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1. Schneppenheim, R; Budde, U; Ruggeri, ZM
   A molecular approach to the classification of von Willebrand disease
   BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
   
   R. Schneppenheim et al., "A molecular approach to the classification of von Willebrand disease", BEST P R C, 14(2), 2001, pp. 281-298
2. Lowenberg, B
   Prognostic factors in acute myeloid leukaemia
   BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
   
   B. Lowenberg, "Prognostic factors in acute myeloid leukaemia", BEST P R C, 14(1), 2001, pp. 65-75
3. Pei, Y
   A 'two-hit' model of cystogenesis in autosomal dominant polycystic kidney disease?
   TRENDS IN MOLECULAR MEDICINE
   
   Y. Pei, "A 'two-hit' model of cystogenesis in autosomal dominant polycystic kidney disease?", TRENDS MO M, 7(4), 2001, pp. 151-156
4. Rougvie, AE
   Control of developmental timing in animals
   NATURE REVIEWS GENETICS
   
   A.E. Rougvie, "Control of developmental timing in animals", NAT REV GEN, 2(9), 2001, pp. 690-701
5. Cronk, QCB
   Plant evolution and development in a post-genomic context
   NATURE REVIEWS GENETICS
   
   Q.C.B. Cronk, "Plant evolution and development in a post-genomic context", NAT REV GEN, 2(8), 2001, pp. 607-619
6. Ostrer, H
   A genetic profile of contemporary Jewish populations
   NATURE REVIEWS GENETICS
   
   H. Ostrer, "A genetic profile of contemporary Jewish populations", NAT REV GEN, 2(11), 2001, pp. 891-898
7. Lalouel, JM; Rohrwasser, A
   Development of genetic hypotheses in essential hypertension
   JOURNAL OF HUMAN GENETICS
   
   J.M. Lalouel e A. Rohrwasser, "Development of genetic hypotheses in essential hypertension", J HUM GENET, 46(6), 2001, pp. 299-306
8. Schaefer, DG
   Gene targeting in Physcomitrella patens
   CURRENT OPINION IN PLANT BIOLOGY
   
   D.G. Schaefer, "Gene targeting in Physcomitrella patens", CUR OPIN PL, 4(2), 2001, pp. 143-150
9. Kato, T
   The other, forgotten genome: mitochondrial DNA and mental disorders
   MOLECULAR PSYCHIATRY
   
   T. Kato, "The other, forgotten genome: mitochondrial DNA and mental disorders", MOL PSYCHI, 6(6), 2001, pp. 625-633
10. Theophilus, BDM; Enayat, MS; Williams, MD; Hill, FGH
    Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A
    HAEMOPHILIA
    
    B.D.M. Theophilus et al., "Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A", HAEMOPHILIA, 7(4), 2001, pp. 381-391
11. Tang, S; Lai, KN
    Gene polymorphism in IgA nephropathy
    NEPHROLOGY
    
    S. Tang e K.N. Lai, "Gene polymorphism in IgA nephropathy", NEPHROLOGY, 6(2), 2001, pp. 63-70
12. Seeman, P; Mazanec, R; Ctvrteckova, M; Smilkova, D
    Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with centralconduction slowing
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    
    P. Seeman et al., "Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with centralconduction slowing", INT J MOL M, 8(4), 2001, pp. 461-468
13. Takashima, H; Boerkoel, CF; Lupski, JR
    Screening for mutations in a genetically heterogeneous disorder: DHPLC versus DNA sequence for mutation detection in multiple genes causing Charcot-Marie-Tooth neuropathy
    GENETICS IN MEDICINE
    
    H. Takashima et al., "Screening for mutations in a genetically heterogeneous disorder: DHPLC versus DNA sequence for mutation detection in multiple genes causing Charcot-Marie-Tooth neuropathy", GENET MED, 3(5), 2001, pp. 335-342
14. Lokki, ML; Laitinen, T
    Role of major histocompatibility complex class III genes in recurrent spontaneous abortions
    FRONTIERS IN BIOSCIENCE
    
