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Journal of Cell Science
|
November 13, 2008
Effect of cell shape and packing density on granulosa cell proliferation and formation of multiple layers during early follicle development in the ovary
Patricia Da Silva-Buttkus, Gayani S Jayasooriya, Jocelyn M Mora, et al.
Cureus
|
October 30, 2025
Adherence to the American Academy of Pediatrics Health Supervision Guidelines for Children With Down Syndrome in a Tertiary Care Institution in Northeastern Colombia
Silvia N Suárez-Mantilla, Martha L Africano-Leon, Victor M Mora-Bautista, et al.
Clinical Transplantation
|
March 20, 2025
Prognostic Utility of the GAP Score in Interstitial Lung Disease Patients Evaluated for Lung Transplantation: A Single-Center Study
Víctor M Mora-Cuesta, Javier Zuazaga-Fuentes, David Iturbe-Fernández, et al.
Glycobiology
|
August 1, 2024
The sunflower jacalin Helja: biological and structural insights of its antifungal activity against Candida albicans
Marianela V Del Río, Melisa B Radicioni, Anabela M Cutine, et al.
ASAIO Transactions
|
July 1, 1990
Biomaterial associated impairment of local neutrophil function
S S Kaplan, R E Basford, R L Kormos, et al.
The Journal of Clinical Investigation
|
January 1, 1994
Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin
K Matsumura, A H Burghes, M Mora, et al.
Neurologia (Barcelona, Spain)
|
February 11, 2005
[Urogenital alterations in hereditary and sporadic neurodegenerative ataxias]
J M Díez Rodríguez, J Salinas Casado, E Fernández del Busto, et al.
Archivos Espanoles De Urologia
|
November 1, 1989
[Vesical actinomycosis: rare tumor of the urachus]
J Jiménez de León, F Burgos, M Mora, et al.
Neuromuscular Disorders : NMD
|
February 17, 2015
Non-coding VMA21 deletions cause X-linked myopathy with excessive autophagy
A Ruggieri, N Ramachandran, P Wang, et al.
Journal of Medical Genetics
|
February 9, 2000
Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations
R Barresi, C Di Blasi, T Negri, et al.
Page
of 68
Search research articles
Search
Showing results (421-430 of 680) with videos related to
Sort By:
Page
of 68
Journal of Cell Science
|
November 13, 2008
Effect of cell shape and packing density on granulosa cell proliferation and formation of multiple layers during early follicle development in the ovary
Patricia Da Silva-Buttkus, Gayani S Jayasooriya, Jocelyn M Mora, et al.
Cureus
|
October 30, 2025
Adherence to the American Academy of Pediatrics Health Supervision Guidelines for Children With Down Syndrome in a Tertiary Care Institution in Northeastern Colombia
Silvia N Suárez-Mantilla, Martha L Africano-Leon, Victor M Mora-Bautista, et al.
Clinical Transplantation
|
March 20, 2025
Prognostic Utility of the GAP Score in Interstitial Lung Disease Patients Evaluated for Lung Transplantation: A Single-Center Study
Víctor M Mora-Cuesta, Javier Zuazaga-Fuentes, David Iturbe-Fernández, et al.
Glycobiology
|
August 1, 2024
The sunflower jacalin Helja: biological and structural insights of its antifungal activity against Candida albicans
Marianela V Del Río, Melisa B Radicioni, Anabela M Cutine, et al.
ASAIO Transactions
|
July 1, 1990
Biomaterial associated impairment of local neutrophil function
S S Kaplan, R E Basford, R L Kormos, et al.
The Journal of Clinical Investigation
|
January 1, 1994
Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin
K Matsumura, A H Burghes, M Mora, et al.
Neurologia (Barcelona, Spain)
|
February 11, 2005
[Urogenital alterations in hereditary and sporadic neurodegenerative ataxias]
J M Díez Rodríguez, J Salinas Casado, E Fernández del Busto, et al.
Archivos Espanoles De Urologia
|
November 1, 1989
[Vesical actinomycosis: rare tumor of the urachus]
J Jiménez de León, F Burgos, M Mora, et al.
Neuromuscular Disorders : NMD
|
February 17, 2015
Non-coding VMA21 deletions cause X-linked myopathy with excessive autophagy
A Ruggieri, N Ramachandran, P Wang, et al.
Journal of Medical Genetics
|
February 9, 2000
Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations
R Barresi, C Di Blasi, T Negri, et al.
Page
of 68