-
1
-
-
0034920620
-
-
Akey J. M., Wang H., Xiong M. [et al.], Interaction between the melanocortin-1 receptor and P genes contributes to inter-individual variation in skin pigmentation phenotypes in a Tibetan population, Human Genetics 2001, 108, 516-520.
-
Akey J. M., Wang H., Xiong M. [et al.], Interaction between the melanocortin-1 receptor and P genes contributes to inter-individual variation in skin pigmentation phenotypes in a Tibetan population, Human Genetics 2001, 108, 516-520.
-
-
-
-
2
-
-
0038383793
-
et al.], Genetics of the serotonergic system in suicidal behavior
-
37
-
Arango V., Huang Y. Y., Underwood M. D. [et al.], Genetics of the serotonergic system in suicidal behavior, Journal of Psychological Research 2003, 37, 375-386.
-
(2003)
Journal of Psychological Research
, pp. 375-386
-
-
Arango, V.1
Huang, Y.Y.2
Underwood, M.D.3
-
3
-
-
0030843448
-
-
Bar W., Brinkmann B., Budowle B. [et al.], recommendations. Further report of the DNA Commission of the ISFH regarding the use of short tandem repeat systems, International Society for Forensic Haemogenetics, International Journal of Legal Medicine 1997, 110, 175-176.
-
Bar W., Brinkmann B., Budowle B. [et al.], recommendations. Further report of the DNA Commission of the ISFH regarding the use of short tandem repeat systems, International Society for Forensic Haemogenetics, International Journal of Legal Medicine 1997, 110, 175-176.
-
-
-
-
5
-
-
0036598550
-
et al.], SNPstream UHT: Ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery
-
74
-
Bell P. A., Chaturvedi S., Gelfand C. A. [et al.], SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery, Biotechniques 2002, 74, 76-77.
-
(2002)
Biotechniques
, pp. 76-77
-
-
Bell, P.A.1
Chaturvedi, S.2
Gelfand, C.A.3
-
6
-
-
0036308132
-
Coding or non-coding, that is the question: Having solved the last technical hurdles to extract DNA information from virtually any biological material, forensic biologists now have to ponder the ethical and social questions of using information from exonic DNA,
-
2002, 3, 498-502
-
Benecke M., Coding or non-coding, that is the question: having solved the last technical hurdles to extract DNA information from virtually any biological material, forensic biologists now have to ponder the ethical and social questions of using information from exonic DNA, The European Molecular Biology Organisation Reports 2002, 3, 498-502.
-
The European Molecular Biology Organisation Reports
-
-
Benecke, M.1
-
9
-
-
33644950802
-
-
Brudnik U., Wojas-Pelc A., Branicki W., Genetyczne uwarunkowania czerniaka, Postȩpy Dermatologii i Alergologii 2006, 23, 21-25.
-
(2006)
Postȩpy Dermatologii i Alergologii
, vol.23
, pp. 21-25
-
-
Brudnik, U.1
Wojas-Pelc, A.2
Branicki, W.3
uwarunkowania czerniaka, G.4
-
10
-
-
0027442475
-
et al.], Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A
-
262
-
Brunner H. G., Nelen M., Breakefield X. O. [et al.], Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A, Science 1993, 262, 578-580.
-
(1993)
Science
, pp. 578-580
-
-
Brunner, H.G.1
Nelen, M.2
Breakefield, X.O.3
-
12
-
-
33845801707
-
The color of a Dalmatian's spots: Linkage evidence to support the TYRP1 gene
-
et al
-
Cargill E. J., Famula T. R., Schnabel R. D. [et al.], The color of a Dalmatian's spots: linkage evidence to support the TYRP1 gene, Biomed Central Veterinary Research 2005, 1, 1.
