Search research articles
Contact Us
Filters
Showing results (41-50 of 79) with videos related to
Page
of 8
Sort By:
International Journal of Endocrinology
|
May 16, 2020
Rare Somatic MEN1 Gene Pathogenic Variant in a Patient Affected by Atypical Parathyroid Adenoma
Luigia Cinque, Flavia Pugliese, Celeste Clemente, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 12, 2020
The Oncosuppressors MEN1 and CDC73 Are Involved in lncRNA Deregulation in Human Parathyroid Tumors
Annamaria Morotti, Irene Forno, Chiara Verdelli, et al.
BMC Medical Genetics
|
September 15, 2017
Erratum to: Large intragenic deletion of CDC73 (exons 4-10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family
Vito Guarnieri, Raewyn M Seaberg, Catherine Kelly, et al.
Cells
|
November 26, 2025
Functional and <i>In Silico</i> Characterization of ALPL Gene Variants Reveals Genotype-Phenotype Correlations in Italian Hypophosphatasia Patients
Giulia Casamassima, Anna Maria Grieco, Tommaso Biagini, et al.
BMC Medical Genetics
|
August 5, 2017
Large intragenic deletion of CDC73 (exons 4-10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family
Vito Guarnieri, Raewyn M Seaberg, Catherine Kelly, et al.
International Journal of Laboratory Hematology
|
May 5, 2021
Occurrence of chronic myeloid leukemia in a patient with CDC73 gene deletion: "Chance or Causality?"
Maria Stella De Candia, Nicola Sgherza, Laura Bernardini, et al.
Journal of Endocrinological Investigation
|
October 31, 2025
Molecular spectrum of autosomal recessive osteogenesis imperfecta in 93 Italian children with bone fragility: a monocentric experience
Vito Guarnieri, Luca Celli, Chiara De Luca, et al.
Stem Cell Research
|
January 13, 2023
Generation of an induced pluripotent stem cell line CSSi015-A (9553), carrying a point mutation c.2915C > T in the human calcium sensing receptor (CasR) gene
Giovannina Rotundo, Elisa Maria Turco, Giorgia Ruotolo, et al.
International Journal of Molecular Sciences
|
March 6, 2021
Yes-Associated Protein 1 Is a Novel Calcium Sensing Receptor Target in Human Parathyroid Tumors
Giulia Stefania Tavanti, Chiara Verdelli, Annamaria Morotti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 23, 2017
Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism
Luigia Cinque, Angelo Sparaneo, Laura Penta, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 79) with videos related to
Sort By:
Page
of 8
International Journal of Endocrinology
|
May 16, 2020
Rare Somatic MEN1 Gene Pathogenic Variant in a Patient Affected by Atypical Parathyroid Adenoma
Luigia Cinque, Flavia Pugliese, Celeste Clemente, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 12, 2020
The Oncosuppressors MEN1 and CDC73 Are Involved in lncRNA Deregulation in Human Parathyroid Tumors
Annamaria Morotti, Irene Forno, Chiara Verdelli, et al.
BMC Medical Genetics
|
September 15, 2017
Erratum to: Large intragenic deletion of CDC73 (exons 4-10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family
Vito Guarnieri, Raewyn M Seaberg, Catherine Kelly, et al.
Cells
|
November 26, 2025
Functional and <i>In Silico</i> Characterization of ALPL Gene Variants Reveals Genotype-Phenotype Correlations in Italian Hypophosphatasia Patients
Giulia Casamassima, Anna Maria Grieco, Tommaso Biagini, et al.
BMC Medical Genetics
|
August 5, 2017
Large intragenic deletion of CDC73 (exons 4-10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family
Vito Guarnieri, Raewyn M Seaberg, Catherine Kelly, et al.
International Journal of Laboratory Hematology
|
May 5, 2021
Occurrence of chronic myeloid leukemia in a patient with CDC73 gene deletion: "Chance or Causality?"
Maria Stella De Candia, Nicola Sgherza, Laura Bernardini, et al.
Journal of Endocrinological Investigation
|
October 31, 2025
Molecular spectrum of autosomal recessive osteogenesis imperfecta in 93 Italian children with bone fragility: a monocentric experience
Vito Guarnieri, Luca Celli, Chiara De Luca, et al.
Stem Cell Research
|
January 13, 2023
Generation of an induced pluripotent stem cell line CSSi015-A (9553), carrying a point mutation c.2915C > T in the human calcium sensing receptor (CasR) gene
Giovannina Rotundo, Elisa Maria Turco, Giorgia Ruotolo, et al.
International Journal of Molecular Sciences
|
March 6, 2021
Yes-Associated Protein 1 Is a Novel Calcium Sensing Receptor Target in Human Parathyroid Tumors
Giulia Stefania Tavanti, Chiara Verdelli, Annamaria Morotti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 23, 2017
Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism
Luigia Cinque, Angelo Sparaneo, Laura Penta, et al.
Page
of 8