    M.L. Lokki e T. Laitinen, "Role of major histocompatibility complex class III genes in recurrent spontaneous abortions", FRONT BIOSC, 6, 2001, pp. E23-E29
15. Highlander, SK
    Molecular genetic analysis of virulence in Mannheimia (Pasteurella) haemolytica
    FRONTIERS IN BIOSCIENCE
    
    S.K. Highlander, "Molecular genetic analysis of virulence in Mannheimia (Pasteurella) haemolytica", FRONT BIOSC, 6, 2001, pp. D1128-D1151
16. Conesa, A; Punt, PJ; van Luijk, N; van den Hondel, CAMJJ
    The secretion pathway in filamentous fungi: A biotechnological view
    FUNGAL GENETICS AND BIOLOGY
    
    A. Conesa et al., "The secretion pathway in filamentous fungi: A biotechnological view", FUNGAL G B, 33(3), 2001, pp. 155-171
17. Zhang, ZJ; Butler, JD; Levin, SW; Wisniewski, KE; Brooks, SS; Mukherjee, AB
    Lysosomal ceroid depletion by drugs: Therapeutic implications for a hereditary neurodegenerative disease of childhood
    NATURE MEDICINE
    
    Z.J. Zhang et al., "Lysosomal ceroid depletion by drugs: Therapeutic implications for a hereditary neurodegenerative disease of childhood", NAT MED, 7(4), 2001, pp. 478-484
18. Srivastava, S; Verma, M; Henson, DE
    Biomarkers for early detection of colon cancer
    CLINICAL CANCER RESEARCH
    
    S. Srivastava et al., "Biomarkers for early detection of colon cancer", CLIN CANC R, 7(5), 2001, pp. 1118-1126
19. Vega, F; Medeiros, LJ
    Marginal-zone B-cell lymphoma of extranodal mucosa-associated lymphoid tissue type: Molecular genetics provides new insights into pathogenesis
    ADVANCES IN ANATOMIC PATHOLOGY
    
    F. Vega e L.J. Medeiros, "Marginal-zone B-cell lymphoma of extranodal mucosa-associated lymphoid tissue type: Molecular genetics provides new insights into pathogenesis", ADV ANAT PA, 8(6), 2001, pp. 313-319
20. Jameson, KA; Highnote, SM; Wasserman, LM
    Richer color experience in observers with multiple photopigment opsin genes
    PSYCHONOMIC BULLETIN & REVIEW
    
    K.A. Jameson et al., "Richer color experience in observers with multiple photopigment opsin genes", PSYCHON B R, 8(2), 2001, pp. 244-261
21. Wirtzfeld, DA; Petrelli, NJ; Rodriguez-Bigas, MA
    Hamartomatous polyposis syndromes: Molecular genetics, neoplastic risk, and surveillance recommendations
    ANNALS OF SURGICAL ONCOLOGY
    
    D.A. Wirtzfeld et al., "Hamartomatous polyposis syndromes: Molecular genetics, neoplastic risk, and surveillance recommendations", ANN SURG O, 8(4), 2001, pp. 319-327
22. Harnevik, L; Fjellstedt, E; Molbaek, A; Tiselius, HG; Denneberg, T; Soderkvist, P
    Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients
    HUMAN MUTATION
    
    L. Harnevik et al., "Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients", HUM MUTAT, 18(6), 2001, pp. 516-525
23. Deltas, CC
    Mutations of the human polycystic kidney disease 2 (PKD2) gene
    HUMAN MUTATION
    
    C.C. Deltas, "Mutations of the human polycystic kidney disease 2 (PKD2) gene", HUM MUTAT, 18(1), 2001, pp. 13-24
24. Duponchel, C; Di Rocco, C; Cicardi, M; Tosi, M
    Rapid detection by fluorescent multiplex PCR of exon deletions and duplications in the C1 inhibitor gene of hereditary angioedema patients
    HUMAN MUTATION
    