-
(2005)
Biomed Central Veterinary Research
, vol.1
, pp. 1
-
-
Cargill, E.J.1
Famula, T.R.2
Schnabel, R.D.3
-
13
-
-
0343091513
-
et al.], DNA commission of the international society for forensic genetics: Guidelines for mitochondrial DNA typing
-
110
-
Carracedo A., Bar W., Lincoln P. [et al.], DNA commission of the international society for forensic genetics: guidelines for mitochondrial DNA typing, Forensic Science International 2000, 110, 79-85.
-
(2000)
Forensic Science International
, pp. 79-85
-
-
Carracedo, A.1
Bar, W.2
Lincoln, P.3
-
15
-
-
0036910868
-
manhunt - an application of Y-chromosome STRs
-
Dettlaff-Ka̧kol A., Pawlowski R., First Polish DNA "manhunt" - an application of Y-chromosome STRs, International Journal of Legal Medicine 2002, 116, 289-291.
-
(2002)
International Journal of Legal Medicine
, vol.116
, pp. 289-291
-
-
Dettlaff-Ka̧kol, A.1
Pawlowski, R.2
First Polish, D.N.A.3
-
16
-
-
25144458042
-
et al.], Validation of a 21-locus autosomal SNP multiplex for forensic identification purposes
-
154
-
Dixon L. A., Murray C. M., Archer E. J. [et al.], Validation of a 21-locus autosomal SNP multiplex for forensic identification purposes, Forensic Science International 2005, 154, 62-77.
-
(2005)
Forensic Science International
, pp. 62-77
-
-
Dixon, L.A.1
Murray, C.M.2
Archer, E.J.3
-
17
-
-
1242307966
-
et al.], Interactive effects of MC1R and OCA2 on melanoma risk phenotype
-
13
-
Duffy D. L., Box N. F., Chen W. [et al.], Interactive effects of MC1R and OCA2 on melanoma risk phenotype. Human Molecular Genetics 2004, 13, 447-461.
-
(2004)
Human Molecular Genetics
, pp. 447-461
-
-
Duffy, D.L.1
Box, N.F.2
Chen, W.3
-
18
-
-
0347361675
-
et al.], Sequences associated with human iris pigmentation
-
165
-
Frudakis T., Thomas M., Gaskin Z. [et al.], Sequences associated with human iris pigmentation, Genetics 2003, 165, 2071-2083.
-
(2003)
Genetics
, pp. 2071-2083
-
-
Frudakis, T.1
Thomas, M.2
Gaskin, Z.3
-
19
-
-
0037711623
-
et al.], A classifier for the SNP-based inference of ancestry
-
48
-
Frudakis T., Venkateswarlu K., Thomas M. J. [et al.], A classifier for the SNP-based inference of ancestry, Journal of Forensic Sciences 2003, 48, 771-782.
-
(2003)
Journal of Forensic Sciences
, pp. 771-782
-
-
Frudakis, T.1
Venkateswarlu, K.2
Thomas, M.J.3
-
20
-
-
0035055939
-
An assessment of the utility of single nucleotide polymorphisms (SNPs) for forensic purposes
-
Gill P., An assessment of the utility of single nucleotide polymorphisms (SNPs) for forensic purposes, International Journal of Legal Medicine 2001, 114, 204-210.
-
(2001)
International Journal of Legal Medicine
, vol.114
, pp. 204-210
-
-
Gill, P.1
-
21
-
-
0842306977
-
-
Gill P., Werrett D. J., Budowle B. [et al.], An assessment of whether SNPs will replace STRs in national DNA databases - joint considerations of the DNA working group of the European Network of Forensic Science Institutes (ENFSI) and the Scientific Working Group on DNA Analysis Methods (SWGDAM), Science and Justice 2004, 44, 51-53.
-
Gill P., Werrett D. J., Budowle B. [et al.], An assessment of whether SNPs will replace STRs in national DNA databases - joint considerations of the DNA working group of the European Network of Forensic Science Institutes (ENFSI) and the Scientific Working Group on DNA Analysis Methods (SWGDAM), Science and Justice 2004, 44, 51-53.
-
-
-
-
22
-
-
14944367557
-
Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation
-
Graf J., Hodgson R., van Daal A., Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation, Human Mutation 2005, 25, 278-284.
