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Results: 1-16 |
Results: 16
MELANOCORTIN-1 RECEPTOR VARIANTS IN AN IRISH POPULATION
Authors: SMITH R HEALY E SIDDIQUI S FLANAGAN N STEIJLEN PM ROSDAHL I JACQUES JP ROGERS S TURNER R JACKSON IJ BIRCHMACHIN MA REES JL
Citation: R. Smith et al., MELANOCORTIN-1 RECEPTOR VARIANTS IN AN IRISH POPULATION, Journal of investigative dermatology, 111(1), 1998, pp. 119-122
THE INHERITANCE OF RED HAIR
Authors: HEALY E FLANAGAN N TODD C JACKSON IJ BIRCHMACHIN MA REES JL
Citation: E. Healy et al., THE INHERITANCE OF RED HAIR, Journal of investigative dermatology, 110(4), 1998, pp. 618-618
MITOCHONDRIAL-DNA AND ULTRAVIOLET-LIGHT EXPOSURE IN HUMAN SKIN
Authors: RAY A TURNER R NIKAIDO O REES JL BIRCHMACHIN MA
Citation: A. Ray et al., MITOCHONDRIAL-DNA AND ULTRAVIOLET-LIGHT EXPOSURE IN HUMAN SKIN, Journal of investigative dermatology, 110(4), 1998, pp. 692-692
MITOCHONDRIAL-DNA DELETIONS IN HUMAN SKIN REFLECT PHOTO RATHER THAN CHRONOLOGICAL AGING
Authors: BIRCHMACHIN MA TINDALL M TURNER R HALDANE F REES JL
Citation: Ma. Birchmachin et al., MITOCHONDRIAL-DNA DELETIONS IN HUMAN SKIN REFLECT PHOTO RATHER THAN CHRONOLOGICAL AGING, Journal of investigative dermatology, 110(2), 1998, pp. 149-152
MONILETHRIX IS CAUSED BY MUTATION IN THE HELIX TERMINATION PEPTIDE OFHUMAN TYPE-II HAIR KERATIN HHB6 IN 3 FAMILIES
Authors: KORGE BP HEALY E TRAUPE H PUNTER C MAUCH C HAMM H BIRCHMACHIN MA BELGAID CE STEPHENSON AM HOLMES SC DARLINGTON S MESSENGER AG REES JL MUNRO CS
Citation: Bp. Korge et al., MONILETHRIX IS CAUSED BY MUTATION IN THE HELIX TERMINATION PEPTIDE OFHUMAN TYPE-II HAIR KERATIN HHB6 IN 3 FAMILIES, Journal of investigative dermatology, 109(3), 1997, pp. 409-409
MITOCHONDRIAL-DNA DELETIONS IN HUMAN SKIN REFLECT PHOTOAGEING RATHER THAN CHRONOLOGICAL AGING
Authors: BIRCHMACHIN MA HALDANE F REES JL
Citation: Ma. Birchmachin et al., MITOCHONDRIAL-DNA DELETIONS IN HUMAN SKIN REFLECT PHOTOAGEING RATHER THAN CHRONOLOGICAL AGING, Journal of investigative dermatology, 109(3), 1997, pp. 436-436
MAPPING OF MONILETHRIX TO THE TYPE-II KERATIN GENE-CLUSTER AT CHROMOSOME 12Q13 IN 3 NEW FAMILIES, INCLUDING ONE WITH VARIABLE EXPRESSIVITY
Authors: BIRCHMACHIN MA HEALY E TURNER R HALDANE F BELGAID CE DARLINGTON S STEPHENSON AM MUNRO C MESSENGER AG REES JL
Citation: Ma. Birchmachin et al., MAPPING OF MONILETHRIX TO THE TYPE-II KERATIN GENE-CLUSTER AT CHROMOSOME 12Q13 IN 3 NEW FAMILIES, INCLUDING ONE WITH VARIABLE EXPRESSIVITY, British journal of dermatology, 137(3), 1997, pp. 339-343
DEFICIENCY OF COMPLEX-II OF THE MITOCHONDRIAL RESPIRATORY-CHAIN IN LATE-ONSET OPTIC ATROPHY AND ATAXIA
Authors: TAYLOR RW BIRCHMACHIN MA SCHAEFER J TAYLOR L SHAKIR R ACKRELL BAC COCHRAN B BINDOFF LA JACKSON MJ GRIFFITHS P TURNBULL DM
Citation: Rw. Taylor et al., DEFICIENCY OF COMPLEX-II OF THE MITOCHONDRIAL RESPIRATORY-CHAIN IN LATE-ONSET OPTIC ATROPHY AND ATAXIA, Annals of neurology, 39(2), 1996, pp. 224-232
HUMAN SKIN MITOCHONDRIAL-DNA DELETIONS ASSOCIATED WITH ULTRAVIOLET-LIGHT EXPOSURE AND AGING SKIN
