Publications: Prof Carol Shoulders
Ruiz-Cantos M, Hutchison CE, Shoulders CC
(
2021
)
.
Musings from the Tribbles Research and Innovation Network
.
Cancers
vol.
13
,
(
18
)
4517
-
4517
.
Andreotti F, Crea F, Patti G, Shoulders CC, Navarese EP, Robishaw J, Maseri A, Hennekens CH
(
2021
)
.
Family history in first degree relatives of patients with premature cardiovascular disease
.
International Journal of Cardiology
vol.
333
,
215
-
218
.
Cegla J, Neely RDG, France M, Ferns G, Byrne CD, Halcox J, Datta D, Capps N et al.
(
2020
)
.
Corrigendum to “HEART UK consensus statement on Lipoprotein(a): A call to action” [Atherosclerosis 291 (2019) 62–70](S002191501931528X)(10.1016/j.atherosclerosis.2019.10.011)
.
Atherosclerosis
vol.
296
,
Johnston JM, Angyal A, Bauer RC, Hamby S, Suvarna SK, Baidžajevas K, Hegedus Z, Dear TN et al.
(
2019
)
.
Myeloid Tribbles 1 induces early atherosclerosis via enhanced foam cell expansion
.
Science Advances
Cegla J, Neely RDG, France M, Ferns G, Byrne CD, Halcox J, Datta D, Capps N et al.
(
2019
)
.
HEART UK consensus statement on Lipoprotein(a): A call to action
.
Atherosclerosis
vol.
291
,
62
-
70
.
Johnston JM, Angyal A, Bauer R, Hamby SE, Suvarna SK, Baidžajevas K, Hegedus Z, Dear NT et al.
(
2018
)
.
P14 MYELOID TRIB1 PROMOTES EXPERIMENTAL ATHEROSCLEROSIS
.
Cardiovascular Research
.
vol.
114
,
s4
-
s4
.
Johnston J, Angyal A, Bauer R, Rader D, Shoulders C, Francis S, Kiss-Toth E
(
2018
)
.
123 Myeloid TRIB1 controls experimental atherosclerosis
.
Heart
.
Conference:
Basic Science
vol.
104
,
Johnston J, Angyal A, Bauer R, Rader D, Shoulders C, Francis S, Kiss-Toth E
(
2018
)
.
Myeloid Tribbles 1 Regulates Experimental Atherosclerosis
.
Atherosclerosis Plus
.
vol.
32
,
France M, Rees A, Datta D, Thompson G, Capps N, Ferns G, Ramaswami U, Seed M et al.
(
2016
)
.
HEART UK statement on the management of homozygous familial hypercholesterolaemia in the United Kingdom
.
Atherosclerosis
Stiles C, Barry S, Gadaleta E, Chelala C, Shoulders CC, Korbonits M
(
2015
)
.
Investigation of the invasive phenotype of AIP-mutated pituitary adenomas
.
Endocrine Abstracts
Mothojakan NB, Stiles CE, Barry S, Shoulders CC, Korbonits M
(
2015
)
.
Silencing of aryl hydrocarbon receptor protein (AIP) up-regulates the small Rho GTPase, CDC42
.
Endocrine Abstracts
Aikio M, Elamaa H, Vicente D, Izzi V, Kaur I, Seppinen L, Speedy HE, Kaminska D et al.
(
2014
)
.
Specific collagen XVIII isoforms promote adipose tissue accrual via mechanisms determining adipocyte number and affect fat deposition
.
Proc Natl Acad Sci U S A
vol.
111
,
(
30
)
E3043
-
E3052
.
Fryer LGD, Jones B, Duncan EJ, Hutchison CE, Ozkan T, Williams PA, Alder O, Nieuwdorp M et al.
(
2014
)
.
The endoplasmic reticulum coat protein II transport machinery coordinates cellular lipid secretion and cholesterol biosynthesis
.
J Biol Chem
vol.
289
,
(
7
)
4244
-
4261
.
Horswell SD, Fryer LGD, Hutchison CE, Zindrou D, Speedy HE, Town M-M, Duncan EJ, Sivapackianathan R et al.
(
2013
)
.
