Genetic Control of the Circulating Concentration of Transforming Growth Factor Type β1 von Grainger, David J., Heathcote, Kirsten, Chiano, Mathias, Snieder, Harold, Kemp, Paul R., Metcalfe, James C., Carter, Nicholas D., Specter, Tim D.

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Molecular Analysis of Berardinelli-Seip Congenital Lipodystrophy in Oman von Kirsten Heathcote, Anna Rajab, Jocelyne Magré, Petros Syrris, Mehran Besti, Michael Patton, Marc Délépine, Mark Lathrop, Jacqueline Capeau, Steve Jeffery

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Common arterial trunk associated with a homeodomain mutation of NKX2.6 von Heathcote, Kirsten, Braybrook, Claire, Abushaban, Lulu, Guy, Michelle, Khetyar, Maher E., Patton, Michael A., Carter, Nicholas D., Scambler, Peter J., Syrris, Petros

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A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350) von Heathcote, Kirsten, Syrris, Petros, Carter, Nicholas D, Patton, Michael A

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Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: Evidence for multiple loci von HEATHEOTE, Kirsten, RAJAB, Anna, MAGRE, Jocelyne, SYRRIS, Petros, BESTI, Mehran, PATTON, Michael, DELEPINE, Marc, LATHROP, Mark, CAPEAU, Jacqueline, JEFFERY, Steve

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Human piebaldism: six novel mutations of the proto-oncogene KIT von Syrris, Petros, Heathcote, Kirsten, Carrozzo, Romeo, Devriendt, Koen, Elçioglu, Nursel, Garrett, Christine, McEntagart, Meriel, Carter, Nicholas D.

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Heterogeneity for congenital generalized lipodystrophy in seventeen patients from Oman von Rajab, Anna, Heathcote, Kirsten, Joshi, Surendra, Jeffery, Steve, Patton, Michael

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Human piebaldism: six novel mutations of the proto-oncogene KIT: MUTATIONS IN BRIEF von Syrris, Petros, Heathcote, Kirsten, Carrozzo, Romeo, Devriendt, Koen, Elçioglu, Nursel, Garrett, Christine, McEntagart, Meriel, Carter, Nicholas D.

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Genetic control of the circulating concentration of transforming growth factor type [beta]1 von Grainger, David J, Heathcote, Kirsten, Chiano, Mathias, Snieder, Harold, Kemp, Paul R, Metcalfe, James C, Carter, Nicholas D, Spector, Tim D

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Diagnose durch Bestimmung von Polymorphismen in der Promoterregion des TGF-Beta 1 Gens von HEATHCOTE, KIRSTEN, GRAINGER, DAVID JOHN, SPECTOR, TIMOTHY DAVID

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DIAGNOSE DURCH BESTIMMUNG VON POLYMORPHISMEN IN DER PROMOTERREGION DES TGF-BETA 1 GENS von HEATHCOTE, KIRSTEN, GRAINGER, DAVID JOHN, SPECTOR, TIMOTHY DAVID

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Use of the determination of polymorphims in the promoter region of the TGF-beta 1 gene in diagnosis von HEATHCOTE, KIRSTEN, GRAINGER, DAVID JOHN, SPECTOR, TIMOTHY DAVID

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In vitro method for diagnosis of osteoporosis, atherosclerosis, cancer and immune disorders and medicaments von HEATHCOTE, KIRSTEN, GRAINGER, DAVID JOHN, SPECTOR, TIMOTHY DAVID

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Diagnostic method and apparatus von TIMOTHY DAVID SPECTOR, DAVID JOHN GRAINGER, KIRSTEN HEATHCOTE

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Methods of diagnosis by detecting polymorphisms in the TGF- beta 1 promoter von GRAINGER, DAVID J, HEATHCOTE, KIRSTEN, SPECTOR, TIMOTHY D

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Use of the determination of polymorphims in the promoter region of the TGF-beta 1 gene in diagnosis von HEATHCOTE, KIRSTEN, GRAINGER, DAVID JOHN, SPECTOR, TIMOTHY DAVID

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Diagnostic method and apparatus von TIMOTHY DAVID SPECTOR, DAVID JOHN GRAINGER, KIRSTEN HEATHCOTE

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DIAGNOSTIC METHOD AND APPARATUS von HEATHCOTE, KIRSTEN, GRAINGER, DAVID JOHN, SPECTOR, TIMOTHY DAVID

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DIAGNOSTIC METHOD AND APPARATUS von HEATHCOTE, KIRSTEN, SPECTOR, TIMOTHY, DAVID, GRAINGER, DAVID, JOHN

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The protein LEM promotes CD8⁺ T cell immunity through effects on mitochondrial respiration von Okoye, Isobel, Wang, Lihui, Pallmer, Katharina, Richter, Kirsten, Ichimura, Takahuru, Haas, Robert, Crouse, Josh, Choi, Onjee, Heathcote, Dean, Lovo, Elena, Mauro, Claudio, Abdi, Reza, Oxenius, Annette, Rutschmann, Sophie, Ashton-Rickardt, Philip G.

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