-
(2005)
Human Mutation
, vol.25
, pp. 278-284
-
-
Graf, J.1
Hodgson, R.2
van Daal, A.3
-
23
-
-
0035500953
-
-
Grimes E. A, Noake P. J., Dixon L. [et al.], Sequence polymorphism in the human melanocortin 1 receptor gene as an indicator of the red hair phenotype, Forensic Science International 2001, 122, 124-129.
-
Grimes E. A, Noake P. J., Dixon L. [et al.], Sequence polymorphism in the human melanocortin 1 receptor gene as an indicator of the red hair phenotype, Forensic Science International 2001, 122, 124-129.
-
-
-
-
24
-
-
0033927855
-
-
Harding R. M., Healy E., Ray A. J. [et al.], Evidence for variable selective pressures at MC1, American Journal of Human Genetics 2000, 66, 1351-1361.
-
Harding R. M., Healy E., Ray A. J. [et al.], Evidence for variable selective pressures at MC1, American Journal of Human Genetics 2000, 66, 1351-1361.
-
-
-
-
25
-
-
0038795172
-
Genetics of melanoma predisposition
-
Hayward N. K., Genetics of melanoma predisposition, Oncogene 2003, 22, 3053-3062.
-
(2003)
Oncogene
, vol.22
, pp. 3053-3062
-
-
Hayward, N.K.1
-
26
-
-
3242725813
-
-
Jiang Y., Wilk J. B., Borecki I. [et al.], Common variants in the 5′ region of the leptin gene are associated with body mass index in men from the National Heart, Lung, and Blood Institute Family Heart Study, American Journal of Human Genetics 2004, 75, 220-230.
-
Jiang Y., Wilk J. B., Borecki I. [et al.], Common variants in the 5′ region of the leptin gene are associated with body mass index in men from the National Heart, Lung, and Blood Institute Family Heart Study, American Journal of Human Genetics 2004, 75, 220-230.
-
-
-
-
27
-
-
0026879472
-
Light is a dominant mouse mutation resulting in premature cell death
-
Johnson R., Jackson I. J., Light is a dominant mouse mutation resulting in premature cell death, Nature Genetics 1992, 1, 226-229.
-
(1992)
Nature Genetics
, vol.1
, pp. 226-229
-
-
Johnson, R.1
Jackson, I.J.2
-
28
-
-
0032006951
-
Using mitochondrial and nuclear DNA markers to reconstruct human evolution
-
Jorde L. B., Bamshad M., Rogers A. R., Using mitochondrial and nuclear DNA markers to reconstruct human evolution, Bioessays 1998, 20, 126-136.
-
(1998)
Bioessays
, vol.20
, pp. 126-136
-
-
Jorde, L.B.1
Bamshad, M.2
Rogers, A.R.3
-
29
-
-
0036181358
-
et al.], A polymorphism in the agouti signaling protein gene is associated with human pigmentation
-
70
-
Kanetsky P. A., Swoyer J., Panossian S. [et al.], A polymorphism in the agouti signaling protein gene is associated with human pigmentation, American Journal of Human Genetics 2002, 70, 770-775.
-
(2002)
American Journal of Human Genetics
, pp. 770-775
-
-
Kanetsky, P.A.1
Swoyer, J.2
Panossian, S.3
-
30
-
-
2942545810
-
-
Kanetsky P. A., Ge F., Najarian D. [et al.], Assessment of polymorphic variants in the melanocortin-1 receptor gene with cutaneous pigmentation using an evolutionary approach, Cancer Epidemiology Biomarkers & Prevention 2004, 13, 808-819.
-
Kanetsky P. A., Ge F., Najarian D. [et al.], Assessment of polymorphic variants in the melanocortin-1 receptor gene with cutaneous pigmentation using an evolutionary approach, Cancer Epidemiology Biomarkers & Prevention 2004, 13, 808-819.
