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16 results on '"Sally A Camper"'

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1. Homozygous CDH2 variant may be associated with hypopituitarism without neurological disorders

2. Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice.

3. PROP1 triggers epithelial-mesenchymal transition-like process in pituitary stem cells

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

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

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

7. Aged PROP1 deficient dwarf mice maintain ACTH production.

8. A transient transgenic RNAi strategy for rapid characterization of gene function during embryonic development.

9. SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice.

10. Knockout mice with pituitary malformations help identify human cases of hypopituitarism

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

12. Multi-omic profiling of pituitary thyrotropic cells and progenitors

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

14. Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulationResearch in context

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

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

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