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Authors: Armand Marie Leroi

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McLachlan, J. 1994.
Medical embryology.
Addison-Wesley, Wokingham

McLaren, A. 1990. What makes a man a man?
Nature
346: 216–17

McMahon, J.A. et al. 1998. Noggin-mediated antatonism of BMP signalling is required for growth and patterning of the neural tube and somite.
Genes and Development
12: 1438–52

McMullen, G. and K. Pearson. 1913. On the inheritance of the deformity known as split-foot or lobster-claw.
Biometrika
9: 381–90

McPherron, A.C. and SJ. Lee. 1997. Doubling muscle in cattle due to mutations in the myostatin gene.
Proceedings of the National Academy of Sciences, USA
94: 12457–61

McPherron, A.C. et al. 1997. Regulation of skeletal muscle mass in mice by a new TGF-Beta superfamily member.
Nature
387: 83–90

Maden, M. 1999. Heads or tails? Retinoic acid will decide.
Bioessays
21: 809–12

Maeder, T. 1998. A few hundred people turned to bone.
The Atlantic
, February, (two parts)

Manoiloff, E.O. 1931. A rare case of hereditary hexadactylism.
American Journal of Physical Anthropology
15: 503–8

Manouvrier-Hanu S. et al. 1999. Genetics of limb anomalies in humans.
Trends in Genetics
15: 409–17

Mansholt, U.J. 1987. The increase in the height of Dutchmen and the attraction of tennis.
Nederlands Tijdschrift voor Geneeskunde
131: 376

Mark, M. et al. 1993. Two rhombomeres are altered in Hoxa-1 mutant mice.
Development
119: 319–38

Maroteaux, P. 1995. Toulouse-Lautrec’s diagnosis.
Nature Genetics
11: 362

Maroteaux, P. and M. Lamy. 1965. The malady of Toulouse Lautrec.
JAMA, Journal of the American Medical Association
191: 111–13

Marshall, H.K. and H.I. Harder. 1958. Testicular feminising syndrome in male pseudohermaphrodite: report of two cases in identical twins.
Obstetrics and Gynecology
12: 284–93

Martin, E. 1880.
Histoire des monstres.
C. Reinwald, Paris

Martin, G. and J. Oshima. 2000. Lessons from human progeroid syndromes.
Nature
408: 263–6

Martinez-Frias, M.-L. 1993. Another way to interpret the description of the Monster of Ravenna of the sixteenth century.
American Journal of Medical Genetics
49: 362

Mascie-Taylor, C.G.N and J.L. Boldsen. 1985. Regional and social analysis of height variation in a contemporary British sample.
Annals of Human Biology
12: 315–24

Mathon, N.F. et al. 2001. Lack of replicative sensecence in normal rodent glia.
Science
291: 872–5

Mayor, A. 2000.
The first fossil hunters.
Princeton University Press, Princeton, N.J.

Medawar, P.B. 1952.
An unsolved problem in biology.
H. K. Lewis. London

Melanchthon, P. and M. Luther. 1523 (1823).
Interpretation of two horrible monsters
[
Deuttung der czwo grewlichï Figuren, etc.
]

Merimee, T.J. et al. 1981. Dwarfism in the pygmy.
New England Journal of Medicine
305: 965–8

Merimee, T.J. et al. 1987. Insulin-like growth factors in pygmies: the role of puberty in determining final stature.
New England Journal of Medicine
316: 906–11

Merke, F. 1993.
History and iconography of endemic goitre and cretinism.
MTP Press, Lancaster

Merlo, G.R. et al. 2002. Mouse model of split hand/foot malformation type 1.
Genesis
33: 97–101

Meyers, E.N. and G.R. Martin. 1999. Differences in left-right axis pathways in mouse and chick: functions of FGF8 and SHH.
Science
285: 403–6

Miller, R. and S. Austad. 1999. Large animals in the fast lane.
Science
285:199

Mills, A.A. et al. 1999. P63 is a P53 homologue required for limb and epidermal morphogenesis.
Nature
398: 708–13

Mittwoch, U. 1973.
Genetics of sex differentiation.
Academic Press, N.Y.

