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B Franco

Showing results (121-130 of 181) with videos related to

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Blood|June 17, 1998
A 5' regulatory sequence containing two Ets motifs controls the expression of the Wiskott-Aldrich syndrome protein (WASP) gene in human hematopoietic cellsA Petrella, I Doti, V Agosti, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22)A Totaro, A Roetto, J M Rommens, et al.
Clinical Anatomy (New York, N.Y.)|January 24, 2023
Innervation of the heart: Anatomical study with application to better understanding pathologies of the cardiac autonomicsMailén L González, Sofía M Pividori, Gregorio Fosser, et al.
Journal of Medical Primatology|November 1, 2023
Effects of atipamezole on selected physiologic parameters in cynomolgus macaques (Macaca fascicularis)K Schwartz, M Zhang, B Franco, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2006
Notch/Delta signaling constrains reengineering of pro-T cells by PU.1Christopher B Franco, Deirdre D Scripture-Adams, Irina Proekt, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesityW Ahmad, M De Fusco, M Faiyaz ul Haque, et al.
Revista Espanola De Enfermedades Digestivas|January 29, 2026
The impact of oral health-related quality of life and country-level context on patients with cirrhosis: a cross-sectional studyJanaina B Medina, Amanda Dos Santos Matioli, Maria Gabriela Haye Biazevic, et al.
American Journal of Medical Genetics|July 27, 2001
Corpus callosum agenesis, multiple cysts, skin defects, and subtle ocular abnormalities with a de novo mutation [45,XX,der(5), t(5;;14) (pter;q11.2)]R Zannolli, R Mostardini, L Pucci, et al.
Blood|October 18, 2011
Reduced mast cell and basophil numbers and function in Cpa3-Cre; Mcl-1fl/fl miceJennifer N Lilla, Ching-Cheng Chen, Kaori Mukai, et al.
American Journal of Human Genetics|August 27, 1998
Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domainK Gaudenz, E Roessler, N Quaderi, et al.
Pageof 19

Showing results (121-130 of 181) with videos related to

Sort By:
Pageof 19
Blood|June 17, 1998
A 5' regulatory sequence containing two Ets motifs controls the expression of the Wiskott-Aldrich syndrome protein (WASP) gene in human hematopoietic cellsA Petrella, I Doti, V Agosti, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22)A Totaro, A Roetto, J M Rommens, et al.
Clinical Anatomy (New York, N.Y.)|January 24, 2023
Innervation of the heart: Anatomical study with application to better understanding pathologies of the cardiac autonomicsMailén L González, Sofía M Pividori, Gregorio Fosser, et al.
Journal of Medical Primatology|November 1, 2023
Effects of atipamezole on selected physiologic parameters in cynomolgus macaques (Macaca fascicularis)K Schwartz, M Zhang, B Franco, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2006
Notch/Delta signaling constrains reengineering of pro-T cells by PU.1Christopher B Franco, Deirdre D Scripture-Adams, Irina Proekt, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesityW Ahmad, M De Fusco, M Faiyaz ul Haque, et al.
Revista Espanola De Enfermedades Digestivas|January 29, 2026
The impact of oral health-related quality of life and country-level context on patients with cirrhosis: a cross-sectional studyJanaina B Medina, Amanda Dos Santos Matioli, Maria Gabriela Haye Biazevic, et al.
American Journal of Medical Genetics|July 27, 2001
Corpus callosum agenesis, multiple cysts, skin defects, and subtle ocular abnormalities with a de novo mutation [45,XX,der(5), t(5;;14) (pter;q11.2)]R Zannolli, R Mostardini, L Pucci, et al.
Blood|October 18, 2011
Reduced mast cell and basophil numbers and function in Cpa3-Cre; Mcl-1fl/fl miceJennifer N Lilla, Ching-Cheng Chen, Kaori Mukai, et al.
American Journal of Human Genetics|August 27, 1998
Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domainK Gaudenz, E Roessler, N Quaderi, et al.
Pageof 19