Authors: BIRCHMACHIN MA REES JL
Citation: Ma. Birchmachin et Jl. Rees, HUMAN SKIN MITOCHONDRIAL-DNA DELETIONS ASSOCIATED WITH ULTRAVIOLET-LIGHT EXPOSURE AND AGING SKIN, Journal of investigative dermatology, 107(3), 1996, pp. 412-412
BIOCHEMICAL INVESTIGATIONS AND IMMUNOBLOT ANALYSES OF 2 UNRELATED PATIENTS WITH AN ISOLATED DEFICIENCY IN COMPLEX-II OF THE MITOCHONDRIAL RESPIRATORY-CHAIN
Authors: BIRCHMACHIN MA MARSAC C PONSOT G PARFAIT B TAYLOR RW RUSTIN P MUNNICH A
Citation: Ma. Birchmachin et al., BIOCHEMICAL INVESTIGATIONS AND IMMUNOBLOT ANALYSES OF 2 UNRELATED PATIENTS WITH AN ISOLATED DEFICIENCY IN COMPLEX-II OF THE MITOCHONDRIAL RESPIRATORY-CHAIN, Biochemical and biophysical research communications, 220(1), 1996, pp. 57-62
NEONATAL FANCONI-SYNDROME DUE TO DEFICIENCY OF COMPLEX III OF THE RESPIRATORY-CHAIN
Authors: MORRIS AAM TAYLOR RW BIRCHMACHIN MA JACKSON MJ COULTHARD MG BINDOFF LA WELCH RJ HOWELL N TURNBULL DM
Citation: Aam. Morris et al., NEONATAL FANCONI-SYNDROME DUE TO DEFICIENCY OF COMPLEX III OF THE RESPIRATORY-CHAIN, Pediatric nephrology, 9(4), 1995, pp. 407-411
AN EVALUATION OF THE MEASUREMENT OF THE ACTIVITIES OF COMPLEXES I-IV IN THE RESPIRATORY-CHAIN OF HUMAN SKELETAL-MUSCLE MITOCHONDRIA
Authors: BIRCHMACHIN MA BRIGGS HL SABORIDO AA BINDOFF LA TURNBULL DM
Citation: Ma. Birchmachin et al., AN EVALUATION OF THE MEASUREMENT OF THE ACTIVITIES OF COMPLEXES I-IV IN THE RESPIRATORY-CHAIN OF HUMAN SKELETAL-MUSCLE MITOCHONDRIA, Biochemical medicine and metabolic biology, 51(1), 1994, pp. 35-42
THE CONTROL OF MITOCHONDRIAL OXIDATIONS BY COMPLEX-III IN RAT MUSCLE AND LIVER-MITOCHONDRIA - IMPLICATIONS FOR OUR UNDERSTANDING OF MITOCHONDRIAL CYTOPATHIES IN MAN
Authors: TAYLOR RW BIRCHMACHIN MA BARTLETT K LOWERSON SA TURNBULL DM
Citation: Rw. Taylor et al., THE CONTROL OF MITOCHONDRIAL OXIDATIONS BY COMPLEX-III IN RAT MUSCLE AND LIVER-MITOCHONDRIA - IMPLICATIONS FOR OUR UNDERSTANDING OF MITOCHONDRIAL CYTOPATHIES IN MAN, The Journal of biological chemistry, 269(5), 1994, pp. 3523-3528
THE CDNA SEQUENCE OF THE FLAVOPROTEIN SUBUNIT OF HUMAN HEART SUCCINATE-DEHYDROGENASE
Authors: MORRIS AAM FARNSWORTH L ACKRELL BAC TURNBULL DM BIRCHMACHIN MA
Citation: Aam. Morris et al., THE CDNA SEQUENCE OF THE FLAVOPROTEIN SUBUNIT OF HUMAN HEART SUCCINATE-DEHYDROGENASE, Biochimica et biophysica acta. Bioenergetics, 1185(1), 1994, pp. 125-128
DEFECTS OF OXIDATIVE-PHOSPHORYLATION IN MAN
Authors: TAYLOR RW BIRCHMACHIN MA LOWERSON S SHERRATT HSA WEST IC BARTLETT K TURNBULL DM
Citation: Rw. Taylor et al., DEFECTS OF OXIDATIVE-PHOSPHORYLATION IN MAN, Biochemical Society transactions, 21(3), 1993, pp. 804-807
SUCCINATE-CYTOCHROME-C REDUCTASE - ASSESSMENT OF ITS VALUE IN THE INVESTIGATION OF DEFECTS OF THE RESPIRATORY-CHAIN
Authors: TAYLOR RW BIRCHMACHIN MA BARTLETT K TURNBULL DM
Citation: Rw. Taylor et al., SUCCINATE-CYTOCHROME-C REDUCTASE - ASSESSMENT OF ITS VALUE IN THE INVESTIGATION OF DEFECTS OF THE RESPIRATORY-CHAIN, Biochimica et biophysica acta, 1181(3), 1993, pp. 261-265
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