    C. Duponchel et al., "Rapid detection by fluorescent multiplex PCR of exon deletions and duplications in the C1 inhibitor gene of hereditary angioedema patients", HUM MUTAT, 17(1), 2001, pp. 61-70
25. Gale, C; Gerami-Nejad, M; McClellan, M; Vandoninck, S; Longtine, MS; Berman, J
    Candida albicans Int1p interacts with the septin ring in yeast and hyphal cells
    MOLECULAR BIOLOGY OF THE CELL
    
    C. Gale et al., "Candida albicans Int1p interacts with the septin ring in yeast and hyphal cells", MOL BIOL CE, 12(11), 2001, pp. 3538-3549
26. Michels-Rautenstrauss, KG; Mardin, CY; Zenker, M; Jordan, N; Gusek-Schneider, GC; Rautenstrauss, BW
    Primary congenital glaucoma: Three case reports on novel mutations and combinations of mutations in the GLC3A (CYP1B1) gene
    JOURNAL OF GLAUCOMA
    
    K.G. Michels-Rautenstrauss et al., "Primary congenital glaucoma: Three case reports on novel mutations and combinations of mutations in the GLC3A (CYP1B1) gene", J GLAUCOMA, 10(4), 2001, pp. 354-357
27. Simonoff, E
    Gene-environment interplay in oppositional defiant and conduct disorder
    CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA
    
    E. Simonoff, "Gene-environment interplay in oppositional defiant and conduct disorder", CH ADOLESC, 10(2), 2001, pp. 351
28. Hsing, AW; Chen, C; Chokkalingam, AP; Gao, YT; Dightman, DA; Nguyen, HT; Deng, J; Cheng, JR; Sesterhenn, IA; Mostofi, FK; Stanczyk, FZ; Reichardt, JKV
    Polymorphic markers in the SRD5A2 gene and prostate cancer risk: A population-based case-control study
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    
    A.W. Hsing et al., "Polymorphic markers in the SRD5A2 gene and prostate cancer risk: A population-based case-control study", CANC EPID B, 10(10), 2001, pp. 1077-1082
29. Bieche, I; Franc, B; Vidaud, D; Vidaud, M; Lidereau, R
    Analyses of MYC, ERBB2, and CCND1 genes in benign and malignant thyroid follicular cell tumors by real-time polymerase chain reaction
    THYROID
    
    I. Bieche et al., "Analyses of MYC, ERBB2, and CCND1 genes in benign and malignant thyroid follicular cell tumors by real-time polymerase chain reaction", THYROID, 11(2), 2001, pp. 147-152
30. Trapp, S; Croteau, R
    Defensive resin biosynthesis in conifers
    ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY
    
    S. Trapp e R. Croteau, "Defensive resin biosynthesis in conifers", ANN R PLANT, 52, 2001, pp. 689-724
31. Hart, LA; Conron, M; du Bois, RM
    Sarcoidosis
    INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE
    
    L.A. Hart et al., "Sarcoidosis", INT J TUBE, 5(9), 2001, pp. 791-806
32. Yagil, Y; Yagil, C
    Genetic models of hypertension in experimental animals
    EXPERIMENTAL NEPHROLOGY
    
    Y. Yagil e C. Yagil, "Genetic models of hypertension in experimental animals", EXP NEPHROL, 9(1), 2001, pp. 1-9
33. Bouba, I; Koptides, M; Mean, R; Costi, CE; Demetriou, K; Georgiou, I; Pierides, A; Siamopoulos, K; Deltas, CC
    Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families
    EUROPEAN JOURNAL OF HUMAN GENETICS
    