CDKN2B expression in adipose tissue of familial combined hyperlipidemia patients
.
J Lipid Res
vol.
54
,
(
12
)
3491
-
3505
.
Motazacker MM, Peter J, Treskes M, Shoulders CC, Kuivenhoven JA, Hovingh GK
(
2013
)
.
Evidence of a polygenic origin of extreme high-density lipoprotein cholesterol levels
.
Arterioscler Thromb Vasc Biol
vol.
33
,
(
7
)
1521
-
1528
.
Salm MPA, Horswell SD, Hutchison CE, Speedy HE, Yang X, Liang L, Schadt EE, Cookson WO et al.
(
2012
)
.
The origin, global distribution, and functional impact of the human 8p23 inversion polymorphism
.
Genome Res
vol.
22
,
(
6
)
1144
-
1153
.
Calandra S, Tarugi P, Speedy HE, Dean AF, Bertolini S, Shoulders CC
(
2011
)
.
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk
.
J LIPID RES
vol.
52
,
(
11
)
1885
-
1926
.
Shoulders CC
(
2010
)
.
A new Thematic Series: Genetics of human lipid diseases
.
J LIPID RES
vol.
51
,
(
7
)
1621
-
1623
.
Ringham HE, Town MM, Horswell SD, Shoulders CC
(
2009
)
.
GPIHBP1 VARIANTS CONTRIBUTE TO LIPID LEVELS IN FAMILIAL COMBINED HYPERLIPIDEMIA
.
ATHEROSCLEROSIS
.
vol.
207
,
E3
-
E3
.
Horswell SD, Ringham HE, Shoulders CC
(
2009
)
.
New technologies for delineating and characterizing the lipid exome: prospects for understanding familial combined hyperlipidemia
.
J Lipid Res
vol.
50 Suppl
,
(
Suppl
)
S370
-
S375
.
Shoulders CC
(
2008
)
.
The FTO (fat mass and obesity-associated) gene: big in adipocyte lipolysis?
.
J Lipid Res
vol.
49
,
(
3
)
495
-
496
.
Lelliott CJ, Ljungberg A, Ahnmark A, William-Olsson L, Ekroos K, Elmgren A, Arnerup G, Shoulders CC et al.
(
2007
)
.
Hepatic PGC-1beta overexpression induces combined hyperlipidemia and modulates the response to PPARalpha activation
.
Arterioscler Thromb Vasc Biol
vol.
27
,
(
12
)
2707
-
2713
.
Plaisier CL, Lusis AJ, Naoumova RP, Shoulders CC, Taskinen M-R, De Bruin TW, Pajukanta P
(
2006
)
.
Fine mapping a region on chromosome 11P for familial combined hyperlipidemia
.
ATHEROSCLEROSIS SUPPLEMENTS
.
vol.
7
,
130
-
130
.
Shoulders CC, Jones B, Jones EL, Bonney SA, Williams PA, Mensenkamp AR, Towney AK, Horswell SD et al.
(
2006
)
.
Genetics of intracellular lipid transport and familial combined hyperlipidemia
.
ATHEROSCLEROSIS SUPPLEMENTS
.
vol.
7
,
21
-
21
.
Shoulders CC
(
2005
)
.
Cardiovascular implications of partial, tissue-specific silencing of MTP
.
Lipids and Atherosclerosis
,
Shoulders CC, Shelness GS
(
2005
)
.
Current biology of MTP: implications for selective inhibition
.
Curr Top Med Chem
vol.
5
,
(
3
)
283
-
300
.
Rigby RJ, Horswell S, Haywood M, Shoulders C, Morley BJ, Vyse TJ
(
2005
)
.
Differential transcript profiling identifies candidate genes in the New Zealand model of systemic lupus erythematosus, including the B-cell transcription factor, Bach2
.
CLINICAL IMMUNOLOGY
.
vol.
115
,
S18
-
S19
.
Shoulders CC, Naoumova RP
(
2004
)
.
USF1 implicated in the aetiology of familial combined hyperlipidaemia and the metabolic syndrome
.
Trends Mol Med
vol.
10
,
(
8
)
362
-
365
.