Monreal, A.W. 1999. Mutations in the human homologue of mouse
dl
cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia.
Nature Genetics
22: 366–9

Montaigne, M. de. 1580 (1958).
Essays
(trans. J.M. Cohen). Penguin Books, Harmondsworth, UK

Montaigne, M. de. 1603 (1998).
Florio’s translation of Montaigne’s essays.
B. R. Schneider (ed.), Renascence Editions, University of Oregon

Moon, A.M. and M.R. Capecchi. 2000. Fgf8 is required for outgrowth and patterning of the limbs.
Nature Genetics
26: 455–9

Morin, A. 1996. La teratologic de Geoffroy Saint-Hilaire á nos jours.
Bulletin de l’Association des Anatomistes
80: 17–31

Morishima, A. et al. 1995. Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens.
Journal of clinical endocrinology and metabolism
80: 3689–98

Mortlock, D.P. and J.W. Innis. 1997. Mutation of Hox a-13 in hand-foot-genital syndrome.
Nature Genetics
15: 179–80

Mortlock, D.P. et al. 1996. The molecular basis of hypodactyly (Hd): a deletion in Hox a-13 leads to arrest of digital arch formation.
Nature Genetics
13: 284–8

Moskovitz, E. 1987.
By the grace of the devil.
Rotem, Ramat-Gan, Israel

Muenke M. and PA. Beachy 2000. Genetics of ventral forebrain development and holoprosencephaly.
Current Opinion in Genetics and Development
10: 262–9

Mundlos, S. 1999. Cleidocranial dysplasia: clinical and molecular genetics.
Journal of Medical Genetics
36: 177–82

Mundlos, S. et al. 1997. Mutations involving the transcription factor CBFAi cause cleiodocranial dysplasia.
Cell
89: 773–9

Muragaki, Y. et al. 1996. Altered growth and branching patters in synpoly-dactyly caused by mutations in Hox d-13.
Science
272: 548–51

Mya-Tu, M. et al. 1962. Tarong pygmies in North Burma.
Nature
195: 131–2

Mya-Tu, M. et al. 1966.
The Tarons in Burma.
Burma Medical Research Institute, Rangoon. Special Report Series No. 1

Nanni, L. et al. 1999. The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
Human Molecular Genetics
8: 2479–88

Nanni, L.et al. 2001. SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.
Journal of Medical Genetics
102: 1–10, 2001

Naski, M.C. et al. 1996. Graded activation of fibroblast growth factor receptor 3 by mutaitons causing achondroplasia and thanatophoric dysplasia.
Nature Genetics
13: 233–7

Naski, M.C. et al. 1998. Repression of hedgehog signalling and BMP4 expression in growth plate cartilage by fibroblast growth factor receptor 3.
Development
125: 4977–88

Naudin ten Gate L., C. Vermeij-Keers, D.A. Smit, T.W. Cohen-Overbeek, K.B. Gerssen-Schoorl, T. Dijkhuisen. 1995. Intracranial teratoma with multiple fetuses. Pre- and post-natal appearance.
Human Pathology
26: 804–7

Neaves, W.B. et al. 1980. Sexual dimorphism of the phallus in spotted hyena (
Crocuta crocuta). Journal of Reproduction and Fertility
59: 509–13

Needham, J. 1959.
A history of embryology.
Cambridge University Press, Cambridge, UK

Netter, A. et al. 1958. Le testicule feminisant.
Annates d’ endocrinologie
9: 994–1014

Neubert, R. et al. 1999. Developmental model for thalidomide action.
Nature
400: 419–20

Newbery, H.J. and CM. Abbott. 2002. Of mice, men and motor neurons.
Trends in Molecular Medicine
8: 88–92

Niccoli, O. 1990.
People and prophecy in renaissance Italy
, (trans. L. G. Cochrane.) Princeton University Press, Princeton

Niswander, L. et al. 1993. FGF-4 replaces the apical ectodermal ridge and directs outgrowth and patterning of the limb.
Cell
75: 579–87

Nonaka, S. et al. 1998. Randomisation of left–right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein.
Cell
95: 839–47

Noramly, S. and B.A. Morgan. 1998. BMPs mediate lateral inhibition at successive stages in feather tract development.
Development
125: 3775–87

O’Connell, H.E. et al. 1998. Anatomical relationship between urethra and clitoris.
Journal of Urology
159: 1892–7

Olbrich, H. et al. 2002. Mutations in DNAH5 cause primary ciliary dyskinesia and randomisation of left–right asymmetry.
Nature Genetics
30: 143–4

Olsen, B.R. et al. 2000. Bone development.
Annual Reviews of Cell and Developmental Biology
16: 191–220

