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Dr. Qin's Published Works

Original research and publications in pediatric endocrinology by Dr. Kenan Qin, MD, FAAP

Original Scientific Articles
21 peer-reviewed publications
1
Naturally labeled 13C-glucose: use for carbohydrate metabolic studies in pediatric diabetes and obesity
J. Stable Isotope. 1987; 2:33-38.
Qin K, Wang D-F
2
Molecular cloning and expression of rat liver 3β-hydroxysteroid dehydrogenase
Mol. Endo. 5:823-828, 1991.
Cheng K-C, White P.C, Qin K
3
Molecular cloning of multiple cDNAs encoding human enzymes structurally related to 3β-hydroxysteroid dehydrogenase
J. Steroid Biochem. Mol. Biol. 1993; 46:673-679.
Qin K, New MI, Cheng K-C
4
Distribution and ontogeny of 3β-hydroxysteroid dehydrogenase in the brain
J. Steroid Biochem. Mol. Biol. 1994; 50:85-89.
Cheng K-C, White PC, Qin K
5
Structure of a gene coding for human dihydrodiol dehydrogenase/bile acid-binding protein
Gene. 1994; 149:357-361.
Qin K, Khanna M, Cheng K-C
6
Structure and tissue-specific expression of the aldo/keto reductase superfamily
Biochemistry. 1994; 33:3223-3228.
Qin K, Cheng K-C
7
Localization of multiple human dihydrodiol dehydrogenase (DDH1 and DDH2) and chlordecone reductase (CHDR) genes in chromosome 10
Genomics. 1995; 25:588-590.
Khanna M, Qin K, Klisak I, et al.
8
Distribution of 3β-hydroxysteroid dehydrogenase in rat brain and molecular cloning
J. Steroid Biochem. Mol. Biol. 1995; 53:41-46.
Khanna M, Qin K, Cheng K-C
9
Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens
J. Clin. Endocrinol. Metab. 1995; 80:3689-3698.
Morishima A, Grumbach MM, Simpson ER, Fisher C, Qin K
10
Substrate specificity, gene structure, and tissue-specific distribution of multiple human of 3β-hydroxysteroid dehydrogenase
J. Biol. Chem. 1995; 270:20162-20168.
Khanna M, Qin K, Wang RW, Cheng K-C
11
Aromatase deficiency in the male. Effect of testosterone and estradiol treatment
N Engl J Med. 1997; 337:91-95.
Carani C, Qin K, Simoni M, et al.
12
Expression of 17β-hydroxysteroid dehydrogenase type 5 in human ovary. A pilot study
J Soc Gynecol Investig 2000; 7:61-64.
Qin K, Rosenfield RL
13
The biochemical basis for increased testosterone production in theca cells propagated from patients with polycystic ovary syndrome
J Clin Endocrinol Metab 2001 Dec;86(12):5925-33.
Nelson VL, Qin K, Rosenfield RL, et al.
14
Bartter syndrome complicated by immune complex nephropathy. Case report and literature review
Pediatr Nephrol. 2003 Sep;18(9):913-8.
Sardani Y, Qin K, Haas M, et al.
15
Characterization of the basal promoter element of the human type 5 17beta-hydroxysteroid dehydrogenase gene
Biochim Biophys Acta 2005; 1728:115-25.
Qin K, Rosenfield RL
16
Identification of a functional polymorphism of the human type 5 17β-hydroxysteroid dehydrogenase gene associated with polycystic ovary syndrome
J Clin Endocrinol Metab. 2006 Jan;91(1):270-6.
Qin K, Ehrmann DA, Cox N, et al.
17
An Alu-mediated rearrangement causing a 3.2 kb deletion and a novel two base pair deletion in AAAS gene as the cause of Triple A syndrome
Mol Genet Metab. 2007 Dec;92(4):359-63.
Qin K, Du X, Rich B
18
KLF15 is a Transcriptional Regulator of The Human 17β-Hydroxysteroid Dehydrogenase Type 5 Gene
J Clin Endocrinol Metab. 2009 Jul;94(7):2594-601.
Du X, Rosenfield RL, Qin K
19
Unique mode of lipogenic activation in rat preputial sebocytes
J Nutr Metab. 2011;2011:163631.
Deplewski D, Qin K, Ciletti N, Rosenfield RL
20
P450c17 Deficiency Caused by Compound Heterozygosity for Two Novel Mutations Presenting as Hypotension in Early Infancy
Horm Res Paediatr. 2011 Aug 4.
Gregg B, Kociolek LK, Qin K, et al.
21
Identification of two novel CYP17A1 mutations as the cause of 46, XY disorders of sex development in Chinese children
JPEM. 2011 (accepted).
Chen Y, Wang W, Qin K, et al.
Chapters & Reviews
7 book chapters and review articles
1
Radioimmunoassay of salivary progesterone and its application
Reproduction & Contraception. 1988; 8:3-9.
Qin K, Wang D-F, Zeng J-S
2
Aromatase expression in health and disease
Recent Progress in Hormone Research. 1997; 52:185-214.
Simpson ER, Zhano Y, Agarwal VR, et al.
3
Role of cytochrome P450c17 in polycystic ovary syndrome
Mol Cell Endocrinol. 1998; 145:111-121.
Qin K, Rosenfield RL
4
Adrenocortical disorders in infancy and childhood
In: Becker K, Bilezikian J, Bremner W, eds. Principle and Practice of Endocrinology and Metabolism. 3rd. Philadelphia: Lippincott, JB, Ch 83; 2001.
Rosenfield RL, Qin K
5
Sexual hormones in human skin
Horm Metab Res. 2007 Feb;39(2):85-95.
Zouboulis CC, Chen WC, Thornton MJ, Qin K, Rosenfield R
6
Book Review for “Adrenal Disease in Childhood” (C.E. Fluck and W.L. Miller, editors)
7
Genetic Defects of Androgen Resistance
In: Roy E. Weiss and Samuel Refetoff, eds. Genetic Diagnosis of Endocrine Disorders. 1st. Elsevier. Ch 22; 2010.
Qin K
Compact Discs
2 UpToDate contributions
1
Normal adrenarche
In: Rose B (ed). UpToDate (CD). Wellesley MA: UpToDate, 1998-.
Rosenfield RL, Qin K
2
Premature adrenarche
In: Rose B (ed). UpToDate (CD). Wellesley MA: UpToDate, 1998-.
Rosenfield RL, Qin K

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