Griffin JL, Bonney SA, Mann C, Hebbachi AM, Gibbons GF, Nicholson JK, Shoulders CC, Scott J
(
2004
)
.
An integrated reverse functional genomic and metabolic approach to understanding orotic acid-induced fatty liver
.
Physiol Genomics
vol.
17
,
(
2
)
140
-
149
.
Shoulders CC, Jones EL, Naoumova RP
(
2004
)
.
Genetics of familial combined hyperlipidemia and risk of coronary heart disease
.
Hum Mol Genet
vol.
13 Spec No 1
,
R149
-
R160
.
Shoulders CC, Stephens DJ, Jones B
(
2004
)
.
The intracellular transport of chylomicrons requires the small GTPase, Sar1b
.
Curr Opin Lipidol
vol.
15
,
(
2
)
191
-
197
.
Mensenkamp AR, Van Luyn MJA, Havinga R, Teusink B, Waterman IJ, Mann CJ, Elzinga BM, Verkade HJ et al.
(
2004
)
.
The transport of triglycerides through the secretory pathway of hepatocytes is impaired in apolipoprotein E deficient mice
.
Journal of Hepatology
vol.
40
,
(
4
)
599
-
606
.
Shoulders CC
(
2004
)
.
USF1 on trial
.
Nature Genetics
vol.
36
,
(
4
)
322
-
323
.
Shoulders CC, Naoumova RP
(
2004
)
.
The genes and proteins of atherogenic lipoprotein production
.
Biochemical Society Transactions
vol.
32
,
(
1
)
70
-
74
.
Shoulders CC, Naoumova RP
(
2004
)
.
The genes and proteins of atherogenic lipoprotein production
.
Biochem Soc Trans
vol.
32
,
(
Pt 1
)
70
-
74
.
Eichenbaum-Voline S, Olivier M, Jones EL, Naoumova RP, Jones B, Gau B, Patel HN, Seed M et al.
(
2004
)
.
Linkage and association between distinct variants of the APOA1/C3/A4/A5 gene cluster and familial combined hyperlipidemia
.
ARTERIOSCL THROM VAS
vol.
24
,
(
1
)
167
-
174
.
Naoumova RP, Bonney SA, Eichenbaum-Voline S, Patel HN, Jones B, Jones EL, Amey J, Colilla S et al.
(
2003
)
.
Confirmed locus on chromosome 11p and candidate loci on 6q and 8p for the triglyceride and cholesterol traits of combined hyperlipidemia
.
ARTERIOSCL THROM VAS
vol.
23
,
(
11
)
2070
-
2077
.
Jones B, Jones EL, Bonney SA, Patel HN, Mensenkamp AR, Eichenbaum-Voline S, Rudling M, Myrdal U et al.
(
2003
)
.
Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders
.
Nat Genet
vol.
34
,
(
1
)
29
-
31
.
Levy E, Stan S, Delvin E, Ménard D, Shoulders C, Garofalo C, Slight I, Seidman E et al.
(
2002
)
.
Localization of microsomal triglyceride transfer protein in the Golgi. Possible role in the assembly of chylomicrons
.
Journal of Biological Chemistry
vol.
277
,
(
19
)
16470
-
16477
.
Griffin JL, Mann CJ, Scott J, Shoulders CC, Nicholson JK
(
2001
)
.
Choline containing metabolites during cell transfection: an insight into magnetic resonance spectroscopy detectable changes
.
FEBS Lett
vol.
509
,
(
2
)
263
-
266
.
Roosbeek S, Vanloo B, Duverger N, Caster H, Breyne J, De Beun I, Patel H, Vandekerckhove J et al.
(
2001
)
.
Three arginine residues in apolipoprotein A-I are critical for activation of lecithin:cholesterol acyltransferase
.
J Lipid Res
vol.
42
,
(
1
)
31
-
40
.
Read J, Anderson TA, Ritchie PJ, Vanloo B, Amey J, Levitt D, Rosseneu M, Scott J et al.
(
2000
)
.
A mechanism of membrane neutral lipid acquisition by the microsomal triglyceride transfer protein
.
J Biol Chem
vol.
