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of 6
pro vyhledávání: '"Holly R. Martin"'
Autor:
Stephen Johnston, Joyce O’Shaughnessy, Miguel Martin, Jens Huober, Masakazu Toi, Joohyuk Sohn, Valérie A. M. André, Holly R. Martin, Molly C. Hardebeck, Matthew P. Goetz
Publikováno v:
npj Breast Cancer, Vol 7, Iss 1, Pp 1-5 (2021)
Abstract In MONARCH 3, continuous dosing of abemaciclib with an aromatase inhibitor (AI) conferred significant clinical benefit to postmenopausal women with HR+, HER2− advanced breast cancer. We report data for clinically prognostic subgroups: live
Externí odkaz:
https://doaj.org/article/cf9cf9b9d25d4a93984071353e442e17
Autor:
Holly R. Martin, Michele D. Poe, Joanne Kurtzberg, Adam Mendizabal, Maria L. Escolar, James M. Provenzale
Publikováno v:
Biology of Blood and Marrow Transplantation. 19(4):616-624
Metachromatic leukodystrophy (MLD) is an inherited demyelinating disease that causes progressive neurologic deterioration, leading to severe motor disability, developmental regression, seizures, blindness, deafness, and death. The disease presents as
Autor:
Matthew M. White, Holly R. Martin
Publikováno v:
Copeia. 2008:579-585
We examined the phylogeography of the Least Brook Lamprey (Lampetra aepyptera) to recognize phylogenetically distinct clades within this species and to estimate the relative contributions of vicariance and dispersal to the distribution of genetic var
Publikováno v:
Pediatrics. 118:e879-e889
OBJECTIVE. Infantile Krabbe disease, a rare neurodegenerative disorder that leads to rapid demyelination, dysmyelination, and death in the first 2 years of life, is responsive to treatment with umbilical cord blood transplantation provided that the p
Autor:
Matthew M. White, Holly R. Martin
Publikováno v:
Journal of molecular evolution. 68(6)
Tandemly repeated sequences are a common feature of vertebrate mitochondrial DNA control regions. However, questions still remain about their mode of evolution, function, and phylogenetic distribution. We report phylogenetic and geographic patterns o
Autor:
Angela Rosenberg, Holly R. Martin, Michele D. Poe, Jackson Roush, Debra B. Reinhartsen, Stacey C. Dusing, Maria L. Escolar, Rebecca Edmondson Pretzel
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 97(457)
Lysosomal storage diseases and related disorders (LSRDs) are a heterogeneous group of rare diseases caused by genetic mutations that result in deficiencies of specific lysosomal enzymes. Some of these enzymes are necessary for normal development of t