On-line Mendelian Inheritance in Man. 2000.
OMIM™.
McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University, Baltimore, MD, and National Center for Biotechnology Information, National Library of Medicine, Bethesda, MD.
http://www.ncbi.nlm.nih.gov/omim/

Oosterhout, van C. et al. 2003. Inbreeding depression and genetic load of sexually selected traits: how the guppy lost its spots.
Journal of Evolutionary Biology
16: 273–81

Oostra, R.–J. et al. 1998a. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. I: syndromes with multiple congenital anomalies.
American Journal of Medical Genetics
77: 100–15

Oostra, R.–J. et al. 1998b. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. II: Skeletal Dysplasias.
American Journal of Medical Genetics
77: 116–34

Oostra, R.–J. et al. 1998c. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. Ill: Primary field defects, sequences and other complex anomalies.
American Journal of Medical Genetics
80: 46–59

Oostra, R.–J. et al. 1998d. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. IV: Closure defects of the neural tube.
American Journal of Medical Genetics
80: 60–73

Oostra, R.–J. et al. 1998e. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. V: Conjoined and acardiac twins.
American Journal of Medical Genetics
80: 74–89

Oro, A.E. and M.P. Scott. 1998. Splitting hairs: dissecting roles of signaling systems in epidermal development.
Cell
95: 575–8

Orr, H.T. 2000. A proposed mechanism of ALS fails the test in vivo.
Nature Neuroscience
5: 287–8

Ortega-Ortiz, J.G. and B. Villa-Ramirez. 2000. Polydactyly and other features of the manus of the vaquita,
Phocoena sinus. Marine Mammal Science
16: 277–86

Paré, A. 1573 (1971).
Des monstres.
J. Céard (ed.) Droz, Geneva

Paré, A. 1573 (1982).
On monsters and marvels
(trans. J
.
L. Pallister) Chicago University Press, Chicago

Park, K. and L. Daston. 1981. Unnatural conceptions: the study of monsters in sixteenth and seventeenth century France and England.
Past and Present
92: 20–54

Parkes, T.L. et al. 1998. Extension
of Drosophila
lifespan by overexpression of human SOD1 in motorneurons.
Nature Genetics
19: 171–4

Partridge, L. and D. Gems. 2002. Mechanisms of ageing: public or private?
Nature Reviews Genetics
3: 165–75

Patronek, G.J. et al. 1997. Comparative longevity of pet dogs and humans: implications for gerontology research.
Journal of Gerontology
52A: B171–8

Pearson, K. et al. 1913.
A monograph on albinism in man.
3 V. text; 3 V. plates. Draper’s company research memoirs, Biometric series X. Dulau & Co. London

Pearson, K. 1908. On the inheritance of the deformity known as split-foot or lobster claw.
Biometrika
6: 69–79

Pearson, K. 1913. Notes on the Honduras piebald.
Biometrika
9: 330–1

Perrett, D.I. et al. 1994. Facial shape and judgements of female attractiveness.
Nature
368: 239–42

Perriton, C. et al. 2002. Sonic hedgehog signalling from the urethral epithelium controls external genital development
Developmental Biology
247: 26–46

Piccolo, S. et al. 1996. Dorsoventral patterning in
Xenopus:
inhibition of ventral signals by direct binding of Chordin to BMP-4.
Cell
86: 589–98

Pinto-Correa, C. 1997.
The ovary of Eve: egg and sperm and preformationism.
Chicago University Press, Chicago

Pletcher, S.D. et al. 2002. Genome-wide transcript profiles in aging and calorically restricted Drosophila melanogaster.
Current Biology
30: 712–23

Posel, D. 2001. Race as common sense: racial classification in twentieth century South Africa.
African Studies Review
44: 87–113

Posner, G. L. and J. Ware. 1986.
Mengele: the complete story.
Futura, London

Power, C. and S. Matthews. 1997. Origins of health inequalities in a national population sample.
Lancet
350: 1584–9

Qu, S. et al. 1998. Mutations in mouse Aristaless-like4 cause Strong’s luxoid Polydactyly.
Development.
125: 2711–21

Quance, E. 1977.
Alexander Graham Bell, human inheritance, and the eugenics movement.
Research Bulletin of the National Historic Parks and Sites Branch, Parks Canada. No. 62

Quigley, C.A. et al. 1992. Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status.
Journal of Clinical Endocrinology and Metabolism
74: 932–3

Ramesar, R.S. et al. 1996. Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity.
Journal of Medical Genetics
33: 511–14

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