275
,
(
39
)
30372
-
30377
.
Scott J, Shoulders C, Navaratnam N, Aitman T
(
2000
)
.
The genetics of the metabolic overlap syndrome
.
Proc Nutr Soc
vol.
59
,
(
3
)
Scott J, Naoumova R, Shoulders CC, Aitman TJ
(
1999
)
.
Use of biochip microarrays to discover genes for dyslipidaemia, insulin resistance and hypertension in rats and humans
.
Nature Genetics
vol.
23
,
(
Suppl 3
)
72
-
72
.
Ritchie PJ, Decout A, Amey J, Mann CJ, Read J, Rosseneu M, Scott J, Shoulders CC
(
1999
)
.
Baculovirus expression and biochemical characterization of the human microsomal triglyceride transfer protein
.
Biochem J
vol.
338 ( Pt 2)
,
(
Pt 2
)
305
-
310
.
Bradbury P, Mann CJ, Köchl S, Anderson TA, Chester SA, Hancock JM, Ritchie PJ, Amey J et al.
(
1999
)
.
A common binding site on the microsomal triglyceride transfer protein for apolipoprotein B and protein disulfide isomerase
.
J Biol Chem
vol.
274
,
(
5
)
3159
-
3164
.
Nicodeme E, Benoist F, McLeod R, Yao Z, Scott J, Shoulders CC, Grand-Perret T
(
1999
)
.
Identification of domains in apolipoprotein B100 that confer a high requirement for the microsomal triglyceride transfer protein
.
Journal of Biological Chemistry
vol.
274
,
(
4
)
1986
-
1993
.
Mann CJ, Anderson TA, Read J, Chester SA, Harrison GB, Köchl S, Ritchie PJ, Bradbury P et al.
(
1999
)
.
The structure of vitellogenin provides a molecular model for the assembly and secretion of atherogenic lipoproteins
.
J Mol Biol
vol.
285
,
(
1
)
391
-
408
.
Aitman TJ, Glazier AM, Wallace CA, Cooper LD, Norsworthy PJ, Wahid FN, Al-Majali KM, Trembling PM et al.
(
1999
)
.
Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats
.
Nat Genet
vol.
21
,
(
1
)
76
-
83
.
Heath KE, Luong LEA, Leonard JV, Chester A, Shoulders CC, Scott J, Middleton-Price HR, Humphries SE et al.
(
1997
)
.
The use of a highly informative CA repeat polymorphism within the abetalipoproteinaemia locus (4q22-24)
.
Prenatal Diagnosis
vol.
17
,
(
12
)
1181
-
1186
.
Shoulders CC, Grantham TT, North JD, Gaspardone A, Tomai F, de Fazio A, Versaci F, Gioffre PA et al.
(
1996
)
.
Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school children
.
Hum Genet
vol.
98
,
(
5
)
557
-
566
.
Webb JC, Patel DD, Shoulders CC, Knight BL, Soutar AK
(
1996
)
.
Genetic variation at a splicing branch point in intron 9 of the low density lipoprotein (LDL)-receptor gene: a rare mutation that disrupts mRNA splicing in a patient with familial hypercholesterolaemia and a common polymorphism
.
Hum Mol Genet
vol.
5
,
(
9
)
1325
-
1331
.
Lamberg A, Jauhiainen M, Metso J, Ehnholm C, Shoulders C, Scott J, Pihlajaniemi T, Kivirikko KI
(
1996
)
.
The role of protein disulphide isomerase in the microsomal triacylglycerol transfer protein does not reside in its isomerase activity
.
Biochemical Journal
vol.
315
,
(
2
)
533
-
536
.
Narcisi TM, Shoulders CC, Chester SA, Read J, Brett DJ, Harrison GB, Grantham TT, Fox MF et al.
(
1995
)
.
Mutations of the microsomal triglyceride-transfer-protein gene in abetalipoproteinemia
.
Am J Hum Genet
vol.
57
,
(
6
)
1298
-
1310
.
Leiper JM, Bayliss JD, Pease RJ, Brett DJ, Scott J, Shoulders CC
(
1994
)
.