    I. Bouba et al., "Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families", EUR J HUM G, 9(9), 2001, pp. 677-684
34. Khadem, M; Rozas, J; Segarra, C; Aguade, M
    DNA variation at the rp49 gene region in Drosophila madeirensis and D-subobscura from Madeira: inferences about the origin of an insular endemic species
    JOURNAL OF EVOLUTIONARY BIOLOGY
    
    M. Khadem et al., "DNA variation at the rp49 gene region in Drosophila madeirensis and D-subobscura from Madeira: inferences about the origin of an insular endemic species", J EVOL BIOL, 14(3), 2001, pp. 379-387
35. Davis, LM; Glenn, TC; Elsey, RM; Dessauer, HC; Sawyer, RH
    Multiple paternity and mating patterns in the American alligator, Alligator mississippiensis
    MOLECULAR ECOLOGY
    
    L.M. Davis et al., "Multiple paternity and mating patterns in the American alligator, Alligator mississippiensis", MOL ECOL, 10(4), 2001, pp. 1011-1024
36. Eizirik, E; Kim, JH; Menotti-Raymond, M; Crawshaw, PG; O'Brien, SJ; Johnson, WE
    Phylogeography, population history and conservation genetics of jaguars (Panthera onca, Mammalia, Felidae)
    MOLECULAR ECOLOGY
    
    E. Eizirik et al., "Phylogeography, population history and conservation genetics of jaguars (Panthera onca, Mammalia, Felidae)", MOL ECOL, 10(1), 2001, pp. 65-79
37. Fretland, AJ; Leff, MA; Doll, MA; Hein, DW
    Functional characterization of human N-acetyltransferase 2 (NAT2) single nucleotide polymorphisms
    PHARMACOGENETICS
    
    A.J. Fretland et al., "Functional characterization of human N-acetyltransferase 2 (NAT2) single nucleotide polymorphisms", PHARMACOGEN, 11(3), 2001, pp. 207-215
38. Dufau, ML; Tsai-Morris, CH; Tang, PZ; Khanum, A
    Regulation of steroidogenic enzymes and a novel testicular RNA helicase
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
    
    M.L. Dufau et al., "Regulation of steroidogenic enzymes and a novel testicular RNA helicase", J STEROID B, 76(1-5), 2001, pp. 187-197
39. Aquadro, CF; DuMont, VB; Reed, FA
    Genome-wide variation in the human and fruitfly: a comparison
    CURRENT OPINION IN GENETICS & DEVELOPMENT
    
    C.F. Aquadro et al., "Genome-wide variation in the human and fruitfly: a comparison", CUR OP GEN, 11(6), 2001, pp. 627-634
40. Charlesworth, D; Wright, SI
    Breeding systems and genome evolution
    CURRENT OPINION IN GENETICS & DEVELOPMENT
    
    D. Charlesworth e S.I. Wright, "Breeding systems and genome evolution", CUR OP GEN, 11(6), 2001, pp. 685-690
41. Fu, Y; Katsuya, T; Higaki, J; Asai, T; Fukuda, M; Takiuchi, S; Hatanaka, Y; Rakugi, H; Ogihara, T
    A common mutation of low-density lipoprotein receptor gene is associated with essential hypertension among Japanese
    JOURNAL OF HUMAN HYPERTENSION
    
    Y. Fu et al., "A common mutation of low-density lipoprotein receptor gene is associated with essential hypertension among Japanese", J HUM HYPER, 15(2), 2001, pp. 125-130
42. Pavelic, K; Gall-Troselj, K
    Recent advances in molecular genetics of breast cancer
    JOURNAL OF MOLECULAR MEDICINE-JMM
    
    K. Pavelic e K. Gall-Troselj, "Recent advances in molecular genetics of breast cancer", J MOL MED-J, 79(10), 2001, pp. 566-573
43. Radner, H; Katenkamp, D; Reifenberger, G; Deckert, M; Pietsch, T; Wiestler, OD
    New developments in the pathology of skull base tumors
    VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
    