-
-
-
-
31
-
-
0041886412
-
et al.], MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2
-
73
-
King R. A., Willaert R. K., Schmidt R. M. [et al.], MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2), American Journal of Human Genetics 2003, 73, 638-645.
-
(2003)
American Journal of Human Genetics
, pp. 638-645
-
-
King, R.A.1
Willaert, R.K.2
Schmidt, R.M.3
-
32
-
-
0031012096
-
-
Koppula S. V., Robbins L. S., Lu D. [et al.], Identification of common polymorphisms in the coding sequence of the human MSH receptor (MCIR) with possible biological effects, Human Mutation 1997, 9, 30-36.
-
Koppula S. V., Robbins L. S., Lu D. [et al.], Identification of common polymorphisms in the coding sequence of the human MSH receptor (MCIR) with possible biological effects, Human Mutation 1997, 9, 30-36.
-
-
-
-
33
-
-
0031838353
-
-
Krude H., Biebermann H., Luck W. [et al.], Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans, Nature Genetics 1998, 19, 155-157.
-
Krude H., Biebermann H., Luck W. [et al.], Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans, Nature Genetics 1998, 19, 155-157.
-
-
-
-
34
-
-
0038389384
-
Mutations in the human proopiomelanocortin gene
-
Krude H., Biebermann H., Gruters A., Mutations in the human proopiomelanocortin gene, Annals of the New York Academy of Sciences 2003, 994, 233-239.
-
(2003)
Annals of the New York Academy of Sciences
, vol.994
, pp. 233-239
-
-
Krude, H.1
Biebermann, H.2
Gruters, A.3
-
35
-
-
2042437650
-
et al.], Initial sequencing and analysis of the human genome
-
409
-
Lander E. S., Linton L. M., Birren B. [et al.], Initial sequencing and analysis of the human genome, Nature 2001, 409, 860-921.
-
(2001)
Nature
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
-
36
-
-
0028942723
-
-
Lee S. T., Nicholls R. D., Jong M. T. [et al.], Organization and sequence of the human P gene and identification of a new family of transport proteins, Genomics 1995, 26, 354-363.
-
Lee S. T., Nicholls R. D., Jong M. T. [et al.], Organization and sequence of the human P gene and identification of a new family of transport proteins, Genomics 1995, 26, 354-363.
-
-
-
-
37
-
-
23844535500
-
et al.], Chocolate coated cats: TYRP1 mutations for brown color in domestic cats
-
16
-
Lyons L. A., Foe I. T., Rah H. C. [et al.], Chocolate coated cats: TYRP1 mutations for brown color in domestic cats, Mammalian Genome 2005, 16, 356-366.
-
(2005)
Mammalian Genome
, pp. 356-366
-
-
Lyons, L.A.1
Foe, I.T.2
Rah, H.C.3
-
38
-
-
0037716741
-
The UK National DNA Database
-
Linacre A., The UK National DNA Database, Lancet 2003, 361, 1841-1842.
-
(2003)
Lancet
, vol.361
, pp. 1841-1842
-
-
Linacre, A.1
-
39
-
-
5044221485
-
Methods developed to identify victims of the world trade center disaster
-
Marchi E. Methods developed to identify victims of the world trade center disaster, American Laboratory 2004, 36, 30-36.
-
(2004)
American Laboratory
, vol.36
, pp. 30-36
-
-
Marchi, E.1
-
40
-
-
34249813199
-
-
Martin-Guerrero I., Callado L. F., Saitua K. [et al.], The N251K functional polymorphism in the alpha(2A)-adrenoceptor gene is not associated with depression: a study in suicide completers, Psychopharmacology 2005, 7, 1-5.
-
Martin-Guerrero I., Callado L. F., Saitua K. [et al.], The N251K functional polymorphism in the alpha(2A)-adrenoceptor gene is not associated with depression: a study in suicide completers, Psychopharmacology 2005, 7, 1-5.
