Sally Camper, Ph. D.

Affiliations: 
Human Genetics University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Pituitary developement
Google:
"Sally Camper"
Mean distance: 16.06 (cluster 32)
 
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Publications

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Brinkmeier ML, Cheung LYM, O'Connell SP, et al. (2025) Nucleoredoxin regulates WNT signaling during pituitary stem cell differentiation. Human Molecular Genetics
Brinkmeier ML, Cheung LYM, O'Connell SP, et al. (2025) Nucleoredoxin regulates WNT signaling during pituitary stem cell differentiation. Biorxiv : the Preprint Server For Biology
Brinkmeier ML, George AS, Cheung LYM, et al. (2024) Long non-coding RNAs expressed in mouse pituitary development and mature hormone-producing cells. Endocrinology
Cheung LYM, Menage L, Rizzoti K, et al. (2023) Novel candidate regulators and developmental trajectory of pituitary thyrotropes. Endocrinology
Winningham AH, Camper SA. (2023) Pituitary Stem Cell Regulation by Zeb2 and BMP Signaling. Endocrinology. 164
Bando H, Brinkmeier ML, Castinetti F, et al. (2022) Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man. Human Molecular Genetics
Brinkmeier ML, Bando H, Camarano AC, et al. (2020) Rathke's cleft-like cysts arise from Isl1 deletion in murine pituitary progenitors. The Journal of Clinical Investigation
Bando H, Gergics P, Bohnsack BL, et al. (2020) otx2b mutant zebrafish have pituitary, eye and mandible defects that model mammalian disease. Human Molecular Genetics
Cheung L, Daly A, Brinkmeier M, et al. (2020) OR16-05 Single-Cell Sequencing Identifies Novel Regulators of Thyrotrope Populations and POU1F1-Independent Thyroid-Stimulating Hormone Expression Journal of the Endocrine Society. 4
Brinkmeier M, Camper SA. (2020) SAT-288 Pituitary Developmental Defects Caused by Haploinsufficiency for the Transcription Factor SIX3 Are Worsened by POU1F1 Deficiency Journal of the Endocrine Society. 4
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