    H. Radner et al., "New developments in the pathology of skull base tumors", VIRCHOWS AR, 438(4), 2001, pp. 321-335
44. McGleenan, T; Wiesing, U
    Insurance and genetics - Options to prevent undesirable consequences
    GESUNDHEITSWESEN
    
    T. McGleenan e U. Wiesing, "Insurance and genetics - Options to prevent undesirable consequences", GESUNDHEITS, 63(10), 2001, pp. 583-590
45. Nakanishi, K; Sweeney, WE; Avner, ED; Murcia, NS
    Expression of the orpk disease gene during kidney development and maturation
    PEDIATRIC NEPHROLOGY
    
    K. Nakanishi et al., "Expression of the orpk disease gene during kidney development and maturation", PED NEPHROL, 16(3), 2001, pp. 219-226
46. Plantaz, D
    Neuroblastoma, one century after Pepper: Which genes?
    ARCHIVES DE PEDIATRIE
    
    D. Plantaz, "Neuroblastoma, one century after Pepper: Which genes?", ARCH PED, 8(9), 2001, pp. 917-921
47. Shinozaki-Kuwahara, N; Hayakawa, M; Shiroza, T; Abiko, Y; Fukushima, K
    Purification and characterization of an oligo-isomaltosaccharide synthase from a Streptococcus sobrinus glucosyltransferase-I deficient mutant.
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
    
    N. Shinozaki-Kuwahara et al., "Purification and characterization of an oligo-isomaltosaccharide synthase from a Streptococcus sobrinus glucosyltransferase-I deficient mutant.", BIOS BIOT B, 65(6), 2001, pp. 1290-1295
48. Zimonjic, DB; Keck-Waggoner, C; Popescu, NC
    Novel genomic imbalances and chromosome translocations involving c-myc gene in Burkitt's lymphoma
    LEUKEMIA
    
    D.B. Zimonjic et al., "Novel genomic imbalances and chromosome translocations involving c-myc gene in Burkitt's lymphoma", LEUKEMIA, 15(10), 2001, pp. 1582-1588
49. Yin, TM; Huang, MR; Wang, MX; Zhu, LH; Zeng, ZB; Wu, RL
    Preliminary interspecific genetic maps of the Populus genome constructed from RAPD markers
    GENOME
    
    T.M. Yin et al., "Preliminary interspecific genetic maps of the Populus genome constructed from RAPD markers", GENOME, 44(4), 2001, pp. 602-609
50. Li, CX; Yeh, FC
    Construction of a framework map in Pinus contorta subsp latifolia using random amplified polymorphic DNA markers
    GENOME
    
    C.X. Li e F.C. Yeh, "Construction of a framework map in Pinus contorta subsp latifolia using random amplified polymorphic DNA markers", GENOME, 44(2), 2001, pp. 147-153
51. Disse-Nicodeme, S; Corvol, P; Jeunemaitre, X; Achard, JM
    Two genes involved in human familial hypertension
    M S-MEDECINE SCIENCES
    
    S. Disse-Nicodeme et al., "Two genes involved in human familial hypertension", M S-MED SCI, 17(8-9), 2001, pp. 959-962
52. Schachter, F; Foulon, M; Poulain, M
    Color vision anomalies and the genetics of aging.
    COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES
    
    F. Schachter et al., "Color vision anomalies and the genetics of aging.", CR AC S III, 324(4), 2001, pp. 327-333
53. Guinand, B; Durand, JD; Laroche, J
    Identifying main evolutionary mechanisms shaping genetic variation of Leuciscus cephalus L. 1758 (Cyprinidae) in Western Greece: discordance between methods
    COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES
    