Microsomal triglyceride transfer protein, the abetalipoproteinemia gene product, mediates the secretion of apolipoprotein B-containing lipoproteins from heterologous cells
.
J Biol Chem
vol.
269
,
(
35
)
21951
-
21954
.
Crea F, Gaspardone A, Tomai F, Shoulders C, De Fazio A, Versaci F, Iamele M, Roncaglioni C et al.
(
1994
)
.
Risk factors in schoolchildren associated with a family history of unheralded myocardial infarction or uncomplicated stable angina in male relatives
.
J Am Coll Cardiol
vol.
23
,
(
6
)
1472
-
1478
.
SHOULDERS CC, NARCISI TME, READ J, CHESTER SA, BRETT DJ, SCOTT J, ANDERSON TA, LEVITT DG et al.
(
1994
)
.
THE ABETALIPOPROTEINEMIA GENE IS A MEMBER OF THE VITELLOGENIN FAMILY AND ENCODES AN ALPHA-HELICAL DOMAIN
.
NATURE STRUCTURAL BIOLOGY
vol.
1
,
(
5
)
285
-
286
.
Shoulders CC
(
1994
)
.
Genetics and molecular biology
.
Current Opinion in Lipidology
vol.
5
,
(
1
)
Shoulders CC, Brett DJ, Bayliss JD, Narcisi TM, Jarmuz A, Grantham TT, Leoni PR, Bhattacharya S et al.
(
1993
)
.
Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein
.
Hum Mol Genet
vol.
2
,
(
12
)
2109
-
2116
.
Narcisi TM, Schotz MC, Scott J, Shoulders CC
(
1993
)
.
Dinucleotide repeat polymorphisms at the lipoprotein lipase (LPL) locus
.
Human Genetics
vol.
92
,
(
3
)
312
-
313
.
Castro Cabezas M, de Bruin TW, de Valk HW, Shoulders CC, Jansen H, Willem Erkelens D
(
1993
)
.
Impaired fatty acid metabolism in familial combined hyperlipidemia. A mechanism associating hepatic apolipoprotein B overproduction and insulin resistance
.
J Clin Invest
vol.
92
,
(
1
)
160
-
168
.
Shoulders CC, Narcisi TME, Jarmuz A, Brett DJ, Bayliss JD, Scott J
(
1993
)
.
Characterization of genetic markers in the 5′ flanking region of the apo A1 gene
.
Human Genetics
vol.
91
,
(
2
)
197
-
198
.
Shoulders CC
(
1993
)
.
Genetics and molecular biology: Editorial comment
.
Current Opinion in Lipidology
vol.
4
,
(
1
)
i
-
i
.
Shoulders CC
(
1993
)
.
Genetics and molecular biology
.
Current Opinion in Lipidology
vol.
4
,
(
1
)
Shoulders CC
(
1992
)
.
Genetics and molecular biology
.
Current Opinion in Lipidology
vol.
3
,
(
4
)
Shoulders CC
(
1991
)
.
Genetics and molecular biology
.
Current Opinion in Lipidology
vol.
2
,
(
4
)
Shoulders CC, Harry PJ, Lagrost L, White SE, Shah NF, North JD, Gilligan M, Gambert P et al.
(
1991
)
.
Variation at the apo AI/CIII/A1V gene complex is associated with elevated plasma levels of apo CIII
.
Atherosclerosis
vol.
87
,
(
2-3
)
239
-
247
.
Shoulders CC
(
1990
)
.
Genetics and molecular biology
.
Current Opinion in Lipidology
vol.
1
,
(
6
)
544
-
547
.
Shoulders CC
(
1990
)
.
Genetics and molecular biology: Editorial comment
.
Current Opinion in Lipidology
vol.
1
,
(
4
)
371
-
373
.
Shoulders CC, Ball MJ, Baralle FE
(
1989
)
.
Variation in the apo AI/CIII/AIV gene complex: its association with hyperlipidemia
.
Atherosclerosis
vol.
80
,
(
2
)
111
-
118
.
Jenner K, Sidoli A, Ball M, Rodriguez JR, Pagani F, Giudici G, Vergani C, Mann J et al.
(
1988
)
.
