Jorge Zamora | Universidad Complutense de Madrid (original) (raw)
Papers by Jorge Zamora
Journal of Wine Research, 2007
... of both genders, and towards a protective attitude of wine culture. It is missing a more effi... more ... of both genders, and towards a protective attitude of wine culture. It is missing a more efficient use of open space and genuine involvement of local communities in the implementation of programs for sustainable wine tourism. ...
Archives of Insect Biochemistry and Physiology, 2002
In Manduca sexta larvae, radioactive free cholesterol is absorbed directly from the midgut into m... more In Manduca sexta larvae, radioactive free cholesterol is absorbed directly from the midgut into mucosal cells where it is stored both in the free form (87% in males and 93% in females) and esterified form (13% in males and 7% in females). Subsequently, cholesterol is transported to fat body via lipophorin in the hemolymph exclusively in the free form. In fat body, the distribution of cholesterol between the free and esterified form varied significantly between genders and developmental stages. Except for the larval stage, males and females were able to store cholesterol in both free and esterified forms in the fat body and in the adult stage cholesterol ester accounted for more than 75% of the stored cholesterol. Placement of radioactive cholesterol at different locations in the gut-foregut, midgut, and hindgut-demonstrated that the midgut is the site where cholesterol is absorbed and released into the hemolymph. Cholesterol-labeled lipophorin injected into larval hemolymph was cleared from the hemolymph with a half-life of 10.2 h. After 17 h, most of the cleared radioactivity was recovered in the fat body (38%). Arch.
European Journal of Medical Genetics, 2006
Journal of Gastroenterology and Hepatology, 2005
It has been postulated that the HFE C282Y mutation (linked to human leukocyte antigen [HLA]-A3-B7... more It has been postulated that the HFE C282Y mutation (linked to human leukocyte antigen [HLA]-A3-B7 haplotype) is not only responsible for hereditary hemochromatosis; HLA class I alleles would also contribute to the disease pathogenesis. In addition, H63D mutation linked to HLA-A29-B44 would also be pathogenetic, particularly in the Mediterranean Basin and throughout the world. However, sporadic porphyria cutanea tarda (s-PCT) has also been linked to these HFE mutations. In the present work, we have studied HFE mutations and HLA genes to test these hypotheses. C282Y and H63D mutations together with HLA genetic typing have been performed in Spanish hereditary hemochromatosis (n = 98) and PCT (n = 63) patients. The etiologic fraction (delta) has been used to determine the absolute strongest gene linkage to both diseases. The Spanish frequent HLA-A29-B44 haplotype is not significantly associated to the H63D mutations in hereditary hemochromatosis patients (although it is found more frequently in patients than in controls). Sporadic porphyria cutanea tarda patients do not show a significant association to H63D mutations, although it is also more frequent than in controls; however, compound H63D/C282Y subjects seem to bear a significant risk to s-PCT. Allelic C282Y (and not H63D) frequencies show a significant association with s-PCT. The postulated additional risk of hereditary hemochromatosis given by class I HLA antigens may be secondary to the HFE gene linkage disequilibrium with certain class I alleles or to the existence of other neighboring genetic pathogenetic factors in our Spanish sample.
Journal of Molecular Evolution, 2001
Journal of Ornithology, 2007
The radiation of canaries (genus Serinus) occurred in Africa and Eurasia during the Miocene Epoch... more The radiation of canaries (genus Serinus) occurred in Africa and Eurasia during the Miocene Epoch (9 million years ago) according to maximum parsimony (MP), neighbor-joining (NJ), maximum likelihood (ML) and Bayesian methodologies. Serinus canaria (wild canary) and S. serinus (European serin) together form one of the several polytomies within the genus Serinus phylogenetic trees. In a relatively late period, a wild ancestor of S. canaria invaded the Canary Islands, and these birds are the origin of all existing cage canaries, including the first genetically engineered animal: the red canary. The present analysis of the major histocompatibility complex (MHC) molecules in the Canary Islands' species S. canaria shows that the evolution of the MHC in this species is overall different and faster than that of continental species – namely, S. thibetanus (Asia) and S. mozambicus (Africa) – but particularly so in the peptide binding region. These data support the hypothesis that oceanic islands may be evolutionary reservoirs and not evolutionary dead ends.
Immunogenetics, 2004
Two theories about MHC allele generation have been put forward: (1) point mutation diversificatio... more Two theories about MHC allele generation have been put forward: (1) point mutation diversification and/or (2) gene conversion events. A model supporting the existence of both of these mechanisms is shown in this paper; the possible evolution of the HLA-B*570101 and HLA-B*5801 alleles (which belong to the HLA-B17 serology group) is studied. The hypothesis favoured is that gene conversion events have originated these alleles, because intron sequences are also analysed. Evolution by point mutation should only be accepted if flanking introns have also been sequenced.