-
-
-
-
41
-
-
0032913013
-
Molecular basis of albinism: Mutations and polymorphisms of pigmentation genes associated with albinism
-
Oetting W. S., King R. A., Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism, Human Mutation 1999, 13, 99-115.
-
(1999)
Human Mutation
, vol.13
, pp. 99-115
-
-
Oetting, W.S.1
King, R.A.2
-
42
-
-
29444456332
-
-
Oetting W. S., Garrett S. S., Brott M. [et al.], P gene mutations associated with oculocutaneous albinism type II (OCA2), Human Mutation 2005, 25, 323-329.
-
Oetting W. S., Garrett S. S., Brott M. [et al.], P gene mutations associated with oculocutaneous albinism type II (OCA2), Human Mutation 2005, 25, 323-329.
-
-
-
-
43
-
-
16344384807
-
Implications of correlations between skin color and genetic ancestry for biomedical research
-
Parra E. J., Kittles R. A., Shriver M. D., Implications of correlations between skin color and genetic ancestry for biomedical research, Nature Genetics 2004, 36, S54-S60.
-
(2004)
Nature Genetics
, vol.36
-
-
Parra, E.J.1
Kittles, R.A.2
Shriver, M.D.3
-
44
-
-
7244247169
-
et al.], Novel MC1R variants in Ligurian melanoma patients and controls
-
24
-
Pastorino L., Cusano R., Bruno W. [et al.], Novel MC1R variants in Ligurian melanoma patients and controls, Human Mutation 2004, 24, 103-111.
-
(2004)
Human Mutation
, pp. 103-111
-
-
Pastorino, L.1
Cusano, R.2
Bruno, W.3
-
45
-
-
0032918729
-
-
Rana B. K., Hewett-Emmett D., Jin L. [et al.], High polymorphism at the human melanocortin 1 receptor locus, Genetics 1999, 151, 1547-1557.
-
Rana B. K., Hewett-Emmett D., Jin L. [et al.], High polymorphism at the human melanocortin 1 receptor locus, Genetics 1999, 151, 1547-1557.
-
-
-
-
46
-
-
0022646577
-
et al.], Effects of melanin-induced free radicals on the isolated rat peritoneal mast cells
-
86
-
Ranadive N. S., Shirwadkar S., Persad S. [et al.], Effects of melanin-induced free radicals on the isolated rat peritoneal mast cells, Journal of Investigative Dermatology 1986, 86, 303-307.
-
(1986)
Journal of Investigative Dermatology
, pp. 303-307
-
-
Ranadive, N.S.1
Shirwadkar, S.2
Persad, S.3
-
47
-
-
0036325172
-
-
Rebbeck T. R., Kanetsky P. A., Walker A. H. [et al.], P gene as an inherited biomarker of human eye color, Cancer Epidemiol Biomarkers & Prevention 2002, 11, 782-784.
-
Rebbeck T. R., Kanetsky P. A., Walker A. H. [et al.], P gene as an inherited biomarker of human eye color, Cancer Epidemiol Biomarkers & Prevention 2002, 11, 782-784.
-
-
-
-
48
-
-
3442879338
-
Assessing the function of genetic variants in candidate gene association studies
-
Rebbeck T. R., Spitz M., Wu X., Assessing the function of genetic variants in candidate gene association studies, Nature Reviews Genetics 2004, 5, 589-597.
-
(2004)
Nature Reviews Genetics
, vol.5
, pp. 589-597
-
-
Rebbeck, T.R.1
Spitz, M.2
Wu, X.3
-
49
-
-
0346786217
-
Genetics of hair and skin color
-
Rees J. L., Genetics of hair and skin color, Annual Review of Genetics 2003, 37, 67-90.
-
(2003)
Annual Review of Genetics
, vol.37
, pp. 67-90
-
-
Rees, J.L.1
-
50
-
-
6344290128
-
The genetics of sun sensitivity in human
-
Rees J. L., The genetics of sun sensitivity in human, American Journal of Human Genetics 2004, 75, 739-751.
