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American Journal of Human Genetics|March 3, 1999
Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22J A Martignetti, R J Desnick, E Aliprandis, et al.
Calcified Tissue International|January 28, 2009
Ablation of cathepsin k activity in the young mouse causes hypermineralization of long bone and growth platesAdele L Boskey, Bruce D Gelb, Eric Pourmand, et al.
Calcified Tissue International|July 23, 2003
Cathepsin K deficiency in pycnodysostosis results in accumulation of non-digested phagocytosed collagen in fibroblastsV Everts, W S Hou, X Rialland, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|November 11, 1991
Pseudoconduction of atrial flutter of a recipient atriumB D Gelb, S Denfield, R Friedman, et al.
Frontiers in Genetics|May 28, 2020
The Phosphatase CSW Controls Life Span by Insulin Signaling and Metabolism Throughout Adult Life in <i>Drosophila</i>Leonardo R Ruzzi, Pablo E Schilman, Alvaro San Martin, et al.
Genomics|April 15, 1997
Structure and chromosomal assignment of the human cathepsin K geneB D Gelb, G P Shi, M Heller, et al.
American Journal of Medical Genetics|April 15, 1994
Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G)G M Pastores, F M Santorelli, S Shanske, et al.
The Journal of Allergy and Clinical Immunology|July 11, 2000
Genetics of peanut allergy: a twin studyS H Sicherer, T J Furlong, H H Maes, et al.
Catheterization and Cardiovascular Diagnosis|February 1, 1993
Transcatheter closure of residual atrial septal defect following cardiac transplantationM P O'Laughlin, J T Bricker, C E Mullins, et al.
Circulation. Genomic and Precision Medicine|June 6, 2022
Prevalence of Genetic Diagnoses in a Cohort With Valvar Pulmonary StenosisK Nicole Weaver, Jing Chen, Amy Shikany, et al.
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