    B. Guinand et al., "Identifying main evolutionary mechanisms shaping genetic variation of Leuciscus cephalus L. 1758 (Cyprinidae) in Western Greece: discordance between methods", CR AC S III, 324(11), 2001, pp. 1045-1060
54. Tauber, E; Kyriacou, BP
    Insect photoperiodism and circadian clocks: Models and mechanisms
    JOURNAL OF BIOLOGICAL RHYTHMS
    
    E. Tauber e B.P. Kyriacou, "Insect photoperiodism and circadian clocks: Models and mechanisms", J BIOL RHYT, 16(4), 2001, pp. 381-390
55. Rubin, BP; Dal Cin, P
    The genetics of lipomatous tumors
    SEMINARS IN DIAGNOSTIC PATHOLOGY
    
    B.P. Rubin e P. Dal Cin, "The genetics of lipomatous tumors", SEM DIAGN P, 18(4), 2001, pp. 286-293
56. Bielawski, JP; Yang, ZH
    Positive and negative selection in the DAZ gene family
    MOLECULAR BIOLOGY AND EVOLUTION
    
    J.P. Bielawski e Z.H. Yang, "Positive and negative selection in the DAZ gene family", MOL BIOL EV, 18(4), 2001, pp. 523-529
57. Andolfatto, P
    Contrasting patterns of X-linked and autosomal nucleotide variation in Drosophila melanogaster and Drosophila simulans
    MOLECULAR BIOLOGY AND EVOLUTION
    
    P. Andolfatto, "Contrasting patterns of X-linked and autosomal nucleotide variation in Drosophila melanogaster and Drosophila simulans", MOL BIOL EV, 18(3), 2001, pp. 279-290
58. Przeworski, M; Wall, JD; Andolfatto, P
    Recombination and the frequency spectrum in Drosophila melanogaster and Drosophila simulans
    MOLECULAR BIOLOGY AND EVOLUTION
    
    M. Przeworski et al., "Recombination and the frequency spectrum in Drosophila melanogaster and Drosophila simulans", MOL BIOL EV, 18(3), 2001, pp. 291-298
59. Aguade, M
    Nucleotide sequence variation at two genes of the phenylpropanoid pathway,the FAH1 and F3H genes, in Arabidopsis thaliana
    MOLECULAR BIOLOGY AND EVOLUTION
    
    M. Aguade, "Nucleotide sequence variation at two genes of the phenylpropanoid pathway,the FAH1 and F3H genes, in Arabidopsis thaliana", MOL BIOL EV, 18(1), 2001, pp. 1-9
60. Dinus, RJ; Payne, P; Sewell, NM; Chiang, VL; Tuskan, GA
    Genetic modification of short rotation popular wood: Properties for ethanol fuel and fiber productions
    CRITICAL REVIEWS IN PLANT SCIENCES
    
    R.J. Dinus et al., "Genetic modification of short rotation popular wood: Properties for ethanol fuel and fiber productions", CR R PLANT, 20(1), 2001, pp. 51-69
61. Jang, KL; Vernon, PA; Livesley, WJ
    Behavioural-genetic perspectives on personality function
    CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE
    
    K.L. Jang et al., "Behavioural-genetic perspectives on personality function", CAN J PSY, 46(3), 2001, pp. 234-244
62. Johnson, TE; de Castro, E; de Castro, SH; Cypser, J; Henderson, S; Tedesco, P
    Relationship between increased longevity and stress resistance as assessedthrough gerontogene mutations in Caenorhabditis elegans
    EXPERIMENTAL GERONTOLOGY
    
    T.E. Johnson et al., "Relationship between increased longevity and stress resistance as assessedthrough gerontogene mutations in Caenorhabditis elegans", EXP GERONT, 36(10), 2001, pp. 1609-1617
63. Petursdottir, V; Moslemi, AR; Persson, M; Nordborg, E; Nordborg, C
    Estrogen receptor alpha in giant cell arteritis: A molecular genetic study
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
    