-
(2004)
American Journal of Human Genetics
, vol.75
, pp. 739-751
-
-
Rees, J.L.1
-
51
-
-
3142631983
-
-
Retz W., Retz-Junginger P., Supprian T. [et al.], Association of serotonin transporter promoter gene polymorphism with violence: relation with personality disorders, impulsivity, and childhood ADHD psychopathology, Behavioral Sciences & The Law 2004, 22, 415-425.
-
Retz W., Retz-Junginger P., Supprian T. [et al.], Association of serotonin transporter promoter gene polymorphism with violence: relation with personality disorders, impulsivity, and childhood ADHD psychopathology, Behavioral Sciences & The Law 2004, 22, 415-425.
-
-
-
-
53
-
-
14644429805
-
et al.], MC1R and the response of melanocytes to ultraviolet radiation
-
571
-
Rouzaud F., Kadekaro A. L., Abdel-Malek Z. A. [et al.], MC1R and the response of melanocytes to ultraviolet radiation, Mutation Research 2005, 571, 133-152.
-
(2005)
Mutation Research
, pp. 133-152
-
-
Rouzaud, F.1
Kadekaro, A.L.2
Abdel-Malek, Z.A.3
-
54
-
-
1042299964
-
Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4
-
Rundshagen U., Zuhlke C., Opitz S., Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4, Human Mutation 2004, 23, 106-110.
-
(2004)
Human Mutation
, vol.23
, pp. 106-110
-
-
Rundshagen, U.1
Zuhlke, C.2
Opitz, S.3
-
55
-
-
0942290488
-
et al.], Twin study of genetic and environmental influences on adult body size, shape, and composition
-
28
-
Schousboe K., Visscher P. M., Erbas B. [et al.], Twin study of genetic and environmental influences on adult body size, shape, and composition, The International Journal of Obesity and Related Metabolic Disorders 2004, 28, 39-48.
-
(2004)
The International Journal of Obesity and Related Metabolic Disorders
, pp. 39-48
-
-
Schousboe, K.1
Visscher, P.M.2
Erbas, B.3
-
56
-
-
0038323985
-
et al.], Skin pigmentation, biogeographical ancestry and admixture mapping
-
112
-
Shriver M. D., Parra E. J., Dios S. [et al.], Skin pigmentation, biogeographical ancestry and admixture mapping, Human Genetics 2003, 112, 387-399.
-
(2003)
Human Genetics
, pp. 387-399
-
-
Shriver, M.D.1
Parra, E.J.2
Dios, S.3
-
57
-
-
14844285310
-
et al.], The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs
-
1
-
Shriver M. D., Kennedy G. C., Parra E. J. [et al.], The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs, Human Genomics 2004, 1, 274-286.
-
(2004)
Human Genomics
, pp. 274-286
-
-
Shriver, M.D.1
Kennedy, G.C.2
Parra, E.J.3
-
58
-
-
18144363563
-
Getting the science and the ethics right in forensic genetics
-
Shriver M., Frudakis T., Budowle B., Getting the science and the ethics right in forensic genetics, Nature Genetics 2005, 37, 449-50.
-
(2005)
Nature Genetics
, vol.37
, pp. 449-450
-
-
Shriver, M.1
Frudakis, T.2
Budowle, B.3
-
59
-
-
0034503342
-
et al.], Genetics of testosterone and the aggression-hostility-anger (AHA) syndrome: A study of middle-aged male twins
-
3
-
Sluyter F., Keijser J. N., Boomsma D. I. [et al.], Genetics of testosterone and the aggression-hostility-anger (AHA) syndrome: a study of middle-aged male twins, Twin Research 2000, 3, 266-276.
-
(2000)
Twin Research
, pp. 266-276
-
-
Sluyter, F.1
Keijser, J.N.2
Boomsma, D.I.3
-
60
-
-
7144254441
-
et al.], Melanocortin 1 receptor variants in an Irish population
-
111
-
Smith R., Healy E., Siddiqui S. [et al.], Melanocortin 1 receptor variants in an Irish population. Journal of Investigative Dermatology 1998, 111, 119-122.