Journal of Gastroenterology and Hepatology, 2005
It has been postulated that the HFE C282Y mutation (linked to human leukocyte antigen [HLA]-A3-B7... more It has been postulated that the HFE C282Y mutation (linked to human leukocyte antigen [HLA]-A3-B7 haplotype) is not only responsible for hereditary hemochromatosis; HLA class I alleles would also contribute to the disease pathogenesis. In addition, H63D mutation linked to HLA-A29-B44 would also be pathogenetic, particularly in the Mediterranean Basin and throughout the world. However, sporadic porphyria cutanea tarda (s-PCT) has also been linked to these HFE mutations. In the present work, we have studied HFE mutations and HLA genes to test these hypotheses. C282Y and H63D mutations together with HLA genetic typing have been performed in Spanish hereditary hemochromatosis (n = 98) and PCT (n = 63) patients. The etiologic fraction (delta) has been used to determine the absolute strongest gene linkage to both diseases. The Spanish frequent HLA-A29-B44 haplotype is not significantly associated to the H63D mutations in hereditary hemochromatosis patients (although it is found more frequently in patients than in controls). Sporadic porphyria cutanea tarda patients do not show a significant association to H63D mutations, although it is also more frequent than in controls; however, compound H63D/C282Y subjects seem to bear a significant risk to s-PCT. Allelic C282Y (and not H63D) frequencies show a significant association with s-PCT. The postulated additional risk of hereditary hemochromatosis given by class I HLA antigens may be secondary to the HFE gene linkage disequilibrium with certain class I alleles or to the existence of other neighboring genetic pathogenetic factors in our Spanish sample.
Journal of Ornithology, 2006
The evolutionary history of three out of four birds traditionally classified into the genus Rhodo... more The evolutionary history of three out of four birds traditionally classified into the genus Rhodopechys birds has been studied by comparing their mitochondrial cytochrome b DNA sequence with that of greenfinches and other genus Carduelis finches. The desert finch (Rhodopechys obsoleta) or a sister extinct species seems to have existed about 6 million years ago in Asian and perhaps African desert-like areas. This bird has no molecular relationship with other Rhodopechys birds and seems to have given rise to the greenfinches radiation, probably by allopatry of marginal or isolated groups; the latter would have evolved to green plumage colours and more simple song modulations (i.e., greenfinches). The possible role of assortative mating and the newly postulated acquired phenotypic characters in greenfinches speciation are discussed.
Molecular Immunology, 2006
Annales De Genetique, 2004
European Journal of Medical Genetics, 2006
Journal of Wine Research, 2007
... of both genders, and towards a protective attitude of wine culture. It is missing a more effi... more ... of both genders, and towards a protective attitude of wine culture. It is missing a more efficient use of open space and genuine involvement of local communities in the implementation of programs for sustainable wine tourism. ...
Archives of Insect Biochemistry and Physiology, 2002
In Manduca sexta larvae, radioactive free cholesterol is absorbed directly from the midgut into m... more In Manduca sexta larvae, radioactive free cholesterol is absorbed directly from the midgut into mucosal cells where it is stored both in the free form (87% in males and 93% in females) and esterified form (13% in males and 7% in females). Subsequently, cholesterol is transported to fat body via lipophorin in the hemolymph exclusively in the free form. In fat body, the distribution of cholesterol between the free and esterified form varied significantly between genders and developmental stages. Except for the larval stage, males and females were able to store cholesterol in both free and esterified forms in the fat body and in the adult stage cholesterol ester accounted for more than 75% of the stored cholesterol. Placement of radioactive cholesterol at different locations in the gut-foregut, midgut, and hindgut-demonstrated that the midgut is the site where cholesterol is absorbed and released into the hemolymph. Cholesterol-labeled lipophorin injected into larval hemolymph was cleared from the hemolymph with a half-life of 10.2 h. After 17 h, most of the cleared radioactivity was recovered in the fat body (38%). Arch.
European Journal of Medical Genetics, 2006
Journal of Gastroenterology and Hepatology, 2005
It has been postulated that the HFE C282Y mutation (linked to human leukocyte antigen [HLA]-A3-B7... more It has been postulated that the HFE C282Y mutation (linked to human leukocyte antigen [HLA]-A3-B7 haplotype) is not only responsible for hereditary hemochromatosis; HLA class I alleles would also contribute to the disease pathogenesis. In addition, H63D mutation linked to HLA-A29-B44 would also be pathogenetic, particularly in the Mediterranean Basin and throughout the world. However, sporadic porphyria cutanea tarda (s-PCT) has also been linked to these HFE mutations. In the present work, we have studied HFE mutations and HLA genes to test these hypotheses. C282Y and H63D mutations together with HLA genetic typing have been performed in Spanish hereditary hemochromatosis (n = 98) and PCT (n = 63) patients. The etiologic fraction (delta) has been used to determine the absolute strongest gene linkage to both diseases. The Spanish frequent HLA-A29-B44 haplotype is not significantly associated to the H63D mutations in hereditary hemochromatosis patients (although it is found more frequently in patients than in controls). Sporadic porphyria cutanea tarda patients do not show a significant association to H63D mutations, although it is also more frequent than in controls; however, compound H63D/C282Y subjects seem to bear a significant risk to s-PCT. Allelic C282Y (and not H63D) frequencies show a significant association with s-PCT. The postulated additional risk of hereditary hemochromatosis given by class I HLA antigens may be secondary to the HFE gene linkage disequilibrium with certain class I alleles or to the existence of other neighboring genetic pathogenetic factors in our Spanish sample.