    V. Petursdottir et al., "Estrogen receptor alpha in giant cell arteritis: A molecular genetic study", CLIN EXP RH, 19(3), 2001, pp. 297-302
64. Veneselli, E; Biancheri, R; Buoni, S; Fois, A
    Clinical and EEG findings in 18 cases of late infantile neuronal ceroid lipofuscinosis
    BRAIN & DEVELOPMENT
    
    E. Veneselli et al., "Clinical and EEG findings in 18 cases of late infantile neuronal ceroid lipofuscinosis", BRAIN DEVEL, 23(5), 2001, pp. 306-311
65. Kawamura, S; Hirai, M; Takenaka, O; Radlwimmer, FB; Yokoyama, S
    Genomic and spectral analyses of long to middle Wavelength-sensitive visual pigments of common marmoset (Callithrix jacchus)
    GENE
    
    S. Kawamura et al., "Genomic and spectral analyses of long to middle Wavelength-sensitive visual pigments of common marmoset (Callithrix jacchus)", GENE, 269(1-2), 2001, pp. 45-51
66. Comabella, M; Waye, JS; Raguer, N; Eng, B; Dominguez, C; Navarro, C; Borras, C; Krivit, W; Montalban, X
    Late-onset metachromatic leukodystrophy clinically presenting as isolated peripheral neuropathy: Compound heterozygosity for the IVS2+1G -> A mutation and a newly identified missense mutation (Thr408Ile) in a Spanish family
    ANNALS OF NEUROLOGY
    
    M. Comabella et al., "Late-onset metachromatic leukodystrophy clinically presenting as isolated peripheral neuropathy: Compound heterozygosity for the IVS2+1G -> A mutation and a newly identified missense mutation (Thr408Ile) in a Spanish family", ANN NEUROL, 50(1), 2001, pp. 108-112
67. Morris, M; Means, S; Oliverio, MI; Coffman, TM
    Enhanced central response to dehydration in mice lacking angiotensin AT(1a) receptors
    AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
    
    M. Morris et al., "Enhanced central response to dehydration in mice lacking angiotensin AT(1a) receptors", AM J P-REG, 280(4), 2001, pp. R1177-R1184
68. Hayashi, T; Yamaguchi, T; Kitahara, K; Sharpe, LT; Jagle, H; Yamade, S; Ueyama, H; Motulsky, AG; Deeb, SS
    The importance of gene order in expression of the red and green visual pigment genes and in color vision
    COLOR RESEARCH AND APPLICATION
    
    T. Hayashi et al., "The importance of gene order in expression of the red and green visual pigment genes and in color vision", COL RES APP, 26, 2001, pp. S79-S83
69. Yamade, S; Hayashi, S; Ueyama, H; Tanabe, S; Hukami, K; Ichikawa, K; Tachibana, M
    Red-green pigment gene analysis as a clinical diagnostic tool
    COLOR RESEARCH AND APPLICATION
    
    S. Yamade et al., "Red-green pigment gene analysis as a clinical diagnostic tool", COL RES APP, 26, 2001, pp. S89-S92
70. Bollinger, K; Bialozynski, C; Neitz, J; Neitz, M
    The importance of deleterious mutations of M pigment genes as a cause of color vision defects
    COLOR RESEARCH AND APPLICATION
    
    K. Bollinger et al., "The importance of deleterious mutations of M pigment genes as a cause of color vision defects", COL RES APP, 26, 2001, pp. S100-S105
71. Carroll, J; Neitz, M; Neitz, J
    Testing hypotheses about visual pigments underlying deutan color vision
    COLOR RESEARCH AND APPLICATION
    
    J. Carroll et al., "Testing hypotheses about visual pigments underlying deutan color vision", COL RES APP, 26, 2001, pp. S106-S111
72. Jacobs, GH; Williams, GA
    The prevalence of defective color vision in Old World monkeys and apes
    COLOR RESEARCH AND APPLICATION
    