-
(1998)
Journal of Investigative Dermatology
, pp. 119-122
-
-
Smith, R.1
Healy, E.2
Siddiqui, S.3
-
61
-
-
0035071957
-
A new statistical method for haplotype reconstruction from population data
-
Stephens M., Smith N. J., Donnelly P., A new statistical method for haplotype reconstruction from population data, American Journal of Human Genetics 2001, 68, 978-989.
-
(2001)
American Journal of Human Genetics
, vol.68
, pp. 978-989
-
-
Stephens, M.1
Smith, N.J.2
Donnelly, P.3
-
62
-
-
0029095104
-
-
Sturm R. A., O'Sullivan B. J., Box N. F. [et al.], Chromosomal structure of the human TYRP1 and TYRP2 loci and comparison of the tyrosinase-related protein gene family, Genomics 1995, 29, 24-34.
-
Sturm R. A., O'Sullivan B. J., Box N. F. [et al.], Chromosomal structure of the human TYRP1 and TYRP2 loci and comparison of the tyrosinase-related protein gene family, Genomics 1995, 29, 24-34.
-
-
-
-
63
-
-
0038727493
-
et al.], Genetic association and cellular function of MC1R variant alleles in human pigmentation
-
994
-
Sturm R. A., Duffy D. L., Box N. F. [et al.], Genetic association and cellular function of MC1R variant alleles in human pigmentation. Annals of the New York Academy Sciences 2003, 994, 348-358.
-
(2003)
Annals of the New York Academy Sciences
, pp. 348-358
-
-
Sturm, R.A.1
Duffy, D.L.2
Box, N.F.3
-
64
-
-
0037902558
-
et al.], The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes
-
16
-
Sturm R. A., Duffy D. L., Box N. F. [et al.], The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes, Pigment Cell Research 2003, 16, 266-272.
-
(2003)
Pigment Cell Research
, pp. 266-272
-
-
Sturm, R.A.1
Duffy, D.L.2
Box, N.F.3
-
65
-
-
3242733252
-
Eye colour: Portals into pigmentation genes and ancestry
-
Sturm R. A, Frudakis T. N., Eye colour: portals into pigmentation genes and ancestry, Trends in Genetics 2004, 20, 327-332.
-
(2004)
Trends in Genetics
, vol.20
, pp. 327-332
-
-
Sturm, R.A.1
Frudakis, T.N.2
-
66
-
-
0028786945
-
-
Valverde P., Healy E., Jackson I. [et al.], Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans, Nature Genetics 1995, 11, 328-330.
-
Valverde P., Healy E., Jackson I. [et al.], Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans, Nature Genetics 1995, 11, 328-330.
-
-
-
-
67
-
-
0029839525
-
et al.], The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma
-
5
-
Valverde P., Healy E., Sikkink S. [et al.], The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma, Human Molecular Genetics 1996, 5, 1663-1666.
-
(1996)
Human Molecular Genetics
, pp. 1663-1666
-
-
Valverde, P.1
Healy, E.2
Sikkink, S.3
-
68
-
-
34249805205
-
Baza danych profili DNA - nowe narzȩdzie dla wymiaru sprawiedliwości
-
Wolańska-Nowak P., Branicki W., Baza danych profili DNA - nowe narzȩdzie dla wymiaru sprawiedliwości, Prokuratura i Prawo 2000, 5, 87-98.
-
(2000)
Prokuratura i Prawo
, vol.5
, pp. 87-98
-
-
Wolańska-Nowak, P.1
Branicki, W.2
-
69
-
-
11144355855
-
et al.], A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15q
-
7
-
Zhu G., Evans D. M., Duffy D. L. [et al.], A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q, Twin Research 2004, 7, 197-210.
-
(2004)
Twin Research
, pp. 197-210
-
-
Zhu, G.1
Evans, D.M.2
Duffy, D.L.3
|