Journal of Molecular Evolution, 2001
Journal of Ornithology, 2007
The radiation of canaries (genus Serinus) occurred in Africa and Eurasia during the Miocene Epoch... more The radiation of canaries (genus Serinus) occurred in Africa and Eurasia during the Miocene Epoch (9 million years ago) according to maximum parsimony (MP), neighbor-joining (NJ), maximum likelihood (ML) and Bayesian methodologies. Serinus canaria (wild canary) and S. serinus (European serin) together form one of the several polytomies within the genus Serinus phylogenetic trees. In a relatively late period, a wild ancestor of S. canaria invaded the Canary Islands, and these birds are the origin of all existing cage canaries, including the first genetically engineered animal: the red canary. The present analysis of the major histocompatibility complex (MHC) molecules in the Canary Islands' species S. canaria shows that the evolution of the MHC in this species is overall different and faster than that of continental species – namely, S. thibetanus (Asia) and S. mozambicus (Africa) – but particularly so in the peptide binding region. These data support the hypothesis that oceanic islands may be evolutionary reservoirs and not evolutionary dead ends.
Immunogenetics, 2004
Two theories about MHC allele generation have been put forward: (1) point mutation diversificatio... more Two theories about MHC allele generation have been put forward: (1) point mutation diversification and/or (2) gene conversion events. A model supporting the existence of both of these mechanisms is shown in this paper; the possible evolution of the HLA-B*570101 and HLA-B*5801 alleles (which belong to the HLA-B17 serology group) is studied. The hypothesis favoured is that gene conversion events have originated these alleles, because intron sequences are also analysed. Evolution by point mutation should only be accepted if flanking introns have also been sequenced.
Journal of Gastroenterology and Hepatology, 2005
It has been postulated that the HFE C282Y mutation (linked to human leukocyte antigen [HLA]-A3-B7... more It has been postulated that the HFE C282Y mutation (linked to human leukocyte antigen [HLA]-A3-B7 haplotype) is not only responsible for hereditary hemochromatosis; HLA class I alleles would also contribute to the disease pathogenesis. In addition, H63D mutation linked to HLA-A29-B44 would also be pathogenetic, particularly in the Mediterranean Basin and throughout the world. However, sporadic porphyria cutanea tarda (s-PCT) has also been linked to these HFE mutations. In the present work, we have studied HFE mutations and HLA genes to test these hypotheses. C282Y and H63D mutations together with HLA genetic typing have been performed in Spanish hereditary hemochromatosis (n = 98) and PCT (n = 63) patients. The etiologic fraction (delta) has been used to determine the absolute strongest gene linkage to both diseases. The Spanish frequent HLA-A29-B44 haplotype is not significantly associated to the H63D mutations in hereditary hemochromatosis patients (although it is found more frequently in patients than in controls). Sporadic porphyria cutanea tarda patients do not show a significant association to H63D mutations, although it is also more frequent than in controls; however, compound H63D/C282Y subjects seem to bear a significant risk to s-PCT. Allelic C282Y (and not H63D) frequencies show a significant association with s-PCT. The postulated additional risk of hereditary hemochromatosis given by class I HLA antigens may be secondary to the HFE gene linkage disequilibrium with certain class I alleles or to the existence of other neighboring genetic pathogenetic factors in our Spanish sample.
Journal of Ornithology, 2006
The evolutionary history of three out of four birds traditionally classified into the genus Rhodo... more The evolutionary history of three out of four birds traditionally classified into the genus Rhodopechys birds has been studied by comparing their mitochondrial cytochrome b DNA sequence with that of greenfinches and other genus Carduelis finches. The desert finch (Rhodopechys obsoleta) or a sister extinct species seems to have existed about 6 million years ago in Asian and perhaps African desert-like areas. This bird has no molecular relationship with other Rhodopechys birds and seems to have given rise to the greenfinches radiation, probably by allopatry of marginal or isolated groups; the latter would have evolved to green plumage colours and more simple song modulations (i.e., greenfinches). The possible role of assortative mating and the newly postulated acquired phenotypic characters in greenfinches speciation are discussed.
Molecular Immunology, 2006
Annales De Genetique, 2004
European Journal of Medical Genetics, 2006