Results 131 to 140 of about 2,236 (206)

Genetic evaluation of pediatric pituitary adenomas and USP8-related genotype-phenotype correlations in Cushing's disease. [PDF]

Pituitary
Zainab R, Kaur S, Lack J, Similuk M, Tandon M, Ghosh R, Seifert BA, Tokita M, Flippo C, Yan J, Walkiewicz M, Chittiboina P, Tatsi C.   +12 more
europepmc   +1 more source

Guest editorial [PDF]

, 2018
Yamashita, Shunichi
core  

Clinical characteristics associated with somatic <i>GNAS</i> mutations in acromegaly: a systematic review and institutional experience. [PDF]

Front Endocrinol (Lausanne)
Dillon BR, Ruddy M, McQuade EC, Shah SN, Twi-Yeboah A, Levinson BA, Agrawal N.   +6 more
europepmc   +1 more source

Single GNAS Droplet-Based Digital Polymerase Chain Reaction Analysis of Pancreatic Cyst Fluid: An Effective Up-Front Strategy for Mucinous Cyst Diagnosis by Endoscopic Ultrasound-Guided Fine-Needle Aspiration. [PDF]

Clin Transl Gastroenterol
Araujo IK, Soy G, Ginès A, Sendino O, Fernández-Esparrach G, Sánchez-Montes C, Cuatrecasas M, Archilla I, Montironi C, Silvia A, Ausania F, Domínguez-Fraile M, Villagrasa V, López-Guerra M, Colomer D, Vaquero EC.   +15 more
europepmc   +1 more source

Gene expression regulation by Ca²⁺ signaling: an updated systematic review. [PDF]

Cell Mol Biol Lett
Zou M, Wang H, Zeng X, Zhang X.
europepmc   +1 more source

Is chromogranin a prohormone? [PDF]

Nature, 1987
openaire   +1 more source

Feasibility of Ex Vivo Ligandomics. [PDF]

Biomolecules
Waduge P, Veettil RA, Zhang B, Huang C, Tian H, Li W.   +5 more
europepmc   +1 more source

Fibrous dysplasia/McCune-Albright syndrome: state-of-the-art advances, pathogenesis, and basic/translational research. [PDF]

Orphanet J Rare Dis
Palmisano B, Berry C, Boyce A, Charles JF, Collins MT, Corsi A, Fierro FA, Heegaard AM, van der Heijden H, Hoffman CS, Hopkins C, Upadhyay J, Wehn PM, Wentworth KL, Yang Y, Zhao X, Hsiao EC, Riminucci M.   +17 more
europepmc   +1 more source

A Dominant Mutation in G_αs-Protein Increases Hair Pigmentation. [PDF]

Pigment Cell Melanoma Res
Goff PS, Budd P, Logan DW, Keighren M, Cantero M, McKie L, Montoliu L, Jackson IJ, Sviderskaya EV.   +8 more
europepmc   +1 more source

Heterodisomy in the <i>GNAS</i> locus is also a cause of pseudohypoparathyroidism type 1B (iPPSD3). [PDF]

Front Endocrinol (Lausanne)
Manero-Azua A, Vado Y, Gonzàlez Morlà J, Mogas E, Pereda A, Perez de Nanclares G.   +5 more
europepmc   +1 more source