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Endocrinology|January 1, 1988
Localization of 7B2, neuromedin B, and neuromedin U in specific cell types of rat, mouse, and human pituitary, in rat hypothalamus, and in 30 human pituitary and extrapituitary tumorsJ H Steel, S Van Noorden, J Ballesta, et al.Neuroscience|July 1, 1986
Calcitonin gene-related peptide immunoreactivity in afferent neurons supplying the urinary tract: combined retrograde tracing and immunohistochemistryH C Su, J Wharton, J M Polak, et al.Journal of Chemical Neuroanatomy|March 18, 2000
Stimulus frequency affects c-fos expression in the rat visual systemJ Correa-Lacárcel, M J Pujante, F F Terol, et al.Anales De Pediatria (Barcelona, Spain : 2003)|October 22, 2008
[Review of 22 patients with 22q11.2 deletion syndrome: phenotype spectrum]M J Ballesta Martínez, E Guillén Navarro, I López Expósito, et al.Journal of Neurochemistry|February 1, 1997
Neuronal nicotinic acetylcholine receptors on bovine chromaffin cells: cloning, expression, and genomic organization of receptor subunitsA Campos-Caro, F I Smillie, E Domínguez del Toro, et al.Journal of Pediatric Gastroenterology and Nutrition|June 12, 2013
Three main factors define changes in fecal microbiota associated with feeding modality in infantsCarolina Gomez-Llorente, Julio Plaza-Diaz, Margarita Aguilera, et al.Pediatric Research|August 19, 2017
Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylationMaría E de la Morena-Barrio, María J Ballesta-Martínez, Raquel López-Gálvez, et al.Clinical Genetics|April 30, 2023
Evolution of clinical and radiological presentations of spondyloepimetaphyseal dysplasia, RPL13-related: Description of 11 further casesFrancisca Díaz-González, Manuel Parrón-Pajares, Elsa Lucas-Castro, et al.American Journal of Human Genetics|February 3, 2016
Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual DisabilityPaul R Kasher, Katherine E Schertz, Megan Thomas, et al.Human Molecular Genetics|July 5, 2020
TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal lociErica E Davis, Ravikumar Balasubramanian, Zachary A Kupchinsky, et al.Pageof 12