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Journal of Medical Genetics
|
August 16, 2003
Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations
J Berg, M Porteous, D Reinhardt, et al.
The Journal of Clinical Investigation
|
June 1, 1992
Serological cross-reactivity between a human Ro/SS-A autoantigen (calreticulin) and the lambda Ral-1 antigen of Onchocerca volvulus
F A Lux, D P McCauliffe, D W Büttner, et al.
Cancer Gene Therapy
|
August 13, 2005
Peritoneal cancer treatment with CYP2B1 transfected, microencapsulated cells and ifosfamide
S Samel, M Keese, A Lux, et al.
Human Mutation
|
March 1, 2000
Novel missense and frameshift mutations in the activin receptor-like kinase-1 gene in hereditary hemorrhagic telangiectasia. Mutations in brief no. 164. Online
D J Klaus, C J Gallione, K Anthony, et al.
Life Sciences
|
November 27, 2012
Sex differences in insulin resistance in GABAB1 knockout mice
M M Bonaventura, D Rodriguez, M L Ferreira, et al.
The Laryngoscope
|
January 16, 2023
In vitro Nasodine Can be an Effective Antibiofilm Agent for Biofilms that May Cause CRS
Samuel J M Hale, Christian A Lux, Raymond Kim, et al.
Life Sciences
|
July 12, 2005
Differential gonadotropin releasing hormone (GnRH) expression, autoregulation and effects in two models of rat luteinized ovarian cells
E M Sorianello, M O Fernandez, P N Catalano, et al.
Eye (London, England)
|
July 21, 2007
Autologous translocation of the choroid and RPE in age-related macular degeneration: 1-year follow-up in 30 patients and recommendations for patient selection
F M A Heussen, N F Fawzy, S Joeres, et al.
Frontiers in Cellular and Infection Microbiology
|
October 1, 2021
Unilateral Intervention in the Sinuses of Rabbits Induces Bilateral Inflammatory and Microbial Changes
Christian A Lux, James J Johnston, Sharon Waldvogel-Thurlow, et al.
Genomics
|
January 15, 1994
Characterization of a microdissection library from human chromosome region 3p14
W Bardenheuer, S Szymanski, A Lux, et al.
Page
of 17
Search research articles
Search
Showing results (121-130 of 166) with videos related to
Sort By:
Page
of 17
Journal of Medical Genetics
|
August 16, 2003
Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations
J Berg, M Porteous, D Reinhardt, et al.
The Journal of Clinical Investigation
|
June 1, 1992
Serological cross-reactivity between a human Ro/SS-A autoantigen (calreticulin) and the lambda Ral-1 antigen of Onchocerca volvulus
F A Lux, D P McCauliffe, D W Büttner, et al.
Cancer Gene Therapy
|
August 13, 2005
Peritoneal cancer treatment with CYP2B1 transfected, microencapsulated cells and ifosfamide
S Samel, M Keese, A Lux, et al.
Human Mutation
|
March 1, 2000
Novel missense and frameshift mutations in the activin receptor-like kinase-1 gene in hereditary hemorrhagic telangiectasia. Mutations in brief no. 164. Online
D J Klaus, C J Gallione, K Anthony, et al.
Life Sciences
|
November 27, 2012
Sex differences in insulin resistance in GABAB1 knockout mice
M M Bonaventura, D Rodriguez, M L Ferreira, et al.
The Laryngoscope
|
January 16, 2023
In vitro Nasodine Can be an Effective Antibiofilm Agent for Biofilms that May Cause CRS
Samuel J M Hale, Christian A Lux, Raymond Kim, et al.
Life Sciences
|
July 12, 2005
Differential gonadotropin releasing hormone (GnRH) expression, autoregulation and effects in two models of rat luteinized ovarian cells
E M Sorianello, M O Fernandez, P N Catalano, et al.
Eye (London, England)
|
July 21, 2007
Autologous translocation of the choroid and RPE in age-related macular degeneration: 1-year follow-up in 30 patients and recommendations for patient selection
F M A Heussen, N F Fawzy, S Joeres, et al.
Frontiers in Cellular and Infection Microbiology
|
October 1, 2021
Unilateral Intervention in the Sinuses of Rabbits Induces Bilateral Inflammatory and Microbial Changes
Christian A Lux, James J Johnston, Sharon Waldvogel-Thurlow, et al.
Genomics
|
January 15, 1994
Characterization of a microdissection library from human chromosome region 3p14
W Bardenheuer, S Szymanski, A Lux, et al.
Page
of 17