Characterization of genetic markers in the 3' end of the apo B gene and their use in family and population studies
.
Atherosclerosis
vol.
69
,
(
1
)
39
-
49
.
Shoulders CC, Ball MJ, Mann JI, Baralle FE, Ferns GAA, Stocks J, Galton DJ
(
1986
)
.
GENETIC MARKER IN APOLIPOPROTEIN AI/CIII GENE COMPLEX ASSOCIATED WITH HYPERCHOLESTEROLAEMIA
.
The Lancet
vol.
328
,
(
8518
)
1286
-
1287
.
SHOULDERS CC, BARALLE FE
(
1986
)
.
GENETIC-POLYMORPHISM IN THE APOA-I/C-III COMPLEX
.
METHODS IN ENZYMOLOGY
vol.
128
,
727
-
745
.
Shoulders CC, Baralle FE
(
1986
)
.
The molecular genetics of hyperlipidemia
.
Horizons in biochemistry and biophysics
vol.
8
,
299
-
340
.
BARALLE FE, SHOULDERS CC
(
1985
)
.
APOLIPOPROTEIN GENES, DNA POLYMORPHISMS AND HYPERLIPIDEMIA
.
BULLETIN OF MOLECULAR BIOLOGY AND MEDICINE
vol.
10
,
(
4
)
343
-
358
.
Shelley CS, Sharpe CR, Baralle FE, Shoulders CC
(
1985
)
.
Comparison of the human apolipoprotein genes. Apo AII presents a unique functional intron-exon junction
.
Journal of Molecular Biology
vol.
186
,
(
1
)
43
-
51
.
REES A, STOCKS J, SHARPE CR, VELLA MA, SHOULDERS CC, KATZ J, JOWETT NI, BARALLE FE et al.
(
1985
)
.
DEOXYRIBONUCLEIC-ACID POLYMORPHISM IN THE APOLIPOPROTEIN-A-1-C-III GENE-CLUSTER - ASSOCIATION WITH HYPERTRIGLYCERIDEMIA
.
J CLIN INVEST
vol.
76
,
(
3
)
1090
-
1095
.
Shoulders CC, Myant NB, Sidoli A, Rodriguez JC, Cortese C, Baralle FE, Cortese R
(
1985
)
.
Molecular cloning of human LDL apolipoprotein B cDNA. Evidence for more than one gene per haploid genome
.
Atherosclerosis
vol.
58
,
(
1-3
)
277
-
289
.
Sharpe CR, Sidoli A, Shelley CS, Lucero MA, Shoulders CC, Baralle FE
(
1984
)
.
Human apohpoprotetas AI, AII, CII and CIII. cDNA sequences and mRNA abundance
.
Nucleic Acids Research
vol.
12
,
(
9
)
3917
-
3932
.
Shoulders CC, Baralle FE
(
1984
)
.
Apolipoprotein genes, DNA polymorphisms and hyperlipidemia
.
Agents and actions. Supplements
vol.
16
,
17
-
33
.
SHARPE CR, SIDOLI A, SHELLEY CS, LUCERO MA, SHOULDERS CC, BARALLE FE
(
1984
)
.
HUMAN APOLIPOPROTEIN-A-I, APOLIPOPROTEIN-AII, APOLIPOPROTEIN-CII AND APOLIPOPROTEIN-CIII - CDNA SEQUENCES AND MESSENGER-RNA ABUNDANCE
.
NUCLEIC ACIDS RESEARCH
vol.
12
,
(
9
)
3917
-
3932
.
Baralle FE, Shoulders CC
(
1984
)
.
Lipoprotein genes and hyperlipidemia
.
Schweizerische Medizinische Wochenschrift
vol.
114
,
(
40
)
1351
-
1358
.
REES A, STOCKS J, SCHOULDERS C, CARLSON LA, BARALLE FE, GALTON DJ
(
1984
)
.
RESTRICTION ENZYME ANALYSIS OF THE APOLIPOPROTEIN A-I-GENE IN FISH EYE DISEASE AND TANGIER DISEASE
.
ACTA MEDICA SCANDINAVICA
vol.
215
,
(
3
)
235
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237
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