PROC ELISA Kit for Human(Homo sapiens) | EIAab.comPROC ELISA Kit for Human(Homo sapiens)

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PROC (Gene name),

Vitamin K-dependent protein C (Protein name ), PROC_HUMAN from NCBI database.

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General Annotation

Antigen Annotation

Predicted Eptitope

Vaild Sequence

Related Databases

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Gene name:

PROC;

Protein name:

Vitamin K-dependent protein C;

Alternative:

Autoprothrombin IIA;Anticoagulant protein C;Blood coagulation factor XIV;

Organism:

Human (Homo sapiens).

General Annotation

Sub Unit:

Synthesized as a single chain precursor, which is cleaved into a light chain and a heavy chain held together by a disulfide bond. The enzyme is then activated by thrombin, which cleaves a tetradecapeptide from the amino end of the heavy chain; this reaction, which occurs at the surface of endothelial cells, is strongly promoted by thrombomodulin.

Function:

Protein C is a vitamin K-dependent serine protease that regulates blood coagulation by inactivating factors Va and VIIIa in the presence of calcium ions and phospholipids.

Subcellular Location:

N/A

Protein Attributes:

Sequence length:

461

Sequence:

50:

100:

150:

200:

250:

300:

350:

400:

450:

461:

DKEAPQKSWA | P

3D Structure:

N/A

Predicted Eptitope:

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Vaild Sequence:

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Related Databases

MIM:

176860

String:

P04070

SMR:

P04070

UniGene:

Hs.224698

Pfam:

PF00594

STRING:

9606.ENSP00000234071

KEGG:

hsa:5624

Uniprot:

P04070

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ELISA Kit for Human Vitamin K-dependent protein C

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E0734h

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ELISA Kit for Human Vitamin K-dependent protein C

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ELISA Kit for Human Vitamin K-dependent protein C

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E0734r

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ELISA Kit for Human Vitamin K-dependent protein C

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E0734p

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ELISA Kit for Human Vitamin K-dependent protein C

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E0734d

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96T

ELISA Kit for Human Vitamin K-dependent protein C

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E0734m

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ELISA Kit for Human Vitamin K-dependent protein C

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E0734b

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96T

CLIA Kit for Human Vitamin K-dependent protein C

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U0734m

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96T

CLIA Kit for Human Vitamin K-dependent protein C

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U0734p

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96T

CLIA Kit for Human Vitamin K-dependent protein C

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U0734r

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96T

CLIA Kit for Human Vitamin K-dependent protein C

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U0734h

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96T

CLIA Kit for Human Vitamin K-dependent protein C

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U0734d

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CLIA Kit for Human Vitamin K-dependent protein C

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CLIA Kit for Human Vitamin K-dependent protein C

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U0734b

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Polyclonal Antibody for Human Vitamin K-dependent protein C

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P0734Rb-r

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40ug/0.2ml

Polyclonal Antibody for Human Vitamin K-dependent protein C

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P0734Rb-h

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Polyclonal Antibody for Human Vitamin K-dependent protein C

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P0734Rb-m

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Polyclonal Antibody for Human Vitamin K-dependent protein C

Monoclonal Antibody for Human Vitamin K-dependent protein C

Protein for Human Vitamin K-dependent protein C

R&D Technical Data

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Precision

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Recovery

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Linearity

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References

1.

"The structure and evolution of a 461 amino acid human protein C precursor and its messenger RNA, based upon the DNA sequence of cloned human liver cDNAs."
Beckmann R.J. , Schmidt R.J. , Santerre R.F. , Plutzky J. , Crabtree G.R. , Long G.L.
Nucleic Acids Res.13:5233-5247(1985) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)
2.

"The nucleotide sequence of the gene for human protein C."
Foster D.C. , Yoshitake S. , Davie E.W.
Proc. Natl. Acad. Sci. U.S.A.82:4673-4677(1985) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA];HYDROXYLATION AT ASP-113;GLYCOSYLATION AT ASN-290; ASN-355 AND ASN-371;GAMMA-CARBOXYGLUTAMATION AT GLU-48; GLU-49; GLU-56; GLU-58; GLU-61; GLU-62; GLU-67; GLU-68 AND GLU-71
3.

"Evolution and organization of the human protein C gene."
Plutzky J. , Hoskins J.A. , Long G.L. , Crabtree G.R.
Proc. Natl. Acad. Sci. U.S.A.83:546-550(1986) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]
4.

