, L. Beyer, S. Camper, 2006, Hearing Research.

Ash1l controls quiescence and self-renewal potential in hematopoietic stem cells.

S. Malek, Y. Dou, T. Cierpicki, 2015, The Journal of clinical investigation.

Ash 1 l controls quiescence and self-renewal potential in hematopoietic stem cells

S. Malek, Y. Dou, T. Cierpicki, 2015 .

Genetic redundancy of GATA factors in the extraembryonic trophoblast lineage ensures the progression of preimplantation and postimplantation mammalian development

S. Camper, Ram P Kumar, P. Fields, 2017, Development.

TCF and Groucho-related genes influence pituitary growth and development.

Hans Clevers, Jan Meeldijk, Michelle L Brinkmeier, 2003, Molecular endocrinology.

The Ames dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage-specific cell proliferation.

S. Camper, M. Brinkmeier, L. Knapp, 1996, Molecular endocrinology.

Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing.

Jun Z. Li, S. Camper, B. Mendonca, 2017, Archives of endocrinology and metabolism.

Growth hormone deficiency with advanced bone age : phenotypic interaction between GHRH receptor and CYP 21 A 2 mutations diagnosed by sanger and whole exome sequencing

Jun Z. Li, S. Camper, B. Mendonca, 2017 .

A Modifier Gene Alleviates Hypothyroidism-Induced Hearing Impairment in Pou1f1dw Dwarf Mice

S. Camper, K. Johnson, L. Gagnon, 2011, Genetics.

A novel modifier of hypothyroidism-induced hearing impairment in Pou1f1 dw dwarf mice

S. Camper, K. Johnson, L. Gagnon, 2011 .

A Modi fi er Gene Alleviates Hypothyroidism-Induced Hearing Impairment in Pou 1 f 1 dw Dwarf Mice

S. Camper, K. Johnson, L. Gagnon, 2011 .

The human and mouse receptors for hyaluronan-mediated motility, RHAMM, genes (HMMR) map to human chromosome 5q33.2-qter and mouse chromosome 11.

J. McPherson, E. Turley, J. Wasmuth, 1995, Genomics.

Anterior pituitary cells defective in the cell-autonomous factor, df, undergo cell lineage specification but not expansion.

S. Camper, T. Saunders, P. Gage, 1996, Development.

gene expression profiling Candidate genes for panhypopituitarism identified by

D. Ghosh, S. Camper, J. MacDonald, 2015 .

Candidate genes for panhypopituitarism identified by gene expression profiling.

D. Ghosh, S. Camper, J. MacDonald, 2011, Physiological genomics.

Lhx4 and Prop1 are required for cell survival and expansion of the pituitary primordia.

Sally A Camper, S. Camper, Lori T Raetzman, 2002, Development.

Identification of members of the Wnt signaling pathway in the embryonic pituitary gland

Mary Anne Potok, Jennifer A. Kennell, P. Eswara, 2001, Mammalian Genome.

Distribution of m6A in mRNA and its Possible Biological Role

T. Nilsen, D. Ayers, S. Camper, 1986 .

The proximal promoter of the bovine luteinizing hormone beta-subunit gene confers gonadotrope-specific expression and regulation by gonadotropin-releasing hormone, testosterone, and 17 beta-estradiol in transgenic mice.

S. Camper, I. Anderson, J. Gorski, 1994, Molecular endocrinology.

The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing

M. Mustapha, T. Friedman, G. Frolenkov, 2015, eLife.

Whirler Mutant Hair Cells Have Less Severe Pathology than Shaker 2 or Double Mutants

Y. Raphael, L. Beyer, M. Mustapha, 2007, Journal of the Association for Research in Otolaryngology.

M. I. Lomax, Yehoash Raphael, Y. Raphael, 2006, Journal of the Association for Research in Otolaryngology.

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.

Donna M. Martin, Y. Raphael, L. Beyer, 2003, Human molecular genetics.

Developmental expression of growth hormone and prolactin genes in the bovine pituitary.

S. Camper, F. Rottman, J. Virgin, 1983, The Journal of biological chemistry.

Research applications of transgenic mice

S. Camper, 1987 .

Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulation

H. Williams, M. Dattani, I. Robinson, 2019, EBioMedicine.

Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man

S. Camper, M. Brinkmeier, F. Albarel, 2022, Human molecular genetics.

Pituitary Neoplasm Nomenclature Workshop: Does Adenoma Stand the Test of Time?

P. Chanson, S. Radovick, A. Mamelak, 2021, Journal of the Endocrine Society.

Pituitary Changes in Prop1 Transgenic Mice: Hormone Producing Tumors and Signet-ring Type Gonadotropes

S. Camper, S. Takekoshi, R. Osamura, 2008, Acta histochemica et cytochemica.

Thyroid Hormone Is Essential for Pituitary Somatotropes and Lactotropes *

D. Watkins-Chow, R. Lloyd, S. Camper, 1999 .

LINE-1 Mediated Insertion into Poc1a (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice

Daniel L Burgess, S. Camper, K. Kozloff, 2015, PLoS genetics.

Cre‐mediated recombination in the pituitary gland

S. Camper, N. Muzyczka, A. Seasholtz, 2000, Genesis.

Nucleotide sequence and expression of the mouse corticotropin-releasing hormone gene

S. Camper, A. Seasholtz, C. E. Harnden, 1991, Molecular and Cellular Neuroscience.

Efficient, specific, developmentally appropriate cre‐mediated recombination in anterior pituitary gonadotropes and thyrotropes

S. Camper, T. Saunders, M. Zeidler, 2013, Genesis.

Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing

S. Camper, G. Iguchi, Masaaki Yamamoto, 2022, Frontiers in Endocrinology.

Regulation of the rat follicle-stimulating hormone beta-subunit promoter by activin.

