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22篇 您的检索式：作者名="Lemmink HH"

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	题名	作者	年代	出处	被引量
1	Mutations in the type Ⅳcollagen alpha-3 (COL4 A3) gene in autosomal recessive Alport syndrome显示文摘	Lemmink HH Mochizuki T van den Heuvel LP	1994	Hum Molec Genet1994，3，：	1
2	Identification ofmutations in the alpha 3 ( IV ) and alpha 4 ( IV ) collagen genes in autosomal recessive Alport syndrome 显示文摘	Mochizuki T Lemmink HH Mariyama M	1994	Nat Genet1994，8，1：	1
3	Benign familial hematuria due to mutation of the type Ⅳ collagen α4 gene显示文摘	Lemmink HH Nillesen WN Mochizuki T	1996	J Clin Invest1996，98，5：	1
4	Benign familial hematuria due to mutation of the type IV collagen alpha 4 gene 显示文摘	Lemmink HH Nillesen WN Mochizuki T	1996	J Clin Invest1996，98，5：	1
5	A missense mutation in KRTI4 causing a derma- topathia pigmentosa retieulafis/Naegeli-Francesehetti-Jadassohn phenotype 显示文摘	Van Steensel MA Lemmink HH	2010	J Eur Acad Dermatol Venereo12010，24，9：	1
6	Identification of LIL - STAT in mono - cytic leukemia cells and monocytes after stimulation with interleukin - 6orinterferon gamma显示文摘	Lemmink HH Tuye L Knd Q	2003	Blood2003，161，13：	1
7	Identification of LIL-STAT in monocytic leukemia cells and monocytes after stimulation with interleukin-6or interferon gamma显示文摘	Lemmink HH Tuye L Knd Q	2001	Blood2001，98，13：	1
8	Benign familial hematufia due to mutation of the type IV collagen alpha4 gene显示文摘	Lemmink HH Nillesen WN Moehizuki T	1996	J Clin Invest1996，98，5：	1
9	Benign familial hematuria due to mutation of the type Ⅳ collagen α4 gene显示文摘	LEMMINK HH NILLESEN WN MOCHIZUKI T	1996	J Clin Invest1996，98，5：	1
10	Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndrome显示文摘	Lemmink HH Mochizuki T van den Heuvel LP	1994	Hum Mol Genet1994，3，8：	1
11	Autosomal dominant Alport syndrome linked to the type 1V collage alpha 3 and alpha 4 genes (COL4A3 and COL4A4)显示文摘	Jefferson JA Lemmink HH Hughes AE	1997	Nephrol Dial Transplant1997，12，8：	1
12	Novel mu- tations in the thiazide-sensitive NaC1 co-transporter gene in patients with Gitelman syndrome with predominant loca- lization to the C-terminal domain 显示文摘	Lemmink HH Knoers NV Karolyi L	1988	Kidney Int1988，54，3：	1
13	Autosomaldominant Alport syndrome linked to the type IV collage alpha3 and alpha 4 genes (COL4A3 and COL4A4) 显示文摘	Jefferson JA Lemmink HH Hughes AE	1997	Nephrol DialTransplant1997，12，8：	1
14	Identification of mutations in thec-3 ( IV ) and ct4 ( IV ) collagen genes in autoso- mal recessive Alport syndrome显示文摘	Mochizuki T Lemmink HH Mariyama M	1994	Nat Genet1994，8，1：	1
15	Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome显示文摘	Konrad M Vollmer M Lemmink HH	2000	J Am Soc Nephrol2000，11，8：	1
16	Novel mutations in the thiazide-sensitive NaC1 cotransporter gene in patients with Gitelman syndrome with predominant localization to the C- terminal domain 显示文摘	LEMMINK HH KNOERS NV K~ROLYI L	1998	Kidney Int1998，54，3：	1
17	Autosomal dominant Alport syndrome linked to the type IV collage alpha 3 and alpha 4 genes ( COIAA3 and COIAA4) 显示文摘	Jefferson JA Lemmink HH Hughes AE Hill CM Smeets HJ Doherty CC	1997	Nephrol Dial Transplant1997，12，8：	1
18	ldentification of LIL2STAT in mono2 cytic leukemia cells and monocytes after stimulation with interleukin26 or interferon gamma显示文摘	Lemmink HH Tuye L Knd Q	2003	Blood2003，161，13：	1
19	Identification of LIL-STAT in monocytic leukemia cells and monocytes after stimulation with interleukin-6or interferon gamma显示文摘	Lemmink HH Tuye L Knd Q	2003	Blood2003，161，13：	1
20	Identification of four novel mutations in the COL4A5 gene of patients with Alport syndrome显示文摘	Lemmink HH Schroder CH Brunner HG	1993	Genomics1993，17，2：	1

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