SeattleSNPs variation discovery resource
Submitted (2001-06) to the EMBL/GenBank/DDBJ databases

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]
5.

"Complete sequencing and characterization of 21,243 full-length human cDNAs."
Ota T. , Suzuki Y. , Nishikawa T. , Otsuki T. , Sugiyama T. , Irie R. , Wakamatsu A. , Hayashi K. , Sato H. , Nagai K. , Kimura K. , Makita H. , Sekine M. , Obayashi M. , Nishi T. , Shibahara T. , Tanaka T. , Ishii S. , more...
Nat. Genet.36:40-45(2004) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2)
tissue: Liver.
6.

"Generation and annotation of the DNA sequences of human chromosomes 2 and 4."
Hillier L.W. , Graves T.A. , Fulton R.S. , Fulton L.A. , Pepin K.H. , Minx P. , Wagner-McPherson C. , Layman D. , Wylie K. , Sekhon M. , Becker M.C. , Fewell G.A. , Delehaunty K.D. , Miner T.L. , Nash W.E. , Kremitzki C. , Oddy L. , Du H. , more...
Nature434:724-731(2005) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]
7.

Mural R.J. , Istrail S. , Sutton G.G. , Florea L. , Halpern A.L. , Mobarry C.M. , Lippert R. , Walenz B. , Shatkay H. , Dew I. , Miller J.R. , Flanigan M.J. , Edwards N.J. , Bolanos R. , Fasulo D. , Halldorsson B.V. , Hannenhalli S. , Turner R. , more...
Submitted (2005-07) to the EMBL/GenBank/DDBJ databases

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]
8.

"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res.14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1)
tissue: Colon.
9.

"Protein C Osaka 10 with aberrant propeptide processing: loss of anticoagulant activity due to an amino acid substitution in the protein C precursor."
Miyata T. , Zheng Y.-Z. , Sakata T. , Kato H.
Thromb. Haemost.74:1003-1008(1995) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: PROTEIN SEQUENCE OF 42-57;VARIANT THPH3 SER-42
tissue: Blood.
10.

"An abnormal protein C (protein C Yonago) with an amino acid substitution of Gly for Arg-15 caused by a single base mutation of C to G in codon 57 (CGG-->GGG). Deteriorated calcium-dependent conformation of the gamma-carboxyglutamic acid domain relevant to a thrombotic tendency."
Mimuro J. , Muramatsu S. , Kaneko M. , Yoshitake S. , Iijima K. , Nakamura K. , Sakata Y. , Matsuda M.
Int. J. Hematol.57:9-14(1993) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 43-64;VARIANT PROC DEFICIENCY GLY-57
11.

"Characterization of a cDNA coding for human protein C."
Foster D.C. , Davie E.W.
Proc. Natl. Acad. Sci. U.S.A.81:4766-4770(1984) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 106-461 (ISOFORM 1)
12.

"Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutations."
Long G.L. , Tomczak J.A. , Rainville I.R. , Dreyfus M. , Schramm W. , Schwarz H.P.
Thromb. Haemost.72:526-533(1994) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 134-178 AND 267-332;VARIANTS THPH4 PRO-178 AND HIS-328
13.

"Beta protein C is not glycosylated at asparagine 329. The rate of translation may influence the frequency of usage at asparagine-X-cysteine sites."
Miletich J.P. , Broze G.J. Jr.
J. Biol. Chem.265:11397-11404(1990) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: GLYCOSYLATION AT ASN-371
14.

"O-linked fucose is present in the first epidermal growth factor domain of factor XII but not protein C."
Harris R.J. , Ling V.T. , Spellman M.W.
J. Biol. Chem.267:5102-5107(1992) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: HYDROXYLATION
15.

"Human plasma N-glycoproteome analysis by immunoaffinity subtraction, hydrazide chemistry, and mass spectrometry."
Liu T. , Qian W.-J. , Gritsenko M.A. , Camp D.G. II , Monroe M.E. , Moore R.J. , Smith R.D.
J. Proteome Res.4:2070-2080(2005) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: GLYCOSYLATION [LARGE SCALE ANALYSIS] AT ASN-290
tissue: Plasma.
16.

"Human urinary glycoproteomics; attachment site specific analysis of N-and O-linked glycosylations by CID and ECD."
Halim A. , Nilsson J. , Ruetschi U. , Hesse C. , Larson G.
Mol. Cell. Proteomics0:0-0(2011) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: GLYCOSYLATION AT THR-19;STRUCTURE OF CARBOHYDRATES;IDENTIFICATION BY MASS SPECTROMETRY
17.