    G.H. Jacobs e G.A. Williams, "The prevalence of defective color vision in Old World monkeys and apes", COL RES APP, 26, 2001, pp. S123-S127
73. Neitz, M; Neitz, J
    A new mass screening test for color-vision deficiencies in children
    COLOR RESEARCH AND APPLICATION
    
    M. Neitz e J. Neitz, "A new mass screening test for color-vision deficiencies in children", COL RES APP, 26, 2001, pp. S239-S249
74. Beesley, CE; Meaney, CA; Greenland, G; Adams, V; Vellodi, A; Young, EP; Winchester, BG
    Mutational analysis of 85 mucopolysaccharidosis type I families: frequencyof known mutations, identification of 17 novel mutations and in vitro expression of missense mutations
    HUMAN GENETICS
    
    C.E. Beesley et al., "Mutational analysis of 85 mucopolysaccharidosis type I families: frequencyof known mutations, identification of 17 novel mutations and in vitro expression of missense mutations", HUM GENET, 109(5), 2001, pp. 503-511
75. Takenaga, M; Horinouchi, K; Shirieda, K; Fukudome, T; Fujimoto, T
    A novel nonsense mutation in the antithrombin III gene (Ser365 to stop) causing deep and mesenteric venous thromboses
    THROMBOSIS AND HAEMOSTASIS
    
    M. Takenaga et al., "A novel nonsense mutation in the antithrombin III gene (Ser365 to stop) causing deep and mesenteric venous thromboses", THROMB HAEM, 85(3), 2001, pp. 570-571
76. Lang-Muritano, M; Biason-Lauber, A; Gitzelmann, C; Belville, C; Picard, Y; Schoenle, EJ
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77. Benjafield, AV; Lin, RCY; Dalziel, B; Gosby, AK; Caterson, ID; Morris, BJ
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78. Mowry, BJ; Nancarrow, DJ
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79. Rawlings, DE
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80. Loke, KY; Lee, YS; Lee, WWR; Poh, LKS
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81. Thierfelder, L
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82. Smit, JWA; Van Zelderen-Bhola, S; Merx, R; De Leeuw, W; Wessels, H; Vink, R; Morreau, H
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83. Todd, R; Donoff, RB; Kim, Y; Wong, DTW
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84. Verma, A; Bradley, WG
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85. Mishra, RK; Mihaly, J; Barges, S; Spierer, A; Karch, F; Hagstrom, K; Schweinsberg, SE; Schedl, P
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86. Lim, CJ; Spiegelman, GB; Weeks, G
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87. Formosa, T; Eriksson, P; Wittmeyer, J; Ginn, J; Yu, YX; Stillman, DJ
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88. Dale, B
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89. Bain, BJ
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90. Allayee, H; de Bruin, TWA; Dominguez, KM; Cheng, LSC; Ipp, E; Cantor, RM; Krass, KL; Keulen, ETP; Aouizerat, BE; Lusis, AJ; Rotter, JI
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91. Danziger, RS
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92. Martinez, A; Soberon-Chavez, G
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93. Werner, M; Becker, KF; Keller, G; Hofler, H
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94. Kaplan, JM; Pigliucci, M
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95. Dessen, P; Zagulski, M; Gromadka, R; Plattner, H; Kissmehl, R; Meyer, E; Betermier, M; Schultz, JE; Linder, JU; Pearlman, RE; Kung, C; Forney, J; Satir, BH; Van Houten, JL; Keller, AM; Froissard, M; Sperling, L; Cohen, J
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96. Araz, M; Yilmaz, N; Gungor, K; Okan, V; Kepekci, Y; Aynacioglu, AS
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97. Kato, T
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98. Doevendans, PA; Jukema, W; Spiering, W; Defesche, JC; Kastelein, JJP
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99. Ramsay, RR; Gandour, RD; van der Leij, FR
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100. Nadol, JB; Merchant, SN
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