S. Camper, T. Woodruff, H. Suh, 2003, Molecular endocrinology.

Hypothalamic β-Catenin Is Essential for FGF8-Mediated Anterior Pituitary Growth: Links to Human Disease.

B. Ellsworth, S. Camper, Alexandre Z. Daly, 2017, Endocrinology.

Postnatal repression of the -fetoprotein gene is enhancer independent

S. Camper, Shirley M. Ti lghman, 2007 .

β-catenin is required in the neural crest and mesencephalon for pituitary gland organogenesis

K. Yamamura, S. Camper, Amanda L. Zacharias, 2016, BMC Developmental Biology.

Differential expression of corticotropin-releasing hormone in developing mouse embryos and adult brain.

J. Herman, S. Camper, C. Keegan, 1994, Endocrinology.

HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype

M. Dattani, S. Camper, B. Mendonca, 2016, Clinical endocrinology.

Influence of a V kappa 8 L chain transgene on endogenous rearrangements and the immune response to the HA(Sb) determinant on influenza virus.

S. Camper, M. Weigert, W. Gerhard, 1991, Journal of immunology.

Hair cells in the inner ear of the pirouette and shaker 2 mutant mice

E. H. Lambert, Y. Raphael, L. Beyer, 2000, Journal of neurocytology.

Expression of Corticotropin-Releasing Hormone Transgenes in Neurons of Adult and Developing Mice

S. Camper, C. Keegan, A. Seasholtz, 1994, Molecular and Cellular Neuroscience.

Cocaine-and Amphetamine Regulated Transcript (CART) Peptide Is Expressed in Precursor Cells and Somatotropes of the Mouse Pituitary Gland

S. Camper, A. Mortensen, 2016, PloS one.

Meeting report: 10th international mouse genome conference

M. Meisler, S. Camper, 1997, Mammalian Genome.

Wnt-3a is critical for caudal embryonic development

S. Camper, T. L. Greco, M. Newhouse, 1994 .

Sox3 and sexual dysfunction: it's in the head

S. Camper, 2004, Nature Genetics.

Runx1 expression defines a subpopulation of displaced amacrine cells in the developing mouse retina

S. Camper, S. Stifani, Mary Anne Potok, 2005, Journal of neurochemistry.

The gene coding for variant hepatic nuclear factor 1 (Tcf-2), maps between the Edp-1 and Erba genes on mouse Chromosome 11

J. Guénet, S. Camper, I. Karolyi, 2004, Mammalian Genome.

DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.

Y. Raphael, T. Friedman, S. Camper, 2000, Advances in oto-rhino-laryngology.

Natriuretic Peptide Signaling Regulates Female Fertility at the Level of the Ovary.

M. Conti, S. Camper, M. Hsieh, 2011 .

Homozygous CDH2 variant may be associated with hypopituitarism without neurological disorders

Jun Z. Li, S. Camper, B. Mendonca, 2023, Endocrine connections.

Biotin-binding Protein from Egg Yolk

S. Camper, H. B. White, Harry W. Me, 2022 .

The Genomic Landscape of the Old Order Amish.

Kaanan P. Shah, A. Shojaie, J. Long, 2011 .

Localization of the thyrotropin-releasing hormone gene, Trh, on mouse Chromosome 6

S. Camper, M. Roller, 1995, Mammalian Genome.

Mapping of the mouse corticotropin-releasing hormone receptor 2 gene (Crhr2) to Chromosome 6

S. Camper, A. Seasholtz, H. L. Burrows, 2009, Mammalian Genome.

Thyroid Hormone Is Essential for Pituitary Somatotropes and Lactotropes *

D. Watkins-Chow, R. Lloyd, S. Camper, 1999 .

Constitutive secretion of transgene-encoded IgG2b autoantibodies leads to symptoms of autoimmune disease.

M. Radic, S. Camper, M. Weigert, 1995, Journal of immunology.

A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death.

S. Camper, S. Cook, W. White, 1994, Human molecular genetics.

Chromosomal localization of the zinc finger protein 15, Zfp15, on Mouse Chromosome 4

S. Camper, M. Roller, 1995, Mammalian Genome.

Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia.

S. Camper, M. Brinkmeier, Péter Gergics, 2015, Molecular endocrinology.

Localization of the corticotropin-releasing hormone receptor gene on mouse Chromosome 11

S. Camper, A. Seasholtz, H. L. Burrows, 2004, Mammalian Genome.

Advances in Skeletal Dysplasia Genetics.

S. Camper, Krista A. Geister, 2015, Annual review of genomics and human genetics.

The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model

S. Camper, R. Reeves, Huiqing Li, 2015, BMC Developmental Biology.

Pituitary tumors and immortalized cell lines generated by cre-inducible expression of SV40 T antigen.

S. Camper, A. Mortensen, Alexandre Z. Daly, 2021, Endocrinology.

Discovery of transcriptional regulators and signaling pathways in the developing pituitary gland by bioinformatic and genomic approaches.

D. Ghosh, J. Kawai, Piero Carninci, 2009, Genomics.

Steroidogenic factor 1 (SF1) is essential for pituitary gonadotrope function.

S. Camper, M. Bakke, K. Parker, 2001, Development.