"Models of the serine protease domain of the human antithrombotic plasma factor activated protein C and its zymogen."
Fisher C.L. , Greengard J.S. , Griffin J.H.
Protein Sci.3:588-599(1994) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: 3D-STRUCTURE MODELING OF 175-450
18.

"The 2.8 A crystal structure of Gla-domainless activated protein C."
Mather T. , Oganessyan V. , Hof P. , Huber R. , Foundling S. , Esmon C. , Bode W.
EMBO J.15:6822-6831(1996) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: X-RAY CRYSTALLOGRAPHY (2.8 ANGSTROMS) OF 84-461
19.

"Protein C deficiency: a database of mutations."
Reitsma P.H. , Poort S.R. , Bernardi F. , Gandrille S. , Long G.L. , Sala N. , Cooper D.N.
Thromb. Haemost.69:77-84(1993) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: REVIEW ON PROC VARIANTS
20.

"Hereditary thrombophilia: identification of nonsense and missense mutations in the protein C gene."
Romeo G. , Hassan H.J. , Staempfli S. , Roncuzzi L. , Cianetti L. , Leonardi A. , Vicente V. , Mannucci P.M. , Bertina R.M. , Peschle C. , Cortese R.
Proc. Natl. Acad. Sci. U.S.A.84:2829-2832(1987) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH3 CYS-444
21.

"Protein C London 1: recurrent mutation at Arg-169 (CGG-->TGG) in the protein C gene causing thrombosis."
Grundy C.B. , Chitolie A. , Talbot S. , Bevan D. , Kakkar V.V. , Cooper D.N.
Nucleic Acids Res.17:10513-10513(1989) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH3 TRP-211
22.

"The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects."
Reitsma P.H. , Poort S.R. , Allaart C.F. , Briet E. , Bertina R.M.
Blood78:890-894(1991) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH3 CYS-272
23.

"Protein CVermont: symptomatic type II protein C deficiency associated with two GLA domain mutations."
Bovill E.G. , Tomczak J.A. , Grant B. , Bhushan F. , Pillemer E. , Rainville I.R. , Long G.L.
Blood79:1456-1465(1992) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS THPH3 ALA-62 AND MET-76
24.

"Protein C deficiency Hong Kong 1 and 2: hereditary protein C deficiency caused by two mutant alleles, a 5-nucleotide deletion and a missense mutation."
Sugahara Y. , Miura O. , Yuen P. , Aoki N.
Blood80:126-133(1992) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH4 ASP-418
25.

"A novel homozygous missense mutation in the protein C (PROC) gene causing recurrent venous thrombosis."
Grundy C.B. , Chisholm M. , Kakkar V.V. , Cooper D.N.
Hum. Genet.89:683-684(1992) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH4 LEU-289
26.

"Two different missense mutations at Arg 178 of the protein C (PROC) gene causing recurrent venous thrombosis."
Grundy C.B. , Schulman S. , Tengborn L. , Kakkar V.V. , Cooper D.N.
Hum. Genet.89:685-686(1992) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS THPH3 GLN-220 AND TRP-220
27.

"Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis."
Gandrille S. , Vidaud M. , Aiach M. , Alhenc-Gelas M. , Fischer A.M. , Gouault-Heilman M. , Toulon P. , Fiessinger J.-N. , Goossens M.
Hum. Mutat.1:491-500(1992) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH3 GLN-220
28.

"Homozygous protein C deficiency: identification of a novel missense mutation that causes impaired secretion of the mutant protein C."
Yamamoto K. , Matsushita T. , Sugiura I. , Takamatsu J. , Iwasaki E. , Wada H. , Deguchi K. , Shirakawa S. , Saito H.
J. Lab. Clin. Med.119:682-689(1992) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH4 SER-334
29.

"Five novel mutations located in exons III and IX of the protein C gene in patients presenting with defective protein C anticoagulant activity."
Gandrille S. , Alhenc-Gelas M. , Gaussem P. , Aillaud M.-F. , Dupuy E. , Juhan-Vague I. , Aiach M.
Blood82:159-168(1993) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS TRP-38; CYS-42; HIS-42; GLN-271 AND ASN-294
30.

