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Journal of Biomedicine & Biotechnology
|
October 19, 2006
Gaucher disease and the synucleinopathies
Kathleen S Hruska, Ozlem Goker-Alpan, Ellen Sidransky
Human Mutation
|
March 14, 2008
Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA)
Kathleen S Hruska, Mary E LaMarca, C Ronald Scott, et al.
Transgenic Research
|
November 7, 2003
Expression of lysostaphin in milk of transgenic mice affects the growth of neonates
Abhijit Mitra, Kathleen S Hruska, Olga Wellnitz, et al.
Biology of Reproduction
|
April 23, 2002
Concurrent pregnancy retards mammary involution: effects on apoptosis and proliferation of the mammary epithelium after forced weaning of mice
Anthony V Capuco, Minglin Li, Ezhou Long, et al.
Biology of Reproduction
|
February 20, 2004
Methoxychlor-induced atresia in the mouse involves Bcl-2 family members, but not gonadotropins or estradiol
Christina Borgeest, Kimberly P Miller, Rupesh Gupta, et al.
Cancer Genetics
|
August 4, 2022
Fibroblast testing can inform medical management in individuals with mosaic variants detected on hereditary cancer panels
Erin G Sutcliffe, Jessica L Mester, Lisa R Susswein, et al.
Neuroscience Letters
|
June 20, 2006
Glucocerebrosidase mutations are not found in association with LRRK2 G2019S in subjects with parkinsonism
Michael J Eblan, Sonja Scholz, Barbara Stubblefield, et al.
American Journal of Medical Genetics. Part A
|
July 21, 2022
Phenotypic continuum between POLE-related recessive disorders: A case report and literature review
Maegan E Roberts, Sarah Nimrichter, Megan L Marshall, et al.
The American Journal of Pathology
|
October 28, 2003
Introduction of estrogen receptor-alpha into the tTA/TAg conditional mouse model precipitates the development of estrogen-responsive mammary adenocarcinoma
Maddalena T Tilli, M Silvina Frech, Mary E Steed, et al.
Molecular Genetics and Metabolism
|
April 28, 2007
Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson disease
Shira G Ziegler, Michael J Eblan, Usha Gutti, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
Journal of Biomedicine & Biotechnology
|
October 19, 2006
Gaucher disease and the synucleinopathies
Kathleen S Hruska, Ozlem Goker-Alpan, Ellen Sidransky
Human Mutation
|
March 14, 2008
Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA)
Kathleen S Hruska, Mary E LaMarca, C Ronald Scott, et al.
Transgenic Research
|
November 7, 2003
Expression of lysostaphin in milk of transgenic mice affects the growth of neonates
Abhijit Mitra, Kathleen S Hruska, Olga Wellnitz, et al.
Biology of Reproduction
|
April 23, 2002
Concurrent pregnancy retards mammary involution: effects on apoptosis and proliferation of the mammary epithelium after forced weaning of mice
Anthony V Capuco, Minglin Li, Ezhou Long, et al.
Biology of Reproduction
|
February 20, 2004
Methoxychlor-induced atresia in the mouse involves Bcl-2 family members, but not gonadotropins or estradiol
Christina Borgeest, Kimberly P Miller, Rupesh Gupta, et al.
Cancer Genetics
|
August 4, 2022
Fibroblast testing can inform medical management in individuals with mosaic variants detected on hereditary cancer panels
Erin G Sutcliffe, Jessica L Mester, Lisa R Susswein, et al.
Neuroscience Letters
|
June 20, 2006
Glucocerebrosidase mutations are not found in association with LRRK2 G2019S in subjects with parkinsonism
Michael J Eblan, Sonja Scholz, Barbara Stubblefield, et al.
American Journal of Medical Genetics. Part A
|
July 21, 2022
Phenotypic continuum between POLE-related recessive disorders: A case report and literature review
Maegan E Roberts, Sarah Nimrichter, Megan L Marshall, et al.
The American Journal of Pathology
|
October 28, 2003
Introduction of estrogen receptor-alpha into the tTA/TAg conditional mouse model precipitates the development of estrogen-responsive mammary adenocarcinoma
Maddalena T Tilli, M Silvina Frech, Mary E Steed, et al.
Molecular Genetics and Metabolism
|
April 28, 2007
Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson disease
Shira G Ziegler, Michael J Eblan, Usha Gutti, et al.
Page
of 4