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A Gal

Showing results (181-190 of 488) with videos related to

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Human Genetics|December 1, 1996
Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285S Y Xu, M Denton, L Sullivan, et al.
Oncogene|August 29, 2007
Sustained TGF beta exposure suppresses Smad and non-Smad signalling in mammary epithelial cells, leading to EMT and inhibition of growth arrest and apoptosisA Gal, T Sjöblom, L Fedorova, et al.
Der Nervenarzt|April 29, 1998
[Adrenoleukodystrophy and adrenomyeloneuropathy. Clinical biochemical and molecular genetic findings]M Vorgerd, H G Benkmann, M Tegenthoff, et al.
Journal of Biomechanics|July 28, 2004
Analysis of human mandibular mechanics based on screw theory and in vivo dataJ A Gal, L M Gallo, S Palla, et al.
Journal of Medical Genetics|October 3, 1999
Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian familyS Gu, G Kumaramanickavel, C R Srikumari, et al.
Nature Genetics|July 1, 1995
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in JapaneseS Fuchs, M Nakazawa, M Maw, et al.
Contributions to Nephrology|November 2, 2001
Angiokeratoma and pain, but not Fabry's disease: considerations for differential diagnosisM Ries, K Wendrich, C Whybra, et al.
Journal of the American Academy of Dermatology|August 1, 1994
Disseminated strongyloidiasis with cutaneous manifestations in an immunocompromised hostS M Gordon, A A Gal, A R Solomon, et al.
Clinical Cardiology|December 1, 1991
Long-term prognostic value of a normal dipyridamole thallium-201 perfusion scanR A Gal, J Gunasekera, T Massardo, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1989
[An at-risk pregnancy of a carrier of cystic fibrosis (mucoviscidosis) with a new partner]J Reiss, M Krawczak, A Gal, et al.
Pageof 49

Showing results (181-190 of 488) with videos related to

Sort By:
Pageof 49
Human Genetics|December 1, 1996
Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285S Y Xu, M Denton, L Sullivan, et al.
Oncogene|August 29, 2007
Sustained TGF beta exposure suppresses Smad and non-Smad signalling in mammary epithelial cells, leading to EMT and inhibition of growth arrest and apoptosisA Gal, T Sjöblom, L Fedorova, et al.
Der Nervenarzt|April 29, 1998
[Adrenoleukodystrophy and adrenomyeloneuropathy. Clinical biochemical and molecular genetic findings]M Vorgerd, H G Benkmann, M Tegenthoff, et al.
Journal of Biomechanics|July 28, 2004
Analysis of human mandibular mechanics based on screw theory and in vivo dataJ A Gal, L M Gallo, S Palla, et al.
Journal of Medical Genetics|October 3, 1999
Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian familyS Gu, G Kumaramanickavel, C R Srikumari, et al.
Nature Genetics|July 1, 1995
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in JapaneseS Fuchs, M Nakazawa, M Maw, et al.
Contributions to Nephrology|November 2, 2001
Angiokeratoma and pain, but not Fabry's disease: considerations for differential diagnosisM Ries, K Wendrich, C Whybra, et al.
Journal of the American Academy of Dermatology|August 1, 1994
Disseminated strongyloidiasis with cutaneous manifestations in an immunocompromised hostS M Gordon, A A Gal, A R Solomon, et al.
Clinical Cardiology|December 1, 1991
Long-term prognostic value of a normal dipyridamole thallium-201 perfusion scanR A Gal, J Gunasekera, T Massardo, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1989
[An at-risk pregnancy of a carrier of cystic fibrosis (mucoviscidosis) with a new partner]J Reiss, M Krawczak, A Gal, et al.
Pageof 49