"Twelve novel and two recurrent mutations in 14 Austrian families with hereditary protein C deficiency."
Poort S.R. , Pabinger-Fasching I. , Mannhalter C. , Reitsma P.H. , Bertina R.M.
Blood Coagul. Fibrinolysis4:273-280(1993) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GLY-14; GLN-211; TYR-244; GLN-253; LEU-321; CYS-328; ILE-385; THR-388 AND VAL-388
31.

"A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis."
Millar D.S. , Grundy C.B. , Bignell P. , Moffat E.H. , Martin R. , Kakkar V.V. , Cooper D.N.
Blood Coagul. Fibrinolysis4:345-347(1993) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH3 TRP-57
32.

"Genetic mutations in ten unrelated American patients with symptomatic type 1 protein C deficiency."
Tsay W. , Greengard J.S. , Montgomery R.R. , McPherson R.A. , Fucci J.C. , Koerper M.A. , Coughlin J. , Griffin J.H.
Blood Coagul. Fibrinolysis4:791-796(1993) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS THPH3 ARG-145; LEU-210; TRP-211; THR-243; LEU-321; MET-340 AND TYR-426
33.

"Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocket."
Marchetti G. , Patracchini P. , Gemmati D. , Castaman G. , Rodeghiero F. , Wacey A. , Cooper D.N. , Tuddenham E.G. , Bernardi F.
Br. J. Haematol.84:285-289(1993) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH3 SER-423
34.

"First de novo mutations in the protein C gene of two patients with type I deficiency: a missense mutation and a splice site deletion."
Gandrille S. , Jude B. , Alhenc-Gelas M. , Emmerich J. , Aiach M.
Blood84:2566-2570(1994) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT PRO-312
35.

"A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancy."
Millar D.S. , Allgrove J. , Rodeck C. , Kakkar V.V. , Cooper D.N.
Blood Coagul. Fibrinolysis5:647-649(1994) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH4 144-ASN-GLY-145 DELINS LYS
36.

"A novel homozygous missense mutation (Val 325-->Ala) in the protein C gene causing neonatal purpura fulminans."
Witt I. , Beck S. , Seydewitz H.H. , Tasangil C. , Schenck W.
Blood Coagul. Fibrinolysis5:651-653(1994) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT THPH4 ALA-367
37.

"Six missense mutations associated with type I and type II protein C deficiency and implications obtained from molecular modelling."
Zheng Y.-Z. , Sakata T. , Matsusue T. , Umeyama H. , Kato H. , Miyata T.
Blood Coagul. Fibrinolysis5:687-696(1994) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS THPH3 LEU-369; ARG-392; ASN-401 AND HIS-441
38.

"Influence of six mutations of the protein C gene on the Gla domain conformation and calcium affinity."
Gaussem P. , Gandrille S. , Duchemin J. , Emmerich J. , Alhenc-Gelas M. , Aillaud M.-F. , Aiach M.
Thromb. Haemost.71:748-754(1994) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT ASP-49
39.

"Three novel mutations in the protein C (PROC) gene causing venous thrombosis."
Millar D.S. , Bevan D. , Chitolie A. , Reynaud J. , Chisholm M. , Kakkar V.V. , Cooper D.N.
Blood Coagul. Fibrinolysis6:138-140(1995) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS CYS-89; PRO-220 AND THR-301
40.

"Six different point mutations in seven Danish families with symptomatic protein C deficiency."
Lind B. , Schwartz M. , Thorsen S.
Thromb. Haemost.73:186-193(1995) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS THPH3 TRP-57; ARG-114; ARG-324; CYS-328 AND LEU-369;VARIANT THR-43
41.

"Two novel (R(-11)C; T394D) and two repeat missense mutations in the protein C gene associated with venous thrombosis in six kindreds."
Ireland H.A. , Boisclair M.D. , Taylor J. , Thompson E. , Thein S.L. , Girolami A. , de Caterina M. , Scopacasa F. , de Stefano V. , Leone G. , Finazzi G. , Cohen H. , Lane D.A.
Hum. Mutat.7:176-179(1996) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS THPH3 CYS-32 AND ASN-436
42.

"Type I protein C deficiency in French Canadians: evidence of a founder effect and association of specific protein C gene mutations with plasma protein C levels."
Couture P. , Demers C. , Morissette J. , Delage R. , Jomphe M. , Couture L. , Simard J.
Thromb. Haemost.80:551-556(1998) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS THPH3 GLN-220 AND MET-340

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